Related Application

This application claims the benefit of the filing date of U.S. Provisional Application No. 61/434,818, filed January 20, 2011. The entire teachings of the referenced application are expressly incorporated herein by reference.

Government Support

This work was made with Government support under Grant AI066013 awarded by the National Institutes of Health. Therefore, the U.S. Government has certain rights in this invention.

I. Background

Pneumococcal disease continues to be a leading cause of sickness and death in the United States and throughout the world. Each year, millions of cases of pneumonia, meningitis, bacteremia, and otitis media are attributed to infection with the pathogen Streptococcus pneumoniae. S. pneumoniae is a Gram-positive encapsulated coccus that colonizes the nasopharynx in about 5-10% of healthy adults and 20-40% of healthy children. Normal colonization becomes infectious when S. pneumoniae is carried into the Eustachian tubes, nasal sinuses, lungs, bloodstream, meninges, joint spaces, bones and peritoneal cavity. S. pneumoniae has several virulence factors that enable the organism to evade the immune system. Examples include a polysaccharide capsule that prevents phagocytosis by host immune cells, proteases that inhibit complement-mediated opsonization, and proteins that cause lysis of host cells. In the polysaccharide capsule, the presence of complex polysaccharides forms the basis for dividing pneumococci into different serotypes. To date, 93 serotypes of S. pneumoniae have been identified.

Various pharmaceutical compositions have been used to harness an immune response against infection by S. pneumoniae. A polyvalent pneumococcal vaccine, PPV-23, was developed for preventing pneumonia and other invasive diseases due to S. pneumoniae in the adult and aging populations. The vaccine contains capsular polysaccharides (CPs) from 23 serotypes of S. pneumoniae. As T cell-independent antigens, these CPs induce only short-lived antibody responses, necessitating repeated doses, which increases the risk of immunological tolerance. The antibodies raised against S. pneumoniae, termed anticapsular antibodies, are recognized as protective in adult and immunocompetent individuals. However, children under 2 years of age and immunocompromised individuals, including the elderly, do not respond well to T cell-independent antigens and, therefore, are not afforded optimal protection by PPV-23.

Another S. pneumoniae vaccine, Prevnar, includes bacterial polysaccharides from 7 S.

pneumoniae strains conjugated to the diphtheria toxoid protein. This vaccine induces both B and T cell responses. However, because it only protects against 7 pneumococcal serotypes, serotype replacement can render Prevnar ineffective. Serotype replacement has already been

demonstrated in several clinical trials and epidemiologic studies, necessitating development of different formulations of these vaccines. An example is the recently introduced Prevnar 13, directed to 13 pneumococcal serotypes. Furthermore, the two Prevnar formulations are expensive to manufacture, greatly limiting their availability in the developing world. PPV-23, which consists of 23 purified but unconjugated polysaccharides, has broader coverage, but does not provide protection to children under the age of 2 years, a population which is at the highest risk for pneumococcal disease.

Thus, there remains a need to design more effective pharmaceutical compositions than the current strategies offer. In particular, such compositions need to incorporate novel or specific antigens that elicit an immune response against S. pneumoniae. II. Summary

Streptococcus pneumoniae is a major health concern, especially in very young, elderly, or immunocompromised patients. While DNA and protein sequence information for S. pneumoniae has been known for some time, and researchers have long attempted to produce vaccines against S. pneumoniae, a major problem was how to identify protective polypeptides from among the approximately 2100 genes in the S. pneumoniae genome. The instant application presents the results of whole-genome screens designed to identify the most immunogenic proteins in the S. pneumoniae genome. Several of the hits from the screen have been shown to protect against S. pneumoniae colonization in a mouse model, and in some instances against both colonization and S. pneumoniae-induced sepsis. Accordingly, the present disclosure provides, inter alia, certain highly effective vaccines against Streptococcus pneumoniae. The vaccines may be used therapeutically or prophylactically. The present disclosure also provides specific antigens and methods for using the antigens to elicit an immune response against S. pneumoniae.

In certain aspects, the present disclosure provides a vaccine formulation comprising a pharmaceutically acceptable carrier and a polypeptide having an amino acid sequence comprising (or consisting of) SEQ ID NO: 265 or 268 or an immunogenic fragment thereof. In some embodiments, the polypeptide comprises an exogenous signal sequence. For instance, the polypeptide may have an amino acid sequence comprising SEQ ID NO: 266 or an

immunogenic fragment thereof. The polypeptide may have an amino acid sequence consisting of SEQ ID NO: 265, 266, or 268.

In some embodiments, the vaccine formulation further comprises a first polypeptide having an amino acid sequence comprising (or consisting of) one of SEQ ID NOS: 1-23, 267, and 269-270 or an immunogenic fragment thereof. In certain embodiments, the vaccine formulation further comprises a second polypeptide having an amino acid sequence comprising any of SEQ ID NOS: 1-23, 267, and 269-270 or an immunogenic fragment thereof.

In certain embodiments, the first and the second polypeptides belong to a different group of (i)-(vi): (i) SEQ ID NO: 1 or an immunogenic fragment thereof, (ii) one of SEQ ID NOS: 2-5 and 14-17 or an immunogenic fragment thereof, (iii) one of SEQ ID NOS: 6-7 and 18-19 or an immunogenic fragment thereof, (iv) SEQ ID NO: 8 or an immunogenic fragment thereof, (v) one of SEQ ID NOS: 9-10 and 20-21 or an immunogenic fragment thereof, and (vi) one of SEQ ID NO: 11-13, 267, and 269-270 or an immunogenic fragment thereof.

In some such embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 9, or SEQ ID NO: 10. In some embodiments, the vaccine formulation comprises a polypeptide consisting of SEQ ID NO: 6 or 7 and a polypeptide consisting of SEQ ID NO: 9 or 10.

In any of the aspects or embodiments herein, the vaccine formulation may comprise a polypeptide of SEQ ID NO: 265, 266, or 268 which is a truncated fragment having from 1-20 amino acid residues removed from the N-terminus, C-terminus, or both. In some embodiments, the vaccine formulation contains substantially no other S. pneumoniae polypeptides other than polypeptides having an amino acid sequence comprising any of SEQ ID NOS: 1-21 and 265-270.

In certain embodiments, the vaccine formulation comprises one or more polypeptides having an amino acid sequence comprising SEQ ID NOS: 22 or 23 or an immunogenic fragment thereof.

In another aspect, the invention provides vaccine formulations comprising a known S. pneumoniae antigen, such as a pneumolysoid, Choline-binding protein A (CbpA), or

Pneumococcal surface protein A (PspA), or derivatives thereof, and one, two, or three polypeptides from Table 1 or Table 2. An exemplary vaccine formulation comprises: (i) a polypeptide having an amino acid sequence comprising (or consisting of) one or more of SEQ ID NOS: 1-23 and 265-270 or an immunogenic fragment thereof, (ii) a pneumolysoid, and (iii) a pharmaceutically acceptable carrier. A further exemplary vaccine formulation comprises: (i) a polypeptide having an amino acid sequence comprising (or consisting of) one or more of SEQ ID NOS: 1-23 and 265-270 or an immunogenic fragment thereof, (ii) CbpA or a derivative thereof, and (iii) a pharmaceutically acceptable carrier. A further exemplary vaccine formulation comprises: (i) a polypeptide having an amino acid sequence comprising (or consisting of) one or more of SEQ ID NOS: 1-23 and 265-270 or an immunogenic fragment thereof, (ii) PspA or a derivative thereof, and (iii) a pharmaceutically acceptable carrier. In some such embodiments, the polypeptide of (i) comprises any one of SEQ ID NO: 2-5, 6, 7, 9-13, and 265-267. In some embodiments, the vaccine formulation further comprises a second polypeptide having an amino acid sequence comprising one of SEQ ID NO: 1-23 and 265-270. In some embodiments, the pneumolysoid is PdT, Pd-A, Pd-B, rPd2, rPd3, Ply8, A6PLY, L460D (see, e.g., US

2009/0285846 and L. Mitchell, Protective Immune Responses to Streptococcus pneumoniae Pneumolysoids, ASM2011 conference abstract, 2011), or a variant thereof. In some

embodiments, the derivative of PspA comprises all or a fragment of the proline-rich region of PspA.

In certain embodiments, the polypeptide is conjugated to an immunogenic carrier. In some embodiments, the vaccine formulation comprises at least one lipidated polypeptide.

In some embodiments, the vaccine formulation further comprises conjugated S.

pneumoniae polysaccharides. The conjugated polysaccharides may be, for example, as described in US Patent 5,623,057, US Patent 5,371,197, or PCT/US2011/023526.

In some embodiments, the vaccine formulation further comprises an adjuvant. The adjuvant may be, for example, an agonist of toll-like receptors (TLRs). The adjuvant may be, for example, alum. In some embodiments, the vaccine formulation comprises 1-1000 μg of each polypeptide and 1-250 μg of the adjuvant.

In certain embodiments, the vaccine formulation induces a ¾17 cell response at least 1.5-fold greater than that induced by a control unrelated antigen after contacting THIV cells. In some embodiments, the vaccine formulation inhibits infection by S. pneumoniae in an uninfected subject. In certain embodiments, the vaccine formulation inhibits S. pneumoniae colonization in an individual. In some embodiments, the vaccine formulation inhibits S. pneumoniae symptoms or sequelae. For instance, the vaccine formulation inhibits S. pneumoniae-induced sepsis.

In certain aspects, the present disclosure provides a method for treating a subject suffering from or susceptible to S. pneumoniae infection, comprising administering an effective amount of any of the vaccine formulations described herein.

In some embodiments, the method inhibits infection by S. pneumoniae in an uninfected subject. In some embodiments, the method inhibits S. pneumoniae colonization in a subject. In some embodiments, the method inhibits S. pneumoniae symptoms or sequelae. An exemplary sequela is sepsis.

In certain embodiments, the method treats a subject with one dose. In other

embodiments, the method treats a subject with two or three doses. In some embodiments, the method treats a subject within three doses.

In certain embodiments, the subject is a human.

The present disclosure provides, for example, a vaccine formulation comprising a pharmaceutically acceptable carrier and one or more polypeptides having an amino acid sequence comprising any of SEQ ID NOS: 1-13, 265, 266 and 267, or an immunogenic fragment thereof.

The present disclosure also provides a vaccine formulation comprising a

pharmaceutically acceptable carrier and at least one polypeptide having an amino acid sequence comprising SEQ ID NO: 6, SEQ ID NO: 10 or SEQ ID NO: 265, or an immunogenic fragment thereof. The present disclosure further provides a vaccine formulation comprising a

pharmaceutically acceptable carrier and at least one polypeptide having an amino acid sequence consisting of SEQ ID NO: 7, SEQ ID NO: 9 or SEQ ID NO: 265, or an immunogenic fragment thereof. Furthermore, the instant application provides a vaccine formulation comprising a pharmaceutically acceptable carrier and one or more polypeptides having an amino acid sequence comprising any of SEQ ID NOS: 14-23, 268, 269 and 270, or an immunogenic fragment thereof.

The present disclosure further provides an immunogenic composition comprising a pharmaceutically acceptable carrier and two or more polypeptides having amino acid sequences comprising any of SEQ ID NOS: 1-13, 265, 266 and 267, or an immunogenic fragment thereof.

The present disclosure also provides a vaccine formulation comprising a

pharmaceutically acceptable carrier and two or more polypeptides having amino acid sequences comprising SEQ ID NO: 6, SEQ ID NO: 10 or SEQ ID NO: 265, or an immunogenic fragment thereof. The present disclosure further provides a vaccine formulation comprising a

pharmaceutically acceptable carrier and two or more polypeptides having amino acid sequences consisting of SEQ ID NO: 7, SEQ ID NO: 9 or SEQ ID NO: 265, or an immunogenic fragment thereof. This disclosure also provides a vaccine formulation comprising a pharmaceutically acceptable carrier and two or more polypeptides having amino acid sequences comprising SEQ ID NO: 6, SEQ ID NO: 9, and SEQ ID NO: 265, or an immunogenic fragment thereof. In addition, this disclosure provides a vaccine formulation comprising a pharmaceutically acceptable carrier and two or more polypeptides having amino acid sequences comprising SEQ ID NO: 7, SEQ ID NO: 10, and SEQ ID NO: 265, or an immunogenic fragment thereof. In some embodiments, the amino acid sequence comprising SEQ ID NO: 265 comprises an exogenous signal sequence.

The present disclosure also provides a vaccine formulation comprising a

pharmaceutically acceptable carrier and three or more polypeptides having amino acid sequences comprising SEQ ID NO: 6, SEQ ID NO: 10 and SEQ ID NO: 265, respectively, or an

immunogenic fragment thereof. The present disclosure further provides a vaccine formulation comprising a pharmaceutically acceptable carrier and three or more polypeptides having amino acid sequences consisting of SEQ ID NO: 7, SEQ ID NO: 9 and SEQ ID NO: 265, respectively, or an immunogenic fragment thereof. III. Brief Description of the Drawings

FIG. 1 shows the concentration of IL-17 generated by blood samples from mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then stimulated with killed, unencapsulated whole cell S. pneumoniae, as described in Example 5. The left panel shows the data in scatter format, and the right panel shows the average and standard deviation for each sample. Immunization group "All 3" represents animals immunized with a combination of SP2108, SP0148, and SP1634.

FIG. 2 shows the concentration of IL-17 generated by blood samples from mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then stimulated with a combination of three proteins (SP2108, SP0148, and SP1634), as described in Example 5.

FIG. 3 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then challenged with intranasal administration of S. pneumoniae, as described in Example 5. 003 represents a control unrelated antigen.

FIG. 4 shows the concentration of IL-17 generated by blood samples from mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then stimulated with killed, unencapsulated whole cell S. pneumoniae, as described in Example 6.

FIG. 5 shows the concentration of IL-17 generated by blood samples from mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then stimulated by the indicated protein(s), as described in Example 6.

FIG. 6 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then challenged with intranasal administration of S. pneumoniae, as described in Example 6. The HSV-2 protein ICP47 with the gene name US12 (NP_044543.1, NC_001798.1; shown in the figure as 003) and ovalbumin (OVA) represent control antigens.

FIG. 7 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then challenged with intranasal administration of S. pneumoniae, as described in Example 7.

FIG. 8 shows the number of S. pneumoniae colonies obtained from a nasal wash in BALB/c mice that were immunized with the indicated protein(s) and cholera toxin adjuvant, then challenged with intranasal administration of S. pneumoniae, as described in Example 8. FIG. 9 shows the concentration of IL-17A generated by blood samples from mice that were immunized with the indicated proteins and cholera toxin adjuvant, then stimulated with the protein of immunization (left panel) or killed, unencapsulated whole cell S. pneumoniae (right panel), as described in Example 9.

FIG. 10 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated proteins and cholera toxin adjuvant, then challenged with intranasal administration of S. pneumoniae, as described in Example 10.

FIG. 11 shows survival of mice that were immunized with the indicated proteins and the adjuvant alum, then underwent aspiration challenge with S. pneumoniae as described in Example 11.

FIG. 12 shows survival of mice that were immunized with the indicated proteins and the adjuvant alum, then underwent aspiration challenge with S. pneumoniae as described in Example 12.

FIG. 13 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated proteins and cholera toxin adjuvant, then challenged with intranasal administration of S. pneumoniae, as described in Example 13.

FIG. 14 shows the concentration of IL-17A generated by blood samples form mice that were immunized with the indicated proteins and alum, then stimulated with the proteins indicated at upper left, as described in Example 14.

FIG. 15 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated proteins and alum or with killed, unencapsulated whole cell S. pneumoniae plus alum (WCV), then challenged with intranasal administration of S.

pneumoniae, as described in Example 15.

FIG. 16 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated proteins and alum or with killed, unencapsulated whole cell S. pneumoniae plus alum (WCV), then challenged with intranasal administration of S.

pneumoniae, in two pooled studies as described in Example 16.

FIG. 17 shows the number of S. pneumoniae colonies obtained from a nasal wash in mice that were immunized with the indicated proteins and alum or with killed, unencapsulated whole cell S. pneumoniae plus alum (WCB), then challenged with intranasal administration of S.

pneumoniae, as described in Example 17. FIG. 18 shows survival of mice that were injected with antibodies or sera specific to the indicated proteins, then underwent aspiration challenge with S. pneumoniae, as described in Example 18.

FIG. 19 shows the percent of animals protected from sepsis in six separate aspiration challenge studies, two of which are described in more detail in Examples 12 and 18.

IV. Detailed Description

A. Specific polypeptides and nucleic acids for use in S. pneumoniae vaccines and immunogenic compositions

This application describes S. pneumoniae vaccines that include one or more of the polypeptides or genes listed in Table 1 , or variants or fragments thereof as described below. The vaccine may include a polypeptide that comprises a sequence of Table 1 or a variant or immunogenic fragment thereof or a polypeptide that consists of a sequence of Table 1 or a variant or immunogenic fragment thereof. The DNA and protein sequence of each gene and polypeptide may be found by searching for the Locus Tag in the publicly available database, Entrez Gene (on the NCBI NIH web site on the World Wide Web, at

www.ncbi.nlm.nih.gov/sites/entrez?db=gene), in the Streptococcus pneumoniae TIGR4 genome, and the indicated sequences are also included in this application.

Table 1. Immunogenic polypeptides for vaccine formulations

sequence

SP0148 lacking signal sequence 6 27 -

SP0148 including signal sequence 7 28 NC_003028.31: 145,513- 146,343*

SP1072 8 NC_003028.31: 1008420- 1010180

SP2108 including signal sequence 9 NC_003028.3I:2020750- 2022021

SP2108 lacking signal sequence 10 29 -

SP0641M 11 30 -

SP0641 12 NC_003028.3I:2020750- 2022021

SP0641N 13 31 -

SP0882 consensus 14 - -

SP0882N consensus 15 - -

SP0882 consensus with exogenous 16

leader

SP0882N consensus with exogenous 17

leader

SP0148 consensus lacking signal 18

sequence

SP0148 consensus including signal 19

sequence

SP2108 consensus lacking signal 20

sequence

SP2108 consensus including signal 21

sequence

SP1634 22 NC_003028.31: 1534348- 1535421

SP0314 23 - NC_003028.3I:287483- 290683

SP1912 265 271 NC_003028.31: 1824672- 1824971

SP1912L 266 272 -

SP0641.1 267 273 -

SP1912 consensus 268 - -

SP0641N consensus 269 - -

SP0641M consensus 270 - -

*NB : The database sequence incorrectly lists TTG (encoding Leu) at nucleotide positions 541-543. The correct sequence, as shown in SEQ ID NO: 28, has TTC at that codon and encodes Phe. The database sequence further does not include a C-terminal Glu found in certain isolates.

Certain polypeptides of Table 1 , and variants thereof, are described in greater detail below.

1. SP1912 (SEQ ID NO: 265) and variants thereof

SP1912 is a hypothetical protein of 99 amino acids. While the protein function is not definitively known, sequence analysis suggests it is a putative thioredoxin.

In some embodiments, vaccines or pharmaceutical compositions comprising an S.

pneumoniae polypeptide include a polypeptide containing at least 20 consecutive amino acid residues selected from SP1912. The polypeptide may also be a variant of the at least 20 residue fragment. In certain embodiments, the polypeptide includes no more than 90, 75, 60, 45 or 30 consecutive amino acids from SP1912.

In some embodiments, the compositions and methods herein call for the use of an SP1912 variant that comprises an exogenous lipidation sequence. In some embodiments, a signal sequence directs lipidation. Thus, the lipidation signal may be, e.g., the signal sequence of SP2108 (SEQ ID NO: 275) or SP0148, or an E. coli signal sequence. The exemplary variant SP1912L, comprising the signal sequence of the E. coli gene RlpB (SEQ ID NO: 276) is represented by polypeptide sequence SEQ ID NO: 266. SP1912 (SEQ ID NO: 265) and

SP1912L (SEQ ID NO: 266) may be encoded, respectively, by nucleic acids according to SEQ ID NO: 271 and 272, although due to degeneracy in the genetic code, other DNA sequences (including codon-optimized sequences) may be used.

Consensus sequences illustrating combinations of SP1912 sequences from different serotypes are provided as SEQ ID NO: 268. Thus, in certain embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising, or consisting of, SEQ ID NO: 268, or an immunogenic fragment thereof (e.g., in place of a polypeptide having an amino acid sequence comprising SEQ ID NO: 265).

2. SP0024 (SEQ ID NO: 1) and variants thereof

SP0024 represents a hypothetical protein of 165 amino acids, containing a conserved carbonic anhydrase domain that extends from amino acid 27 to amino acid 163. Based on this consensus motif, SP0024 may be a zinc-binding protein.

In some embodiments, vaccines or pharmaceutical compositions comprising an S.

pneumoniae polypeptide include a polypeptide containing at least 20 consecutive amino acid residues selected from SP0024. The polypeptide may also be a variant of the at least 20 residue fragment. In certain embodiments, the polypeptide includes no more than 150, 125, or 100 consecutive amino acids from SP0024.

3. SP0882 (SEQ ID NO: 2) and variants thereof

SP0882 is a conserved hypothetical protein of 274 amino acids. Much of the protein (amino acids 2-270) forms an esterase or lipase-like region.

In some embodiments, vaccines or pharmaceutical compositions comprising an S.

pneumoniae polypeptide include a polypeptide containing at least 20 consecutive amino acid residues selected from SP0882. The polypeptide may also be a variant of the at least 20 residue fragment. In certain embodiments, the polypeptide includes no more than 250, 275, 200, 175, 150, 125, or 100 consecutive amino acids from SP0882.

One particular truncation variant named SP0882N consists of the N-terminal 130 amino acids of SP0882, and is shown as SEQ ID NO: 3. SP0882N includes a region that is particularly well conserved among different serotypes. In certain embodiments, a polypeptide comprising SP0882 or SP0882N, or an immunogenic fragment of either, also comprises an exogenous signal sequence. In some embodiments, the signal sequence is an E. coli or S. pneumoniae signal sequence. The signal sequence may be, for example, the signal sequence of SP2108. Two exemplary such polypeptides are SEQ ID NOS: 4 and 5. Variants of DNA and protein sequences of SP0882 are described, inter alia, in US Patent Application Publication No. 2009/0215149 and International Applications WO2002/077021, W098/18931, and WO2007/106407. A variant of SP0882N is disclosed in International Application WO2008/146164.

Sequence variation occurs at the protein level between different S. pneumoniae serotypes, and consensus sequences illustrating combinations of SP0882 sequences from different S.

pneumoniae serotypes are provided as SEQ ID NOS: 14-17. Accordingly, in certain

embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising, or consisting of, any of SEQ ID NOS: 14-17, or an immunogenic fragment thereof (e.g., in place of a polypeptide having an amino acid sequence comprising one of SEQ ID NOS: 2-5).

Nucleic acid sequences encoding different variants of SP0882 (SEQ ID NOS: 2-5) are provided as SEQ ID NOS: 24-26, although due to degeneracy in the genetic code, other DNA sequences (including codon-optimized sequences) could encode these polypeptides.

4. SP0148 (SEQ ID NO: 7) and variants thereof

The protein SP0148 is named "ABC transporter, substrate-binding protein". Proteins of this class are typically extracellular proteins that interact transiently with a transmembrane protein complex. Such complexes use energy generated by ATP hydrolysis to translocate specific substrates across a cell membrane. SP0148 is a 276 or 277 (depending on the isolate) amino acid protein that contains a conserved PBPb (periplasmic binding protein) domain, spanning amino acids 40-246, which is typical of membrane-bound transport complexes. In addition, SP0148 has a bacterial extracellular solute-binding proteins family 3 domain which is largely co-extensive with the PBPb domain and extends from amino acid 40 to 244. In some embodiments, a vaccine or other composition comprises a truncation mutant of SP0148 comprising or lacking one or more of said domains and motifs.

In some embodiments, vaccines or pharmaceutical compositions comprising an S.

pneumoniae polypeptide include a polypeptide containing at least 20 consecutive amino acid residues selected from SP0148. The polypeptide may also be a variant of the at least 20 residue fragment. In certain embodiments, the polypeptide includes no more than 250, 275, 200, 175, 150, 125, or 100 consecutive amino acids from SP0148. Endogenous SP0148 comprises a signal sequence that directs its secretion and potential lipidation. In some embodiments, the signal sequence of the polypeptide of SEQ ID NO: 7 is partially or fully processed by an expression host, e.g. E. coli. In some embodiments, a variant of SP0148 that lacks the signal sequence (SEQ ID NO: 6) is used. The polypeptide of SEQ ID NO: 6 is encoded by the nucleic acid of SEQ ID NO: 27, although other nucleic acid sequences (including codon-optimized sequences) may be used. SEQ ID NO: 28 encodes the full length sequence of SP0148 used in the screens herein.

Variants of the amino acid sequence and nucleotide sequence of SP0148 may be found in U.S.Patent Application Publication No. 2005/0020813, U.S. Patent Nos. 7,378,514 and

7,504,110, and European Patent Application No. EP1572868 and EP1855717.

Consensus sequences illustrating combinations of SP0148 sequences from different S. pneumoniae serotypes are provided as SEQ ID NOS: 18 and 19. Accordingly, in certain embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising, or consisting of, either of SEQ ID NOS: 18-19, or an immunogenic fragment thereof (e.g., in place of a polypeptide having an amino acid sequence comprising one of SEQ ID NOS: 6 or 7).

5. SP1072 (SEQ ID NO: 8) and variants thereof

SP1072, also known as dnaG, is a DNA primase enzyme that catalyzes formation of an RNA primer which allows DNA polymerase to initiate DNA replication. A protein of 586 amino acids, SP1072 contains several conserved motifs. Beginning at the N-terminus, amino acids 2 - 96 form a zinc finger domain, the DNA primase catalytic core spans amino acids 122 - 250, and a highly conserved topoisomerase-primase (TORPIM) nucleotidyl transferase/hydrolase domain region extends from amino acid 258 to 330. In some embodiments, a vaccine or other composition comprises a truncation mutant of SP1072 comprising or lacking one or more of said domains and motifs.

In some embodiments, vaccines or pharmaceutical compositions comprising an S.

pneumoniae polypeptide include a polypeptide containing at least 20 consecutive amino acid residues selected form SP1072. The polypeptide may also be a variant of the at least 20 residue fragment. In certain embodiments, the polypeptide includes no more than 550, 500, 450, 400, 350, 300, 250, 200, 150, or 100 consecutive amino acids from SP1072. 6. SP2108 (SEQ ID NO: 9) and variants thereof

The polypeptide SP2108 is 423 amino acids in length and is alternatively known as MalX, maltose/maltodextrin ABC transporter, or maltose/maltodextrin-binding protein. Much of the protein (amino acids 3-423) is classified as a MalE (Maltose-binding periplasmic) domain. In addition, SP2108 contains a signal sequence that directs its secretion and potential lipidation. In some embodiments, the signal sequence of the polypeptide of SEQ ID NO: 9 is partially or fully processed by an expression host, e.g. E. coli. In some embodiments, a vaccine or other composition comprises a truncation mutant of SP2108 comprising one or more of said domains and motifs.

In some embodiments, the compositions and methods herein call for the use of an

SP2108 variant that lacks the signal sequence. This variant is represented by polypeptide sequence SEQ ID NO: 10 and may be encoded by, for example, a nucleic acid according to SEQ ID NO: 29, although due to degeneracy in the genetic code, other DNA sequences (including codon-optimized sequences) may be used.

In some embodiments, vaccines or pharmaceutical compositions comprising an S.

pneumoniae polypeptide include a polypeptide containing at least 20 consecutive amino acid residues selected from SP2108. The polypeptide may also be a variant of the at least 20 residue fragment. In certain embodiments, the polypeptide includes no more than 400, 350, 300, 250, 200, 150, or 100 consecutive amino acids from SP2108.

Consensus sequences illustrating combinations of SP2108 sequences from different serotypes are provided as SEQ ID NOS: 20 and 21. Thus, in certain embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising, or consisting of, either of SEQ ID NOS: 20-21, or an immunogenic fragment thereof (e.g., in place of a polypeptide having an amino acid sequence comprising one of SEQ ID NOS: 9 or 10).

7. SP0641 (SEQ ID NO: 12) and variants thereof

At 2144 amino acids in length, SP0641 is also known as PrtA, a cell wall-associated serine protease. Full-length SP0641 contains a number of conserved motifs: the PA_2 motif, extending between amino acids 485 and 597, which may form a protein binding surface; the Fn3- like domain (amino acids 800 - 939); and two predicted catalytic domains of the S8 C5a type located at amino acids 226 - 449 and 639 - 777. In some embodiments, a vaccine or other composition comprises a truncation mutant of SP0641 comprising or lacking one or more of said domains and motifs.

In some embodiments, vaccines or pharmaceutical compositions comprising an S.

pneumoniae polypeptide include a polypeptide containing at least 20 consecutive amino acid residues selected from SP0641. The polypeptide may also be a variant of the at least 20 residue fragment. In certain embodiments, the polypeptide includes no more than 1000, 900, 800, 700, 600, 500, 400, 300, 200, or 100 consecutive amino acids from SP0641.

Certain other truncation mutants of SP0641 may also be used. For instance, the polypeptide designated SP0641N (SEQ ID NO: 13) consists of 661 amino acids corresponding to amino acids 24-684 near the N-terminus of SP0641. Roughly adjacent to SP0641N (and corresponding to amino acids 686-1333 of SP0641) lies the 648 residue region captured by the truncation variant SP0641M (SEQ ID NO: 11). The polypeptide designated SP0641.1 (SEQ ID NO: 267) consists of 978 amino acids corresponding to amino acids 28-1006 of SP0641.

Variants of SP0641 are disclosed in, for example, U.S. Patents No. 7,338,786, 6,573,082, and 7,132,107, as well as International Application WO00/06738.

SEQ ID NOS: 30, 31 and 273 display the DNA sequences of SP0641M (SEQ ID NO: 11), SP0641N (SEQ ID NO: 13) and SP641.1 (SEQ ID NO: 267), respectively, although due to degeneracy in the genetic code, other DNA sequences (including codon-optimized sequences) could encode these SP0641 variants.

Consensus sequences illustrating combinations of SP0641N and SP0641M sequences from different S. pneumoniae serotypes are provided as SEQ ID NOS: 269 and 270.

Accordingly, in certain embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising, or consisting of, either of SEQ ID NOS: 269 or 270, or an immunogenic fragment thereof (e.g., in place of a polypeptide having an amino acid sequence comprising one of SEQ ID NOS: 11 or 13).

Polypeptides homologous to the polypeptides of Tables 1 and 2 (for example, SP1912, SP1912L, SP0024, SP0882, SP0882N, SP0148 with or without a signal sequence, SP1072, SP2108 with or without a signal sequence, SP0641, SP0641M, SP0641N, or SP0641.1) may also be used in the compositions and methods disclosed herein. Individual strains of S. pneumoniae contain numerous mutations relative to each other, and some of these result in different protein sequences between the different strains. One of skill in the art may readily substitute an amino acid sequence, or a portion thereof, with the homologous amino acid sequence from a different S. pneumoniae strain. In certain aspects, this application provides immunogenic polypeptides with at least 90%, 95%, 97%, 98%, 99%, or 99.5% identity to the polypeptides of Tables 1 and 2 or an immunogenic fragment thereof. Serotypic variation may be used to design such variants of the polypeptides of Tables 1 and 2.

In some embodiments, the vaccine compositions herein comprise a fragment of a protein of Table 1 or 2 (for example, fragments of SP1912, SP1912L, SP0024, SP0882, SP0882N, 0SP148 with or without a signal sequence, SP1072, SP2108 with or without a signal sequence, SP0641, SP0641M, SP0641N, or SP0641.1). In some embodiments, this application provides truncation mutants that are close in size to the polypeptide of Table 1 or 2 (for example, one of SEQ ID NOS: 1-13, 265, 266 or 267). For example, they may lack at most one, two three, four, five, ten, or twenty amino acids from one or both termini. Internal deletions, e.g., of 1-10, 11-20, 21-30, or 31-40 amino acids, are also contemplated.

In certain embodiments the vaccine formulation comprises one or more polypeptides having an amino acid sequence comprising, or consisting of, any of SEQ ID NOS: 14-21, 268, 269 and 270. In certain embodiments, the fragment is a truncated fragment of any of SEQ ID NOS: 14-21, 268, 269 and 270, wherein from 1-5, 1-10, or 1-20 amino acid residues are removed from the N-terminus, C-terminus, or both. In certain embodiments, the fragment is a truncated fragment of any of SEQ ID NOS: 14-21, 268, 269 and 270, wherein from 1-10 amino acid residues are removed from the N-terminus, C-terminus, or both. For instance, 10 amino acid residues may be removed from each of the N-terminus and C-terminus resulting in a protein with 20 amino acid residues removed.

In certain embodiments, the vaccine formulations provided herein comprise or further comprise one or more, or two or more, known S. pneumoniae antigens. In some instances, the known S. pneumoniae antigens are predominantly antibody targets. In some instances, the known S. pneumoniae antigens protect from S. pneumoniae colonization, or from S pneumoniae- induced sepsis. One appropriate art-recognized class of S. pneumoniae antigen is the

pneumolysoids. Pneumolysoids have homology to the S. pneumoniae protein pneumolysin (PLY), but have reduced toxicity compared to pneumolysin. Pneumolysoids can be naturally occurring or engineered derivatives of pneumolysin. In some embodiments, a pneumolysoid has at least 70%, 80%, 85%, 90%, 95%, 97%, 98%, or 99% identity to pneumolysin. In some embodiments, the pneumolysoid demonstrates less than 1/2, 1/5, 1/10, 1/20, 1/50, 1/100, 1/200, 1/500, or 1/1000 the toxicity of pneumolysin in an assay for one or both of hemolytic activity towards erythrocytes and inhibition of polymorphonuclear leukocytes. Both assays are described in Saunders F.K. et al. ("Pneumolysin, the thiol-activated toxin of Streptococcus pneumoniae, does not require a thiol group for in vitro activity" Infect Immun. 1989 Aug;57(8):2547-52.). Exemplary pneumolysoids include PdT (a triple mutant further described in Berry, A.M. et al. (1995) Infection and Immunity 63: 1969-74); Pd-A and Pd-B (Paton J.C. et al. "Purification and immunogenicity of genetically obtained pneumolysin toxoids and their conjugation to

Streptococcus pneumoniae type 19F polysaccharide" Infect Immun. 1991 Jul ;59(7): 2297-304); rPd2 and rPd3 (Ferreira et al. "DNA vaccines based on genetically detoxified derivatives of pneumolysin fail to protect mice against challenge with Streptococcus pneumoniae" FEMS Immunol Med Microbiol (2006) 46: 291-297); Ply8, A6PLY, L460D, or a variant thereof. In some embodiments, the pneumolysin has a mutation in the catalytic center, such as at amino acid 428 or 433 or the vicinity.

Other appropriate S. pneumoniae antigens for combination vaccines include

Pneumococcal surface protein A (PspA); derivatives of PspA, Choline-binding protein A (CbpA) and derivatives thereof (AD Ogunniyi et al., "Protection against Streptococcus pneumoniae elicited by immunization with pneumolysin and CbpA," Infect Immun. 2001 Oct;69(10):5997- 6003); Pneumococcal surface adhesin A (PsaA); caseinolytic protease; sortase A (SrtA); pilus 1 RrgA adhesin; PpmA; PrtA; PavA; LytA; Stk-PR; PcsB; RrgB and derivatives thereof.

Derivatives of PspA include proline-rich segments with the non-proline block (PR+NPB, further described below as well as in Daniels, C.C. et al. (2010) Infection and Immunity

78:2163-72) and related constructs comprising all or a fragment of the proline-rich region of PspA (e.g., regions containing one or more of the sequences PAPAP, PKP, PKEPEQ and PEKP and optionally including a non-proline block). An example of the non-proline-block has the exemplary sequence EKSADQQAEEDYARRSEEEYNRLTQQQ (SEQ ID NO: 306), which generally has no proline residues in an otherwise proline-rich area of the non-coiled region of PspA. Other embodiments of non-proline block (NPB) sequences include SEQ ID NOs: 307 and 308. PspA and its derivatives can include genes expressing similar proline-rich structures (i.e. PKP, PKEPEQ and PEKP), with or without the NPB. The amino acids at either end of the NPB mark the boundaries of the proline-rich region. In one example, the amino-terminal boundary to the PR-region is DLKKAVNE (SEQ ID NO: 309), and the carboxy-terminal boundary is (K/G)TGW(K/G)QENGMW (SEQ ID NO: 310). Peptides containing the NPB are particularly immunogenic, suggesting that the NPB may be an important epitope. Exemplary immunogenic PspA polypeptide derivatives containing the coiled-coil structure include SEQ ID NOs: 301 and 302. Particular embodiments of the immunogenic PspA polypeptide derivatives lacking the coiled-coil structure have the amino acid sequences shown as SEQ ID NOS: 303-305.

Immunogenic PspA polypeptides SEQ ID NO: 301, 303 and 305 include both PR and NPB sequences (PR+NPB). Immunogenic PspA polypeptides of SEQ ID NOS: 302 and 304 include only a PR sequence (PR only) and lack the NPB.

In some cases, the other appropriate S. pneumoniae antigen is at least at least 70%, 80%, 85%, 90%, 95%, 97%, 98%, or 99% identity to the corresponding wild-type S. pneumoniae protein. Sequences of the above-mentioned polypeptides, and nucleic acids that encode them, are known; see, for example, the S. pneumoniae ATCC 700669 complete genome sequence under GenBank accession number FM211187.1 and linked polypeptide sequences therein.

Further S. pneumoniae antigens for combination vaccines include conjugated S.

pneumoniae polysaccharides. The conjugated polysaccharides may be, for example, as described in US Patent 5,623,057, US Patent 5,371,197, or PCT/US2011/023526.

In addition to those nucleic acids and polypeptides described in Table 1 above, this application also provides immunogenic compositions that include one or more of the

polypeptides or genes listed in Table 2, or variants or fragments thereof as described herein. The DNA and protein sequence of each gene and protein may be found by searching for the Locus Tag in the publicly available database, Entrez Gene, as described above.

Table 2. Immunogenic proteins identified in human and mouse screens

SP0605 AAK74757.1 NC_003028.3l:571604-572485

SP1177 AAK75286.1 NC_003028.3l:cl l l5580-1115317

SP0335 AAK74510.1 NC_003028.3l:306559-306876

SP0906 AAK75031.1 NC_003028.3l:c859160-859029

SP1828 AAK75901.1 NC_003028.3l:cl740010-1739000

SP2157 AAK76211.1 NC_003028.3l:c2072146-2070995

SP1229 AAK75335.1 NC_003028.3l:cl l63388-1161718

SP1128 AAK75238.1 NC_003028.31: 1061773-1063077

SP1836 AAK75909.1 NC_003028.31: 1746104-1746280

SP1865 AAK75937.1 NC_003028.3l:cl772987-1771923

SP0904 AAK75029.1 NC_003028.3l:c858126-857311

SP0765 AAK74903.1 NC_003028.3l:724170-725207

SP1634 AAK75714.1 NC_003028.31: 1534348-1535421

SP0418 AAK74581.1 NC_003028.3I:396692-396916

SP1923 AAK75991.1 NC_003028.3l:cl833311-1831896

SP1313 AAK75991.1 NC_003028.3l:cl833311-1831896

SP0775 AAK74913.1 NC_003028.3l:731798-732070

SP0314 AAK74491.1 NC_003028.3l:287483-290683

SP0912 AAK75037.1 NC_003028.3l:864707-865465

SP0159 AAK74341.1 NC_003028.3l:cl57554-156292

SP0910 AAK75035.1 NC_003028.3l:863462-863734

SP2148 AAK76205.1 NC_003028.3l:2062144-2063373

SP1412 AAK75510.1 NC_003028.3l:cl332393-1331605

SP0372 AAK74539.1 NC_003028.3l:350268-350597

SP1304 AAK75407.1 NC_003028.3l:cl232491-1232390

SP2002 AAK76069.1 NC_003028.3l:cl906183-1905446

SP0612 AAK74764.1 NC_003028.3l:579708-579806

SP1988 AAK76055.1 NC_003028.3l:cl892598-1890565

SP0484 AAK74643.1 NC_003028.3l:465572-466402

SP0847 AAK74978.1 NC_003028.3l:794144-795202 SP1527 AAK75616.1 NC_003028.3l:cl439494-1437536

SP0542 AAK74699.1 NC_003028.3I:515940-516059

SP0441 AAK74602.1 NC_003028.3I:414869-415057

SP0350 AAK74523.1 NC_003028.3l:323990-324625

SP0014 AAK74207.1 NC_003028.31: 14450-14929

SP1965 AAK76032.1 NC_003028.3l:cl873279-1873073

SP0117 AAK74303.1 NC_003028.31: 118423-120657

SP0981 AAK75102.1 NC_003028.3I:927115-928056

SP2229 AAK76277.1 NC_003028.3l:c2148627-2147602

SP2136 AAK76194.1 NC_003028.3l:c2048521-2046656

SP1179 AAK75288.1 NC_003028.31: 1116230-1118389

SP1174 AAK75283.1 NC_003028.3l:cl 110717-1108258

SP2216 AAK76264.1 NC_003028.3l:c2136445-2135267

SP1393 AAK75491.1 NC_003028.3I: 1316756-1318027

SP1384 AAK75482.1 NC_003028.3l:cl309464-1308967

SP2032 AAK76097.1 NC_003028.3l:cl939994-1938321

Typically, the polypeptides present in compounds of the invention are immunogenic, either alone or as a variant, which includes polypeptides fused to another polypeptide or mixed with or complexed to an adjuvant. Variants also include sequences with less than 100% sequence identity, as described herein. In certain embodiments, an antigen of Table 1 or 2 is provided as a full length polypeptide. In addition, one may use fragments, precursors and analogs that have an appropriate immunogenicity.

These polypeptides may be immunogenic in mammals, for example mice, guinea pigs, or humans. An immunogenic polypeptide is typically one capable of raising a significant immune response in an assay or in a subject. The immune response may be innate, humoral, cell- mediated, or mucosal (combining elements of innate, humoral and cell-mediated immunity). For instance, an immunogenic polypeptide may increase the amount of IL-17 produced by T cells. The IL-17 assay described in Examples 1-4 is an example of an assay that may be used to identify an immunogenic polypeptide. Alternatively or additionally, an immunogenic polypeptide may(i) induce production of antibodies, e.g., neutralizing antibodies, that bind to the polypeptide and/or the whole bacteria, (ii) induce TH17 immunity, (iii) activate the CD4 ⁺ T cell response, for example by increasing CD4 ⁺ T cells and/or increasing localization of CD4 ⁺ T cells to the site of infection or reinfection, (iv) activate the CD8 ⁺ CTL response, for example by increasing CD8 ⁺ T cells and/or increasing localization of CD8 ⁺ T cells to the site of infection or reinfection, (v) induce Tjjl immunity, and/or (vi) activate innate immunity. In some embodiments, an immunogenic polypeptide causes the production of a detectable amount of antibody specific to that antigen.

In certain embodiments, polypeptides have less than 20%, 30%, 40%, 50%, 60% or 70% identity to human autoantigens and/or gut commensal bacteria (e.g., certain Bacteroides, Clostridium, Fusobacterium, Eubacterium, Ruminococcus, Peptococcus, Peptostreptococcus, Bifidobacterium, Escherichia and Lactobacillus species). Examples of human autoantigens include insulin, proliferating cell nuclear antigen, cytochrome P450, and myelin basic protein.

The present invention also provides an immunogenic composition comprising a pharmaceutically acceptable carrier, a polypeptide having an amino acid sequence comprising SEQ ID NO: 265, 266, or 268 or an immunogenic fragment thereof, and one or more polypeptides having amino acid sequences comprising any of SEQ ID NOS: 1-23 and SP1574, SP1655, SP2106, SP1473, SP0605, SP1177, SP0335, SP0906, SP1828, SP2157, SP1229, SP1128, SP1836, SP1865, SP0904, SP0765, SP1634, SP0418, SP1923, SP1313, SP0775, SP0314, SP0912, SP0159, SP0910, SP2148, SP1412, SP0372, SP1304, SP2002, SP0612, SP1988, SP0484, SP0847, SP1527, SP0542, SP0441, SP0350, SP0014, SP1965, SP0117,

SP0981, SP2229, SP2136, SP1179, SP1174, SP2216, SP1393, SP0641.1, SP1384, and SP2032, or an immunogenic fragment thereof.

In some embodiments, the vaccine formulation comprises at least two polypeptides, each polypeptide belonging to a different group of (i)-(vii): (i) SEQ ID NO: 1 or an immunogenic fragment thereof, (ii) one of SEQ ID NOS: 2-5 and 14-17 or an immunogenic fragment thereof, (iii) one of SEQ ID NOS: 6-7 and 18-19 or an immunogenic fragment thereof, (iv) SEQ ID NO: 8 or an immunogenic fragment thereof, (v) one of SEQ ID NOS: 9-10 and 20-21 or an immunogenic fragment thereof, (vi) one of SEQ ID NOS: 11-13, 267, and 269-270 or an immunogenic fragment thereof, and (vii) one of SEQ ID NOS: 265-266 and 268 or an immunogenic fragment thereof. Examples of such combinations are listed below. Additional combinations may be made by replacing one of the sequences below with the corresponding consensus sequence, e.g. , one of SEQ ID NOS: 14-21 or 268-270. In some embodiments, one of the polypeptides is one of SEQ ID NOS: 265-266 and 268 or an immunogenic fragment thereof. In some embodiments, the vaccine formulation further comprises a pneumolysoid. In some embodiments, the vaccine formulation further comprises CbpA or a derivative thereof. In some embodiments, the vaccine formulation further comprises PspA or a derivative thereof comprising all or a fragment of the proline-rich region of PspA.

SEQ ID NO: 1 and SEQ ID NO: 2

SEQ ID NO: 1 and SEQ ID NO: 3

SEQ ID NO: 1 and SEQ ID NO: 4

SEQ ID NO: 1 and SEQ ID NO: 5

SEQ ID NO: 1 and SEQ ID NO: 6

SEQ ID NO: 1 and SEQ ID NO: 7

SEQ ID NO: 1 and SEQ ID NO: 8

SEQ ID NO: 1 and SEQ ID NO: 9

SEQ ID NO: 1 and SEQ ID NO: 10

SEQ ID NO: 1 and SEQ ID NO: 11

SEQ ID NO: 1 and SEQ ID NO: 12

SEQ ID NO: 1 and SEQ ID NO: 13

SEQ ID NO: 1 and SEQ ID NO: 265

SEQ ID NO: 1 and SEQ ID NO: 266

SEQ ID NO: 1 and SEQ ID NO: 267

SEQ ID NO: 2 and SEQ ID NO: 6

SEQ ID NO: 2 and SEQ ID NO: 7

SEQ ID NO: 2 and SEQ ID NO: 8

SEQ ID NO: 2 and SEQ ID NO: 9

SEQ ID NO: 2 and SEQ ID NO: 10

SEQ ID NO: 2 and SEQ ID NO: 11

SEQ ID NO: 2 and SEQ ID NO: 12

SEQ ID NO: 2 and SEQ ID NO: 13 SEQ ID NO: 2 and SEQ ID NO: 265

SEQ ID NO: 2 and SEQ ID NO: 266

SEQ ID NO: 2 and SEQ ID NO: 267

SEQ ID NO: 3 and SEQ ID NO: 6

SEQ ID NO: 3 and SEQ ID NO: 7

SEQ ID NO: 3 and SEQ ID NO: 8

SEQ ID NO: 3 and SEQ ID NO: 9

SEQ ID NO: 3 and SEQ ID NO: 10

SEQ ID NO: 3 and SEQ ID NO: 11

SEQ ID NO: 3 and SEQ ID NO: 12

SEQ ID NO: 3 and SEQ ID NO: 13

SEQ ID NO: 3 and SEQ ID NO: 265

SEQ ID NO: 3 and SEQ ID NO: 266

SEQ ID NO: 3 and SEQ ID NO: 267

SEQ ID NO: 4 and SEQ ID NO: 6

SEQ ID NO: 4 and SEQ ID NO: 7

SEQ ID NO: 4 and SEQ ID NO: 8

SEQ ID NO: 4 and SEQ ID NO: 9

SEQ ID NO: 4 and SEQ ID NO: 10

SEQ ID NO: 4 and SEQ ID NO: 11

SEQ ID NO: 4 and SEQ ID NO: 12

SEQ ID NO: 4 and SEQ ID NO: 13

SEQ ID NO: 4 and SEQ ID NO: 265

SEQ ID NO: 4 and SEQ ID NO: 266

SEQ ID NO: 4 and SEQ ID NO: 267 SEQ ID NO: 5 and SEQ ID NO: 6

SEQ ID NO: 5 and SEQ ID NO: 7

SEQ ID NO: 5 and SEQ ID NO: 8

SEQ ID NO: 5 and SEQ ID NO: 9

SEQ ID NO: 5 and SEQ ID NO: 10

SEQ ID NO: 5 and SEQ ID NO: 11

SEQ ID NO: 5 and SEQ ID NO: 12

SEQ ID NO: 5 and SEQ ID NO: 13

SEQ ID NO: 5 and SEQ ID NO: 265

SEQ ID NO: 5 and SEQ ID NO: 266

SEQ ID NO: 5 and SEQ ID NO: 267

SEQ ID NO: 6 and SEQ ID NO: 8

SEQ ID NO: 6 and SEQ ID NO: 9

SEQ ID NO: 6 and SEQ ID NO: 10

SEQ ID NO: 6 and SEQ ID NO: 11

SEQ ID NO: 6 and SEQ ID NO: 12

SEQ ID NO: 6 and SEQ ID NO: 13

SEQ ID NO: 6 and SEQ ID NO: 265

SEQ ID NO: 6 and SEQ ID NO: 266

SEQ ID NO: 6 and SEQ ID NO: 267

SEQ ID NO: 7 and SEQ ID NO: 8

SEQ ID NO: 7 and SEQ ID NO: 9

SEQ ID NO: 7 and SEQ ID NO: 10

SEQ ID NO: 7 and SEQ ID NO: 11

SEQ ID NO: 7 and SEQ ID NO: 12

SEQ ID NO: 7 and SEQ ID NO: 13

SEQ ID NO: 7 and SEQ ID NO: 265 SEQ ID NO: 7 and SEQ ID NO: 266

SEQ ID NO: 7 and SEQ ID NO: 267

SEQ ID NO: 8 and SEQ ID NO: 9

SEQ ID NO: 8 and SEQ ID NO: 10

SEQ ID NO: 8 and SEQ ID NO: 11

SEQ ID NO: 8 and SEQ ID NO: 12

SEQ ID NO: 8 and SEQ ID NO: 13

SEQ ID NO: 8 and SEQ ID NO: 265

SEQ ID NO: 8 and SEQ ID NO: 266

SEQ ID NO: 8 and SEQ ID NO: 267

SEQ ID NO: 9 and SEQ ID NO: 11

SEQ ID NO: 9 and SEQ ID NO: 12

SEQ ID NO: 9 and SEQ ID NO: 13

SEQ ID NO: 9 and SEQ ID NO: 265

SEQ ID NO: 9 and SEQ ID NO: 266

SEQ ID NO: 9 and SEQ ID NO: 267

SEQ ID NO: 10 and SEQ ID NO: 11

SEQ ID NO: 10 and SEQ ID NO: 12

SEQ ID NO: 10 and SEQ ID NO: 13

SEQ ID NO: 10 and SEQ ID NO: 265

SEQ ID NO: 10 and SEQ ID NO: 266

SEQ ID NO: 10 and SEQ ID NO: 267

SEQ ID NO: 11 and SEQ ID NO: 265

SEQ ID NO: 11 and SEQ ID NO: 266 SEQ ID NO: 12 and SEQ ID NO: 265

SEQ ID NO: 12 and SEQ ID NO: 266

SEQ ID NO: 13 and SEQ ID NO: 265

SEQ ID NO: 13 and SEQ ID NO: 266

In certain embodiments, the vaccine formulation comprises at least three different polypeptides having an amino acid sequence comprising any of SEQ ID NOS: 1-13, 265, 266, and 267, or an immunogenic fragment thereof, each polypeptide belonging to a different group of (i)-(vii): (i) SEQ ID NO: 1 or an immunogenic fragment thereof, (ii) one of SEQ ID NOS: 2-5 or an immunogenic fragment thereof, (iii) one of SEQ ID NOS: 6-7 or an immunogenic fragment thereof, (iv) SEQ ID NO: 8 or an immunogenic fragment thereof, (v) one of SEQ ID NOS: 9-10 or an immunogenic fragment thereof, (vi) one of SEQ ID NO: 11-13 and 267, or an

immunogenic fragment thereof, and (vii) one of SEQ ID NOS: 265-266 or an immunogenic fragment thereof. Examples of such combinations are listed below. Additional combinations may be made by replacing one of the sequences below with the corresponding consensus sequence, e.g. , one of SEQ ID NOS: 14-21 or 268-270. In some embodiments, one of the polypeptides is one of SEQ ID NOS: 265-266 and 268 or an immunogenic fragment thereof. In some embodiments, the vaccine formulation further comprises a pneumolysoid. In some embodiments, the vaccine formulation further comprises CbpA or a derivative thereof. In some embodiments, the vaccine formulation further comprises PspA or a derivative thereof comprising all or a fragment of the proline-rich reg ion of PspA.

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 6

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 7

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 8

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 9

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 10

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 11

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 12

SEQ ID NO 1, SEQ ID NO: 2, and SEQ ID NO: 13 SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 6

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 7

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 8

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 9

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 10

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 3, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 6

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 7

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 8

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 9

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 10

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 4; and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 4, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 4, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 4, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 6

SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 7

SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 8 SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 9

SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 10

SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 5; and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 5, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 5, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 5, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 6; and SEQ ID NO: 8

SEQ ID NO: 1, SEQ ID NO: 6; and SEQ ID NO: 9

SEQ ID NO: 1, SEQ ID NO: 6; and SEQ ID NO: 10

SEQ ID NO: 1, SEQ ID NO: 6; and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 6; and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 6; and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 6, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 6, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 6, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 7; and SEQ ID NO: 8

SEQ ID NO: 1, SEQ ID NO: 7; and SEQ ID NO: 9

SEQ ID NO: 1, SEQ ID NO: 7; and SEQ ID NO: 10

SEQ ID NO: 1, SEQ ID NO: 7; and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 7; and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 7; and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 7, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 7, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 7, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 8; and SEQ ID NO: 9

SEQ ID NO: 1, SEQ ID NO: 8; and SEQ ID NO: 10 SEQ ID NO: 1, SEQ ID NO: 8; and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 8; and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 8; and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 8, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 8, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 8, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 9, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 9, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 10; and SEQ ID NO: 11

SEQ ID NO: 1, SEQ ID NO: 10; and SEQ ID NO: 12

SEQ ID NO: 1, SEQ ID NO: 10; and SEQ ID NO: 13

SEQ ID NO: 1, SEQ ID NO: 10, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 10, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 1, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 1, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 1, SEQ ID NO: 267, and SEQ ID NO: 265 SEQ ID NO: 1, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 6; and SEQ ID NO: 8

SEQ ID NO: 2, SEQ ID NO: 6; and SEQ ID NO: 9

SEQ ID NO: 2, SEQ ID NO: 6; and SEQ ID NO: 10

SEQ ID NO: 2, SEQ ID NO: 6; and SEQ ID NO: 11

SEQ ID NO: 2, SEQ ID NO: 6; and SEQ ID NO: 12

SEQ ID NO: 2, SEQ ID NO: 6; and SEQ ID NO: 13

SEQ ID NO: 2, SEQ ID NO: 6, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 6, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 6, and SEQ ID NO: 267

SEQ ID NO: 2, SEQ ID NO: 7; and SEQ ID NO: 8

SEQ ID NO: 2, SEQ ID NO: 7; and SEQ ID NO: 9

SEQ ID NO: 2, SEQ ID NO: 7; and SEQ ID NO: 10

SEQ ID NO: 2, SEQ ID NO: 7; and SEQ ID NO: 11

SEQ ID NO: 2, SEQ ID NO: 7; and SEQ ID NO: 12

SEQ ID NO: 2, SEQ ID NO: 7; and SEQ ID NO: 13

SEQ ID NO: 2, SEQ ID NO: 7, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 7, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 7, and SEQ ID NO: 267

SEQ ID NO: 2, SEQ ID NO: 8; and SEQ ID NO: 9

SEQ ID NO: 2, SEQ ID NO: 8; and SEQ ID NO: 10

SEQ ID NO: 2, SEQ ID NO: 8; and SEQ ID NO: 11

SEQ ID NO: 2, SEQ ID NO: 8; and SEQ ID NO: 12

SEQ ID NO: 2, SEQ ID NO: 8; and SEQ ID NO: 13

SEQ ID NO: 2, SEQ ID NO: 8, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 8, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 8, and SEQ ID NO: 267 SEQ ID NO: 2, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: 2, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: 2, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: 2, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 9, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 9, and SEQ ID NO: 267

SEQ ID NO: 2, SEQ ID NO: 10; and SEQ ID NO: 11

SEQ ID NO: 2, SEQ ID NO: 10; and SEQ ID NO: 12

SEQ ID NO: 2, SEQ ID NO: 10; and SEQ ID NO: 13

SEQ ID NO: 2, SEQ ID NO: 10, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 10, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 2, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 2, SEQ ID NO: 267, and SEQ ID NO: 265

SEQ ID NO: 2, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 6; and SEQ ID NO: 8

SEQ ID NO: 3, SEQ ID NO: 6; and SEQ ID NO: 9

SEQ ID NO: 3, SEQ ID NO: 6; and SEQ ID NO: 10 SEQ ID NO: 3, SEQ ID NO: 6; and SEQ ID NO: 11

SEQ ID NO: 3, SEQ ID NO: 6; and SEQ ID NO: 12

SEQ ID NO: 3, SEQ ID NO: 6; and SEQ ID NO: 13

SEQ ID NO: 3, SEQ ID NO: 6, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 6, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 6, and SEQ ID NO: 267

SEQ ID NO: 3, SEQ ID NO: 7; and SEQ ID NO: 8

SEQ ID NO: 3, SEQ ID NO: 7; and SEQ ID NO: 9

SEQ ID NO: 3, SEQ ID NO: 7; and SEQ ID NO: 10

SEQ ID NO: 3, SEQ ID NO: 7; and SEQ ID NO: 11

SEQ ID NO: 3, SEQ ID NO: 7; and SEQ ID NO: 12

SEQ ID NO: 3, SEQ ID NO: 7; and SEQ ID NO: 13

SEQ ID NO: 3, SEQ ID NO: 7, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 7, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 7, and SEQ ID NO: 267

SEQ ID NO: 3, SEQ ID NO: 8; and SEQ ID NO: 9

SEQ ID NO: 3, SEQ ID NO: 8; and SEQ ID NO: 10

SEQ ID NO: 3, SEQ ID NO: 8; and SEQ ID NO: 11

SEQ ID NO: 3, SEQ ID NO: 8; and SEQ ID NO: 12

SEQ ID NO: 3, SEQ ID NO: 8; and SEQ ID NO: 13

SEQ ID NO: 3, SEQ ID NO: 8, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 8, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 8, and SEQ ID NO: 267

SEQ ID NO: 3, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: 3, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: 3, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: 3, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 9, and SEQ ID NO: 266 SEQ ID NO: 3, SEQ ID NO: 9, and SEQ ID NO: 267

SEQ ID NO: 3, SEQ ID NO: 10; and SEQ ID NO: 11

SEQ ID NO: 3, SEQ ID NO: 10; and SEQ ID NO: 12

SEQ ID NO: 3, SEQ ID NO: 10; and SEQ ID NO: 13

SEQ ID NO: 3, SEQ ID NO: 10, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 10, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 3, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 3, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 3, SEQ ID NO: 267, and SEQ ID NO: 265 SEQ ID NO: 3, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 6; and SEQ ID NO: 8

SEQ ID NO: 4, SEQ ID NO: 6; and SEQ ID NO: 9

SEQ ID NO: 4, SEQ ID NO: 6; and SEQ ID NO: 10

SEQ ID NO: 4, SEQ ID NO: 6; and SEQ ID NO: 11

SEQ ID NO: 4, SEQ ID NO: 6; and SEQ ID NO: 12

SEQ ID NO: 4, SEQ ID NO: 6; and SEQ ID NO: 13

SEQ ID NO: 4, SEQ ID NO: 6, and SEQ ID NO: 265

SEQ ID NO: 4, SEQ ID NO: 6, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 6, and SEQ ID NO: 267 SEQ ID NO: 4, SEQ ID NO: 7; and SEQ ID NO: 8

SEQ ID NO: 4, SEQ ID NO: 7; and SEQ ID NO: 9

SEQ ID NO: 4, SEQ ID NO: 7; and SEQ ID NO: 10

SEQ ID NO: 4, SEQ ID NO: 7; and SEQ ID NO: 11

SEQ ID NO: 4, SEQ ID NO: 7; and SEQ ID NO: 12

SEQ ID NO: 4, SEQ ID NO: 7; and SEQ ID NO: 13

SEQ ID NO: 4, SEQ ID NO: 7, and SEQ ID NO: 265

SEQ ID NO: 4, SEQ ID NO: 7, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 7, and SEQ ID NO: 267

SEQ ID NO: 4, SEQ ID NO: 8; and SEQ ID NO: 9

SEQ ID NO: 4, SEQ ID NO: 8; and SEQ ID NO: 10

SEQ ID NO: 4, SEQ ID NO: 8; and SEQ ID NO: 11

SEQ ID NO: 4, SEQ ID NO: 8; and SEQ ID NO: 12

SEQ ID NO: 4, SEQ ID NO: 8; and SEQ ID NO: 13

SEQ ID NO: 4, SEQ ID NO: 8, and SEQ ID NO: 265

SEQ ID NO: 4, SEQ ID NO: 8, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 8, and SEQ ID NO: 267

SEQ ID NO: 4, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: 4, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: 4, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: 4, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: 4, SEQ ID NO: 9, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 9, and SEQ ID NO: 267

SEQ ID NO: 4, SEQ ID NO: 10; and SEQ ID NO: 11

SEQ ID NO: 4, SEQ ID NO: 10; and SEQ ID NO: 12

SEQ ID NO: 4, SEQ ID NO: 10; and SEQ ID NO: 13

SEQ ID NO: 4, SEQ ID NO: 10, and SEQ ID NO: 265 SEQ ID NO: 4, SEQ ID NO: 10, and SEQ ID NO: 266 SEQ ID NO: 4, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 4, SEQ ID NO: 11, and SEQ ID NO: 265 SEQ ID NO: 4, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 12, and SEQ ID NO: 265 SEQ ID NO: 4, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 13, and SEQ ID NO: 265 SEQ ID NO: 4, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 4, SEQ ID NO: 267, and SEQ ID NO: 265 SEQ ID NO: 4, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 6; and SEQ ID NO: 8

SEQ ID NO: 5, SEQ ID NO: 6; and SEQ ID NO: 9

SEQ ID NO: 5, SEQ ID NO: 6; and SEQ ID NO: 10

SEQ ID NO: 5, SEQ ID NO: 6; and SEQ ID NO: 11

SEQ ID NO: 5, SEQ ID NO: 6; and SEQ ID NO: 12

SEQ ID NO: 5, SEQ ID NO: 6; and SEQ ID NO: 13

SEQ ID NO: 5, SEQ ID NO: 6, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 6, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 6, and SEQ ID NO: 267

SEQ ID NO: 5, SEQ ID NO: 7; and SEQ ID NO: 8

SEQ ID NO: 5, SEQ ID NO: 7; and SEQ ID NO: 9

SEQ ID NO: 5, SEQ ID NO: 7; and SEQ ID NO: 10

SEQ ID NO: 5, SEQ ID NO: 7; and SEQ ID NO: 11

SEQ ID NO: 5, SEQ ID NO: 7; and SEQ ID NO: 12 SEQ ID NO: 5, SEQ ID NO: 7; and SEQ ID NO: 13

SEQ ID NO: 5, SEQ ID NO: 7, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 7, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 7, and SEQ ID NO: 267

SEQ ID NO: 5, SEQ ID NO: 8; and SEQ ID NO: 9

SEQ ID NO: 5, SEQ ID NO: 8; and SEQ ID NO: 10

SEQ ID NO: 5, SEQ ID NO: 8; and SEQ ID NO: 11

SEQ ID NO: 5, SEQ ID NO: 8; and SEQ ID NO: 12

SEQ ID NO: 5, SEQ ID NO: 8; and SEQ ID NO: 13

SEQ ID NO: 5, SEQ ID NO: 8, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 8, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 8, and SEQ ID NO: 267

SEQ ID NO: 5, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: 5, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: 5, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: 5, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 9, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 9, and SEQ ID NO: 267

SEQ ID NO: 5, SEQ ID NO: 10; and SEQ ID NO: 11

SEQ ID NO: 5, SEQ ID NO: 10; and SEQ ID NO: 12

SEQ ID NO: 5, SEQ ID NO: 10; and SEQ ID NO: 13

SEQ ID NO: 5, SEQ ID NO: 10, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 10, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 5, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 11, and SEQ ID NO: 266 SEQ ID NO: 5, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 5, SEQ ID NO: 267, and SEQ ID NO: 265

SEQ ID NO: 5, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 6, SEQ ID NO: 8; and SEQ ID NO: 9

SEQ ID NO: 6, SEQ ID NO: 8; and SEQ ID NO: 10

SEQ ID NO: 6, SEQ ID NO: 8; and SEQ ID NO: 11

SEQ ID NO: 6, SEQ ID NO: 8; and SEQ ID NO: 12

SEQ ID NO: 6, SEQ ID NO: 8; and SEQ ID NO: 13

SEQ ID NO: 6, SEQ ID NO: 8, and SEQ ID NO: 265

SEQ ID NO: 6, SEQ ID NO: 8, and SEQ ID NO: 266

SEQ ID NO: 6, SEQ ID NO: 8, and SEQ ID NO: 267

SEQ ID NO: 6, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: 6, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: 6, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: 6, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: 6, SEQ ID NO: 9, and SEQ ID NO: 266

SEQ ID NO: 6, SEQ ID NO: 9, and SEQ ID NO: 267

SEQ ID NO: 6, SEQ ID NO 10; and SEQ ID NO: 11

SEQ ID NO: 6, SEQ ID NO 10; and SEQ ID NO: 12

SEQ ID NO: 6, SEQ ID NO 10; and SEQ ID NO: 13

SEQ ID NO: 6, SEQ ID NO 10, and SEQ ID NO: 265

SEQ ID NO: 6, SEQ ID NO 10, and SEQ ID NO: 266 SEQ ID NO: 6, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 6, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: 6, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 6, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 6, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 6, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 6, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 6, SEQ ID NO: 267, and SEQ ID NO: 265

SEQ ID NO: 6, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: v, SEQ ID NO: 8; and SEQ ID NO: 9

SEQ ID NO: v, SEQ ID NO: 8; and SEQ ID NO: 10

SEQ ID NO: v, SEQ ID NO: 8; and SEQ ID NO: 11

SEQ ID NO: v, SEQ ID NO: 8; and SEQ ID NO: 12

SEQ ID NO: v, SEQ ID NO: 8; and SEQ ID NO: 13

SEQ ID NO: v, SEQ ID NO: 8, and SEQ ID NO: 265

SEQ ID NO: v, SEQ ID NO: 8, and SEQ ID NO: 266

SEQ ID NO: v, SEQ ID NO: 8, and SEQ ID NO: 267

SEQ ID NO: v, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: v, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: v, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: v, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: v, SEQ ID NO: 9, and SEQ ID NO: 266

SEQ ID NO: v, SEQ ID NO: 9, and SEQ ID NO: 267 SEQ ID NO: v, SEQ ID NO: 10; and SEQ ID NO: 11

SEQ ID NO: v, SEQ ID NO: 10; and SEQ ID NO: 12

SEQ ID NO: v, SEQ ID NO: 10; and SEQ ID NO: 13

SEQ ID NO: v, SEQ ID NO: 10, and SEQ ID NO: 265

SEQ ID NO: v, SEQ ID NO: 10, and SEQ ID NO: 266

SEQ ID NO: v, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: v, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: v, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: v, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: v, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: v, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: v, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: v, SEQ ID NO: 267, and SEQ ID NO: 265

SEQ ID NO: v, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 8, SEQ ID NO: 9; and SEQ ID NO: 11

SEQ ID NO: 8, SEQ ID NO: 9; and SEQ ID NO: 12

SEQ ID NO: 8, SEQ ID NO: 9; and SEQ ID NO: 13

SEQ ID NO: 8, SEQ ID NO: 9, and SEQ ID NO: 265

SEQ ID NO: 8, SEQ ID NO: 9, and SEQ ID NO: 266

SEQ ID NO: 8, SEQ ID NO: 9, and SEQ ID NO: 267

SEQ ID NO: 8, SEQ ID NO: 10; and SEQ ID NO: 11

SEQ ID NO: 8, SEQ ID NO: 10; and SEQ ID NO: 12

SEQ ID NO: 8, SEQ ID NO: 10; and SEQ ID NO: 13

SEQ ID NO: 8, SEQ ID NO: 10, and SEQ ID NO: 265 SEQ ID NO: 8, SEQ ID NO: 10, and SEQ ID NO: 266

SEQ ID NO: 8, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 8, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: 8, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 8, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 8, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 8, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 8, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 8, SEQ ID NO: 267, and SEQ ID NO: 265

SEQ ID NO: 8, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 9, SEQ ID NO: 10, and SEQ ID NO: 265

SEQ ID NO: 9, SEQ ID NO: 10, and SEQ ID NO: 266

SEQ ID NO: 9, SEQ ID NO: 10, and SEQ ID NO: 267

SEQ ID NO: 9, SEQ ID NO: 11, and SEQ ID NO: 265

SEQ ID NO: 9, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 9, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 8, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 9, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 9, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 9, SEQ ID NO: 267, and SEQ ID NO: 265

SEQ ID NO: 9, SEQ ID NO: 267, and SEQ ID NO: 266

SEQ ID NO: 10, SE( ID NO: 11, and SEQ ID NO: 265 SEQ ID NO: 10, SEQ ID NO: 11, and SEQ ID NO: 266

SEQ ID NO: 10, SEQ ID NO: 12, and SEQ ID NO: 265

SEQ ID NO: 10, SEQ ID NO: 12, and SEQ ID NO: 266

SEQ ID NO: 10, SEQ ID NO: 13, and SEQ ID NO: 265

SEQ ID NO: 10, SEQ ID NO: 13, and SEQ ID NO: 266

SEQ ID NO: 10, SEQ ID NO: 267, and SEQ ID NO: 265

SEQ ID NO: 10, SEQ ID NO: 267, and SEQ ID NO: 266

In some embodiments, the vaccine formulation comprises at least two different polypeptides having an amino acid sequence comprising any of SEQ ID NOS: 14-21, 268, 269 and 270, or an immunogenic fragment thereof. In certain such embodiments, the vaccine formulation comprises at least two polypeptides, each polypeptide belonging to a different group of (i)-(v): (i) one of SEQ ID NOS: 14-17 or an immunogenic fragment thereof, (ii) one of SEQ ID NOS: 18-19 or an immunogenic fragment thereof; (iii) one of SEQ ID NOS: 20-21 or an immunogenic fragment thereof, (iv) one of SEQ ID NO: 268 or an immunogenic fragment thereof, and (v) one of SEQ ID NOS: 269-279 or an immunogenic fragment thereof. Examples of such combinations are listed below. The combinations below specify consensus sequences. However, additional combinations may be made by replacing one of the consensus sequences with the corresponding non-consensus sequence, e.g., one of SEQ ID NOS: 1-13 or 266-267. In some embodiments, one of the polypeptides is SEQ ID NO: 268 or an immunogenic fragment thereof. In some embodiments, the vaccine formulation further comprises a pneumolysoid. In some embodiments, the vaccine formulation further comprises CbpA or a derivative thereof. In some embodiments, the vaccine formulation further comprises PspA or a derivative thereof comprising all or a fragment of the proline-rich region of PspA.

SEQ ID NO: 14 and SEQ ID NO: 18

SEQ ID NO: 14 and SEQ ID NO: 19

SEQ ID NO: 14 and SEQ ID NO: 20

SEQ ID NO: 14 and SEQ ID NO: 21 SEQ ID NO: 14 and SEQ ID NO: 268

SEQ ID NO: 14 and SEQ ID NO: 269

SEQ ID NO: 14 and SEQ ID NO: 270

SEQ ID NO: 15 and SEQ ID NO: 18

SEQ ID NO: 15 and SEQ ID NO: 19

SEQ ID NO: 15 and SEQ ID NO: 20

SEQ ID NO: 15 and SEQ ID NO: 21

SEQ ID NO: 15 and SEQ ID NO: 268

SEQ ID NO: 15 and SEQ ID NO: 269

SEQ ID NO: 15 and SEQ ID NO: 270

SEQ ID NO: 16 and SEQ ID NO: 18

SEQ ID NO: 16 and SEQ ID NO: 19

SEQ ID NO: 16 and SEQ ID NO: 20

SEQ ID NO: 16 and SEQ ID NO: 21

SEQ ID NO: 16 and SEQ ID NO: 268

SEQ ID NO: 16 and SEQ ID NO: 269

SEQ ID NO: 16 and SEQ ID NO: 270

SEQ ID NO: 17 and SEQ ID NO: 18

SEQ ID NO: 17 and SEQ ID NO: 19

SEQ ID NO: 17 and SEQ ID NO: 20

SEQ ID NO: 17 and SEQ ID NO: 21

SEQ ID NO: 17 and SEQ ID NO: 268

SEQ ID NO: 17 and SEQ ID NO: 269

SEQ ID NO: 17 and SEQ ID NO: 270 SEQ ID NO: 18 and SEQ ID NO: 20

SEQ ID NO: 18 and SEQ ID NO: 21

SEQ ID NO: 18 and SEQ ID NO: 268

SEQ ID NO: 18 and SEQ ID NO: 269

SEQ ID NO: 18 and SEQ ID NO: 270

SEQ ID NO: 19 and SEQ ID NO: 20

SEQ ID NO: 19 and SEQ ID NO: 21

SEQ ID NO: 19 and SEQ ID NO: 268

SEQ ID NO: 19 and SEQ ID NO: 269

SEQ ID NO: 19 and SEQ ID NO: 270

SEQ ID NO: 20 and SEQ ID NO: 268

SEQ ID NO: 20 and SEQ ID NO: 269

SEQ ID NO: 20 and SEQ ID NO: 270

SEQ ID NO: 21 and SEQ ID NO: 268

SEQ ID NO: 21 and SEQ ID NO: 269

SEQ ID NO: 21 and SEQ ID NO: 270

SEQ ID NO: 268 and SEQ ID NO: 269

SEQ ID NO: 268 and SEQ ID NO: 270

In some embodiments, the fragment is a truncated fragment of any of SEQ ID NOS: 14- 21 and 268-270 wherein from 1-20 amino acid residues are removed from the N-terminus, C- terminus, or both.

In some embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising any of SEQ ID NOS: 14-17. In some embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising either of SEQ ID NOS: 18-19. In some embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising either of SEQ ID NOS: 20-21. In some embodiments, the vaccine formulation comprises a polypeptide having an amino acid sequence comprising any of SEQ ID NOS: 268-270.

In some aspects, a vaccine formulation comprising one or more of SEQ ID NOS: 14-21, 268, 269 and 270 further comprises a polypeptide having an amino acid sequence comprising any of SEQ ID NOS: 1-13, 265, 266 and 267.

In certain embodiments, the vaccine formulation comprises at least three different polypeptides having an amino acid sequence comprising any of SEQ ID NOS: 14-21, 268, 269 and 270, or an immunogenic fragment thereof. In certain such embodiments, the vaccine formulation comprises three of (i)-(v): (i) one of SEQ ID NOS: 14-17 or an immunogenic fragment thereof, (ii) one of SEQ ID NOS: 18-19 or an immunogenic fragment thereof; and (iii) one of SEQ ID NOS: 20-21 or an immunogenic fragment thereof, (iv) one of SEQ ID NO: 268 or an immunogenic fragment thereof, and (v) one of SEQ ID NOS: 269-270 or an immunogenic fragment thereof. Examples of such combinations are listed below. The combinations below specify consensus sequences. However, additional combinations may be made by replacing one of the consensus sequences with the corresponding non-consensus sequence, e.g., one of SEQ ID NOS: 1-13 or 266-267. In some embodiments, one of the polypeptides is SEQ ID NO: 268 or an immunogenic fragment thereof. In some embodiments, the vaccine formulation further comprises a pneumolysoid. In some embodiments, the vaccine formulation further comprises CbpA or a derivative thereof. In some embodiments, the vaccine formulation further comprises PspA or a derivative thereof comprising all or a fragment of the proline-rich region of PspA.

SEQ ID NO 14, SEQ ID NO 18, and SEQ ID NO: 20

SEQ ID NO 14, SEQ ID NO 18, and SEQ ID NO: 21

SEQ ID NO 14, SEQ ID NO 18, and SEQ ID NO: 268

SEQ ID NO 14, SEQ ID NO 18, and SEQ ID NO: 269

SEQ ID NO 14, SEQ ID NO 18, and SEQ ID NO: 270 SEQ ID NO: 14, SEQ ID NO: 19, and SEQ ID NO: 20

SEQ ID NO: 14, SEQ ID NO: 19, and SEQ ID NO: 21 SEQ ID NO: 14, SEQ ID NO: 19, and SEQ ID NO: 268 SEQ ID NO: 14, SEQ ID NO: 19, and SEQ ID NO: 269 SEQ ID NO: 14, SEQ ID NO: 19, and SEQ ID NO: 270 SEQ ID NO: 14, SEQ ID NO: 268, and SEQ ID NO: 269

SEQ ID NO: 14, SEQ ID NO: 268, and SEQ ID NO: 270

SEQ ID NO: 15, SEQ ID NO: 18, and SEQ ID NO: 20

SEQ ID NO: 15, SEQ ID NO: 18, and SEQ ID NO: 21

SEQ ID NO: 15, SEQ ID NO: 18, and SEQ ID NO: 268

SEQ ID NO: 15, SEQ ID NO: 18, and SEQ ID NO: 269

SEQ ID NO: 15, SEQ ID NO: 18, and SEQ ID NO: 270

SEQ ID NO: 15, SEQ ID NO: 19, and SEQ ID NO: 20

SEQ ID NO: 15, SEQ ID NO: 19, and SEQ ID NO: 21

SEQ ID NO: 15, SEQ ID NO: 19, and SEQ ID NO: 268

SEQ ID NO: 15, SEQ ID NO: 19, and SEQ ID NO: 269

SEQ ID NO: 15, SEQ ID NO: 19, and SEQ ID NO: 270

SEQ ID NO: 15, SEQ ID NO: 268, and SEQ ID NO: 269 SEQ ID NO: 15, SEQ ID NO: 268, and SEQ ID NO: 270

SEQ ID NO: 16, SEQ ID NO: 18, and SEQ ID NO: 20

SEQ ID NO: 16, SEQ ID NO: 18, and SEQ ID NO: 21

SEQ ID NO: 16, SEQ ID NO: 18, and SEQ ID NO: 268

SEQ ID NO: 16, SEQ ID NO: 18, and SEQ ID NO: 269

SEQ ID NO: 16, SEQ ID NO: 18, and SEQ ID NO: 270

SEQ ID NO: 16, SEQ ID NO: 19, and SEQ ID NO: 20

SEQ ID NO: 16, SEQ ID NO: 19, and SEQ ID NO: 21

SEQ ID NO: 16, SEQ ID NO: 19, and SEQ ID NO: 268 SEQ ID NO: 16, SEQ ID NO: 19, and SEQ ID NO: 269 SEQ ID NO: 16, SEQ ID NO: 19, and SEQ ID NO: 270

SEQ ID NO: 16, SEQ ID NO: 268, and SEQ ID NO: 269 SEQ ID NO: 16, SEQ ID NO: 268, and SEQ ID NO: 270

SEQ ID NO: IV, SEQ ID NO: 18, and SEQ ID NO: 20

SEQ ID NO: IV, SEQ ID NO: 18, and SEQ ID NO: 21

SEQ ID NO: IV, SEQ ID NO: 18, and SEQ ID NO: 268

SEQ ID NO: IV, SEQ ID NO: 18, and SEQ ID NO: 269

SEQ ID NO: IV, SEQ ID NO: 18, and SEQ ID NO: 270

SEQ ID NO: IV, SEQ ID NO: 19, and SEQ ID NO: 20

SEQ ID NO: IV, SEQ ID NO: 19, and SEQ ID NO: 21

SEQ ID NO: IV, SEQ ID NO: 19, and SEQ ID NO: 268

SEQ ID NO: IV, SEQ ID NO: 19, and SEQ ID NO: 269

SEQ ID NO: IV, SEQ ID NO: 19, and SEQ ID NO: 270

SEQ ID NO: 17, SEQ ID NO: 268, and SEQ ID NO: 269 SEQ ID NO: 17, SEQ ID NO: 268, and SEQ ID NO: 270

SEQ ID NO: 18, SEQ ID NO: 20, and SEQ ID NO: 268

SEQ ID NO: 18, SEQ ID NO: 20, and SEQ ID NO: 269

SEQ ID NO: 18, SEQ ID NO: 20, and SEQ ID NO: 270

SEQ ID NO: 18, SEQ ID NO: 21, and SEQ ID NO: 268

SEQ ID NO: 18, SEQ ID NO: 21, and SEQ ID NO: 269

SEQ ID NO: 18, SEQ ID NO: 21, and SEQ ID NO: 270

SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 268 SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 269

SEQ ID NO: 19, SEQ ID NO: 20, and SEQ ID NO: 270

SEQ ID NO: 19, SEQ ID NO: 21, and SEQ ID NO: 268

SEQ ID NO: 19, SEQ ID NO: 21, and SEQ ID NO: 269

SEQ ID NO: 19, SEQ ID NO: 21, and SEQ ID NO: 270

SEQ ID NO: 20, SEQ ID NO: 268, and SEQ ID NO: 269

SEQ ID NO: 20, SEQ ID NO: 268, and SEQ ID NO: 270

SEQ ID NO: 21, SEQ ID NO: 268, and SEQ ID NO: 269

SEQ ID NO: 21, SEQ ID NO: 268, and SEQ ID NO: 270

A polypeptide may comprise one or more immunogenic portions and one or more non- immunogenic portions. The immunogenic portions may be identified by various methods, including protein microarrays, ELISPOT/ELISA techniques, and/or specific assays on different deletion mutants (e.g., fragments) of the polypeptide in question. Immunogenic portions may also be identified by computer algorithms. Some such algorithms, like EpiMatrix (produced by EpiVax), use a computational matrix approach. Other computational tools for identifying antigenic epitopes include PEPVAC (Promiscuous EPitope-based VACcine, hosted by Dana Farber Cancer Institute on the world wide web at immunax.dfci.harvard.edu/PEPVAC), MHCPred (which uses a partial least squares approach and is hosted by The Jenner Institute on the world wide web at www.jenner.ac.uk/MHCPred), and Immune Epitope Database algorithms on the world wide web at tools.immuneepitope.org. An immunogenic fragment of a polypeptide described herein comprises at least one immunogenic portion, as measured experimentally or identified by algorithm. Peptides identified by the tools described above include the following: SP2108 SP0148 SP1634 SP0882 SP0314

Fragments Fragments Fragments Fragments Fragments

(SEQ ID NOS 34- (SEQ ID NOS (SEQ ID NOS (SEQ ID NOS (SEQ ID NOS

57, respectively, in 58-82, 83-109, 110-130, 131-169, order of respectively, in respectively, respectively, in respectively, in appearance) order of in order of order of order of

appearance) appearance) appearance) appearance)

AIIDGPWKA ALGLVAAGV RLLDLAPQV HLDNLVLKV MLKDKIAFL

VMMAPYDRV ELTGYEIEV MLEIPAHQI DLIAGRVHL SLADYTYKV

SIAGINYAK AVNNLSYTK KNFFAHHPK ILLPKDYEK FLLLGAFYL

VWDPAKNML TYLPAEADI KVILAGHSK EYQDQIGCL VLIDGLSQL

QPLPNISQM RYNMAVNNL SFDNLVSTL YFHDGQNVF ILASLGFLL

APYDRVGSL DFQQIMVRL YYDLPLNEL NPDISRMIV GLSQLLPVI

APAVIESLV EHTDNPTIL YFDLFFGTI IPWSENLPD FLLNHYMTV

FYYTYGLLA APIAQNPNV ALEYIHHLF QFGGKGVEY MLIPNVDRA

SKYAFAGE LPSDQQPYV LPLNELDIL IGLEYQDQI KLEEMAKQV

TEGAGNLI YVYPLLAQG IPQGSIIGM VYFHDGQN VLKRGVYTI

LADWTNFYY QGLDNLKVI DPELQKQFA MEVVKPFI KVIAGLLRK

SLVMYYNKD KYLYAAPI AVYTFDAPG YLKMKEHKL TLNYEHMNK

KEAGVKVTL GELTGYEI QSLTPEERE KLSPDQRIF NIGYFFFKK

KSTAVLGTV NPNVLVVKK AIYAASQI RIFIYVGTE KYTDVIEKF

GAKTDDTTK KLSKQFFGD LEIPAHQI FIDETYRTK KYDDSVSTI

SQKFVDFLV GSPRPFIYE LLDLAPQVP DTDRSYPVV TFNQMIKEL

QAFKDAKVN AVNNLSYTK WQIEDKHFV YIDSSLCYY DYPETQSVF

AVIESLVMY KIFDKIGVE TLGRLTQLL TQFIGLEYQ TPRAINNTL

DAKTAANDA MVRLSDGQF LYFDLFFGT KDTDRSYPV APLLVNGEL

YGVATIPTL YVYPLLAQG SINDLASLK LCYYHDLIA YIDHTNVAY

KTAAIIDGP VVQATTSAK SINDLASLK NVFNSKESF KQNGDSYGY

KAYEKEAGV TLEKLSKQF YYDLPLNEL FLLNHYMTV AGNGAYVFG VAAGVLAAC QKVILAGHS FYLYNGDLS

AWVIPQAVK LDNLKVIEL GTDDSIIGW KSFAPLLV

NMAVNNLSY TYLSFDNLV DETVVRTV

FGTILDAGI YIDHTNVAY

NQITAVYTF MLKDKIAFL

KLRFKIKTD

KLELFYETG

KIAFLGSNI

SVPRTSYLS

FGFGLSLFS

STIRSIEQV

FRKTTDNPF

TVVRTVRDS

STIRSIEQV

DGLSQLLPV

FGFGLSLFS

KLVDQGEGF

KPKTRVAIV DAAKFYHAI EGQGRNRKL ALLGIGSLALATKKVAK

LHGQLNLPL DTALEELER EIKGAGDLR KMWMAGLALLGIG

LHVAQALGL EEYQGVPFI EPIAEGQYF SDMGEIATLYVQVYE

DMGEIATLYVQVYES

LPLKPKTRV EFLEKIAPL EVSELKPHR

AGLALLGIGSLALAT

MGTREIVVL EFQVLYDLL GAFFDKSKI

MGEIATLYVQVYESS

MQLLIESPL EHVEHLKRL GDLKWDGLI

KKMWMAGLALLGIGS

QANQAYVAL ELSEVEMTR GEVEKNLEV

GMKAKKMWMAGLALL

QFMQANQAY ESPLVLNDY IHFESVEEM

MKAKKMWMAGLALLG

QLNLPLKPK GEKTPSFNV IMFIVGIFL HFSDMGEIATLYVQV

QQMGTREIV GLCPFHGEK IPGTLNKGI MNGMKAKKMWMAGLA

REIVVLHHT IGDMPVQIV IRYQVFTFK MWMAGLALLGIGSLA

SPLIPDDVI ITMPVTKQL ISDKGGFNW DHFSDMGEIATLYVQ

SRLHVAQAL KALLNQDNM IVSEEDFIL RDHFSDMGEIATLYV

TEDMIRSLV KRLTKKLVL KEIGVEEAI NGMKAKKMWMAGLAL

VDVSDQDFL LTKTRISPI KIVVKDFAR

VSDQDFLPF LVLVYDGDK KKINFQPSL

VTEDMIRSL MRAEAHLLY KLKFVYIGK

NGPEDLAYL KVYYGNNYK

QTEEVERAW KYWQAIRAL

SEIYLMEGF LHIDNTRDF

SPHQALYDM MRFKKEDLK

VDKQVIEEI NESVVDNYL

VEMTRNKAL NEVWYAGAA

VLYDLLGQY NINDIVDGL

VPFIEAVQI QYLLKDNII

WYQVLAQDL SPRQQGAGL

YLMEGFMDV SRSKTLGGY

SSLKNTKVL

TAAVILAAY

WTELPAMGY Thus, in some aspects, this application provides an immunogenic fragment of an antigen described herein. The fragments, in some instances, are close in size to the full-length polypeptide or the polypeptide of Table 1 or 2. For example, they may lack at most one, two, three, four, five, ten, twenty, or thirty amino acids from one or both termini. In certain embodiments, the polypeptide is 100-500 amino acids in length, or 150-450, or 200-400, or 250- 250 amino acids in length. In some embodiments, the polypeptide is 100-200, 150-250, 200- 300, 250-350, 300-400, 350-450, or 400-500 amino acids in length. In certain embodiments, the fragments result from processing, or partial processing, of signal sequences by an expression host, e.g. E. coli, an insect cell line (e.g., the baculovirus expression system), or a mammalian (e.g., human or Chinese Hamster Ovary) cell line. The fragments described above or sub- fragments thereof (e.g., fragments of 8-50, 8-30, or 8-20 amino acid residues) preferably have one of the biological activities described below, such as increasing the amount of IL-17 released by at least 1.5 fold or 2 fold or more (e.g., either as an absolute measure or relative to an immunologically inactive protein). A fragment may be used as the polypeptide in the vaccines described herein or may be fused to another protein, protein fragment or a polypeptide.

In some embodiments, the fragment is a truncated fragment of any of SEQ ID NOS: 1-21 or 265-270, having from 1-5, 1-10, or 1-20 amino acid residues removed from the N-terminus, C-terminus, or both. In some such embodiments, the same number of residues is removed from the N-terminus and the C-terminus, while in other embodiments, a different number of residues is removed from the N-terminus compared to the C-terminus.

In certain aspects, this application provides immunogenic polypeptides with at least 90%, 95%, 97%, 98%, 99%, or 99.5% identity to a polypeptide of Table 1 or 2. In certain

embodiments, the vaccine formulation comprises at least two different polypeptides having an amino acid sequence comprising a sequence at least 90%, 95%, 98%, or 99% identical to any of SEQ ID NOS: 1-21 or 265-270, or an immunogenic fragment thereof.

In some embodiments, one or more, e.g., two, three, four, or more polypeptides from Table 1 or 2 or immunogenic fragments or variants thereof are provided in a mixture. In some embodiments, the mixture contains both full-length polypeptides and fragments resulting from processing, or partial processing, of signal sequences by an expression host, e.g. E. coli, an insect cell line (e.g., the baculovirus expression system), or a mammalian (e.g., human or Chinese Hamster Ovary) cell line. In some embodiments, rather than being in a simple physical mixture, two, three, four, or more polypeptides from Table 1 or 2 or immunogenic fragments or variants thereof are covalently bound to each other, e.g. as a fusion protein. In some embodiments, the vaccine formulation contains substantially no other S. pneumoniae polypeptides other than polypeptides having an amino acid sequence comprising any of SEQ ID NOS: 1-23 or 265-270. In some embodiments, the vaccine formulation contains substantially no other S. pneumoniae

polypeptides other than polypeptides of Table 1. In some embodiments, the vaccine formulation contains substantially no other S. pneumoniae polypeptides other than polypeptides of Tables 1 and/or 2.

In certain embodiments, vaccine formulations or immunogenic compositions contain substantially no other S. pneumoniae polypeptides other than polypeptides having an amino acid sequence comprising any of SEQ ID NO: 1-23 or 265-270. In certain such embodiments, vaccine formulations or immunogenic compositions contain substantially no other S.

pneumoniae polypeptides other than polypeptides having an amino acid sequence consisting of any of SEQ ID NO: 1-23 or 265-270. In some embodiments, vaccine formulations or immunogenic compositions contain substantially no other S. pneumoniae polypeptides other than polypeptides having an amino acid sequence comprising (or consisting of) any of the amino acid sequences of the polypeptides of Tables 1 and/or 2. Substantially, in this context, refers to less than 50%, less than 40%, less than 30%, less than 20%, less than 10%, less than 5%, less than 3%, less than 2, or even less than 1% of the other S. pneumoniae polypeptides.

In certain embodiments, the vaccine composition induces a ¾17 cell response at least 1.5-fold greater than that induced by a control unrelated antigen (such as the HSV-2 protein ICP47 with the gene name US 12) after contacting ¾17 cells. In some embodiments, the vaccine formulation inhibits infection by S. pneumoniae in an uninfected subject. In certain

embodiments, the vaccine formulation reduces occurrence or duration of S. pneumoniae nasopharyngeal colonization in an individual infected by S. pneumoniae. In some embodiments, the vaccine formulation inhibits development of sepsis in an individual infected by S.

pneumoniae. In some embodiments, the vaccine formulation inhibits development of pneumonia, meningitis, otitis media, sinusitis or infection of other sites or organs with S.

pneumoniae. In certain embodiments, this application provides nucleic acids encoding one or more of the polypeptides described above, such as DNA, RNA, or an analog thereof. The underlying DNA sequences for the polypeptides described above may be modified in ways that do not affect the sequence of the protein product, and such sequences are included in the invention. For instance, the DNA sequence may be codon-optimized to improve expression in a host such as E. coli, an insect cell line (e.g., using the baculovirus expression system), or a mammalian (e.g., human or Chinese Hamster Ovary) cell line.

In certain embodiments, this application provides nucleic acids (such as DNA, RNA, or an analog thereof) that are at least 70%, 80%, 90%, 95%, 97%, 98%, 99%, or 100% identical to a gene in Table 1 or 2, or a variant or portion of said gene. In certain embodiments, the nucleic acid is 600-2000, 800-1800, 1000-1600, 1200-1400 nucleotides in length. In some

embodiments, the nucleic acid is 600-1600, 800-1800, or 1000-2000 nucleotides in length. The nucleic acids may be used, for example, for recombinant production of the polypeptides of Tables 1 and 2, or immunogenic fragments thereof.

In some embodiments, the vaccine or immunogenic composition may comprise fusion proteins and/or fusion DNA constructs. The polypeptides described herein may be used without modification. In certain embodiments, when smaller related polypeptides are used, such as fragments or the like, and their molecular weight is less than about 5000 daltons, e.g., 1500 to 5000 daltons, modification may be useful in eliciting the desired immune response. For example, the smaller polypeptides can be conjugated to an appropriate immunogenic carrier such as tetanus toxoid, pneumolysin, keyhole limpet hemocyanin or the like.

In certain embodiments, the vaccine formulation comprises at least one lipidated polypeptide. Conjugation to the lipid moiety may be direct or indirect (e.g., via a linker). The lipid moiety may be synthetic or naturally produced. In certain embodiments, a polypeptide from Table 1 or 2 may be chemically conjugated to a lipid moiety. In certain embodiments, a construct may comprise a gene or polypeptide from Table 1 or 2, or an immunogenic fragment or variant thereof, and a lipidation sequence including a lipobox motif. A canonical lipobox motif is shown as SEQ ID NO: 274. A lipidation sequence may be N-terminal or C-terminal to the protein, and may be embedded in a signal or other sequence, or in a fusion protein. Exemplary lipidation sequences include the signal sequence of SP2108 (SEQ ID NO: 275) and the signal sequence of the E. coli gene RlpB (SEQ ID NO: 276). A signal sequence may be, for example, an E. coli or S. pneumoniae signal sequence. Exemplary E. coli signal sequences include the mlpA signal sequence (Lin, J.J. et al., "An Escherichia coli mutant with an amino acid alteration within the signal sequence of outer membrane prolipoprotein" Proc Natl Acad Sci U S A. 1978 Oct;75(10):4891-5 ), the lamB signal sequence (Emr, S.D. et al. "Mutations altering the cellular localization of the phage lambda receptor, an Escherichia coli outer membrane protein", Proc Natl Acad Sci U S A. 1978 Dec;75(12):5802-6), the MBP signal sequence (Bassford, P.J., "Use of gene fusion to study secretion of maltose-binding protein into Escherichia coli periplasm" J Bacteriol. 1979 Jul;139(l): 19-31). Lpp is an exemplary E. coli signal sequence that directs lipidation (Cullen, P.A. et al. "Construction and evaluation of a plasmid vector for the expression of recombinant lipoproteins in Escherichia coi Plasmid. 2003 Jan;49(l): 18-29.) E. coli signal sequences that direct lipidation are also described in Legrain, M. et al. ("Production of lipidated meningococcal transferrin binding protein 2 in Escherichia coli" Protein Expr Purif. 1995 Oct;6(5):570-8), e.g. the signal sequence of the gene RlpB (SEQ ID NO: 276) Numerous S. pneumoniae signal sequences are known in the art. One such signal sequence is SEQ ID NO: 275.

In other embodiments, a construct may comprise a gene or protein from Table 1 or 2, or an immunogenic fragment or variant thereof, and a tag. A tag may be N-terminal or C-terminal. For instance, tags may be added to the nucleic acid or polypeptide to facilitate purification, detection, solubility, or confer other desirable characteristics on the protein or nucleic acid. For instance, a purification tag may be a peptide, oligopeptide, or polypeptide that may be used in affinity purification. Examples include His, GST, TAP, FLAG, myc, HA, MBP, VSV-G, thioredoxin, V5, avidin, streptavidin, BCCP, Calmodulin, Nus, S tags, lipoprotein D, and β galactosidase. Particular exemplary His tags include HHHHHH (SEQ ID NO: 32) and

MSYYHHHHHH (SEQ ID NO: 33). In other embodiments, the polypeptide is free of tags such as protein purification tags, and is purified by a method not relying on affinity for a purification tag. In some embodiments, the fused portion is short. This, in some instances, the fusion protein comprises no more than 1, 2, 3, 4, 5, 10, or 20 additional amino acids on one or both termini of the polypeptide of Table 1 or 2. B. Immunogenic compositions

The present disclosure also provides pharmaceutical compositions containing

immunogenic polypeptides or polynucleotides encoding these immunogenic polypeptides together with a pharmaceutical carrier. Antigens from S. pneumoniae were identified by screening immune cells from mice infected with S. pneumoniae, or from healthy human donors. The human donors had presumably been exposed to S. pneumoniae at some point during their lifetimes, because S. pneumoniae is a very common disease and colonizing pathogen. Briefly, a library of S. pneumoniae antigens was expressed in bacteria and mixed with antigen presenting cells (APCs). The APCs, in turn, presented S. pneumoniae-dehved polypeptides to lymphocytes that had been isolated from mice or from human donors. Lymphocyte responses were assayed for reactivity to S. pneumoniae. Human donors, as well as mice immunized with S. pneumoniae, produced lymphocytes specific to S. pneumoniae antigens. Thus, the present disclosure contemplates compositions of the S. pneumoniae antigens that elicit a strong immune response in immunized or infected mice or humans for counteracting infection by S. pneumoniae.

Tables 1 and 2 list the protein sequence and corresponding nucleotide sequence for S. pneumoniae antigens identified according to the screening methods described herein. The antigens were identified in screens of mouse and human T cells. In the screens of mouse T cells, the identified antigens were subjected to at least two rounds of screening: a genome-wide round to identify pools of 4 antigens that elicited an immune response, followed by a deconvolution round to individually test and identify single antigens that elicited an immune response from a pool identified in the genome- wide round. In contrast, in the screens of human T cells, two different sets of antigen pools were created, such that a polypeptide was combined with different polypeptides between the first and second pools. Consequently, it is possible to determine which polypeptides are antigens by identifying which polypeptides are in positive pools in both the first and second sets. Table 1 lists antigens (and variants thereof) that were identified by one of the above screening methods, and were subsequently subjected to further testing in the mouse models described in Examples 5-12. Thus, compositions according to this disclosure may include one or two or more of the genes listed in Table 1 or 2, or the corresponding gene products.

An immunogenic composition may also comprise portions of said Streptococcus polypeptides, for example deletion mutants, truncation mutants, oligonucleotides, and peptide fragments. In some embodiments, the portions of said polypeptides are immunogenic. The immunogenicity of a portion of a protein is readily determined using the same assays that are used to determine the immunogenicity of the full-length protein. In some embodiments, the portion of the polypeptide has substantially the same immunogenicity as the full-length proteins. In some embodiments, the immunogenicity is no more than 10%, 20%, 30%, 40%, or 50% less than that of the full-length protein (e.g., polypeptides of Tables 1 and 2). The peptide fragments may be, for example, linear, circular, or branched.

Some embodiments of the vaccine formulations and immunogenic compositions described herein include an immunogenic polypeptide (e.g., a polypeptide of Table 1 or 2) that contains a membrane translocating sequence (MTS), to facilitate introduction of the polypeptide into the mammalian cell and subsequent stimulation of the cell-mediated immune response. Exemplary membrane translocating sequences include hydrophobic region in the signal sequence of Kaposi fibroblast growth factor, the MTS of a-synuclein, β-synuclein, or γ-synuclein, the third helix of the Antennapedia homeodomain, SN50, integrin β3 h-region, HIV Tat, pAntp, PR- 39, abaecin, apidaecin, Bac5, Bac7, P. berghei CS protein, and those MTSs described in US Patents 6,248,558, 6,432,680 and 6,248,558.

In certain embodiments, an antigen (e.g., a polypeptide of Table 1 or 2) is covalently bound to another molecule. This may, for example, increase the half-life, solubility,

bioabailability, or immunogenicity of the antigen. Molecules that may be covalently bound to the antigen include a carbohydrate, biotin, poly(ethylene glycol) (PEG), polysialic acid, N- propionylated polysialic acid, nucleic acids, polysaccharides, and PLGA. There are many different types of PEG, ranging from molecular weights of below 300 g/mol to over 10,000,000 g/mol. PEG chains can be linear, branched, or with comb or star geometries. In some embodiments, the naturally produced form of a protein is covalently bound to a moeity that stimulates the immune system. An example of such a moeity is a lipid moeity. In some instances, lipid moieties are recognized by a Toll-like receptor (TLR) such as TLR-2 or TLR-4, and activate the innate immune system.

C. Antibodies specific to the proteins of Tables 1 and 2

Another aspect disclosed herein is an antibody preparation generated against an antigenic composition (e.g., one of the proteins listed in Table 1 or 2 or an immunogenic fragment thereof). For instance, this disclosure provides combinations of two, three, four, or five antibodies each recognizing a different protein of Table 1 or 2. Any of a variety of antibodies are included. Such antibodies include, e.g., polyclonal, monoclonal, recombinant, humanized or partially humanized, single chain, Fab, and fragments thereof, etc. The antibodies can be of any isotype, e.g., IgG, various IgG isotypes such as IgGl, IgG2, IgG2a, IgG2b, IgG3, IgG4, etc.; and they can be from any animal species that produces antibodies, including goat, rabbit, mouse, chicken or the like. In some embodiments, Fab molecules are expressed and assembled in a genetically transformed host like E. coli. A lambda vector system is available thus to express a population of Fab's with a potential diversity equal to or exceeding that of subject generating the predecessor antibody. See Huse et al. (1989), Science 246, 1275-81.

D. Components of a vaccine or immunogenic composition comprising S. pneumoniae antigens or antibodies recognizing the same

In certain embodiments, the vaccine or immunogenic composition comprises an antigen and one or more of the following: an adjuvant, stabilizer, buffer, surfactant, controlled release component, salt, preservative, and/or an antibody specific to said antigen.

1. Adjuvants

The vaccine formulations and immunogenic compositions described herein may include an adjuvant. Adjuvants can be broadly separated into two classes, based on their principal mechanisms of action: vaccine delivery systems and immunostimulatory adjuvants (see, e.g., Singh et al. , Curr. HIV Res. 1 :309-20, 2003). In many vaccine formulations, the adjuvant provides a signal to the immune system so that it generates a response to the antigen, and the antigen is required for driving the specificity of the response to the pathogen. Vaccine delivery systems are often particulate formulations, e.g., emulsions, microparticles, immune-stimulating complexes (ISCOMs), nanoparticles, which may be, for example, particles and/or matrices, and liposomes. In contrast, immunostimulatory adjuvants are sometimes derived from pathogens and can represent pathogen associated molecular patterns (PAMP), e.g., lipopolysaccharides (LPS), monophosphoryl lipid (MPL), or CpG-containing DNA, which activate cells of the innate immune system.

Alternatively, adjuvants may be classified as organic and inorganic. Inorganic adjuvants include alum salts such as aluminum phosphate, amorphous aluminum hydroxyphosphate sulfate, and aluminum hydroxide, which are commonly used in human vaccines. Organic adjuvants comprise organic molecules including macromolecules. An example of an organic adjuvant is cholera toxin.

Adjuvants may also be classified by the response they induce. In some embodiments, the adjuvant induces the activation of Tjjl cells or TJJ2 cells. In other embodiments, the adjuvant induces the activation of B cells. In yet other embodiments, the adjuvant induces the activation of antigen-presenting cells. These categories are not mutually exclusive; in some cases, an adjuvant activates more than one type of cell.

In certain embodiments, the adjuvant induces the activation of THIV cells. It may promote the CD4 ⁺ or CD8 ⁺ T cells to secrete IL-17. In some embodiments, an adjuvant that induces the activation of THIV cells is one that produces at least a 2-fold, and in some cases a 10- fold, experimental sample to control ratio in the following assay. In the assay, an experimenter compares the IL-17 levels secreted by two populations of cells: (1) cells from animals immunized with the adjuvant and a polypeptide known to induce THIV activation, and (2) cells from animals treated with the adjuvant and an irrelevant (control) polypeptide. An adjuvant that induces the activation of THIV cells may cause the cells of population (1) to produce more than 2-fold, or more than 10-fold more IL-1V than the cells of population (2). IL-1V may be measured, for example, by ELISA or ELISPOT. Certain toxins, such as cholera toxin and labile toxin (produced by enterotoxigenic E. coli, or ETEC), activate a THIV response. Thus, in some embodiments, the adjuvant is a toxin. Cholera toxin was successfully used in the mouse model to induce protective immunity in conjunction with certain polypeptides from Table 1 (see Examples 5-8). One form of labile toxin is produced by Intercell. Mutant derivates of labile toxin that are active as adjuvants but significantly less toxic can be used as well. Exemplary detoxified mutant derivatives of labile toxin include mutants lacking ADP-ribosyltransferase activity. Particular detoxified mutant derivatives of labile toxin include LTKV (Douce et al. , "Mutants of Escherichia coli heat-labile toxin lacking ADP-ribosyltransferase activity act as nontoxic, mucosal adjuvants" PNAS Vol. 92, pp. 1644-1648, February 1995) and LTK63 (Williams et al. , "Innate Imprinting by the Modified Heat-Labile Toxin of Escherichia coli (LTK63) Provides Generic Protection against Lung Infectious Disease" The Journal of

Immunology, 2004, 1V3: 7435-V443), LT-G192 (Douce et al. "Genetically detoxified mutants of heat-labile toxin from Escherichia coli are able to act as oral adjuvants" Infect Immun. 1999 Sep;67(9):4400-6), and LTR72 ("Mucosal adjuvanticity and immunogenicity of LTR72, a novel mutant of Escherichia coli heat-labile enterotoxin with partial knockout of ADP- ribosyltransferase activity." J Exp Med. 1998 Apr 6;187(7): 1123-32).

In some embodiments, the adjuvant comprises a VLP (virus-like particle). One such adjuvant platform, Alphavirus replicons, induces the activation of TH17 cells using alphavirus and is produced by Alphavax. In certain embodiments of the Alphavirus replicon system, alphavirus may be engineered to express an antigen of interest, a cytokine of interest (for example, IL-17 or a cytokine that stimulates IL-17 production), or both, and may be produced in a helper cell line. More detailed information may be found in U.S. Patent Nos. 5,643,576 and 6,783,939. In some embodiments, a vaccine formulation is administered to a patient in combination with a nucleic acid encoding a cytokine.

Certain classes of adjuvants activate toll-like receptors (TLRs) in order to activate a ¾17 response. TLRs are well known proteins that may be found on leukocyte membranes, and recognize foreign antigens (including microbial antigens). Administering a known TLR ligand together with an antigen of interest (for instance, as a fusion protein) can promote the development of an immune response specific to the antigen of interest. One exemplary adjuvant that activates TLRs comprises Monophosphoryl Lipid A (MPL). Traditionally, MPL has been produced as a detoxified lipopolysaccharide (LPS) endotoxin obtained from gram negative bacteria, such as S. minnesota. In particular, sequential acid and base hydrolysis of LPS produces an immunoactive lipid A fraction (which is MPL), and lacks the saccharide groups and all but one of the phosphates present in LPS. A number of synthetic TLR agonists (in particular, TLR-4 agonists) are disclosed in Evans JT et al. "Enhancement of antigen-specific immunity via the TLR-4 ligands MPL adjuvant and Ribi.529." Expert Rev Vaccines 2003 Apr;2(2):219-29. Like MPL adjuvants, these synthetic compounds activate the innate immune system via TLR. Another type of TLR agonist is a synthetic phospholipid dimer, for example E6020 (Ishizaka ST et al. "E6020: a synthetic Toll-like receptor 4 agonist as a vaccine adjuvant." Expert Rev.

Vaccines. 2007 Oct; 6(5):773-84.). Various TLR agonists (including TLR-4 agonists) have been produced and/or sold by, for example, the Infectious Disease Research Institute (IRDI), Corixa, Esai, Avanti Polar Lipids, Inc., and Sigma Aldrich. Another exemplary adjuvant that activates TLRs comprises a mixture of MPL, Trehalose Dicoynomycolate (TDM), and dioctadecyldimethylammonium bromide (DDA). Another TLR-activating adjuvant is R848 (resiquimod).

In some embodiments, the adjuvant is or comprises a saponin. Typically, the saponin is a triterpene glycoside, such as those isolated from the bark of the Quillaja saponaria tree. A saponin extract from a biological source can be further fractionated (e.g., by chromatography) to isolate the portions of the extract with the best adjuvant activity and with acceptable toxicity. Typical fractions of extract from Quillaja saponaria tree used as adjuvants are known as fractions A and C.

A particular form of saponins that may be used in vaccine formulations described herein is immunostimulating complexes (ISCOMs). ISCOMs are an art-recognized class of adjuvants, that generally comprise Quillaja saponin fractions and lipids (e.g., cholesterol and phospholipids such as phosphatidyl choline). In certain embodiments, an ISCOM is assembled together with a polypeptide or nucleic acid of interest. However, different saponin fractions may be used in different ratios. In addition, the different saponin fractions may either exist together in the same particles or have substantially only one fraction per particle (such that the indicated ratio of fractions A and C are generated by mixing together particles with the different fractions). In this context, "substantially" refers to less than 20%, 15%, 10%, 5%, 4%, 3%, 2% or even 1%. Such adjuvants may comprise fraction A and fraction C mixed into a ratio of 70-95 A: 30-5 C, such as 70 A : 30 C to 75 A : 5 C, 75 A : 5 C to 80 A : 20 C, 80 A : 20 C to 85 A : 15 C, 85 A : 15 C to 90 A : 10 C, 90 A : 10 C to 95 A : 5 C, or 95 A : 5 C to 99 A : 1 C.

In certain embodiments, combinations of adjuvants are used. Three exemplary combinations of adjuvants are MPL and alum, E6020 and alum, and MPL and an ISCOM.

Adjuvants may be covalently bound to antigens. In some embodiments, the adjuvant may comprise a protein which induces inflammatory responses through activation of antigen- presenting cells (APCs). In some embodiments, one or more of these proteins can be recombinantly fused with an antigen of choice, such that the resultant fusion molecule promotes dendritic cell maturation, activates dendritic cells to produce cytokines and chemokines, and ultimately, enhances presentation of the antigen to T cells and initiation of T cell responses (see Wu et al., Cancer Res 2005; 65(11), pp 4947-4954). In certain embodiments, a polypeptide described herein is presented in the context of the trivalent conjugate system, comprising a fusion protein of S. pneumoniae Pneumococcal surface adhesin A (PsaA) with the pneumolysoid PdT and a cell wall polysaccharide (PsaA:PdT-CPs), described in Lu et al. ("Protection against Pneumococcal colonization and fatal pneumonia by a trivalent conjugate of a fusion protein with the cell wall polysaccharide." Infect Immun. 2009 May;77(5):2076-83). PdT carries three amino acid substitutions (W433F, D385N, and C428G) which render the molecule nontoxic but do not interfere with its TLR-4-mediated inflammatory properties. Conjugation of a polysaccharide to the fusion of a polypeptide to the TLR-4-agonist PdT results in greatly enhances immunological response to the polypeptide. In some embodiments, one or more polypeptides described herein are used in place of PsaA in the trivalent conjugate. The trivalent conjugate system typically includes alum and is usually administered parenterally. Other exemplary adjuvants that may be covalently bound to antigens comprise polysaccharides, pneumolysin, synthetic peptides, lipopep tides, and nucleic acids.

Typically, the same adjuvant or mixture of adjuvants is present in each dose of a vaccine. Optionally, however, an adjuvant may be administered with the first dose of vaccine and not with subsequent doses (i.e., booster shots). Alternatively, a strong adjuvant may be administered with the first dose of vaccine and a weaker adjuvant or lower dose of the strong adjuvant may be administered with subsequent doses. The adjuvant can be administered before the administration of the antigen, concurrent with the administration of the antigen or after the administration of the antigen to a subject (sometimes within 1, 2, 6, or 12 hours, and sometimes within 1, 2, or 5 days). Certain adjuvants are appropriate for human patients, non-human animals, or both.

2. Additional components of a vaccine or immunogenic composition

In addition to the antigens and the adjuvants described above, a vaccine formulation or immunogenic composition may include one or more additional components.

In certain embodiments, the vaccine formulation or immunogenic composition may include one or more stabilizers such as sugars (such as sucrose, glucose, or fructose), phosphate (such as sodium phosphate dibasic, potassium phosphate monobasic, dibasic potassium phosphate, or monosodium phosphate), glutamate (such as monosodium L-glutamate), gelatin (such as processed gelatin, hydrolyzed gelatin, or porcine gelatin), amino acids (such as arginine, asparagine, histidine, L-histidine, alanine, valine, leucine, isoleucine, serine, threonine, lysine, phenylalanine, tyrosine, and the alkyl esters thereof), inosine, or sodium borate.

In certain embodiments, the vaccine formulation or immunogenic composition includes one or more buffers such as a mixture of sodium bicarbonate and ascorbic acid. In some embodiments, the vaccine formulation may be administered in saline, such as phosphate buffered saline (PBS), or distilled water.

In certain embodiments, the vaccine formulation or immunogenic composition includes one or more surfactants such as polysorbate 80 (Tween 80), Triton X-100, Polyethylene glycol tert-octylphenyl ether t-Octylphenoxypolyethoxyethanol 4-(l,l,3,3-Tetramethylbutyl)phenyl- polyethylene glycol (TRITON X-100); Polyoxyethylenesorbitan monolaurate Polyethylene glycol sorbitan monolaurate (TWEEN 20); and 4-(l,l,3,3-Tetramethylbutyl)phenol polymer with formaldehyde and oxirane (TYLOXAPOL). A surfactant can be ionic or nonionic.

In certain embodiments, the vaccine formulation or immunogenic composition includes one or more salts such as sodium chloride, ammonium chloride, calcium chloride, or potassium chloride.

In certain embodiments, a preservative is included in the vaccine or immunogenic composition. In other embodiments, no preservative is used. A preservative is most often used in multi-dose vaccine vials, and is less often needed in single-dose vaccine vials. In certain embodiments, the preservative is 2-phenoxyethanol, methyl and propyl parabens, benzyl alcohol, and/or sorbic acid.

In certain embodiments, the vaccine formulation or immunogenic composition is a controlled release formulation.

E. DNA vaccines

In certain aspects, the vaccine comprises one or more of the nucleic acids disclosed herein or corresponding to the polypeptides described herein. When a nucleic acid vaccine is administered to a patient, the corresponding gene product (such as a desired antigen) is produced in the patient's body. In some embodiments, nucleic acid vaccine vectors that include optimized recombinant polynucleotides can be delivered to a mammal (including humans) to induce a therapeutic or prophylactic immune response. The nucleic acid may be, for example, DNA, RNA, or a synthetic nucleic acid. The nucleic acid may be single stranded or double stranded.

Nucleic acid vaccine vectors (e.g., adenoviruses, liposomes, papillomaviruses, retroviruses, etc.) can be administered directly to the mammal for transduction of cells in vivo. The nucleic acid vaccines can be formulated as pharmaceutical compositions for administration in any suitable manner, including parenteral administration. Plasmid vectors are typically more efficient for gene transfer to muscle tissue. The potential to deliver DNA vectors to mucosal surfaces by oral administration has also been reported (PLGA encapsulated Rotavirus and Hepatitis B) and DNA plasmids have been utilized for direct introduction of genes into other tissues. DNA vaccines have been introduced into animals primarily by intramuscular injection, by gene gun delivery, or by electroporation. After being introduced, the plasmids are generally maintained episomally without replication. Expression of the encoded proteins has been shown to persist for extended time periods, providing stimulation of B and T cells.

In determining the effective amount of the vector to be administered in the treatment or prophylaxis of an infection or other condition, the physician evaluates vector toxicities, progression of the disease, and the production of anti- vector antibodies, if any. Often, the dose equivalent of a naked nucleic acid from a vector is from about 1 μg to 1 mg for a typical 70 kilogram patient, and doses of vectors used to deliver the nucleic acid are calculated to yield an equivalent amount of therapeutic nucleic acid. Administration can be accomplished via single or divided doses. The toxicity and therapeutic efficacy of the nucleic acid vaccine vectors can be determined using standard pharmaceutical procedures in cell cultures or experimental animals.

A nucleic acid vaccine can contain DNA, RNA, a modified nucleic acid, or a

combination thereof. In some embodiments, the vaccine comprises one or more cloning or expression vectors; for instance, the vaccine may comprise a plurality of expression vectors each capable of autonomous expression of a nucleotide coding region in a mammalian cell to produce at least one immunogenic polypeptide. An expression vector often includes a eukaryotic promoter sequence, such as the nucleotide sequence of a strong eukaryotic promoter, operably linked to one or more coding regions. The compositions and methods herein may involve the use of any particular eukaryotic promoter, and a wide variety are known; such as a CMV or RSV promoter. The promoter can be heterologous with respect to the host cell. The promoter used may be a constitutive promoter.

A vector useful in the present compositions and methods can be circular or linear, single- stranded or double stranded and can be a plasmid, cosmid, or episome. In a suitable

embodiment, each nucleotide coding region is on a separate vector; however, it is to be understood that one or more coding regions can be present on a single vector, and these coding regions can be under the control of a single or multiple promoters. Numerous plasmids may be used for the production of nucleic acid vaccines. Suitable embodiments of the nucleic acid vaccine employ constructs using the plasmids VR1012 (Vical Inc., San Diego Calif.), pCMVI.UBF3/2 (S. Johnston, University of Texas) or pcDNA3.1 (InVitrogen Corporation, Carlsbad, Calif.) as the vector. In addition, the vector construct can contain immunostimulatory sequences (ISS), such as unmethylated dCpG motifs, that stimulate the animal's immune system. The nucleic acid vaccine can also encode a fusion product containing the immunogenic polypeptide. Plasmid DNA can also be delivered using attenuated bacteria as delivery system, a method that is suitable for DNA vaccines that are administered orally. Bacteria are transformed with an independently replicating plasmid, which becomes released into the host cell cytoplasm following the death of the attenuated bacterium in the host cell.

DNA vaccines, including the DNA encoding the desired antigen, can be introduced into a host cell in any suitable form including, the fragment alone, a linearized plasmid, a circular plasmid, a plasmid capable of replication, an episome, RNA, etc. Preferably, the gene is contained in a plasmid. In certain embodiments, the plasmid is an expression vector. Individual expression vectors capable of expressing the genetic material can be produced using standard recombinant techniques. See e.g., Maniatis et al., 1985 Molecular Cloning: A Laboratory Manual or DNA Cloning, Vol. I and II (D. N. Glover, ed., 1985) for general cloning methods.

Routes of administration include, but are not limited to, intramuscular, intranasal, intraperitoneal, intradermal, subcutaneous, intravenous, intraarterially, intraoccularly and oral as well as topically, transdermally, by inhalation or suppository or to mucosal tissue such as by lavage to vaginal, rectal, urethral, buccal and sublingual tissue. Typical routes of administration include intramuscular, intraperitoneal, intradermal and subcutaneous injection. Genetic constructs may be administered by means including, but not limited to, traditional syringes, needleless injection devices, "microprojectile bombardment gene guns", or other physical methods such as electroporation ("EP"), "hydrodynamic method", or ultrasound. DNA vaccines can be delivered by any method that can be used to deliver DNA as long as the DNA is expressed and the desired antigen is made in the cell.

In some embodiments, a DNA vaccine is delivered via known transfection reagents such as cationic liposomes, fluorocarbon emulsion, cochleate, tubules, gold particles, biodegradable microspheres, or cationic polymers. Cochleate delivery vehicles are stable phospholipid calcium precipitants consisting of phosphatidyl serine, cholesterol, and calcium; this nontoxic and noninflammatory transfection reagent can be present in a digestive system. Biodegradable microspheres comprise polymers such as poly(lactide-co-glycolide), a polyester that can be used in producing microcapsules of DNA for transfection. Lipid-based microtubes often consist of a lipid of spirally wound two layers packed with their edges joined to each other. When a tubule is used, the nucleic acid can be arranged in the central hollow part thereof for delivery and controlled release into the body of an animal.

In some embodiments, DNA vaccine is delivered to mucosal surfaces via microspheres. Bioadhesive microspheres can be prepared using different techniques and can be tailored to adhere to any mucosal tissue including those found in eye, nasal cavity, urinary tract, colon and gastrointestinal tract, offering the possibilities of localized as well as systemic controlled release of vaccines. Application of bioadhesive microspheres to specific mucosal tissues can also be used for localized vaccine action. In some embodiments, an alternative approach for mucosal vaccine delivery is the direct administration to mucosal surfaces of a plasmid DNA expression vector which encodes the gene for a specific protein antigen.

The DNA plasmid vaccines according to the present invention are formulated according to the mode of administration to be used. In some embodiments where DNA plasmid vaccines are injectable compositions, they are sterile, and/or pyrogen free and/or particulate free. In some embodiments, an isotonic formulation is preferably used. Generally, additives for isotonicity can include sodium chloride, dextrose, mannitol, sorbitol and lactose. In some embodiments, isotonic solutions such as phosphate buffered saline are preferred. In some embodiments, stabilizers include gelatin and albumin. In some embodiments, a vasoconstriction agent is added to the formulation. In some embodiments, a stabilizing agent that allows the formulation to be stable at room or ambient temperature for extended periods of time, such as LGS or other polycations or polyanions is added to the formulation.

In some embodiments, the DNA vaccine may further comprises a pharmacologically acceptable carrier or diluent. Suitable carriers for the vaccine are well known to those skilled in the art and include but are not limited to proteins, sugars, etc. Such carriers may be aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non-aqueous carriers are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose and sodium chloride, lactated Ringer's or fixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers such as those based on Ringer's dextrose, and the like. Preservatives and antimicrobials include antioxidants, chelating agents, inert gases and the like. Preferred preservatives include formalin, thimerosal, neomycin, polymyxin B and amphotericin B.

An alternative approach to delivering the nucleic acid to an animal involves the use of a viral or bacterial vector. Examples of suitable viral vectors include adenovirus, polio virus, pox viruses such as vaccinia, canary pox, and fowl pox, herpes viruses, including catfish herpes virus, adenovirus-associated vector, and retroviruses. Exemplary bacterial vectors include attenuated forms of Salmonella, Shigella, Edwardsiella ictaluri, Yersinia ruckerii, and Listeria monocytogenes. In some embodiments, the nucleic acid is a vector, such as a plasmid, that is capable of autologous expression of the nucleotide sequence encoding the immunogenic polypeptide.

F. Use of Vaccines

The S. pneumoniae vaccines described herein may be used for prophylactic and/or therapeutic treatment of S. pneumoniae. Accordingly, this application provides a method for treating a subject suffering from or susceptible to S. pneumoniae infection, comprising administering an effective amount of any of the vaccine formulations described herein. In some aspects, the method inhibits S. pneumoniae colonization in an individual. In some aspects, the method inhibits S. pneumoniae symptoms or sequelae, such as sepsis. The subject receiving the vaccination may be a male or a female, and may be a child or adult. In some embodiments, the subject being treated is a human. In other embodiments, the subject is a non-human animal. 1. Prophylactic use

In prophylactic embodiments, the vaccine is administered to a subject to induce an immune response that can help protect against the establishment of S. pneumoniae, for example by protecting against colonization, the first and necessary step in disease. Thus, in some aspects, the method inhibits infection by S. pneumoniae in a non-colonized or uninfected subject. In another aspect, the method may reduce the duration of colonization in an individual who is already colonized.

In some embodiments, the vaccine compositions of the invention confer protective immunity, allowing a vaccinated individual to exhibit delayed onset of symptoms or sequelae, or reduced severity of symptoms or sequelae, as the result of his or her exposure to the vaccine. In certain embodiments, the reduction in severity of symptoms or sequelae is at least 25%, 40%, 50%, 60%, 70%, 80% or even 90%. In particular embodiments, vaccinated individuals may display no symptoms or sequelae upon contact with S. pneumoniae, do not become colonized by S. pneumoniae, or both. Protective immunity is typically achieved by one or more of the following mechanisms: mucosal, humoral, or cellular immunity. Mucosal immunity is primarily the result of secretory IgA (sIGA) antibodies on mucosal surfaces of the respiratory,

gastrointestinal, and genitourinary tracts. The sIGA antibodies are generated after a series of events mediated by antigen-processing cells, B and T lymphocytes, that result in sIGA production by B lymphocytes on mucosa-lined tissues of the body. Humoral immunity is typically the result of IgG antibodies and IgM antibodies in serum. Cellular immunity can be achieved through cytotoxic T lymphocytes or through delayed-type hypersensitivity that involves macrophages and T lymphocytes, as well as other mechanisms involving T cells without a requirement for antibodies. In particular, cellular immunity may be mediated by Tjjl or ¾17 cells.

Essentially any individual has a certain risk of becoming infected with S. pneumoniae.

However, certain sub-populations have an increased risk of infection. In some embodiments, a vaccine formulation as described herein (e.g., a composition comprising one or more

polypeptides from Table 1 or 2, or nucleic acids encoding the polypeptides, or antibodies reactive with the polypeptides) is administered to patients that are immunocompromised.

An immunocompromising condition arising from a medical treatment is likely to expose the individual in question to a higher risk of infection with S. pneumoniae. It is possible to treat an infection prophylactically in an individual having the immunocompromised condition before or during treatments known to compromise immune function. By prophylactically treating with an antigenic composition (e.g., two or more antigens from Table 1 or 2, or nucleic acids encoding the antigens), or with antibodies reactive to two or more antigens from Table 1 or 2, before or during a treatment known to compromise immune function, it is possible to prevent a subsequent S. pneumoniae infection or to reduce the risk of the individual contracting an infection due to the immunocompromised condition. Should the individual contract an S.

pneumoniae infection e.g., following a treatment leading to an immunocompromised condition it is also possible to treat the infection by administering to the individual an antigen composition.

The following groups are at increased risk of pneumococcal disease or its complications, and therefore it is advantageous for subjects falling into one or more of these groups to receive a vaccine formulation described herein: children, especially those from 1 month to 5 years old or 2 months to 2 years old; children who are at least 2 years of age with asplenia, splenic dysfunction or sickle-cell disease; children who are at least 2 years of age with nephrotic syndrome, chronic cerebrospinal fluid leak, HIV infection or other conditions associated with immunosuppression.

In another embodiment, at least one dose of the pneumococcal antigen composition is given to adults in the following groups at increased risk of pneumococcal disease or its complications: all persons 65 years of age; adults with asplenia, splenic dysfunction or sickle-cell disease; adults with the following conditions: chronic cardiorespiratory disease, cirrhosis, alcoholism, chronic renal disease, nephrotic syndrome, diabetes mellitus, chronic cerebrospinal fluid leak, HIV infection, AIDS and other conditions associated with immunosuppression (Hodgkin's disease, lymphoma, multiple myeloma, immunosuppression for organ

transplantation), individuals with cochlear implants; individuals with long-term health problems such as heart disease and lung disease, as well as individuals who are taking any drug or treatment that lowers the body's resistance to infection, such as long-term steroids, certain cancer drugs, radiation therapy; Alaskan natives and certain Native American populations.

2. Therapeutic use

In therapeutic applications, the vaccine may be administered to a patient suffering from S. pneumoniae infection, in an amount sufficient to treat the patient. Treating the patient, in this case, refers to reducing S. pneumoniae symptoms and/or bacterial load and/or sequelae bin an infected individual. In some embodiments, treating the patient refers to reducing the duration of symptoms or sequelae, or reducing the intensity of symptoms or sequelae. In some

embodiments, the vaccine reduces transmissibihty of S. pneumoniae from the vaccinated patient. In certain embodiments, the reductions described above are at least 25%, 30%, 40%, 50%, 60%, 70%, 80% or even 90%. In therapeutic embodiments, the vaccine is administered to an individual post-infection. The vaccine may be administered shortly after infection, e.g. before symptoms or sequelae manifest, or may be administered during or after manifestation of symptoms or sequelae.

A therapeutic S. pneumoniae vaccine can reduce the intensity and/or duration of the various symptoms or sequelae of S. pneumoniae infection. Symptoms or sequelae of S.

pneumoniae infection can take many forms. In some cases, an infected patient develops pneumonia, acute sinusitis, otitis media (ear infection), meningitis, bacteremia, sepsis, osteomyelitis, septic arthritis, endocarditis, peritonitis, pericarditis, cellulitis, or brain abscess.

Sepsis is a rare but life-threatening complication of S. pneumoniae infection, where the bacterium invades the bloodstream and systemic inflammation results. Typically, fever is observed and white blood cell count increases. A further description of sepsis is found in Goldstein, B. et al. "International pediatric sepsis consensus conference: definitions for sepsis and organ dysfunction in pediatrics." Pediatr Crit Care Med. Jan 2005;6(l):2-8.

3. Assaying vaccination efficacy

The efficacy of vaccination with the vaccines disclosed herein may be determined in a number of ways, in addition to the clinical outcomes described above. First, one may assay IL- 17 levels (particularly IL-17 A) by stimulating T cells derived from the subject after vaccination. The IL-17 levels may be compared to IL-17 levels in the same subject before vaccination.

Increased IL-17 (e.g., IL-17A) levels, such as a 1.5 fold, 2-fold, 5-fold, 10-fold, 20-fold, 50-fold or 100-fold or more increase, would indicate an increased response to the vaccine. Alternatively (or in combination), one may assay neutrophils in the presence of T cells or antibodies from the patient for pneumococcal killing. Increased pneumococcal killing, such as a 1.5 fold, 2-fold, 5- fold, 10-fold, 20-fold, 50-fold or 100-fold or more increase, would indicate an increased response to the vaccine. In addition, one may measure ¾17 cell activation, where increased T _H 17 cell activation, such as a 1.5 fold, 2-fold, 5-fold, 10-fold, 20-fold, 50-fold or 100-fold or more increase, correlates with an increased response to the vaccine. One may also measure levels of an antibody specific to the vaccine, where increased levels of the specific antibody, such as a 1.5 fold, 2-fold, 5-fold, 10-fold, 20-fold, 50-fold or 100-fold or more increase, are correlated with increased vaccine efficacy. In certain embodiments, two or more of these assays are used. For example, one may measure IL-17 levels and the levels of vaccine- specific antibody. Alternatively, one may follow epidemiological markers such as incidence of, severity of, or duration of pneumococcal infection in vaccinated individuals compared to unvaccinated individuals.

Vaccine efficacy may also be assayed in various model systems such as the mouse model. For instance, BALB/c or C57BL/6 strains of mice may be used. After administering the test vaccine to a subject (as a single dose or multiple doses), the experimenter administers a challenge dose of S. pneumoniae. In some cases, a challenge dose administered intranasally is sufficient to cause S. pneumoniae colonization (especially nasal colonization) in an unvaccinated animal, and in some cases a challenge dose administered via aspiration is sufficient to cause sepsis and a high rate of lethality in unvaccinated animals. One can then measure the reduction in colonization or the reduction in lethality in vaccinated animals. Examples 5-8 and 10 show the efficacy of polypeptides of Table 1 in inhibiting S. pneumoniae nasal colonization following intranasal challenge in the mouse model. Examples 11 and 12 show the efficacy of polypeptides of Table 1 in protecting against sepsis and death following infection with S. pneumoniae via aspiration in the mouse model.

G. Use of Immunogenic Compositions

1. Defense against S. pneumoniae infection

The immunogenic compositions of the present disclosure are designed to elicit an immune response against S. pneumoniae. Compositions described herein (e.g., ones comprising one or more polypeptides of Table 1 or 2, or nucleic acids encoding the polypeptides) may stimulate an antibody response or a cell-mediated immune response, or both, in the mammal to which it is administered. In some embodiments, the composition stimulates a Tjjl-biased CD4 ⁺ T cell response, a Tjjl7-biased CD4 ⁺ T cell response and/or a CD8 ⁺ T cell response. In some embodiments, the composition stimulates an antibody response. In some embodiments, the composition stimulates a Tjjl-biased CD4 ⁺ T cell response, Tjjl7-biased CD4 ⁺ T cell response and/or a CD8 ⁺ T cell response, and an antibody response.

In certain embodiments, the composition (e.g., one comprising one or more polypeptides of Table 1 or 2, or nucleic acids encoding the polypeptides, or antibodies reactive with the peptides) includes a cytokine or nucleotide coding region encoding a cytokine such as IL-17, to provide additional stimulation to the immune system of the mammal. In certain embodiments, the composition comprises a cytokine such as IL-17. While not wishing to be bound by theory, in some embodiments a ¾17 cell response is desirable in mounting an immune response to the compositions disclosed herein, e.g., ones comprising one or more polypeptides of Table 1 or 2. In certain embodiments, an active THIV response is beneficial in clearing a pneumococcal infection. For instance, mice lacking the IL- 17A receptor show decreased whole cell vaccine-based protection from a pneumococcal challenge (Lu et ah, "Interleukin-17A mediates acquired immunity to pneumococcal colonization." PLoS Pathog. 2008 Sep 19;4(9)).

Thus, herein is provided a method of increasing IL-17 production by administering the compositions described herein (e.g., ones comprising one or more polypeptides of Table 1 or 2) to a subject. Furthermore, this application provides a method of activating ¾17 cells by administering said compositions to a subject. In certain embodiments, increased IL-17A levels result in increased pneumococcal killing by neutrophils or neutrophil-like cells, for instance by inducing recruitment and activation of neutrophils of neutrophil-like cells. In certain embodiments, this pneumococcal killing is independent of antibodies and complement.

However, specific antibody production and complement activation may be useful additional mechanisms that contribute to clearing of a pneumococcal infection.

Immunogenic compositions containing immunogenic polypeptides or polynucleotides encoding immunogenic polypeptides together with a pharmaceutical carrier are also provided.

In some instances, the immunogenic composition comprises one or more nucleic acids encoding one or more polypeptides of SEQ ID NOS: 1-13, 265, 266 and 267, such as one or more nucleic acids selected from SEQ ID Nos. 24-31, 271, 272 and 273. In some embodiments these nucleic acids are expressed in the immunized individual, producing the encoded S.

pneumoniae antigens, and the S. pneumoniae antigens so produced can produce an

immunostimulatory effect in the immunized individual.

Such a nucleic acid-containing immunostimulatory composition may comprise, for example, an origin of replication, and a promoter that drives expression of one or more nucleic acids encoding one or more polypeptides of SEQ ID NOS: 1-13, 265, 266 and 267. Such a composition may also comprise a bacterial plasmid vector into which is inserted a promoter (sometimes a strong viral promoter), one or more nucleic acids encoding one or more polypeptides of SEQ ID NOS: 1-13, 265, 266 and 267, and a polyadenylation/transcriptional termination sequence. In some instances, the nucleic acid is DNA. H. Diagnostic uses

This application provides, inter alia, a rapid, inexpensive, sensitive, and specific method for detection of S. pneumoniae in patients. In this respect it should be useful to all hospitals and physicians examining and treating patients with or at risk for S. pneumoniae infection. Detection kits can be simple enough to be set up in any local hospital laboratory, and the antibodies and antigen-binding portions thereof can readily be made available to all hospitals treating patients with or at risk for S. pneumoniae infection. As used herein, "patient" refers to an individual (such as a human) that either has an S. pneumoniae infection or has the potential to contract an S. pneumoniae infection. A patient may be an individual (such as a human) that has an S.

pneumoniae infection, has the potential to contract an S. pneumoniae infection, who has recovered from S. pneumoniae infection, and/or an individual whose infection status is unknown.

In some embodiments, one may perform a diagnostic assay using two or more antibodies, each of which binds one of the antigens of Table 1 or 2 to detect S. pneumoniae in an individual. In some embodiment, one of the antigens is SEQ ID NO: 265, 266, or 268. The instant disclosure also provides a method of phenotyping biological samples from patients suspected of having a S. pneumoniae infection: (a) obtaining a biological sample from a patient; (b) contacting the sample with two or more S. pneumoniae -specific antibodies or antigen-binding portions thereof under conditions that allow for binding of the antibody or antigen-binding portion to an epitope of S. pneumoniae; where binding indicates the presence of S. pneumoniae in the sample. In some embodiments, the binding to the biological sample is compared to binding of the same antibody to a negative control tissue, wherein if the biological sample shows the presence of S. pneumoniae as compared to the negative control tissue, the patient is identified as likely having a S. pneumoniae infection. In some cases, binding of one antibody indicates the presence of S. pneumoniae; in other cases, the binding of two or more antibodies indicates the presence of S. pneumoniae. The aforementioned test may be appropriately adjusted to detect other bacterial infections, for instance by using an antibody immunoreactive a homolog (from another bacterial species) of one of the proteins described in Table 1. In some embodiments, the antibodies raised against a S. pneumoniae protein in Table 1 or 2 will also bind the homolog in another Streptococcus species, especially if the homologs have a high percentage sequence identity. Alternatively, one may use an antigen of Table 1 or 2 (such as SEQ ID NO: 265, 266, or 268) to detect anti-S. pneumoniae antibodies in an individual. The instant disclosure also provides a method of phenotyping biological samples from patients suspected of having a S. pneumoniae infection: (a) obtaining a biological sample from a patient; (b) contacting the sample with two or more S. pneumoniae -specific antigens selected from Table 1 or 2 or portions thereof under conditions that allow for binding of the antigen (or portion thereof) to any host antibodies present in the sample; where binding indicates the presence of anti-S. pneumoniae antibodies in the sample. In some embodiments, the binding to the biological sample is compared to binding of the same antigen to a negative control tissue, wherein if the biological sample shows the presence of anti-S. pneumoniae antibodies as compared to the negative control tissue, the patient is identified as likely either (1) having a S. pneumoniae infection, or (2) having had a S.

pneumoniae infection in the past. In some cases, detecting one antibody indicates a current or past infection with S. pneumoniae; in other cases, detecting two or more antibodies indicates a current or past infection with S. pneumoniae. The aforementioned test may be appropriately adjusted to detect other bacterial infections, for instance by using a homolog (from another bacterial species (e.g., a Streptococcal species) of the proteins described in Table 1.

In some embodiments, the immune cell response of a mammalian cell may be quantified ex vivo. A method for such quantification comprises administering the compositions herein disclosed to a mammalian T cell ex vivo, and quantifying the change in cytokine production of the mammalian T cell in response to the composition. In these methods, the cytokine may be, for example, IL-17.

The binding of an S. pneumoniae antibody to an antigen (e.g., a polypeptide of Table 1 or 2, such as SEQ ID NO: 265, 266, or 268) may be measured using any appropriate method. Such methods include ELISA (enzyme-linked immunosorbent assay), Western blotting, competition assay, and spot-blot. The detection step may be, for instance, chemiluminescent, fluorescent, or colorimetric. One suitable method for measuring antibody-protein binding is the Luminex xMAP system, where peptides are bound to a dye-containing microsphere. Certain systems, including the xMAP system, are amenable to measuring several different markers in multiplex, and could be used to measure levels of antibodies at once. In some embodiments, other systems are used to assay a plurality of markers in multiplex. For example, profiling may be performed using any of the following systems: antigen microarrays, bead microarrays, nanobarcodes particle technology, arrayed proteins from cDNA expression libraries, protein in situ array, protein arrays of living transformants, universal protein array, lab-on-a-chip microfluidics, and peptides on pins. Another type of clinical assay is a chemiluminescent assay to detect antibody binding. In some such assays, including the VITROS Eci anti-HCV assay, antibodies are bound to a solid-phase support made up of microparticles in liquid suspension, and a surface fluorometer is used to quantify the enzymatic generation of a fluorescent product.

In some embodiments, if the biological sample shows the presence of S. pneumoniae (e.g., by detecting one or more polypeptide of Table 1 or 2, such as SEQ ID NO: 265, 266, or 268, or an antibody that binds one of said polypeptides), one may administer a therapeutically effective amount of the compositions and therapies described herein to the patient. The biological sample may comprise, for example, blood, semen, urine, vaginal fluid, mucus, saliva, feces, urine, cerebrospinal fluid, or a tissue sample. In some embodiments, the biological sample is an organ intended for transplantation. In certain embodiments, before the detection step, the biological sample is subject to culture conditions that promote the growth of S. pneumoniae.

The diagnostic tests herein (e.g., those that detect a polypeptide of Table 1 or 2, such as

SEQ ID NO: 265, 266, or 268, or an antibody that binds one of said polypeptides) may be used to detect S. pneumoniae in a variety of samples, including samples taken from patients and samples obtained from other sources. For example, the diagnostic tests may be used to detect S. pneumoniae in food, drink, or ingredients for food and drink; on objects such as medical instruments, medical devices such as cochlear implants and pacemakers, shoes, clothing, furniture including hospital furniture, and drapes including hospital drapes; or in samples taken from the environment such as plant samples. In some embodiments, the tests herein may be performed on samples taken from animals such as agricultural animals (cows, pigs, chickens, goats, horses and the like), companion animals (dogs, cats, birds, and the like), or wild animals. In certain embodiments, the tests herein may be performed on samples taken from cell cultures such as cultures of human cells that produce a therapeutic protein, cultures of bacteria intended to produce a useful biological molecule, or cultures of cells grown for research purposes.

This disclosure also provides a method of determining the location of a S. pneumoniae infection in a patient comprising: (a) administering a pharmaceutical composition comprising a labeled S. pneumoniae antibody or antigen-binding portion thereof to the patient, and (b) detecting the label, wherein binding indicates a S. pneumoniae infection in a particular location in the patient. Such a diagnostic may also comprise comparing the levels of binding in the patient to a control. In certain embodiments, the method further comprises, if the patient has a S. pneumoniae infection, treating the infection by administering a therapeutically effective amount of a S. pneumoniae -binding antibody or antigen-binding portion thereof to the patient. In certain embodiments, the method further comprises, if the patient has a S. pneumoniae infection, treating the infection by administering a therapeutically effective amount of a S. pneumoniae protein of Table 1 or 2, or immunogenic portion thereof, to the patient. The method may further comprise determining the location and/or volume of the S. pneumoniae in the patient. This method may be used to evaluate the spread of S. pneumoniae in the patient and determine whether a localized therapy is appropriate.

In some embodiments, the anti-S. pneumoniae antibodies or T cells described herein may be used to make a prognosis of the course of infection. In some embodiments, the anti-S.

pneumoniae antibodies or T cells herein may be detected in a sample taken from a patient. If antibodies or T cells are present at normal levels, it would indicate that the patient has raised an immune response against anti-S. pneumoniae. If antibodies or T cells are absent, or present at reduced levels, it would indicate that the patient is failing to raise a sufficient response against anti-S. pneumoniae, and a more aggressive treatment would be recommended. In some embodiments, antibodies or T cells present at reduced levels refers to antibodies that are present at less than 50%, 20%, 10%, 5%, 2%, or 1% the level of antibodies or T cells typical in a patient with a normal immune system. Antibodies may be detected by affinity for any of the antigens described herein (e.g., those in Table 1 and/or 2), for example using ELISA. T cells may be detected by ex vivo responses for any of the antigens described herein (e.g., those in Table 1 and/or 2), for example using ELISA or ELISPOT assays.

In some embodiments, detection of specific S. pneumoniae antigens (e.g., those in Table 1 and/or 2, such as SEQ ID NO: 265, 266, or 268) may be used to predict the progress and symptoms of S. pneumoniae infection in a patient. It will be understood by one of skill in the art that the methods herein are not limited to detection of S. pneumoniae. Other embodiments include the detection of related bacteria including bacteria with proteins homologous to the proteins described in Table 1 or 2. Such related bacteria include, for example, other strains of Streptococcus. I. Doses and Routes of Administration

1. Dosage forms, amounts, and timing

The amount of antigen in each vaccine or immunogenic composition dose is selected as an effective amount, which induces a prophylactic or therapeutic response, as described above, in either a single dose or over multiple doses. Preferably, the dose is without significant adverse side effects in typical vaccinees. Such amount will vary depending upon which specific antigen is employed. Generally, it is expected that a dose will comprise 1-1000 μg of each protein, in some instances 2-100 μg, for instance 4-40 μg. In some aspects, the vaccine formulation comprises 1-1000 μg of the polypeptide and 1-250 μg of the adjuvant. In some embodiments, the appropriate amount of antigen to be delivered will depend on the age, weight, and health (e.g. immunocompromised status) of a subject. When present, typically an adjuvant will be present in amounts from 1 μg - 250 μg per dose, for example 50-150 μg, 75-125 μg or 100 μg.

In some embodiments, only one dose of the vaccine is administered to achieve the results described above. In other embodiments, following an initial vaccination, subjects receive one or more boost vaccinations, for a total of two, three, four or five vaccinations. Advantageously, the number is three or fewer. A boost vaccination may be administered, for example, about 1 month, 2 months, 4 months, 6 months, or 12 months after the initial vaccination, such that one vaccination regimen involves administration at 0, 0.5-2 and 4-8 months. It may be advantageous to administer split doses of vaccines which may be administered by the same or different routes.

The vaccines and immunogenic compositions described herein may take on a variety of dosage forms. In certain embodiments, the composition is provided in solid or powdered (e.g., lyophilized) form; it also may be provided in solution form. In certain embodiments, a dosage form is provided as a dose of lyophilized composition and at least one separate sterile container of diluent.

In some embodiments, the composition will be administered in a dose escalation manner, such that successive administrations of the composition contain a higher concentration of composition than previous administrations. In some embodiments, the composition will be administered in a manner such that successive administrations of the composition contain a lower concentration of composition than previous administrations.

In therapeutic applications, compositions are administered to a patient suffering from a disease in an amount sufficient to treat the patient. Therapeutic applications of a composition described herein include reducing transmissibility, slowing disease progression, reducing bacterial viability or replication, or inhibiting the expression of proteins required for toxicity, such as by 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20% or 10% of the levels at which they would occur in individuals who are not treated with the composition.

In prophylactic embodiments, compositions are administered to a human or other mammal to induce an immune response that can inhibit the establishment of an infectious disease or other condition. In some embodiments, a composition may partially block the bacterium from establishing an infection.

In some embodiments, the compositions are administered in combination with antibiotics. This co-administration is particularly appropriate when the pharmaceutical composition is administered to a patient who has recently been exposed (or is suspected of having been recently exposed) to S. pneumoniae. Many antibiotics are used to treat pneumococcal infections, including penicillin, amoxicillin, amoxicillin/clavulanate, cefuroxime, cefotaxime, ceftriaxone, and vancomycin. The appropriate antibiotic may be selected based on the type and severity of the infection, as well as any known antibiotic resistance of the infection (Jacobs MR "Drug- resistant Streptococcus pneumoniae: rational antibiotic choices" Am J Med. 1999 May

3;106(5A): 19S-25S).

2. Routes of administration

The vaccine formulations and pharmaceutical compositions herein can be delivered by administration to an individual, typically by systemic administration (e.g., intravenous, intraperitoneal, intramuscular, intradermal, subcutaneous, subdermal, transdermal, intracranial, intranasal, mucosal, anal, vaginal, oral, buccal route or they can be inhaled) or they can be administered by topical application. In some embodiments, the route of administration is intramuscular. In other embodiments, the route of administration is subcutaneous. In yet other embodiments, the route of administration is mucosal. In certain embodiments, the route of administration is transdermal or intradermal

Certain routes of administration are particularly appropriate for vaccine formulations and immunogenic compositions comprising specified adjuvants. In particular, transdermal administration is one suitable route of administration for S. pneumoniae vaccines comprising toxins (e.g. cholera toxin or labile toxin); in other embodiments, the administration is intranasal. Vaccines formulated with Alphavirus replicons may be administered, for example, by the intramuscular or the subcutaneous route. Vaccines comprising Monophosphory Lipid A (MPL), Trehalose Dicoynomycolate (TDM), and dioctadecyldimethylammonium bromide (DDA) are suitable (inter alia) for intramuscular and subcutaneous administration. A vaccine comprising resiquimod may be administered topically or subcutaneously, for example.

3. Formulations

The vaccine formulation or immunogenic composition may be suitable for administration to a human patient, and vaccine or immunogenic composition preparation may conform to USFDA guidelines. In some embodiments, the vaccine formulation or immunogenic composition is suitable for administration to a non-human animal. In some embodiments, the vaccine or immunogenic composition is substantially free of either endotoxins or exotoxins.

Endotoxins may include pyrogens, such as lipopolysaccharide (LPS) molecules. The vaccine or immunogenic composition may also be substantially free of inactive protein fragments which may cause a fever or other side effects. In some embodiments, the composition contains less than 1%, less than 0.1 %, less than 0.01%, less than 0.001 %, or less than 0.0001% of endotoxins, exotoxins, and/or inactive protein fragments. In some embodiments, the vaccine or

immunogenic composition has lower levels of pyrogens than industrial water, tap water, or distilled water. Other vaccine or immunogenic composition components may be purified using methods known in the art, such as ion-exchange chromatography, ultrafiltration, or distillation. In other embodiments, the pyrogens may be inactivated or destroyed prior to administration to a patient. Raw materials for vaccines, such as water, buffers, salts and other chemicals may also be screened and depyrogenated. All materials in the vaccine may be sterile, and each lot of the vaccine may be tested for sterility. Thus, in certain embodiments the endotoxin levels in the vaccine fall below the levels set by the USFDA, for example 0.2 endotoxin (EU)/kg of product for an intrathecal injectable composition; 5 EU/kg of product for a non-intrathecal injectable composition, and 0.25-0.5 EU/mL for sterile water.

In certain embodiments, the preparation comprises less than 50%, 20%, 10%, or 5% (by dry weight) contaminating protein. In certain embodiments, the desired molecule is present in the substantial absence of other biological macromolecules, such as other proteins (particularly other proteins which may substantially mask, diminish, confuse or alter the characteristics of the component proteins either as purified preparations or in their function in the subject reconstituted mixture). In certain embodiments, at least 80%, 90%, 95%, 99%, or 99.8% (by dry weight) of biological macromolecules of the same type present (but water, buffers, and other small molecules, especially molecules having a molecular weight of less than 5000, can be present). In some embodiments, the vaccine or immunogenic composition comprising purified subunit proteins contains less than 5%, 2%, 1%, 0.5%, 0.2%, 0.1% of protein from host cells in which the subunit proteins were expressed, relative to the amount of purified subunit. In some embodiments, the desired polypeptides are substantially free of nucleic acids and/or

carbohydrates. For instance, in some embodiments, the vaccine or immunogenic composition contains less than 5%, less than 2%, less than 1%, less than 0.5%, less than 0.2%, or less than 0.1% host cell DNA and/or RNA. In certain embodiments, at least 80%, 90%, 95%, 99%, or 99.8% (by dry weight) of biological macromolecules of the same type are present in the preparation (but water, buffers, and other small molecules, especially molecules having a molecular weight of less than 5000, can be present).

It is preferred that the vaccine or immunogenic composition has low or no toxicity, within a reasonable risk-benefit ratio. In certain embodiments, the vaccine or immunogenic composition comprises ingredients at concentrations that are less than LD ₅₀ measurements for the animal being vaccinated. LD ₅₀ measurements may be obtained in mice or other experimental model systems, and extrapolated to humans and other animals. Methods for estimating the LD ₅₀ of compounds in humans and other animals are well-known in the art. A vaccine formulation or immunogenic composition, and any component within it, might have an LD ₅₀ value in rats of greater than 100 g/kg, greater than 50g/kg, greater than 20 g/kg, greater than 10 g/kg, greater than 5 g/kg, greater than 2 g/kg, greater than 1 g/kg, greater than 500 mg/kg, greater than 200 mg/kg, greater than 100 mg/kg, greater than 50 mg/kg, greater than 20 mg/kg, or greater than 10 mg/kg. A vaccine formulation or immunogenic composition that comprises a toxin such as botulinum toxin (which can be used as an adjuvant) should contain significantly less than the LD ₅₀ of botulinum toxin.

The formulations suitable for introduction of the vaccine formulations or pharmaceutical composition vary according to route of administration. Formulations suitable for parenteral administration, such as, for example, by intraarticular (in the joints), intravenous, intramuscular, intradermal, intraperitoneal, intranasal, and subcutaneous routes, include aqueous and non- aqueous, isotonic sterile injection solutions, which can contain antioxidants, buffers,

bacteriostats, and solutes that render the formulation isotonic with the blood of the intended recipient, and aqueous and non-aqueous sterile suspensions that can include suspending agents, solubilizers, thickening agents, stabilizers, and preservatives. The formulations can be presented in unit-dose or multi-dose sealed containers, such as ampoules and vials.

Injection solutions and suspensions can be prepared from sterile powders, granules, and tablets of the kind previously described. In the case of adoptive transfer of therapeutic T cells, the cells can be administered intravenously or parenterally.

Formulations suitable for oral administration can consist of (a) liquid solutions, such as an effective amount of the polypeptides or packaged nucleic acids suspended in diluents, such as water, saline or PEG 400; (b) capsules, sachets or tablets, each containing a predetermined amount of the active ingredient, as liquids, solids, granules or gelatin; (c) suspensions in an appropriate liquid; and (d) suitable emulsions. Tablet forms can include one or more of lactose, sucrose, mannitol, sorbitol, calcium phosphates, corn starch, potato starch, tragacanth, microcrystalline cellulose, acacia, gelatin, colloidal silicon dioxide, croscarmellose sodium, talc, magnesium stearate, stearic acid, and other excipients, colorants, fillers, binders, diluents, buffering agents, moistening agents, preservatives, flavoring agents, dyes, disintegrating agents, and pharmaceutically compatible carriers. Lozenge forms can comprise the active ingredient in a flavor, usually sucrose and acacia or tragacanth, as well as pastilles comprising the active ingredient in an inert base, such as gelatin and glycerin or sucrose and acacia emulsions, gels, and the like containing, in addition to the active ingredient, carriers known in the art. The pharmaceutical compositions can be encapsulated, e.g., in liposomes, or in a formulation that provides for slow release of the active ingredient.

The antigens, alone or in combination with other suitable components, can be made into aerosol formulations (e.g., they can be "nebulized") to be administered via inhalation. Aerosol formulations can be placed into pressurized acceptable propellants, such as

dichlorodifluoromethane, propane, nitrogen, and the like. Aerosol formulations can be delivered orally or nasally.

Suitable formulations for vaginal or rectal administration include, for example, suppositories, which consist of the polypeptides or packaged nucleic acids with a suppository base. Suitable suppository bases include natural or synthetic triglycerides or paraffin

hydrocarbons. In addition, it is also possible to use gelatin rectal capsules which consist of a combination of the polypeptides or packaged nucleic acids with a base, including, for example, liquid triglycerides, polyethylene glycols, and paraffin hydrocarbons.

J. Preparation and Storage of Vaccine Formulations and Immunogenic Compositions The S. pneumoniae vaccines and immunogenic compositions described herein may be produced using a variety of techniques. For example, a polypeptide may be produced using recombinant DNA technology in a suitable host cell. A suitable host cell may be bacterial, yeast, mammalian, or other type of cell. The host cell may be modified to express an exogenous copy of one of the relevant polypeptide genes. Typically, the gene is operably linked to appropriate regulatory sequences such as a strong promoter and a polyadenylation sequence. In some embodiments, the promoter is inducible or repressible. Other regulatory sequences may provide for secretion or excretion of the polypeptide of interest or retention of the polypeptide of interest in the cytoplasm or in the membrane, depending on how one wishes to purify the polypeptide. The gene may be present on an extrachromosomal plasmid, or may be integrated into the host genome. One of skill in the art will recognize that it is not necessary to use a nucleic acid 100% identical to the naturally-occurring sequence. Rather, some alterations to these sequences are tolerated and may be desirable. For instance, the nucleic acid may be altered to take advantage of the degeneracy of the genetic code such that the encoded polypeptide remains the same. In some embodiments, the gene is codon-optimized to improve expression in a particular host. The nucleic acid may be produced, for example, by PCR or by chemical synthesis.

Once a recombinant cell line has been produced, a polypeptide may be isolated from it. The isolation may be accomplished, for example, by affinity purification techniques or by physical separation techniques (e.g., a size column).

In a further aspect of the present disclosure, there is provided a method of manufacture comprising mixing one or more polypeptides or an immunogenic fragment or variant thereof with a carrier and/or an adjuvant.

In some embodiments, antigens for inclusion the vaccine formulations and immunogenic compositions may be produced in cell culture. One method comprises providing one or more expression vectors and cloning nucleotides encoding one or more polypeptides selected from polypeptides having an amino acid sequence of Table 1 or 2, such as SEQ ID NO: 265, 266, or 268, then expressing and isolating the polypeptides. The immunogenic polypeptides described herein, and nucleic acid compositions that express the polypeptides, can be packaged in packs, dispenser devices, and kits for administering nucleic acid compositions to a mammal. For example, packs or dispenser devices that contain one or more unit dosage forms are provided. Typically, instructions for administration of the compounds will be provided with the packaging, along with a suitable indication on the label that the compound is suitable for treatment of an indicated condition, such as those disclosed herein.

V. Examples

Example 1. Antigen identification and pooled murine screens

Each open reading frame predicted in the S. pneumoniae TIGR4 genome was cloned into an expression vector comprising a tag that is able to be presented by the major histocompatibility complex (MHC). Each construct was then expressed in E. coli, and full-length expression validated by a surrogate assay that identifies the tag in the context of MHC. The screen is described in more detail in International Application WO 2010/002993. In order to facilitate screening the large library, the library was pooled such that four induced library clones were present in each well. In order to screen T cells from mice immunized against S. pneumoniae, an aliquot of the pooled library was added to peritoneal-derived macrophages. The macrophages were allowed to bind the tagged S. pneumoniae antigens via the MHC. After 2 hr at 37°C, the macrophages were washed with PBS. The macrophages were then fixed with 1%

paraformaldehyde for 15 min and washed extensively with PBS. 10 ⁵ T cells were added to each well in 200 μΕ of RP-10 media. The T cells had previously been isolated from mice that had been immunized 2 times with killed S. pneumoniae bacteria with cholera toxin adjuvant. The assay plates were incubated for 72 hrs at 37°C. The amount of IL-17 in the supernatant of each well was determined through the use of an IL-17 ELISA assay. The threshold for a positive result was set at two standard deviations above the mean of all samples.

Example 2. Deconvolution of the positive murine pools

A secondary screen was used to determine which antigen(s) out of the four clones in each well induced the positive response observed in the pooled screen described in Example 1. All the clones in each positive pool were pulsed individually onto peritoneal macrophages in duplicate wells. T cells isolated from immunized mice from the same genetic background as the initial screen were used to screen the pulsed macrophages using the IL-17 assay described in Example 1. Individual antigens that induced an average response in the duplicate wells greater than two standard deviations above the mean of negative control samples were considered positive responses. The library plasmids present in these positive clones were sequenced to confirm the identity of the antigen. The antigens SP1574, SP1655, SP2106, SP0148, SP1473, SP0605, SP1177, SP0335, SP0906, SP1828, SP2157, SP1229, SP1128, SP1836, SP1865, SP0904, SP0882, SP0765, SP1634, SP0418, SP1923, SP1313, SP0775, SP0314, SP0912, SP0159, SP0910, SP2148, SP1412, SP0372, SP1304, SP2002, SP0612, SP1988, SP0484, SP0847, SP1527, SP0542, SP0441, SP0350, SP0014, SP1965, SP0117, and SP2108 were confirmed using this method.

Example 3. Antigen identification and pooled human screens

CD4+ T cells and CD14 ⁺ monocytes were isolated from peripheral blood acquired from human donors. The monocytes were differentiated into dendritic cells by culturing them in GM- CSF and IL-4 containing media, essentially as described in Tedder TF and Jansen PJ (1997 "Isolation and generation of human dendritic cells." Current Protocols in Immunology Supp 23: 7.32.1-7.32.16). After five days in culture, the dendritic cells were seeded into 384 well plates. The CD4 ⁺ T cells were non-specifically expanded in culture to ensure sufficient quantities.

Each open reading frame predicted in the S. pneumoniae TIGR4 genome was cloned into an expression vector comprising a tag that is able to be presented by the major histocompatibility complex (MHC). Each construct was then expressed in E. coli, and full-length expression validated by a surrogate assay that identifies the tag in the context of MHC. In order to facilitate screening the large library, the library was pooled such that four induced library clones were present in each well. In order to screen the human T cells, an aliquot of the pooled library was added to the seeded dendritic cells in 384-well plates. After 2 hr at 37°C, the dendritic cells were fixed with 1% paraformaldehyde for 15 min and washed extensively with phosphate buffer and lysine buffer. 40,000 of the CD4 ⁺ T cells in 70 μΕ of RP-10 media were added to each well of a 384-well plate. The assay plates were incubated for 3 days at 37°C. The amount of IL-17 in the supernatant of each well was determined through the use of an IL-17 ELISA assay. In different iterations of the screen, the threshold for a positive result was set at two standard deviations above the mean of all samples, two standard deviations above the mean of negative controls, or 1.78 times the median absolution deviation of the data set. Positive pools were then

deconvoluted as described in Example 4. Example 4. Deconvolution of the positive human pools

For all antigens, deconvolution was performed by comparing the results of two pool screens. In this method, two different sets of pools were prepared, so that a polypeptide was with three different polypeptides between the first and second pools. Consequently, it is possible to determine which polypeptides are antigens by identifying which polypeptides are in positive pools in both the first and second sets. In this deconvolution method, a pool was identified as positive if it was at least 1.78 times the median absolution deviation of the data set.

An antigen was identified as a positive hit if it was positive in at least two repeated secondary screens. The antigens SP2108, SP0641, SP1393, SP0024, SP0641.1, SP1072, SP1384 and SP2032 were identified using the above approach.

Example 5

SP2108, SP0148 and SP1634 polypeptides

The SP2108 polypeptide (SEQ ID NO: 9), SP0148 polypeptide (SEQ ID NO: 7) and SP1634 polypeptide (see Table 2) were formulated as vaccine compositions using 4 μg of the polypeptide in combination with 1 μg cholera toxin adjuvant (CT). For combinations, 4 μg of each polypeptide was used. The compositions were administered intranasally to C57BL/6 mice three times, one week apart. The subjects were then allowed to rest for 3 weeks, and bled at that time for immunogenicity. For this assay, heparinized whole blood was collected from the retrograde orbital sinus. The total PBMC were stimulated with either killed, unencapsulated whole cell S. pneumoniae (WCC) or a combination of the three polypeptides in round bottomed tubes for three days. The supernatants were then harvested and evaluated by ELISA for IL-17 levels. Cholera toxin alone (CT) or an unrelated antigen from HSV (003) were used as negative controls. Results of the IL-17 immunogenicity assay are shown in FIGS. 1 and 2, where the left panels show data in scatter format, and the right panels show data as averages with standard deviations. The subjects were allowed to rest an additional 2 weeks, at which time they were challenged with intranasal administration of live, encapsulated S. pneumoniae. The subjects were sacrificed a week later, and the number of colony-forming units (CFU) was counted from nasal washes. Results of the colonization assay are shown in FIG. 3.

Example 6

SP0882 and SP0314 polypeptides This example used the same protocols as Example 5, except that only two doses of the vaccine composition were administered. In these experiments, the SP0882 polypeptide (SEQ ID NO: 2) and SP0314 polypeptides (see Table 2) were tested in parallel with two of the three polypeptides tested in Example 5. Results of the IL-17 immunogenicity assay are shown in FIGS. 4 and 5. Results of the colonization assay are shown in FIG. 6.

Example 7

SP1072, SP0641N, and SP0024 polypeptides

This example used a protocol similar to that of Example 5, except that two doses of the vaccine compositions were administered, one week apart. Vaccine compositions comprised the polypeptides SP1072 (SEQ ID NO: 8), SP0641N (SEQ ID NO: 13) or SP0024 (SEQ ID NO: 1), and cholera toxin adjuvant (CT). Four weeks after the last immunization, the mice were challenged intranasally with live type 6B S. pneumoniae. One week later the bacterial burden was assessed in each mouse by plating a nasal lavage on selective media and counting resultant CFU. The number of CFU isolated from each mouse is plotted for each immunized cohort. The results of this colonization assay are shown in FIG. 7. Statistically significant results are indicated in the figure (* = p- value < 0.05).

Example 8

SP0148, SP0314, SP0882, and SP2108 polypeptides tested in the BALB/c mouse

To determine whether similar immune responses were seen across different mouse genotypes, vaccine compositions were administered to BALB/c mice. Vaccine compositions comprised the polypeptides SP0148 (SEQ ID NO: 2), SP0314 (see Table 2), SP0882 (SEQ ID NO: 2) or SP2108 (SEQ ID NO: 9), and cholera toxin adjuvant (CT). Using a protocol similar to that of Example 5, the mice were immunized, challenged intranasally with S. pneumoniae, and the number of CFU was recorded. The results of this colonization experiment are shown in FIG. 8. Example 9

SP1912, SP2108 and SP0148 polypeptides: IL-17A immunogenicity assay

The polypeptides SP1912 (SEQ ID NO: 265), SP2108 (SEQ ID NO: 9) or SP0148 (SEQ ID NO: 7) were formulated as vaccine compositions with cholera toxin adjuvant (CT). The vaccine compositions were administered to mice two times, one week apart. The positive control was killed, unencapsulated whole cell S. pneumoniae + CT (WCB), and the negative controls were

CT alone or recombinant proteins without CT (with the exception of SP1912). Three weeks after the last immunization, peripheral blood was collected from the retroorbital sinus and evaluated in a whole blood assay. Briefly, the heparizined whole blood was diluted in media and then cultured in duplicate with A) the protein of immunization, or B) the whole cell vaccine for six days. The supernatants were harvested and IL-17A levels measured by ELISA. Results of the IL-17A immunogenicity assay are shown in FIG. 9. Each symbol in the graph represents responses from individual mice, and the line indicates the median response of the group.

Example 10

SP1912, SP2108 and SP0148 polypeptides: colonization assay

Animals were immunized with vaccine formulations comprising the polypeptides SP1912 (SEQ ID NO: 265), SP2108 (SEQ ID NO: 9) or SP0148 (SEQ ID NO: 7) and cholera toxin adjuvant η

(CT) as described in Example 9, and then challenged intranasally with 10 live type 6B S.

pneumoniae four weeks after the last immunization (and one week after retroorbital blood collection). Seven days after challenge, animals were euthanized and the nasopharyngeal cavities lavaged and cultured on permissive media to evaluate the S. pneumoniae titers. Results are shown in FIG. 10 as the colony forming units of bacteria (CFU) per lavage. Each symbol represents a titer from an individual mouse response, and the horizontal line represents the median of the group. (*** = p-value <0.05).

Example 11

SP1912 polypeptide: aspiration challenge (sepsis assay)

Polypeptide SP1912 was evaluated for its ability to protect mice from sepsis. Groups of ten mice were subcutaneously immunized three times, two weeks apart with vaccine compositions comprising either the SP1912 polypeptide (SEQ ID NO: 265) or pneumolysoid (PdT) adsorbed to alum. The positive control was killed, unencapsulated whole cell S. pneumoniae + alum (WCB), and the negative control was alum alone. Three weeks after the final immunization, blood was collected for evaluation of IL-17A response and antibody levels, and then one week η

later, the mice underwent aspiration challenge with 10 live strain 0603 (type 6B) S. pneumoniae. Animals were monitored for survival for eight days. Results of the aspiration challenge are shown in FIG. 11 as survival curves for each immunized group.

Example 12

Pneumolysoid PdT, SP0148 and SP0641N polypeptides: aspiration challenge (sepsis assay) Polypeptide SP0148 was evaluated for its ability to protect mice from sepsis when immunized singly or in combination with SP0641N and/or pneumolysoid (PdT). Groups of ten mice were subcutaneously immunized three times, two weeks apart with vaccine compositions comprising polypeptide SP0148 (SEQ ID NO: 7), singly or in combination with polypeptide SP0641N (SEQ ID NO: 13) and/or PdT, adsorbed to alum. The positive control was killed, unencapsulated whole cell S. pneumoniae + alum (WCB), and the negative control was alum alone. Three weeks after the final immunization, blood was collected for evaluation of IL-17 and antibody, and then one week later, the mice underwent aspiration challenge with 10 live strain 0603 (type 6B) S. pneumoniae. Animals were monitored for survival for eight days. The data are shown in FIG. 12 as survival curves for each immunized group.

Example 13

SP1912, SP2108 and SP0148 polypeptides: colonization assay

Additional studies were performed essentially as described in Example 10, for a total of four separate studies. Briefly, animals were immunized with vaccine formulations comprising the polypeptides SP1912 (SEQ ID NO: 265), SP2108 (SEQ ID NO: 9), SP0148 (SEQ ID NO: 7), or additionally SP2108 plus SP0148, and cholera toxin adjuvant (CT) as described in Example 9. Control animals were immunized with killed, unencapsulated whole cell S. pneumoniae plus CT (WCB), or CT alone. Immunized animals were challenged intranasally with 10 live type 6B S. pneumoniae four weeks after the last immunization. Seven days after challenge, animals were euthanized and the nasopharyngeal cavities lavaged and cultured on permissive media to evaluate the S. pneumoniae titers. Pooled results of four studies are shown in FIG. 13 as the colony forming units of bacteria (CFU) per lavage. Each symbol represents a titer from an individual mouse response, and the horizontal line represents the median of the group. (*** = p- value <0.05). N indicates the total number of animals evaluated. Percentages refer to the number of animals protected from colonization.

Example 14

SP1912 and SP0148 polypeptides: IL-17A immunogenicity assay

Groups of ten mice were subcutaneously immunized twice, two weeks apart with vaccine compositions comprising either SP1912 polypeptide (SEQ ID NO: 265), SP0148 polypeptide (SEQ ID NO: 7), or both adsorbed to alum. Control animals were immunized with alum alone. Three weeks after the last immunization, heparinized blood was collected by cardiac puncture and evaluated for IL-17A levels in a whole blood assay. Briefly, the heparizined whole blood was diluted in media and then cultured for six days with the protein(s) of immunization. The supernatants were harvested and IL-17A levels measured by ELISA. Results of the IL-17A immunogenicity assay are shown in FIG. 14. Each symbol in the graph represents responses from individual mice, and the line indicates the median response of the group.

Example 15

SP1912 and SP0148 polypeptides: colonization assay

Animals were subcutaneously immunized three times, two weeks apart with vaccine

formulations comprising the polypeptides SP0148 (SEQ ID NO: 7) at different doses plus and minus SP1912 (SEQ ID NO: 265), adsorbed to alum. Control animals were immunized with killed, unencapsulated whole cell S. pneumoniae plus alum (WCV), or alum alone. Immunized animals were challenged intranasally with 10 live type 6B S. pneumoniae four weeks after the last immunization. Seven days after challenge, animals were euthanized and the nasopharyngeal cavities lavaged and cultured on permissive media to evaluate the S. pneumoniae titers. Results are shown in FIG. 15 as the colony forming units of bacteria (CFU) per lavage. Each symbol represents a titer from an individual mouse response, and the horizontal line represents the median of the group. The number of animals protected from colonization out of the number of animals in the group is indicated at the top of the figure.

Example 16

SP1912, SP0148, and SP2108 polypeptides: colonization assay

In two separate studies, animals were subcutaneously immunized three times, two weeks apart with vaccine formulations comprising the polypeptides SP0148 (SEQ ID NO: 7) and SP0148 plus SP1912 (SEQ ID NO: 265), or additionally with SP2108 (SEQ ID NO: 9), SP2108 plus SP0148, and SP2108 plus SP1912, adsorbed to alum. Control animals were immunized with killed, unencapsulated whole cell S. pneumoniae plus alum (WCV), or alum alone. Immunized η

animals were challenged intranasally with 10 live type 6B S. pneumoniae four weeks after the last immunization. Seven days after challenge, animals were euthanized and the nasopharyngeal cavities lavaged and cultured on permissive media to evaluate the S. pneumoniae titers. Pooled results of the two studies are shown in FIG. 16 as the colony forming units of bacteria (CFU) per lavage. Each symbol represents a titer from an individual mouse response, and the horizontal line represents the median of the group. The number of animals protected from colonization out of the number of animals in the group and corresponding percentage of animals protected from colonization are indicated at the top of the figure. (*p<0.05, **p<0.01, ***p<0.001 Dunn's Multiple Comparison Test compared to Alum control)

Example 17

Pneumolysoid L460D, PspA derivative PR+NPB, SP1912, SP0148, and SP2108

polypeptides: colonization assay

Animals were subcutaneously immunized three times, two weeks apart with vaccine

formulations comprising the polypeptides SP0148 (SEQ ID NO: 7), SP2108 (SEQ ID NO: 9), SP0148 plus SP2108, and SP0148 plus SP2108 in combination with SP1912 (SEQ ID NO: 265) or known S. pneumoniae antigens L460D plus PR+NPD, adsorbed to alum. Two separate studies were conducted. Control animals were immunized with alum alone. Immunized animals were challenged intranasally with 10 live type 6B S. pneumoniae four weeks after the last immunization. Seven days after challenge, animals were euthanized and the nasopharyngeal cavities lavaged and cultured on permissive media to evaluate the S. pneumoniae titers. Results of the second study are shown in FIG. 17 as the colony forming units of bacteria (CFU) per lavage. Each symbol represents a titer from an individual mouse response, and the horizontal line represents the median of the group. The number of animals protected from colonization out of the number of animals in the group is indicated at the top of the figure.

The chart below shows the absolute number and corresponding percentage of animals protected from colonization in the four studies described in Examples 16 and 17.

2108 + 1912 3/10 10 30%

0148 + 2108 + 1912 8/9 8/10 6/10 22/29 76%

0148 + 2108 + L460D +

2/10 6/10 8/20 40% PR+N PB

Example 18

PspA, SP0148 and SP2108 passive antibody transfer and aspiration challenge (sepsis assay)

Groups of ten mice were injected with monoclonal antibodies specific for PspA, heat-inactivated rabbit sera specific for SP0148, SP2108, or combinations of these. Antibody and antisera concentrations and total injection volumes were adjusted with normal rabbit serum (NRS) and PBS. Control animals were injected with NRS, or serum against killed, unencapsulated whole cell S. pneumoniae (WCB). One day after injection, the mice underwent aspiration challenge with 10 ⁶ live S. pneumoniae type WU-2 (ST-3). Animals were monitored for survival for eight days. The data are shown in FIG. 18 as survival curves for each immunized group.

FIG. 19 shows the percent of animals protected from sepsis in the studies described in Examples

12 and 18, as well as two additional studies.

SEQUENCES

SEQ ID NO: 1

SP0024

>gi I 14971488 I g I AAK74215.1 I conserved hypothetical protein Streptococcus pneumoniae TIGR4

MSYFEQFMQANQAYVALHGQLNLPLKPKTRVAIVTCMDSRLHVAQALGLALGDAHILRNA GGRVTEDMIRSLVISQQ QMGTRE IWLHHTDCGAQTFENEPFQEYLKEELGVDVSDQDFLPFQDIEESVREDMQLLIESPLIPD DVI ISGAIYN VDTGSMTWEL

SEQ ID NO: 2

SP0882

>gi I 14972356 I g I AAK75009.1 I conserved hypothetical protein (Streptococcus pneumoniae TIGR4)

MNQSYFYLKMKEHKLKVPYTGKERRVRILLPKDYEKDTDRSYPWYFHDGQNVFNSKESF IGHSWKI IPAIKRNPDI SRMIWAIDNDGMGRMNEYAAWKFQESPIPGQQFGGKGVEYAEFVMEVVKPFIDETYRTKA DCQHTAMIGSSLGGNI TQF IGLEYQDQIGCLGVFSSANWLHQEAFNRYFECQKLSPDQRIF IYVGTEEADDTDKTLMDGNIKQAYIDSSLCYY HDL IAGGVHLDNLVLKVQSGAIHSEIPWSENLPDCLRFFAEKW SEQ ID NO: 3

SP0882N

MNQSYFYLKMKEHKLKVPYTGKERRVRILLPKDYEKDTDRSYPWYFHDGQNVFNSKESF IGHSWKI IPAIKRNPDI SRMIWAIDNDGMGRMNEYAAWKFQESPIPGQQFGGKGVEYAEFVMEVVKPFI

SEQ ID NO: 4

SP0882 with exogenous signal seguence

MSSKFMKSAAVLGTATLASLLLVACMNQSYFYLKMKEHKLKVPYTGKERRVRILLPKDYE KDTDRSYPVVYFHDGQN VFNSKESFIGHSWKI IPAIKRNPDISRMIVVAIDNDGMGRMNEYAAWKFQESPIPGQQFGGKGVEYAEFVMEWKP F IDETYRTKADCQHTAMIGSSLGGNITQFIGLEYQDQIGCLGVFSSANWLHQEAFNRYFEC QKLSPDQRIFIYVGTEE ADDTDKTLMDGNIKQAYIDSSLCYYHDLIAGGVHLDNLVLKVQSGAIHSEIPWSENLPDC LRFFAEKW

SEQ ID NO: 5

SP0882N with exogenous signal seguence

MSSKFMKSAAVLGTATLASLLLVACMNQSYFYLKMKEHKLKVPYTGKERRVRILLPKDYE KDTDRSYPVVYFHDGQN VFNSKESFIGHSWKI IPAIKRNPDISRMIVVAIDNDGMGRMNEYAAWKFQESPIPGQQFGGKGVEYAEFVMEWKP F I

SEQ ID NO: 6

SP0148 lacking signal seguence

MCSGGAKKEGEAASKKEI IVATNGSPKPFIYEENGELTGYEIEWRAIFKDSDKYDVKFEKTEWSGVFAGLDADRYN MAVNNLSYTKERAEKYLYAAPIAQNPNVLVVKKDDSSIKSLDDIGGKSTEVVQATTSAKQ LEAYNAEHTDNPTILNY TKADFQQIMVRLSDGQFDYKIFDKIGVETVIKNQGLDNLKVIELPSDQQPYVYPLLAQGQ DELKSFVDKRIKELYKD GTLEKLSKQFFGDTYLPAEADIKE

SEQ ID NO: 7

SP0148 including signal seguence (277 amino acids with N-terminal E)

MKKIVKYSSLAALALVAAGVLAACSGGAKKEGEAASKKE I IVATNGSPKPF IYEENGELTGYE IEVVRAIFKDSDKY DVKFEKTEWSGVFAGLDADRYNMAVNNLSYTKERAEKYLYAAPIAQNPNVLWKKDDSSIK SLDDIGGKSTEWQAT TSAKQLEAYNAEHTDNPT ILNYTKADFQQIMVRLSDGQFDYKIFDKIGVETVIKNQGLDNLKVIELPSDQQPYVYPL LAQGQDELKSFVDKRIKELYKDGTLEKLSKQFFGDTYLPAEADIKE

SEQ ID NO: 8

SP1072

>gi I 14972547 I g I AAK75185.1 I DNA primase Streptococcus pneumoniae TIGR4 MVDKQVIEE IKNNANIVEVIGDVI SLQKAGRNYLGLCPFHGEKTPSFNWEDKQFYHCFGCGRSGDVFKFIEEYQGV PFIEAVQILGQRVGIEVEKPLYSEQKSASPHQALYDMHEDAAKFYHAILMTTTMGEEARN YLYQRGLTDEVLKHFWI GLAPPERNYLYQRLSDQYREEDLLDSGLFYLSDANQFVDTFHNRIMFPLTNDQGKVIAFS GRIWQKTDSQTSKYKNS RSTAIFNKSYELYHMDRAKRSSGKASE IYLMEGFMDVIAAYRAGIENAVASMGTALSREHVEHLKRLTKKLVLVYDG DKAGQAATLKALDEIGDMPVQIVSMPDNLDPDEYLQKNGPEDLAYLLTKTRISPIEFYIH QYKPENSENLQAQIEFL EKIAPL IVQEKS IAAQNSYIHILADSLASFDYTQIEQIVNESRQVQRQNRMEGI SRPTPITMPVTKQLSAIMRAEAH LLYRMMESPLVLNDYRLREDFAFATPEFQVLYDLLGQYGNLPPEVLAEQTEEVERAWYQV LAQDLPAEI SPQELSEV EMTRNKALLNQDNMRIKKKVQEASHVGDTDTALEELERL ISQKRRME

SEQ ID NO: 9

SP2108 including signal seguence

>gi I 14973620 I g I AAK76167.1 I maltose/maltodextrin ABC transporter,

maltose/maltodextrin-binding protein (Streptococcus pneumoniae TIGR4)

MSSKFMKSAAVLGTATLASLLLVACGSKTADKPADSGSSEVKELTVYVDEGYKSYIE EVAKAYEKEAGVKVTLKTGD ALGGLDKLSLDNQSGNVPDVMMAPYDRVGSLGSDGQLSEVKLSDGAKTDDTTKSLVTAAN GKVYGAPAVIESLVMYY NKDLVKDAPKTFADLENLAKDSKYAFAGEDGKTTAFLADWTNFYYTYGLLAGNGAYVFGQ NGKDAKDIGLANDGS IV GINYAKSWYEKWPKGMQDTEGAGNLIQTQFQEGKTAAI IDGPWKAQAFKDAKVNYGVATIPTLPNGKEYAAFGGGKA WVIPQAVKNLEASQKFVDFLVATEQQKVLYDKTNEIPANTEARSYAEGKNDELTTAVIKQ FKNTQPLPNISQMSAVW DPAKNMLFDAVSGQKDAKTAANDAVTL IKETIKQKFGE

SEQ ID NO: 10

SP2108 lacking signal seguence

MCGSKTADKPADSGSSEVKELTVYVDEGYKSYIEEVAKAYEKEAGVKVTLKTGDALGGLD KLSLDNQSGNVPDVMMA PYDRVGSLGSDGQLSEVKLSDGAKTDDTTKSLVTAANGKVYGAPAVIESLVMYYNKDLVK DAPKTFADLENLAKDSK YAFAGEDGKTTAFLADWTNFYYTYGLLAGNGAYVFGQNGKDAKDIGLANDGSIVGINYAK SWYEKWPKGMQDTEGAG NLIQTQFQEGKTAAI IDGPWKAQAFKDAKVNYGVAT IPTLPNGKEYAAFGGGKAWVIPQAVKNLEASQKFVDFLVAT EQQKVLYDKTNE IPANTEARSYAEGKNDELTTAVIKQFKNTQPLPNISQMSAVWDPAKNMLFDAVSGQKDAK TAAND AVTLIKETIKQKFGE

SEQ ID NO: 11

SP0641M

MSGTSMATPIVAASTVLIRPKLKEMLERPVLKNLKGDDKIDLTSLTKIALQNTARPMMDA TSWKEKSQYFASPRQQG AGL INVANALRNEWATFKNTDSKGLVNSYGSI SLKEIKGDKKYFTIKLHNTSNRPLTFKVSASAITTDSLTDRLKL DETYKDEKSPDGKQIVPEIHPEKVKGANITFEHDTFTIGANSSFDLNAVINVGEAKNKNK FVESFIHFESVEEMEAL NSNGKKINFQPSLSMPLMGFAGNWNHEPILDKWAWEEGSRSKTLGGYDDDGKPKIPGTLN KGIGGEHGIDKFNPAGV IQNRKDKNTTSLDQNPELFAFNNEGINAPSSSGSKIANIYPLDSNGNPQDAQLERGLTPS PLVLRSAEEGLI SIVNT NKEGENQRDLKVISREHF IRGILNSKSNDAKGIKSSKLKVWGDLKWDGLIYNPRGREENAPESKDNQDPATKIRGQF EPIAEGQYFYKFKYRLTKDYPWQVSYIPVKIDNTAPKIVSVDFSNPEKIKL ITKDTYHKVKDQYKNETLFARDQKEH PEKFDE IANEVWYAGAALVNEDGEVEKNLEVTYAGEGQGRNRKLDKDGNTIYEIKGAGDLRGKI IEVIALDGSSNFT KIHRIKFANQADEKGMISYYLVDPDQDSSKYQ

SEQ ID NO: 12

SP0641

>gi I 14972117 I g I AAK74791.1 I serine protease, subtilase family [Streptococcus pneumoniae TIGR4]

MKKSTVLSLTTAAVILAAYAPNEVVLADTSSSEDALNISDKEKVAENKEKHENIHSAMET SQDFKEKKTAVIKEKEV VSKNPVIDNNTSNEEAKIKEENSNKSQGDYTDSFVNKNTENPKKEDKVVYIAEFKDKESG EKAIKELSSLKNTKVLY TYDRIFNGSAIETTPDNLDKIKQIEGI SSVERAQKVQPMMNHARKEIGVEEAIDYLKSINAPFGKNFDGRGMVISNI DTGTDYRHKAMRIDDDAKASMRFKKEDLKGTDKNYWLSDKIPHAFNYYNGGKITVEKYDD GRDYFDPHGMHIAGILA GNDTEQDIKNFNGIDGIAPNAQIFSYKMYSDAGSGFAGDETMFHAIEDSIKHNVDWSVSS GFTGTGLVGEKYWQAI RALRKAGIPMWATGNYATSASSSSWDLVANNHLKMTDTGNVTRTAAHEDAIAVASAKNQT VEFDKVNIGGESFKYR NIGAFFDKSKITTNEDGTKAPSKLKFVYIGKGQDQDLIGLDLRGKIAVMDRIYTKDLKNA FKKAMDKGARAIMWNT VNYYNRDNWTELPAMGYEADEGTKSQVFSI SGDDGVKLWNMINPDKKTEVKRNNKEDFKDKLEQYYPIDMESFNSNK PNVGDEKEIDFKFAPDTDKELYKEDI IVPAGSTSWGPRIDLLLKPDVSAPGKNIKSTLNVINGKSTYGYMSGTSMAT PIVAASTVL IRPKLKEMLERPVLKNLKGDDKIDLTSLTKIALQNTARPMMDATSWKEKSQYFASPRQQG AGL INVAN ALRNEVVATFKNTDSKGLVNSYGS ISLKEIKGDKKYFTIKLHNTSNRPLTFKVSASAITTDSLTDRLKLDETYKDEK SPDGKQIVPEIHPEKVKGANITFEHDTFTIGANSSFDLNAVINVGEAKNKNKFVESF IHFESVEEMEALNSNGKKIN FQPSLSMPLMGFAGNWNHEPILDKWAWEEGSRSKTLGGYDDDGKPKIPGTLNKGIGGEHG IDKFNPAGVIQNRKDKN TTSLDQNPELFAFNNEGINAPSSSGSKIANIYPLDSNGNPQDAQLERGLTPSPLVLRSAE EGL ISIVNTNKEGENQR DLKVISREHFIRGILNSKSNDAKGIKSSKLKVWGDLKWDGLIYNPRGREENAPESKDNQD PATKIRGQFEPIAEGQY FYKFKYRLTKDYPWQVSYIPVKIDNTAPKIVSVDFSNPEKIKLITKDTYHKVKDQYKNET LFARDQKEHPEKFDE IA NEVWYAGAALVNEDGEVEKNLEVTYAGEGQGRNRKLDKDGNT IYE IKGAGDLRGKI IEVIALDGSSNFTKIHRIKFA NQADEKGMI SYYLVDPDQDSSKYQKLGEIAESKFKNLGNGKEGSLKKDTTGVEHHHQENEESIKEKSSF TIDRNI ST IRDFENKDLKKL IKKKFREVDDFTSETGKRMEEYDYKYDDKGNI IAYDDGTDLEYETEKLDEIKSKIYGVLSPSKDG HFE ILGKISNVSKNAKVYYGNNYKSIE IKATKYDFHSKTMTFDLYANINDIVDGLAFAGDMRLFVKDNDQKKAEIKI RMPEKIKETKSEYPYVSSYGNVIELGEGDLSKNKPDNLTKMESGKIYSDSEKQQYLLKDN I ILRKGYALKVTTYNPG KTDMLEGNGVYSKEDIAKIQKANPNLRALSETT IYADSRNVEDGRSTQSVLMSALDGFNI IRYQVFTFKMNDKGEAI DKDGNLVTDSSKLVLFGKDDKEYTGEDKFNVEAIKEDGSMLF IDTKPVNLSMDKNYFNPSKSNKIYVRNPEFYLRGK ISDKGGFNWELRVNESWDNYLIYGDLHIDNTRDFNIKLNVKDGDIMDWGMKDYKANGFPD KVTDMDGNVYLQTGYS DLNAKAVGVHYQFLYDNVKPEVNIDPKGNTSIEYADGKSWFNINDKRNNGFDGEIQEQHI YINGKEYTSFNDIKQI IDKTLNIKIWKDFARNTTVKEFILNKDTGEVSELKPHRVTVTIQNGKEMSSTIVSEEDFI LPVYKGELEKGYQFDG WEI SGFEGKKDAGYVINLSKDTFIKPVFKKIEEKKEEENKPTFDVSKKKDNPQVNHSQLNESH RKEDLQREEHSQKS DSTKDVTATVLDKNNISSKSTTNNPNKLPKTGTASGAQTLLAAGIMFIVGIFLGLKKKNQ D

SEQ ID NO: 13 SP0641N

MWLADTSSSEDALNISDKEKVAENKEKHENIHSAMETSQDFKEKKTAVIKEKEWSKNPVI DNNTSNEEAKIKEEN SNKSQGDYTDSFVNKNTENPKKEDKWYIAEFKDKESGEKAIKELSSLKNTKVLYTYDRIF NGSAIETTPDNLDKIK QIEGISSVERAQKVQPMMNHARKE IGVEEAIDYLKS INAPFGKNFDGRGMVISNIDTGTDYRHKAMRIDDDAKASMR FKKEDLKGTDKNYWLSDKIPHAFNYYNGGKITVEKYDDGRDYFDPHGMHIAGILAGNDTE QDIKNFNGIDGIAPNAQ IFSYKMYSDAGSGFAGDETMFHAIEDS IKHNVDVVSVSSGFTGTGLVGEKYWQAIRALRKAGIPMVVATGNYATSAS SSSWDLVANNHLKMTDTGNVTRTAAHEDAIAVASAKNQTVEFDKVNIGGESFKYRNIGAF FDKSKITTNEDGTKAPS KLKFVYIGKGQDQDL IGLDLRGKIAVMDRI YTKDLKNAFKKAMDKGARAIMWNTVNYYNRDNWTELPAMGYEADEG TKSQVFSISGDDGVKLWNMINPDKKTEVKRNNKEDFKDKLEQYYPIDMESFNSNKPNVGD EKE IDFKFAPDTDKELY KEDI IVPAGSTSWGPRIDLLLKPDVSAPGKNIKSTLNVINGKSTYG

SEQ ID NO: 14

SP0882 consensus

MNQSYFYLKMKEHKLKVPYTGKERRVRILLPKDYEKDTDRSYPWYFHDGQNVFNSKESF I Y

IGHSWKI IPAIKRNPDISRMIWAIDNDGMGRMNEYAAWKFQESPIPGQQFGGKGVEYAE Y H E E

FVMEWKPF IDETYRTKADCQHTAMIGSSLGGNITQFIGLEYQDQIGCLGVFSSANWLHQ

EK

EAFNRYFECQKLSPDQRIFIYVGTEEADDTDKTLMDGNIKQAYIDSSLCYYHDL IAGGVH I H R

LDNLVLKVQSGAIHSEIPWSENLPDCLRFFAEKW

SEQ ID NO: 15

SP0882N consensus

MNQSYFYLKMKEHKLKVPYTGKERRVRILLPKDYEKDTDRSYPWYFHDGQNVFNSKESF I Y

IGHSWKI IPAIKRNPD I SRMIWAIDNDGMGRMNEYAAWKFQESPIPGQQFGGKGVEYAE Y H E E

FVMEWKPF I SEQ ID NO: 16

SP0882 consensus with exogenous signal seguence

MSSKFMKSAAVLGTATLASLLLVACMNQSYFYLKMKEHKLKVPYTGKERRVRILLPK DYE T T V I

KDTDRSYPVVYFHDGQNVFNSKESFIGHSWKI IPAIKRNPDI SRMIWAIDNDGMGRMNE

Y Y H

YAAWKFQESPIPGQQFGGKGVEYAEFVMEVVKPFIDETYRTKADCQHTAMIGSSLGG NIT E E

QFIGLEYQDQIGCLGVFSSANWLHQEAFNRYFECQKLSPDQRIFIYVGTEEADDTDK TLM EK I H

DGNIKQAYIDSSLCYYHDLIAGGVHLDNLVLKVQSGAIHSEIPWSENLPDCLRFFAE KW

R

SEQ ID NO: 17

SP0882N consensus with exogenous signal seguence

MSSKFMKSAAVLGTATLASLLLVACMNQSYFYLKMKEHKLKVPYTGKERRVRILLPK DYE T T V I

KDTDRSYPVVYFHDGQNVFNSKESFIGHSWKI IPAIKRNPDI SRMIWAIDNDGMGRMNE

Y Y H

YAAWKFQESPIPGQQFGGKGVEYAEFVMEVVKPFI E E

SEQ ID NO: 18

SP0148 consensus lacking signal seguence

MCSGGAKKEGEAASKKEI IVATNGSPKPFIYEENGELTGYEIEWRAIFKDSDKYDVKFE Q S R N N X

KTEWSGVFAGLDADRYNMAVNNLSYTKERAEKYLYAAPIAQNPNVLWKKDDSS IKSLDD

I E IGGKSTEWQATTSAKQLEAYNAEHTDNPT ILNYTKADLQQIMVRLSDGQFDYKIFDKIG

F

VETVIKNQGLDNLKVIELPSDQQPYVYPLLAQGQDELKSFVDKRIKELYKDGTLEKL SKQ Y S

FFGDTYLPAEADIK (E)

SEQ ID NO: 19

SP0148 consensus including signal seguence

MKKIVKYSSLAALALVAAGVLAACSGGAKKEGEAASKKE I IVATNGSPKPF IYEENGELT G L Q S R N

GYE IEVVRAIFKDSDKYDVKFEKTEWSGVFAGLDADRYNMAVNNLSYTKERAEKYLYAAP N X I

IAQNPNVLVVKKDDSSIKSLDDIGGKSTEWQATTSAKQLEAYNAEHTDNPTILNYTK AD E

LQQIMVRLSDGQFDYKIFDKIGVETVIKNQGLDNLKVIELPSDQQPYVYPLLAQGQD ELK F Y S

SFVDKRIKELYKDGTLEKLSKQFFGDTYLPAEADIK (E)

SEQ ID NO: 20

SP2108 consensus lacking signal seguence

MCGSKTADKPADSGSSEVKELTVYVDEGYKSYIEEVAKAYEKEAGVKVTLKTGDALGGLD A I

KLSLDNQSGNVPDVMMAPYDRVGSLGSDGQLSEVKLSDGAKTDDTTKSLVTAANGKV YGA I X T

PAVIESLVMYYNKDLVKDAPKTFADLENLAKDSKYAFAGEDGKTTAFLADWTNFYYT YGL

A LAGNGAYVFGQNGKDAKDIGLANDGSIVGINYAKSWYEKWPKGMQDTEGAGNLIQTQFQE G P A X H

GKTAAI IDGPWKAQAFKDAKVNYGVAT IPTLPNGKEYAAFGGGKAWVIPQAVKNLEASQK

A

FVDFLVATEQQKVLYDKTNEIPANTEARSYAEGKNDELTTAVIKQFKNTQPLPNISQ MSA S A S

VWDPAKNMLFDAVSGQKDAKTAANDAVTLIKET IKQKFGE

SEQ ID NO: 21

SP2108 consensus including signal seguence

MSSKFMKSAAVLGTATLASLLLVACGSKTADKPADSGSSEVKELTVYVDEGYKSYIEEVA T T V A

KAYEKEAGVKVTLKTGDALGGLDKLSLDNQSGNVPDVMMAPYDRVGSLGSDGQLSEV KLS I I X

DGAKTDDTTKSLVTAANGKVYGAPAVIESLVMYYNKDLVKDAPKTFADLENLAKDSK YAF T

AGEDGKTTAFLADWTNFYYTYGLLAGNGAYVFGQNGKDAKDIGLANDGSIVGINYAK SWY

A G P A X

EKWPKGMQDTEGAGNLIQTQFQEGKTAAI IDGPWKAQAFKDAKVNYGVATIPTLPNGKEY

H

AAFGGGKAWVIPQAVKNLEASQKFVDFLVATEQQKVLYDKTNEIPANTEARSYAEGK NDE

A S A

LTTAVIKQFKNTQPLPNI SQMSAVWDPAKNMLFDAVSGQKDAKTAANDAVTLIKETIKQK S

FGE SEQ ID NO: 22

SP1634

>gi I 14973124 I g I AAK75714.1 I hypothetical protein SP_1634 Streptococcus pneumoniae TIGR4

MANIFDYLKDVAYDSYYDLPLNELDILTLIEITYLSFDNLVSTLPQRLLDLAPQVPRDPT MLTSKNRLQLLDELAQH KRFKNCKLSHFINDIDPELQKQFAAMTYRVSLDTYL IVFRGTDDS I IGWKEDFHLTYMKE IPAQKHALRYLKNFFAH HPKQKVILAGHSKGGNLAIYAASQIEQSLQNQITAVYTFDAPGLHQELTQTAGYQRIMDR SKIFIPQGSIIGMMLEI PAHQIIVQSTALGGIAQHDTFSWQIEDKHFVQLDKTNSDSQQVDTTFKEWVATVPDEELQ LYFDLFFGTILDAGISS INDLASLKALEYIHHLFVQAQSLTPEERETLGRLTQLLIDTRYQAWKNR

SEQ ID NO: 23

SP0314

>gi I 14971788 I g I AAK74491.1 I hyaluronidase Streptococcus pneumoniae

TIGR4MQTKTKKLIVSLSSLVLSGFLLNHYMTIGAEETTTNTIQQSQKEVQYQQRDT KNLVENGDFGQTEDGSSPWT GSKAQGWSAWVDQKNSADASTRVIEAKDGAITI SSHEKLRAALHRMVPIEAKKKYKLRFKIKTDNKIGIAKVRI IEE SGKDKRLWNSATTSGTKDWQT IEADYSPTLDVDKIKLELFYETGTGTVSFKDIELVEVADQLSEDSQTDKQLEEKID LPIGKKHVFSLADYTYKVENPDVASVKNGILEPLKEGTTNVIVSKDGKEVKKIPLKILAS VKDAYTDRLDDWNGI IA GNQYYDSKNEQMAKLNQELEGKVADSLSSI SSQADRTYLWEKFSNYKTSANLTATYRKLEEMAKQVTNPSSRYYQDE TVVRTVRDSMEWMHKHVYNSEKSIVGNWWDYEIGTPRAINNTLSLMKEYFSDEE IKKYTDVIEKFVPDPEHFRKTTD NPFKALGGNLVDMGRVKVIAGLLRKDDQEI SST IRS IEQVFKLVDQGEGFYQDGSYIDHTNVAYTGAYGNVL IDGLS QLLPVIQKTKNPIDKDKMQTMYHWIDKSFAPLLVNGELMDMSRGRSISRANSEGHVAAVE VLRGIHRIADMSEGETK QCLQSLVKT IVQSDSYYDVFKNLKTYKDISLMQSLLSDAGVASVPRPSYLSAFNKMDKTAMYNAEKGFG FGLSLFSS RTLNYEHMNKENKRGWYTSDGMFYLYNGDLSHYSDGYWPTVNPYKMPGTTETDAKRADSD TGKVLPSAFVGTSKLDD ANATATMDFTNWNQTLTAHKSWFMLKDKIAFLGSNIQNTSTDTAATTIDQRKLESGNPYK VYVNDKEASLTEQEKDY PETQSVFLESFDSKKNIGYFFFKKSSI SMSKALQKGAWKDINEGQSDKEVENEFLTI SQAHKQNRDSYGYML IPNVD RATFNQMIKELESSL IENNETLQSVYDAKQGVWGIVKYDDSVSTI SNQFQVLKRGVYTIRKEGDEYKIAYYNPETQE SAPDQEVFKKLEQAAQPQVQNSKEKEKSEEEKNHSDQKNLPQTGEGQSILASLGFLLLGA FYLFRRGKNN

SEQ ID NO: 24

SP0882N DNA

ATGAATCAATCCTACTTTTATCTAAAAATGAAAGAACACAAACTCAAGGTTCCTTATACA GGTAAGGAGCGCCGTGT ACGTATTCTTCTTCCTAAAGATTATGAGAAAGATACAGACCGTTCCTATCCTGTTGTATA CTTTCATGACGGGCAAA ATGTTTTTAATAGCAAAGAGTCTTTCATTGGACATTCATGGAAGATTATCCCAGCTATCA AACGAAATCCGGATATC AGTCGCATGATTGTCGTTGCTATTGACAATGATGGTATGGGGCGGATGAATGAGTATGCG GCTTGGAAGTTCCAAGA ATCTCCTATCCCAGGGCAGCAGTTTGGTGGTAAGGGTGTGGAGTATGCTGAGTTTGTCAT GGAGGTGGTCAAGCCTT TTATC SEQ ID NO: 25

SP0882 with exogenous signal seguence (nucleotides)

ATGTCATCTAAATTTATGAAGAGCGCTGCGGTGCTTGGAACTGCTACACTTGCTAGCTTG CTTTTGGTAGCTTGCAT GAATCAATCCTACTTTTATCTAAAAATGAAAGAACACAAACTCAAGGTTCCTTATACAGG TAAGGAGCGCCGTGTAC GTATTCTTCTTCCTAAAGATTATGAGAAAGATACAGACCGTTCCTATCCTGTTGTATACT TTCATGACGGGCAAAAT GTTTTTAATAGCAAAGAGTCTTTCATTGGACATTCATGGAAGATTATCCCAGCTATCAAA CGAAATCCGGATATCAG TCGCATGATTGTCGTTGCTATTGACAATGATGGTATGGGGCGGATGAATGAGTATGCGGC TTGGAAGTTCCAAGAAT CTCCTATCCCAGGGCAGCAGTTTGGTGGTAAGGGTGTGGAGTATGCTGAGTTTGTCATGG AGGTGGTCAAGCCTTTT ATCGATGAGACCTATCGTACAAAAGCAGACTGCCAGCATACGGCTATGATTGGTTCCTCA CTAGGAGGCAATATTAC CCAGTTTATCGGTTTGGAATACCAAGACCAAATTGGTTGCTTGGGCGTTTTTTCATCTGC AAACTGGCTCCACCAAG AAGCCTTTAACCGCTATTTCGAGTGCCAGAAACTATCGCCTGACCAGCGCATCTTCATCT ATGTAGGAACAGAAGAA GCAGATGATACAGACAAGACCTTGATGGATGGCAATATCAAACAAGCCTATATCGACTCG TCGCTTTGCTATTACCA TGATTTGATAGCAGGGGGAGTACATCTGGATAATCTTGTGCTAAAAGTTCAGTCTGGTGC CATCCATAGTGAAATCC CTTGGTCAGAAAATCTACCAGATTGTCTGAGATTTTTTGCAGAAAAATGGTAA

SEQ ID NO: 26

SP0882N with exogenous signal seguence (nucleotides)

ATGTCATCTAAATTTATGAAGAGCGCTGCGGTGCTTGGAACTGCTACACTTGCTAGCTTG CTTTTGGTAGCTTGCAT GAATCAATCCTACTTTTATCTAAAAATGAAAGAACACAAACTCAAGGTTCCTTATACAGG TAAGGAGCGCCGTGTAC GTATTCTTCTTCCTAAAGATTATGAGAAAGATACAGACCGTTCCTATCCTGTTGTATACT TTCATGACGGGCAAAAT GTTTTTAATAGCAAAGAGTCTTTCATTGGACATTCATGGAAGATTATCCCAGCTATCAAA CGAAATCCGGATATCAG TCGCATGATTGTCGTTGCTATTGACAATGATGGTATGGGGCGGATGAATGAGTATGCGGC TTGGAAGTTCCAAGAAT CTCCTATCCCAGGGCAGCAGTTTGGTGGTAAGGGTGTGGAGTATGCTGAGTTTGTCATGG AGGTGGTCAAGCCTTTT ATC

SEQ ID NO: 27

SP0148 lacking signal seguence (nucleotides)

ATGTGCTCAGGGGGTGCTAAGAAAGAAGGAGAAGCAGCTAGCAAGAAAGAAATCATCGTT GCAACCAATGGATCACC AAAGCCATTTATCTATGAAGAAAATGGCGAATTGACTGGTTACGAGATTGAAGTCGTTCG CGCTATCTTTAAAGATT CTGACAAATATGATGTCAAGTTTGAAAAGACAGAATGGTCAGGTGTCTTTGCTGGTCTTG ACGCTGATCGTTACAAT ATGGCTGTCAACAATCTTAGCTACACTAAAGAACGTGCGGAGAAATACCTCTATGCCGCA CCAATTGCCCAAAATCC TAATGTCCTTGTCGTGAAGAAAGATGACTCTAGTATCAAGTCTCTCGATGATATCGGTGG AAAATCGACGGAAGTCG TTCAAGCCACTACATCAGCTAAGCAGTTAGAAGCATACAATGCTGAACACACGGACAACC CAACTATCCTTAACTAT ACTAAGGCAGACTTCCAACAAATCATGGTACGTTTGAGCGATGGACAATTTGACTATAAG ATTTTTGATAAAATCGG TGTTGAAACAGTGATCAAGAACCAAGGTTTGGACAACTTGAAAGTTATCGAACTTCCAAG CGACCAACAACCGTACG TTTACCCACTTCTTGCTCAGGGTCAAGATGAGTTGAAATCGTTTGTAGACAAACGCATCA AAGAACTTTATAAAGAT GGAACTCTTGAAAAATTGTCTAAACAATTCTTCGGAGACACTTATCTACCGGCAGAAGCT GATATTAAAGAGTAA SEQ ID NO: 28

SP0148 including signal seguence (nucleotides)

ATGAAAAAAATCGTTAAATACTCATCTCTTGCAGCCCTTGCTCTTGTTGCTGCAGGTGTG CTTGCGGCTTGCTCAGG GGGTGCTAAGAAAGAAGGAGAAGCAGCTAGCAAGAAAGAAATCATCGTTGCAACCAATGG ATCACCAAAGCCATTTA TCTATGAAGAAAATGGCGAATTGACTGGTTACGAGATTGAAGTCGTTCGCGCTATCTTTA AAGATTCTGACAAATAT GATGTCAAGTTTGAAAAGACAGAATGGTCAGGTGTCTTTGCTGGTCTTGACGCTGATCGT TACAATATGGCTGTCAA CAATCTTAGCTACACTAAAGAACGTGCGGAGAAATACCTCTATGCCGCACCAATTGCCCA AAATCCTAATGTCCTTG TCGTGAAGAAAGATGACTCTAGTATCAAGTCTCTCGATGATATCGGTGGAAAATCGACGG AAGTCGTTCAAGCCACT ACATCAGCTAAGCAGTTAGAAGCATACAATGCTGAACACACGGACAACCCAACTATCCTT AACTATACTAAGGCAGA CTTCCAACAAATCATGGTACGTTTGAGCGATGGACAATTTGACTATAAGATTTTTGATAA AATCGGTGTTGAAACAG TGATCAAGAACCAAGGTTTGGACAACTTGAAAGTTATCGAACTTCCAAGCGACCAACAAC CGTACGTTTACCCACTT CTTGCTCAGGGTCAAGATGAGTTGAAATCGTTTGTAGACAAACGCATCAAAGAACTTTAT AAAGATGGAACTCTTGA AAAATTGTCTAAACAATTCTTCGGAGACACTTATCTACCGGCAGAAGCTGATATTAAAGA GTAA

SEQ ID NO: 29

SP2108 lacking signal seguence (nucleotides)

ATGTGCGGAAGCAAAACTGCTGATAAGCCTGCTGATTCTGGTTCATCTGAAGTCAAAGAA CTCACTGTATATGTAGA CGAGGGATATAAGAGCTATATTGAAGAGGTTGCTAAAGCTTATGAAAAAGAAGCTGGAGT AAAAGTCACTCTTAAAA CTGGTGATGCTCTAGGAGGTCTTGATAAACTTTCTCTTGACAACCAATCTGGTAATGTCC CTGATGTTATGATGGCT CCATACGACCGTGTAGGTAGCCTTGGTTCTGACGGACAACTTTCAGAAGTGAAATTGAGC GATGGTGCTAAAACAGA CGACACAACTAAATCTCTTGTAACAGCTGCTAATGGTAAAGTTTACGGTGCTCCTGCCGT TATCGAGTCACTTGTTA TGTACTACAACAAAGACTTGGTGAAAGATGCTCCAAAAACATTTGCTGACTTGGAAAACC TTGCTAAAGATAGCAAA TACGCATTCGCTGGTGAAGATGGTAAAACTACTGCCTTCCTAGCTGACTGGACAAACTTC TACTATACATATGGACT TCTTGCCGGTAACGGTGCTTACGTCTTTGGCCAAAACGGTAAAGACGCTAAAGACATCGG TCTTGCAAACGACGGTT CTATCGTAGGTATCAACTACGCTAAATCTTGGTACGAAAAATGGCCTAAAGGTATGCAAG ATACAGAAGGTGCTGGA AACTTAATCCAAACTCAATTCCAAGAAGGTAAAACAGCTGCTATCATCGACGGACCTTGG AAAGCTCAAGCCTTTAA AGATGCTAAAGTAAACTACGGAGTTGCAACTATCCCAACTCTTCCAAATGGAAAAGAATA TGCTGCATTCGGTGGTG GTAAAGCTTGGGTCATTCCTCAAGCCGTTAAGAACCTTGAAGCTTCTCAAAAATTTGTAG ACTTCCTTGTTGCAACT GAACAACAAAAAGTATTATATGATAAGACTAACGAAATCCCAGCTAATACTGAGGCTCGT TCATACGCTGAAGGTAA AAACGATGAGTTGACAACAGCTGTTATCAAACAGTTCAAGAACACTCAACCACTGCCAAA CATCTCTCAAATGTCTG CAGTTTGGGATCCAGCGAAAAATATGCTCTTTGATGCTGTAAGTGGTCAAAAAGATGCTA AAACAGCTGCTAACGAT GCTGTAACATTGATCAAAGAAACAATCAAACAAAAATTTGGTGAATAA

SEQ ID NO: 30

SP0641M (nucleotides)

ATGTCAGGAACTAGTATGGCGACTCCAATCGTGGCAGCTTCTACTGTTTTGATTAGACCG AAATTAAAGGAAATGCT TGAAAGACCTGTATTGAAAAATCTTAAGGGAGATGACAAAATAGATCTTACAAGTCTTAC AAAAATTGCCCTACAAA ATACTGCGCGACCTATGATGGATGCAACTTCTTGGAAAGAAAAAAGTCAATACTTTGCAT CACCTAGACAACAGGGA GCAGGCCTAATTAATGTGGCCAATGCTTTGAGAAATGAAGTTGTAGCAACTTTCAAAAAC ACTGATTCTAAAGGTTT GGTAAACTCATATGGTTCCATTTCTCTTAAAGAAATAAAAGGTGATAAAAAATACTTTAC AATCAAGCTTCACAATA CATCAAACAGACCTTTGACTTTTAAAGTTTCAGCATCAGCGATAACTACAGATTCTCTAA CTGACAGATTAAAACTT GATGAAACATATAAAGATGAAAAATCTCCAGATGGTAAGCAAATTGTTCCAGAAATTCAC CCAGAAAAAGTCAAAGG AGCAAATATCACATTTGAGCATGATACTTTCACTATAGGCGCAAATTCTAGCTTTGATTT GAATGCGGTTATAAATG TTGGAGAGGCCAAAAACAAAAATAAATTTGTAGAATCATTTATTCATTTTGAGTCAGTGG AAGAAATGGAAGCTCTA AACTCCAACGGGAAGAAAATAAACTTCCAACCTTCTTTGTCGATGCCTCTAATGGGATTT GCTGGGAATTGGAACCA CGAACCAATCCTTGATAAATGGGCTTGGGAAGAAGGGTCAAGATCAAAAACACTGGGAGG TTATGATGATGATGGTA AACCGAAAATTCCAGGAACCTTAAATAAGGGAATTGGTGGAGAACATGGTATAGATAAAT TTAATCCAGCAGGAGTT ATACAAAATAGAAAAGATAAAAATACAACATCCCTGGATCAAAATCCAGAATTATTTGCT TTCAATAACGAAGGGAT CAACGCTCCATCATCAAGTGGTTCTAAGATTGCTAACATTTATCCTTTAGATTCAAATGG AAATCCTCAAGATGCTC AACTTGAAAGAGGATTAACACCTTCTCCACTTGTATTAAGAAGTGCAGAAGAAGGATTGA TTTCAATAGTAAATACA AATAAAGAGGGAGAAAATCAAAGAGACTTAAAAGTCATTTCGAGAGAACACTTTATTAGA GGAATTTTAAATTCTAA AAGCAATGATGCAAAGGGAATCAAATCATCTAAACTAAAAGTTTGGGGTGACTTGAAGTG GGATGGACTCATCTATA ATCCTAGAGGTAGAGAAGAAAATGCACCAGAAAGTAAGGATAATCAAGATCCTGCTACTA AGATAAGAGGTCAATTT GAACCGATTGCGGAAGGTCAATATTTCTATAAATTTAAATATAGATTAACTAAAGATTAC CCATGGCAGGTTTCCTA TATTCCTGTAAAAATTGATAACACCGCCCCTAAGATTGTTTCGGTTGATTTTTCAAATCC TGAAAAAATTAAGTTGA TTACAAAGGATACTTATCATAAGGTAAAAGATCAGTATAAGAATGAAACGCTATTTGCGA GAGATCAAAAAGAACAT CCTGAAAAATTTGACGAGATTGCGAACGAAGTTTGGTATGCTGGCGCCGCTCTTGTTAAT GAAGATGGAGAGGTTGA AAAAAATCTTGAAGTAACTTACGCAGGTGAGGGTCAAGGAAGAAATAGAAAACTTGATAA AGACGGAAATACCATTT ATGAAATTAAAGGTGCGGGAGATTTAAGGGGAAAAATCATTGAAGTCATTGCATTAGATG GTTCTAGCAATTTCACA AAGATTCATAGAATTAAATTTGCTAATCAGGCTGATGAAAAGGGGATGATTTCCTATTAT CTAGTAGATCCTGATCA AGATTCATCTAAATATCAA

SEQ ID NO: 31

SP0641N (nucleotides)

ATGGTAGTCTTAGCAGACACATCTAGCTCTGAAGATGCTTTAAACATCTCTGATAAAGAA AAAGTAGCAGAAAATAA AGAGAAACATGAAAATATCCATAGTGCTATGGAAACTTCACAGGATTTTAAAGAGAAGAA AACAGCAGTCATTAAGG AAAAAGAAGTTGTTAGTAAAAATCCTGTGATAGACAATAACACTAGCAATGAAGAAGCAA AAATCAAAGAAGAAAAT TCCAATAAATCCCAAGGAGATTATACGGACTCATTTGTGAATAAAAACACAGAAAATCCC AAAAAAGAAGATAAAGT TGTCTATATTGCTGAATTTAAAGATAAAGAATCTGGAGAAAAAGCAATCAAGGAACTATC CAGTCTTAAGAATACAA AAGTTTTATATACTTATGATAGAATTTTTAACGGTAGTGCCATAGAAACAACTCCAGATA ACTTGGACAAAATTAAA CAAATAGAAGGTATTTCATCGGTTGAAAGGGCACAAAAAGTCCAACCCATGATGAATCAT GCCAGAAAGGAAATTGG AGTTGAGGAAGCTATTGATTACCTAAAGTCTATCAATGCTCCGTTTGGGAAAAATTTTGA TGGTAGAGGTATGGTCA TTTCAAATATCGATACTGGAACAGATTATAGACATAAGGCTATGAGAATCGATGATGATG CCAAAGCCTCAATGAGA TTTAAAAAAGAAGACTTAAAAGGCACTGATAAAAATTATTGGTTGAGTGATAAAATCCCT CATGCGTTCAATTATTA TAATGGTGGCAAAATCACTGTAGAAAAATATGATGATGGAAGGGATTATTTTGACCCACA TGGGATGCATATTGCAG GGATTCTTGCTGGAAATGATACTGAACAAGACATCAAAAACTTTAACGGCATAGATGGAA TTGCACCTAATGCACAA ATTTTCTCTTACAAAATGTATTCTGACGCAGGATCTGGGTTTGCGGGTGATGAAACAATG TTTCATGCTATTGAAGA TTCTATCAAACACAACGTTGATGTTGTTTCGGTATCATCTGGTTTTACAGGAACAGGTCT TGTAGGTGAGAAATATT GGCAAGCTATTCGGGCATTAAGAAAAGCAGGCATTCCAATGGTTGTCGCTACGGGTAACT ATGCGACTTCTGCTTCA AGTTCTTCATGGGATTTAGTAGCAAATAATCATCTGAAAATGACCGACACTGGAAATGTA ACACGAACTGCAGCACA TGAAGATGCGATAGCGGTCGCTTCTGCTAAAAATCAAACAGTTGAGTTTGATAAAGTTAA CATAGGTGGAGAAAGTT TTAAATACAGAAATATAGGGGCCTTTTTCGATAAGAGTAAAATCACAACAAATGAAGATG GAACAAAAGCTCCTAGT AAATTAAAATTTGTATATATAGGCAAGGGGCAAGACCAAGATTTGATAGGTTTGGATCTT AGGGGCAAAATTGCAGT AATGGATAGAATTTATACAAAGGATTTAAAAAATGCTTTTAAAAAAGCTATGGATAAGGG TGCACGCGCCATTATGG TTGTAAATACTGTAAATTACTACAATAGAGATAATTGGACAGAGCTTCCAGCTATGGGAT ATGAAGCGGATGAAGGT ACTAAAAGTCAAGTGTTTTCAATTTCAGGAGATGATGGTGTAAAGCTATGGAACATGATT AATCCTGATAAAAAAAC TGAAGTCAAAAGAAATAATAAAGAAGATTTTAAAGATAAATTGGAGCAATACTATCCAAT TGATATGGAAAGTTTTA ATTCCAACAAACCGAATGTAGGTGACGAAAAAGAGATTGACTTTAAGTTTGCACCTGACA CAGACAAAGAACTCTAT AAAGAAGATATCATCGTTCCAGCAGGATCTACATCTTGGGGGCCAAGAATAGATTTACTT TTAAAACCCGATGTTTC AGCACCTGGTAAAAATATTAAATCCACGCTTAATGTTATTAATGGCAAATCAACTTATGG C

SEQ ID NO : 32

HHHHHH

SEQ ID NO : 33

MSYYHHHHHH

SEQ ID NO : 265

SP1912

MNGMKAKKMWMAGLALLGIGSLALATKKVADDRKLMKTQEELTE IVRDHFSDMGE IATLYVQVYES SLE SLVGGVIF EDGRHYTFVYENEDLVYEEEVL

SEQ ID NO : 266

SP1912 L

MRYLATLLL SLAVL I TAGCKKVADDRKLMKTQEELTE IVRDHFSDMGE IATLYVQVYESSLESLVGGVIFEDGRHYT FVYENEDLVYEEEVL

SEQ ID NO : 26 7

SP06 41 . 1

DTS SSEDALNI SDKEKVAENKEKHENIHSAMET SQDFKEKKTAVIKEKEWSKNPVI DNNTSNEEAKIKEENSNKSQ GDYTDSFVNKNTENPKKEDKVVYIAEFKDKESGEKAIKELSSLKNTKVLYTYDRIFNGSA IETTPDNLDKIKQIEGI SSVERAQKVQPMMNHARKE IGVEEAIDYLKS INAPFGKNFDGRGMVI SNIDTGTDYRHKAMRI DDDAKASMRFKKED LKGTDKNYWLSDKIPHAFNYYNGGKITVEKYDDGRDYFDPHGMHIAGI LAGNDTEQD IKNFNGIDGIAPNAQ IFSYK MYSDAGSGFAGDETMFHAIEDS IKHNVDWSVS SGFTGTGLVGEKYWQAIRALRKAGIPMWATGNYAT SAS SSSWD LVANNHLKMTDTGNVTRTAAHEDAIAVASAKNQTVEFDKVNIGGESFKYRNIGAFFDKSK ITTNEDGTKAPSKLKFV YIGKGQDQDLIGLDLRGKIAVMDRIYTKDLKNAFKKAMDKGARAIMWNTVNYYNRDNWTE LPAMGYEADEGTKSQV FSI SGDDGVKLWNMINPDKKTEVKRNNKEDFKDKLEQYYPIDMESFNSNKPNVGDEKEIDFKF APDTDKELYKEDI I VPAGSTSWGPRIDLLLKPDVSAPGKNIKSTLNVINGKSTYGYMSGTSMATPIVAASTVLI RPKLKEMLERPVLKNLK GDDKIDLTSLTKIALQNTARPMMDATSWKEKSQYFASPRQQGAGL INVANALRNEWATFKNTDSKGLVNSYGSI SL KEIKGDKKYFTIKLHNTSNRPLTFKVSASAITTDSLTDRLKLDETYKDEKSPDGKQIVPE IHPEKVKGANITFEHDT FTIGANSSFDLNAVINVGEAKNKNKFVESF IHFESVEEMEALNSNGKKINFQPSLSMPLMGFAGNWNHEPILDKWAW EEGSRSKTLGGYDDDGKPKIPGTLNKGIGGEHGIDKFNPAGVIQNRKDKNTTSL

SEQ ID NO: 268

SP1912 consensus

MNGMKAKKMWMAGLALLGIGSLALATKKVADDRKLMKTQEELTEIVRDHFSDMGEIATLY VQVYESSLESLVGGVIF

H A L I L S

EDGRHYTFVYENEDLVYEEEVL I

SEQ ID NO: 269

SP641N consensus

MWLADTSSSEDALNISDKEKVA ENKEKHENIHSAMETSQDFKEKKTAVIKEKEVVSKNPVIDNNTSNEEAK

N S WDKET KD N I K TE TI EG A T TK R

L

IKEENSNKSQGDYTDSFVNKNTENPKKEDKWYIAEFKDKESGEKAIKELSSLKNTKV LYTYDRIFNGSAIETTPDN

D- Q H Q S Q N G Q

NAH SA G RL G

LDKIKQIEGISSVERAQKVQPMMNHARKEIGVEEAIDYLKSINAPFGKNFDGRGMVI SNIDTGTDYRHKAMRIDDDA T I

KASMRFKKEDLKGTDKNYWLSDKIPHAFNYYNGGKITVEKYDDGRDYFDPHGMHIAG ILAGNDTEQDIKNFNGIDGI

APNAQIFSYKMYSDAGSGFAGDETMFHAIEDSIKHNVDVVSVSSGFTGTGLVGEKYW QAIRALRKAGIPMWATGNY

ATSASSSSWDLVANNHLKMTDTGNVTRTAAHEDAIAVASAKNQTVEFDKVNIGGESF KYRNIGAFFDKSKITTNEDG

Q N TKAPSKLKFVYIGKGQDQDLIGLDLRGKIAVMDRIYTKDLKNAFKKAMDKGARAIMVVNT VNYYNRDNWTELPAMGY

EADEGTKSQVFSISGDDGVKLWNMINPDKKTEVKRNNKEDFKDKLEQYYPIDMESFN SNKPNVGDEKEIDFKFAPDT

N

DKELYKEDI IVPAGSTSWGPRIDLLLKPDVSAPGKNIKSTLNVINGKSTYG

SEQ ID NO: 270

SP641M consensus

MSGTSMATPIVAASTVLIRPKLKEMLERPVLKNLKGDDKIDLTSLTKIALQNTARPM MDATSWKEKSQYFASPRQQG

K T

AGL INVANALRNEWATFKNTDSKGLVNSYGSI SLKEIKGDKKYFTIKLHNTSNRPLTFKVSASAITTDSLTDRLKL

V

DETYKDEKSPDGKQIVPEIHPEKVKGANITFEHDTFTIGANSSFDLNAVINVGEAKN KNKFVESFIHFESVEEMEAL Y R A

NSNGKKINFQPSLSMPLMGFAGNWNHEPILDKWAWEEGSRSKTLGGYDDDGKPKIPG TLNKGIGGEHGIDKFNPAGV S TD K ME

IQNRKDKNTTSLDQNPELFAFNNEGINAPSSSGSKIANIYPLDSNGNPQDAQLERGL TPSPLVLRSAEEGLI SIVNT R D D Q VH E T

NKEGENQRDLKVISREHF IRGILNSKSNDAKGIKSSKLKVWGDLKWDGLIYNPRGREENAPESKDNQDPATKIRGQF K V G

EPIAEGQYFYKFKYRLTKDYPWQVSYIPVKIDNTAPKIVSVDFSNPEKIKL ITKDTYHKVKDQYKNETLFARDQKEH

PEKFDE IANEVWYAGAALVNEDGEVEKNLEVTYAGEGQGRNRKLDKDGNTIYEIKGAGDLRGKI IEVIALDGSSNFT

S A

KIHRIKFANQADEKGMISYYLVDPDQDSSKYQ DH K A E

SEQ ID NO: 271

SP1912 (nucleotides)

ATGAATGGTATGAAAGCTAAAAAAATGTGGATGGCAC ICTTC^

GAAAAAAGTTGCAGATGACCGTAAGCTCAIO AGACTCAGGAAGAGTTGACAGAGATTGTGCGAGACCATTTTTCCG ACATGGGGGAAATTGCGACCCIIIA GTTCAAGTTTACGAAAGCAGIC GGAGAGCTTGGTTGGTGGCGICA TT GAGGATGGCCGTC;ATTATACX^TTTGTC ATGAAAATGAAGACX A(;TI^TATGAGGAGGAAGTC;TTA GA

SEQ ID NO: 272

SP1912L (nucleotides)

ATGAGATACCTGGCAACATTGTTGTTATCTCTGGCGGTGTTAATCACCGCCGGGTGCAAA AAAGTT6CAGAIGACCG

TAAGCTCATGAAGACTCAGGAAGAGTTGAC GAGATTGTGCXjAGACXlATTTTTCCGACATGGG^^

TTTA GTTCAAGTTTACGAAAGCAGTCTGGAGAGCTTGGTTGGTGGCGTCATTTTTGAGGATGGC CGTCATTATACC

TTTGTCTATGAAAATGAAGACCTAGTC GAGGAGGAAGTCTTATGA

SEQ ID NO: 273

SP0641.1 (nucleotides)

GACACATCTAGCTCTGAAGATGCTTTAAACATCTCTGATAAAGAAAAAGTAGCAGAAAAT AAAGAGAAACATGAAAA TATCCATAGTGCTATGGAAACTTCACAGGATTTTAAAGAGAAGAAAACAGCAGTCATTAA GGAAAAAGAAGTTGTTA GTAAAAATCCTGTGATAGACAATAACACTAGCAATGAAGAAGCAAAAATCAAAGAAGAAA ATTCCAATAAATCCCAA GGAGATTATACGGACTCATTTGTGAATAAAAACACAGAAAATCCCAAAAAAGAAGATAAA GTTGTCTATATTGCTGA ATTTAAAGATAAAGAATCTGGAGAAAAAGCAATCAAGGAACTATCCAGTCTTAAGAATAC AAAAGTTTTATATACTT ATGATAGAATTTTTAACGGTAGTGCCATAGAAACAACTCCAGATAACTTGGACAAAATTA AACAAATAGAAGGTATT TCATCGGTTGAAAGGGCACAAAAAGTCCAACCCATGATGAATCATGCCAGAAAGGAAATT GGAGTTGAGGAAGCTAT TGATTACCTAAAGTCTATCAATGCTCCGTTTGGGAAAAATTTTGATGGTAGAGGTATGGT CATTTCAAATATCGATA CTGGAACAGATTATAGACATAAGGCTATGAGAATCGATGATGATGCCAAAGCCTCAATGA GATTTAAAAAAGAAGAC TTAAAAGGCACTGATAAAAATTATTGGTTGAGTGATAAAATCCCTCATGCGTTCAATTAT TATAATGGTGGCAAAAT CACTGTAGAAAAATATGATGATGGAAGGGATTATTTTGACCCACATGGGATGCATATTGC AGGGATTCTTGCTGGAA ATGATACTGAACAAGACATCAAAAACTTTAACGGCATAGATGGAATTGCACCTAATGCAC AAATTTTCTCTTACAAA ATGTATTCTGACGCAGGATCTGGGTTTGCGGGTGATGAAACAATGTTTCATGCTATTGAA GATTCTATCAAACACAA CGTTGATGTTGTTTCGGTATCATCTGGTTTTACAGGAACAGGTCTTGTAGGTGAGAAATA TTGGCAAGCTATTCGGG CATTAAGAAAAGCAGGCATTCCAATGGTTGTCGCTACGGGTAACTATGCGACTTCTGCTT CAAGTTCTTCATGGGAT TTAGTAGCAAATAATCATCTGAAAATGACCGACACTGGAAATGTAACACGAACTGCAGCA CATGAAGATGCGATAGC GGTCGCTTCTGCTAAAAATCAAACAGTTGAGTTTGATAAAGTTAACATAGGTGGAGAAAG TTTTAAATACAGAAATA TAGGGGCCTTTTTCGATAAGAGTAAAATCACAACAAATGAAGATGGAACAAAAGCTCCTA GTAAATTAAAATTTGTA TATATAGGCAAGGGGCAAGACCAAGATTTGATAGGTTTGGATCTTAGGGGCAAAATTGCA GTAATGGATAGAATTTA TACAAAGGATTTAAAAAATGCTTTTAAAAAAGCTATGGATAAGGGTGCACGCGCCATTAT GGTTGTAAATACTGTAA ATTACTACAATAGAGATAATTGGACAGAGCTTCCAGCTATGGGATATGAAGCGGATGAAG GTACTAAAAGTCAAGTG TTTTCAATTTCAGGAGATGATGGTGTAAAGCTATGGAACATGATTAATCCTGATAAAAAA ACTGAAGTCAAAAGAAA TAATAAAGAAGATTTTAAAGATAAATTGGAGCAATACTATCCAATTGATATGGAAAGTTT TAATTCCAACAAACCGA ATGTAGGTGACGAAAAAGAGATTGACTTTAAGTTTGCACCTGACACAGACAAAGAACTCT ATAAAGAAGATATCATC GTTCCAGCAGGATCTACATCTTGGGGGCCAAGAATAGATTTACTTTTAAAACCCGATGTT TCAGCACCTGGTAAAAA TATTAAATCCACGCTTAATGTTATTAATGGCAAATCAACTTATGGCTATATGTCAGGAAC TAGTATGGCGACTCCAA TCGTGGCAGCTTCTACTGTTTTGATTAGACCGAAATTAAAGGAAATGCTTGAAAGACCTG TATTGAAAAATCTTAAG GGAGATGACAAAATAGATCTTACAAGTCTTACAAAAATTGCCCTACAAAATACTGCGCGA CCTATGATGGATGCAAC TTCTTGGAAAGAAAAAAGTCAATACTTTGCATCACCTAGACAACAGGGAGCAGGCCTAAT TAATGTGGCCAATGCTT TGAGAAATGAAGTTGTAGCAACTTTCAAAAACACTGATTCTAAAGGTTTGGTAAACTCAT ATGGTTCCATTTCTCTT AAAGAAATAAAAGGTGATAAAAAATACTTTACAATCAAGCTTCACAATACATCAAACAGA CCTTTGACTTTTAAAGT TTCAGCATCAGCGATAACTACAGATTCTCTAACTGACAGATTAAAACTTGATGAAACATA TAAAGATGAAAAATCTC CAGATGGTAAGCAAATTGTTCCAGAAATTCACCCAGAAAAAGTCAAAGGAGCAAATATCA CATTTGAGCATGATACT TTCACTATAGGCGCAAATTCTAGCTTTGATTTGAATGCGGTTATAAATGTTGGAGAGGCC AAAAACAAAAATAAATT TGTAGAATCATTTATTCATTTTGAGTCAGTGGAAGAAATGGAAGCTCTAAACTCCAACGG GAAGAAAATAAACTTCC AACCTTCTTTGTCGATGCCTCTAATGGGATTTGCTGGGAATTGGAACCACGAACCAATCC TTGATAAATGGGCTTGG GAAGAAGGGTCAAGATCAAAAACACTGGGAGGTTATGATGATGATGGTAAACCGAAAATT CCAGGAACCTTAAATAA GGGAATTGGTGGAGAACATGGTATAGATAAATTTAATCCAGCAGGAGTTATACAAAATAG AAAAGATAAAAATACAA CATCCCTG

SEQ ID NO: 274

Canonical lipobox motif

[LIVMFESTAGPC] - [LVIAMFTG] - [ IVMSTAGCP] - [AGS] -C

SEQ ID NO: 275

SP2108 signal sequence

MSSKFMKSAAVLGTATLASLLLVAC

SEQ ID NO: 276

E. coli RlpB signal sequence

MRYLATLLLSLAVLITAG [C]

SEQ ID NO: 301

Immunogenic PspA/PspC polypeptides including the coiled-coil structure (PR + NPB)

MSDKI IHLTDDSFDTDVLKADGAILVDFWAEWCGPCKMIAPILDE IADEYQGKLTVA KLNIDQNPGTAPKYGIRGIPTLLLFKNGEVAATKVGALSKGQLKEFLDANLAGSGSG HMHHHHHHSSGLVPRGSGMKETAAAKFERQHMDSPDLGTDDDDKAMADLKKAVNE PEKPAEEPENPAPAPKPAPAPQPEKPAPAPAPKPEKSADQQAEEDYARRSEEEYNRLTQQ QPPKAEKPAPAPVPKPEQPAPAPKTGWGQENGMWCRQACGRTRAPPPPPLRSGC

SEQ ID NO: 302

Immunogenic PspA/PspC polypeptides including the coiled-coil structure (E only)

MSDKI IHLTDDSFDTDVLKADGAILVDFWAEWCGPCKMIAPILDE IADEYQGKLTVA

KLNIDQNPGTAPKYGIRGIPTLLLFKNGEVAATKVGALSKGQLKEFLDANLAGSGSG

HMHHHHHHSSGLVPRGSGMKETAAAKFERQHMDSPDLGTDDDDKAMADLKKAVNE

PETPAPAPAPAPAPAPTPEAPAPAPAPAPKPAPAPKPAPAPKPAPAPKPAPAPKPAP APKP

APAPAPAPKPEKPAEKPAPAPKPETPKTGWKQENGMWCRQACGRTRAPPPPPLRSG

SEQ ID NO: 303

Immunogenic PspA/PspC polypeptides lacking the coiled-coil structure (PR NPB)

DLKKAVNEPEKPAEEPENPAPAPKPAPAPQPEKPAPAPAPKPEKSADQQAEEDYARR SEEEYNRLTQQQPPKAEKPAPAPVPKPEQPAPAPKTGWGQENGMW

SEQ ID NO: 304

Immunogenic PspA/PspC polypeptides lacking the coiled-coil structure (PR only)

DLKKAVNEPETPAPAPAPAPAPAPTPEAPAPAPAPAPKPAPAPKPAPAPKPAPAPKPA PAPKPAPAPKPAPAPAPAPKPEKPAEKPAPAPKPETPKTGWKQENGMW

SEQ ID NO: 305

Immunogenic PspA/PspC polypeptides lacking the coiled-coil structure (PR NPB)

MAKKAELEKTPEKPAEEPENPAPAPQPEKSADQQAEEDYARRSEEEYNRLTQQQPPKA

SEQ ID NO: 306

Non-proline Block (NPB)

EKSADQQAEEDYARRSEEEYNRLTQQQ

SEQ ID NO: 307

Non-proline Block (NPB)

DQQAEEDYARRSEEEYNRLTQQQ

SEQ ID NO: 308

Non-proline Block (NPB)

MEKSADQQAEEDYARRSEEEYNRLTQQQ

SEQ ID NO: 309 Amino-terminal boundary to the PR-region

DLKKAVNE

SEQ ID NO: 310

Carboxy-terminal boundary to the PR-region ( K/G) TGW ( K/G ) QENGMW