RELATED PATENT APPLICATION

This application claims the priority to and benefit of Indian Patent Application No. 201841049814 filed on December 29, 2018; the disclosure of which are incorporated herein by reference.

FIELD OF THE INVENTION

This invention relates to creation of new virus strain by adapting to cell substrate recommended for vaccine production and utilizing the new strain for generating vaccines and as a diagnostic tool.

BACKGROUND OF THE INVENTION

Enterovirus 68 or Enterovirus D68 is an emerging enterovirus that causes respiratory illness with mild to severe symptoms often showing flu like symptoms and neurological diseases like acute flaccid myelitis (AFM). Enterovirus 68 is a positive-sense, single stranded RNA virus and it belongs to D species of the Enterovirus genus and Picomavirideae family. Though first isolated way back in 1962 in USA (Schieble et ah, Am J Epidemiol 1967, 85:297-310), the pathogen was not reported frequently until early 21 ^st century (Oberste et ah, J Gen Virol 2004, 85:2577-2584). Thereafter, outbreaks caused by Enterovirus D68 were reported worldwide (Eshaghi et ah, Front Microbiol 2017, 8: 257). In 2014, a massive outbreak occurred due to Enterovirus D68 spreading to different parts of USA which led to 1153 infections and 14 deaths (CDC. Non-Polio Enterovirus: Enterovirus D68; Midgley et ah, MMWR Morb Mortal Wkly Rep 2014, 63:798-9). At the same time period upsurge of Enterovirus infections were reported in Canada (Skowronski et ah, Euro Surveill 2015, 20:1-14; Edwin et ah, Can CommunDis Rep 2015, 41 Suppl 1:2-8). Subsequently, respiratory infections caused by Enterovirus D68 were reported from different countries (Dyrdak et ah, Euro Surveill 2016, 21; Knoester et ah, Emerg Infec Dis 2017, 23:140-143; Wang et ah, SciRep 2017, 7:1242).

US20160312314A1 discloses a method for detection of enterovirus D68, through contacting nucleic acid obtained from the sample with an oligonucleotide primer, exposing the contacted sample to a DNA amplification process that provides for production of a 98 nucleotide amplification product of the enterovirus D68 VP1 gene and thereafter detecting the 98 nucleotide amplification product, wherein the presence of said amplification product indicates that the sample contained enterovirus D68.

US20160355897A1 discloses methods and compositions for detection of enterovirus D in a sample, particularly detection of enterovirus D68. The methods include contacting a sample with at least one primer (such as a forward primer and/or a reverse primer) capable of specifically amplifying an EV-D68 viral protein 1 (VP1) nucleic acid or a portion thereof and/or a detectably labeled probe capable of specifically hybridizing to an EV-D68 VP1 nucleic acid, under conditions sufficient for specific amplification of the EV-D68 VP1 nucleic acid by the at least one primer and/or under conditions sufficient for specific hybridization of the probe to the EV-D68 nucleic acid. The amplification of the EV-D68 VP1 nucleic acid and/or the hybridization of the probe to the EV-D68 VP1 nucleic acid is detected, thereby identifying presence of EV-D68 in the sample.

The prior arts fail to teach the known Enterovirus D68 to adapt and propagate in Vero Cells, the cell substrate which is recommended for virus propagation for use in vaccine production. Furthermore, the prior arts are limited to the methods of detection of the enterovirus D viral strains and fails to disclose any composition that may be used as a vaccine/immunogenic composition to give protection against the virus. The vaccine against this dreadful emerging vims is warranted but is not available till date. The present invention discloses method of adaptation of Enterovirus D68 for propagation in Vero cells. The present invention also discloses an Enterovirus strain containing mutated nucleic acid sequence that translates into proteins which acts as antigens suitable to be used in a vaccine composition. The present invention also discloses suitable vaccine compositions.

OBJECTIVES OF THE INVENTION

The main objective of the present invention is to provide a method of adapting the Enterovirus D68 strain(s) in cell substrate recommended for vaccine production e.g. Vero cells.

Another objective of the present invention is to provide a new Enterovirus D68 strain(s) which is/are adapted to propagate on Vero cells and can be produced in high titers on Vero cells.

Yet another objective of the present invention is to provide inactivated vaccine formulations against Enterovirus D68 infections comprising the virus strain.

Another objective of the present invention discloses the usage of recombinant proteins of Enterovirus D68 or the whole Enterovirus D68 virus adapted to Vero cells for raising antibodies against the respective recombinant proteins or the whole virus that can be utilized for diagnosis of the respective antigen.

SUMMARY OF THE INVENTION

One aspect of the invention is to provide the process of adapting Enterovirus D68 in cell substrate recommended for vaccine production.

In some embodiment, there is provided an Enterovirus D68 adapted to propagate to high titers in Vero cells encoded by a cDNA molecule having the nucleotide sequence of SEQ ID No 1. In some other embodiment, there is provided a nucleotide sequence encoding the Vero cell adapted Enterovirus D68 polyprotein disclosed in SEQ ID No 2. In yet another embodiment, there is provided an amino acid sequence of Vero cell adapted Enterovirus D68 polyprotein disclosed in SEQ ID No 3.

Another aspect of the invention is to provide the amino acid level changes (V341L, E647G, M699K, E719K, D1355N, T1406S, H2110Q) in Vero cell adapted Enterovirus D68 virus.

In some embodiment, there is provided a method of adapting Enterovirus D68 to propagate in Vero cells to high titer comprising of the following steps:

(a) infecting the virus by adsorbing for about 60-120 minutes at 32-35°C, more precisely at 32-33°C; (b) propagating the virus after addition of the maintenance media at 32-35°C, more precisely at 32-33°C;

(c) diluting the virus stock obtained from each passage at 1:3 to 1:10 dilution to infect the next batches of Vero cells for initial passages of the vims at 32-35°C, more precisely at 32-33°C;

(d) diluting the virus at 1:20-1:500 dilution to infect the Vero cells during later/subsequent passages at 32-35°C, more precisely at 32-33°C; and

(e) harvesting the virus during every passage when 90% or more cytopathic effect has been achieved or within 6 days of infection.

In some other embodiment, there is provided a method of adapting Enterovirus D68 to propagate in Vero cells to high titer wherein Enterovirus D68 virus undergoes plaque assay comprising the steps:

(a) plating of 3 to 4 million Vero cells per 12 well plate or 6 well plate to reach the confluency suitable for plaque assay;

(b) adsorption of the virus of different dilution in different wells in duplicate, triplicate or quadruplicate for 1-2 hours at 32-35°C, more precisely at 32-33°C;

(c) overlaying with <0.6% carboxymethylcellulose or 0.8-E8% Avicel RC 591 as overlay media;

(d) fixing of the cells with 10% formalin after 5-7 days post-infection with carboxymethylcellulose as overlay or 3-4 days post-infection with Avicel RC 591 as overlay;

(e) removal of the fixative solution after fixation and washing of the cells with phosphate buffer saline; and

(f) addition of freshly made staining solution-crystal violet solution dropwise to the fixed cells and staining for 30 mins to 1 hour or 2 hours at room temperature.

In some other embodiment, there is provided a method of inactivating Enterovirus D68 containing cDNA encoded from SEQ ID No. 1 for immunization comprising the steps:

(a) sterile filtration of the harvested Enterovirus D68 vims;

(b) removal of the host nucleic acid using nuclease treatment and concentrated by tangential flow filtration using 100 kDa filter;

(c) inactivation using 1/2000-1/4000 formalin for upto 3 weeks at temperature varying from 25-37°C or with BPL at 4-25°C for upto 120 hours or with 0.005% to 3% hydrogen peroxide at 25+ 5°C for upto 6 hours; and

(d) purification of inactivated antigen or purification before inactivation of the viral antigen using gel filtration using Sepharose CL-4B followed by anion exchange chromatography using DEAE resins or by double steps/two rounds of size exclusion chromatography or by cellufine sulphate followed by anion exchange chromatography or by mixed mode resins like CHT Type II (Biorad) alone or in combination with other resins or combination of chromatography methods.

In yet another aspect of the invention there is provided formulation for inactivated Enterovirus D68 monovalent vaccine where inactivating agents for the Enterovirus D68 includes chemical agents like Formalin, Beta-propiolactone, Hydrogen peroxide (H2O2) or various physical agents like UV, X-ray and gamma irradiation.

In some embodiment, there is provided an immunogenic composition comprising inactivated Enterovirus D68 virus antigen in a physiological acceptable vehicle and optionally one or more pharmaceutically acceptable excipients selected from adjuvants, stabilizers or preservatives.

Another aspect of the invention is to provide formulation for combination vaccines comprising of inactivated Enterovirus D68 and other Enteroviruses. In some embodiment, the immunogenic composition according to invention further comprises other Enteroviruses including EV71, polioviruses or combination thereof.

Another aspect of the invention relates to inactivated Enterovirus D68 vaccine capable of inducing Enterovirus D68 specific humoral immune response where inactivated vaccine can be adjuvanted or unadjuvanted.

Yet another aspect of the invention relates to Enterovirus D68 vaccine capable of eliciting significant neutralizing antibody response.

In some embodiment, there is provided an amino acid sequence belonging to Enterovirus D68 having amino acid in the polyprotein selected from L341, G647, K699, K719, N1355, S1406, Q2110 or combination thereof. In some embodiment, there is provided an immunogenic composition comprising inactivated Enterovirus D68 vims antigen in a physiological acceptable vehicle, wherein the Enterovirus D68 is having amino acid in the polyprotein selected from L341, G647, K699, K719, N1355, S1406, Q2110 or combination thereof.

In some embodiment, the immunogenic composition according to present invention are stable for at least 6 months at 2-8°C and for at least 1 month at 37°C.

BRIEF DESCRIPTION OF THE FIGURES

Figure 1: Adaptation of Enterovirus 68 in Vero cells.

1A: Mock infected Vero cells

IB: Vero cells infected with EV68 displaying cytopathic effect on 3 ^rd day post infection.

Figure 2: Titer of Enterovirus D68(US/KY/14- 18953) in Vero cells during different passages.

Figure 3: Confirmation of Vero cell adapted EV68 virus by RT-PCR. RNAs were isolated from EV68 virus from two different passages in Vero cells after adaptation and were reverse transcribed and then detected using EV68 specific primer pair (A) (Lane 1:

1Kb Marker (NEB), Lane 2, 3-Vero adapted US-KY/14-18953 (US-KY/14-18953-Vero) vims and with pan-Enterovims primer), (B) (Lane 1 and 2: Vero adapted US-KY/14- 18953/US-KY/14- 18953- Vero, Lane 3: Negative control, Lane 4: 100 bp marker from NEB).

Figure 4: Plaque assay of Vero adapted EVD68 using two different overlay media.

(A) Avicel (0.8% and 1.2%) and (B) CMC (0.6%) was tested as overlay media for plaque assay development of Enterovims D68 for different time periods.

Figure 5: Expression of Vero adapted EVD68 proteins. Expression of VP1 and VP2 protein of EVD68 was checked by Western Blot using VP1 and VP2 antibodies specific to EVD68. Positions and molecular weight of individual bands of protein ladder has been mentioned.

Figure 6: Stability of Vero cell adapted EVD68 antigens. Stability of Vero cell adapted EVD68 antigen was expressed as percentage of stability after exposing the EVD68 antigen at 2-8°C for 1 month, 3 month and 6 months (A) and at 37°C for 7 days, 15 days and 1 month (B).

Figure 7: Enterovirus D68 specific IgG titer in Balb/c mice serum induced by formalin inactivated Enterovirus D68 strain US/KY/14-18953-Vero. 6-8 weeks female Balb/c mice was immunized subcutaneously with formalin inactivated Enterovirus D68 strain US/KY/14-18953-Vero formulated with or without alum thrice in three weeks interval. Blood was collected and serum was separated before and after each immunization. ELISA was performed to detect Enterovirus D68 specific IgG titer in the serum.

Figure 8: Enterovirus D68 specific IgG Titer in Balb/c mice serum induced by Beta-propiolactone inactivated Enterovirus D68 strain US/KY/14-18953-Vero. 6-8 weeks female Balb/c mice was immunized subcutaneously with Beta-propiolactone inactivated Enterovirus D68 strain US/KY/14-18953-Vero formulated with or without alum thrice in three weeks interval. Blood was collected and serum was separated before and after each immunization. ELISA was performed to detect Enterovirus D68 specific IgG titer in the serum.

Figure 9: Ratio of IgGl and IgG2a in serum collected from mice immunized with beta-propiolactone and formalin inactivated Enterovirus D68 antigens formulated in presence or absence of alum. 6-8 weeks female Balb/c mice were immunized subcutaneously with formalin and beta-propiolactone inactivated Enterovirus D68 strain US/KY/14-18953-Vero formulated with or without alum thrice in three weeks interval. IgGl/IgG2a ratio was determined from the serum collected from immunized mice after 2 weeks of the third immunization.

DETAILED DESCRIPTION OF THE INVENTION

Vero cells are World Health Organization (WHO) recommended most commonly used cell substrate for vaccine production in recent years. Major advantage of Vero cells is the infinite life span (continuous cell line) with proven safety and suitability for large scale production of vaccines (Barrett et al., Expert Rev Vaccines 2009, 8:607-618). Thus, Vero cell is valuable for rapid production of human vaccines. We have adapted a clinical Enterovirus D68 strain isolated from USA (US/KY/14- 18953) in Vero cells after procuring from ATCC (ATCC, VR-1825).

In some embodiment, there is provided an Enterovirus D68 adapted to propagate to high titers in Vero cells encoded by a cDNA molecule having the nucleotide sequence of SEQ ID No 1. In some other embodiment, there is provided a nucleotide sequence encoding the Vero cell adapted Enterovirus D68 polyprotein disclosed in SEQ ID No 2. In yet another embodiment, there is provided an amino acid sequence of Vero cell adapted Enterovirus D68 polyprotein disclosed in SEQ ID No 3.

In some embodiment, there is provided a method of adapting Enterovirus D68 to propagate in Vero cells to high titer comprising of the following steps:

(a) infecting the virus by adsorbing for about 60-120 minutes at 32-35°C, more precisely at 32-33°C;

(b) propagating the virus after addition of the maintenance media at 32-35°C, more precisely at 32-33°C;

(c) diluting the virus stock obtained from each passage at 1:3 to 1:10 dilution to infect the next batches of Vero cells for initial passages of the virus at 32-35°C, more precisely at 32-33°C;

(d) diluting the virus at 1:20-1:500 dilution to infect the Vero cells during later/subsequent passages at 32-35°C, more precisely at 32-33°C; and

(e) harvesting the virus during every passage when 90% or more cytopathic effect has been achieved or within 6 days of infection.

Initially, the parent Enterovirus D68 strain US/KY/14-18953 did not propagate in Vero cells and did not show any sign of infection in the form of cytopathic effect or any cell deformities. Thus, the parent strain did not show any sign of adaptation. Later high infectious doses of virus were used for subsequent few passages. The temperature for the entire process of infection was kept around 32-34°C and was never allowed to go above 35°C. With this strategy, the strain started to adapt in Vero cells and displayed partial cytopathic effect from 3 ^rd passage onwards. By 5 ^th passage complete cytopathic effect (CPE) was observed in Vero cells. Further continued passage of the Enterovirus D68 strain with gradual decrease of infectious doses for infection to determine whether or not the strain stably adapted in Vero cells. The Enterovirus D68 strain, as disclosed in the present invention, does get adapted in Vero cells and has been used as a vaccine candidate strain to produce vaccine using Vero cells as substrate for vims propagation.

The present invention hereby discloses a process for adaptation of any Enterovirus D68 strain in Vero cells for making it suitable for vaccines production. In particular, one embodiment of the present invention describes the process of adapting Enterovirus D68 in new cell e.g. Vero cells.

Further, the invention also discloses the polynucleotide sequence/s of the Vero adapted Enterovirus D68 strain/s disclosed as SEQ ID No. 1, and SEQ ID No. 2, and amino acid sequence/s of the Vero adapted Enterovirus D68 strain disclosed as SEQ ID No. 3.

Invention further discloses the nucleotide sequences of the individual structural proteins of EV68 disclosed as SEQ ID No 4, SEQ ID No. 6, SEQ ID No. 8, SEQ ID No. 10 and amino acids sequences of the individual structural proteins of EV68 disclosed as SEQ ID No. 5, SEQ ID No. 7, SEQ ID No. 9, and SEQ ID No. 11, that can be used to make recombinant proteins. The nucleotide sequence of SEQ ID No 4 translates to give amino acid sequence of SEQ ID No. 5, the nucleotide sequence of SEQ ID No. 6 translates to give amino acid sequence of SEQ ID No. 7, the nucleotide sequence of SEQ ID No. 8 translates to give amino acid sequence of SEQ ID No. 9, and the nucleotide sequence of SEQ ID No. 10 translates to give amino acid sequence of SEQ ID No. 11. The recombinant proteins can be expressed in bacterial, yeast or mammalian system after codon optimization of the nucleotide sequences suitable for each expression system and cloning into respective expression vectors. Antibody raised after immunizing the expressed recombinant proteins can be used for diagnosing whole virus or respective protein antigen.

In another embodiment, the invention discloses the process of standardization of the plaque assay of the Vero cells adapted Enterovirus D68 strain in Vero cells which may be utilized to determine the titer of the vims as Plaque forming units and especially for determining the Plaque reduction neutralization titer (PRNT) for vaccine efficacy study. In some other embodiment, there is provided a method of adapting Enterovirus D68 to propagate in Vero cells to high titer wherein Enterovirus D68 virus undergoes plaque assay comprising the steps:

(a) plating of 3 to 4 million Vero cells per 12 well plate or 6 well plate to reach the confluency suitable for plaque assay;

(b) adsorption of the virus of different dilution in different wells in duplicate, triplicate or quadruplicate for 1-2 hours at 32-35°C, more precisely at 32-33°C;

(c) overlaying with <0.6% carboxymethylcellulose or 0.8-E8% Avicel RC 591 as overlay media;

(d) fixing of the cells with 10% formalin after 5-7 days post-infection with carboxymethylcellulose as overlay or 3-4 days post-infection with Avicel RC 591 as overlay;

(e) removal of the fixative solution after fixation and washing of the cells with phosphate buffer saline; and

(f) addition of freshly made staining solution-crystal violet solution dropwise to the fixed cells and staining for 30 mins to 1 hour or 2 hours at room temperature.

The invention also discloses the preparation of antigen from the adapted vims and formulation of the same as vaccine composition to elicit antibodies against Enterovirus D68. The vaccine antigen of Vero cell adapted EV68 can be prepared by inactivation using chemical methods like formalin, beta-propiolactone (BPL), oxidizing agents like hydrogen peroxide, physical methods including but not limited to UV or X-radiation or gamma irradiation.

In some other embodiment, there is provided a method of inactivating Enterovirus D68 containing cDNA encoded from SEQ ID No. 1 for immunization comprising the steps:

(a) sterile filtration of the harvested Enterovirus D68 vims;

(b) removal of the host nucleic acid using nuclease treatment and concentrated by tangential flow filtration using lOOkDa filter;

(c) inactivation using 1/2000-1/4000 formalin for upto 3 weeks at temperature varying from 25-37°C or with BPL at 4-25°C for upto 120 hours or with 0.005% to 3% hydrogen peroxide at 25+ 5°C for upto 6 hours; and

(d) purification of inactivated antigen or purification before inactivation of the viral antigen using gel filtration using Sepharose CL-4B followed by anion exchange chromatography using DEAE resins or by double steps/two rounds of size exclusion chromatography or by cellufine sulphate followed by anion exchange chromatography or by mixed mode resins like CHT Type II (Biorad) alone or in combination with the resins mentioned earlier or any combinations of chromatography steps mentioned above.

In yet another embodiment, the inactivated vaccine antigen can be formulated either in presence or absence of adjuvants. The adjuvants include but not limited to alum (aluminium hydroxide, aluminium phosphate), emulsions like oil in a water adjuvants or water -in oil adjuvants, Toll-like receptors (TLR) ligands like monophosphoryl lipid A (MPL), flagellin either whole or truncated, adjuvant including bacterial cell components, squalene-based adjuvants like MF59 or AddaVax, montanide etc., Ribi adjuvants, CpG and non-CpG containing oligonucleotides, saponins like QS-21, Immune stimulating complexes (ISCOM), ISCOMATRIX etc, vitamins, immunomodulants including cytokines.

In some embodiment, there is provided an immunogenic composition comprising inactivated Enterovirus D68 virus antigen in a physiological acceptable vehicle and optionally one or more pharmaceutically acceptable excipients selected from adjuvants, stabilizers or preservatives.

In another embodiment, Enterovirus 68 vaccine can be formulated with other Enterovirus-based vaccine/s to make one or more combination vaccine/s where the other enterovirus includes but not limited to Enterovirus 71, Coxsackieviruses including coxsackievirus A16, coxsackievirus A6, coxsackievirus A10, rhinoviruses and polioviruses. Vaccine formulations may also include Enterovirus 68 vaccine in combination with flaviviruses, orthomyxoviruses or any other viruses that can cause respiratory diseases, encephalitis or meningitis.

In some embodiment, there is provided an amino acid sequence belonging to Enterovirus D68 having amino acid in the polyprotein selected from L341, G647, K699, K719, N1355, S1406, Q2110 or combination thereof. In some embodiment, there is provided an immunogenic composition comprising inactivated Enterovirus D68 virus antigen in a physiological acceptable vehicle, wherein the Enterovirus D68 is having amino acid in the polyprotein selected from L341, G647, K699, K719, N1355, S1406, Q2110 or combination thereof.

In some embodiment, the immunogenic composition according to present invention are stable for at least 6 months at 2-8°C and for at least 1 month at 37°C.

EXAMPLES

EXAMPLE 1: Virus Propagation

Enterovirus D68 strain in high infectious dose was used for infecting Vero cells. Initially, virus was allowed to adsorb in T25 cm ² flask with occasional shaking for about 60 to 120 mins followed by the addition of the DMEM as maintenance medium. About 1:3 - 1:10 dilution from the virus stock obtained from each passage was used to infect the next batches for initial passages. During later/subsequent passages, virus with higher dilution of the stock vims from previous passages ranging from 1:20 - 1:500 was used for the infection. The virus was harvested when 90% or more cytopathic effect was achieved or within 6 days of infection, whichever is earlier. The entire process of propagating Enterovirus D68 was performed at temperature not higher than 35°C and ideally at 32-33°C. Titer of the vims in different passages were determined by TCID50 assay and/or plaque assay, and is depicted in Figure 2.

The entire process of selecting lower dilution of vims for infection which will not be toxic for the Vero cells during initial passages followed by higher dilution of vims for infection in later passages under controlled temperature range of 32-35°C, preferably 32- 33°C as described above has allowed the successful adaptation of the Enterovirus D68 vims in Vero cells. Figure 1 illustrates adaptation of Enterovirus 68 in Vero cells, wherein Figure 1A shows mock infected Vero cells and Figure 1 B shows Vero cells infected with EV68 displaying cytopathic effect on 3 ^rd day post infection. After successful adaptation, scaling up of vims production was performed serially in T75 cm ² flasks, T175 cm ² flasks and then in Cell stacks or in roller bottle.

EXAMPLE 2: RNA isolation and RT-PCR

RNA has been isolated by Trizol method according to the standard procedure from the cell free supernatant having the infectious virus after harvesting. Briefly, 750m1 of Trizol has been used for 250m1 of the virus containing supernatant. If required to obtain high amount of virus nucleic acid material, Trizol isolation method was preceded by concentrating the virus supernatant either by PEG6000 or PEG8000 (Merck, India) or ultrafiltration using lOOkDa cut off membrane (Merck, India). Isolated RNA was reverse transcribed to complementary cDNA (cDNA) using RevertAid First Strand cDNA synthesis kit (Thermo Fisher Scientific). The presence of viral RNA was confirmed using virus specific primers as depicted in Figure 3. The primer sequences are provided below:

Enterovirus D68 specific primers (Calvo et ah, Pediatr Infect Dis J 2016, 35:45-49):

(F)- 1 : GTTC YTT AAT AGGRTTCRT AGC AGC

(R)- 1 :CTCTATTRCCAATTATGGCATTRAG

Pan-enterovirus primers (Thao et ah, J. Virol. Methods 2010, 170:134-139)

(F): 5’ -C AAGCACTTCTGTTTCCCCGG-3’

(R): 5’-ATTGTCACCATAAGCAGCCA-3’

EXAMPLE 3: Sequencing

For genome wide sequencing, RNA sequencing libraries were prepared with Illumina- compatible NEBNext® UltraTM Directional RNA Fibrary Prep Kit (New England BioFabs, MA, USA). The sequencing library was initially quantified by Qubit fluorometer (Thermo Fisher Scientific, MA, U.S.A.) and its fragment size distribution was analyzed on Agilent TapeStation. Finally, the sequencing library was accurately quantified by quantitative PCR using Kapa Fibrary Quantification Kit (Kapa Biosystems, Wilmington, MA, U.S.A.). The qPCR quantified libraries were pooled in equimolar amounts to create a final multiplexed library pool for sequencing on Illumina NextSeq (150 x 2 chemistry).

Below Table 1 provides Amino acids difference and the corresponding nucleotide level difference between parent Enterovirus D68 virus strain US/KY/14- 18953 and Vero cells adapted virus strain US/KY/14- 18953- Vero:

Table 1: Sequencing summary

EXAMPLE 4: Plaque assay of Enterovirus D68 No comprehensive literature is available in support of Enterovirus D68 plaque assay. The present invention discloses standardized plaque assay procedure for Enterovirus D68. About 3 to 4 million of Vero cells were plated per 12 well plate or 6 well plate (Greiner bio-one) to reach the confluency suitable for plaque assay. Different dilutions of virus were adsorbed in different wells in duplicate, triplicate or quadruplicate for 1-2 hours. 0.8% carboxymethylcellulose (CMC) (Merck, India) semisolid overlay was added subsequently. Carboxymethylcellulose of 0.6-0.5% concentration was also used alternatively as overlay media. Alternatively, Avicel RC 591(FMC Corporation, USA) of 0.8-1.8% concentration was used as overlay. For convenience, Avicel RC 591 will be termed as Avicel hereafter.

The cells were fixed with 10% formaldehyde for 1 hour after 4 to 6 day post infection when CMC was used as overlay or after 2 to 4 days post infection when Avicel was used as overlay. After fixation, the fixative solution was removed and the cells were washed with phosphate buffer saline (PBS). After washing, freshly made crystal violet solution was added dropwise to the fixed cells and was allowed to be stained for 30 minutes to 1 hour at room temperature. Plaques got visible by 5 ^th day of infections when CMC was used as overlay or within 48 hours when Avicel was used. Results are depicted in Figure 4. Plaques were more distinct after 3 days of infection when Avicel was used as overlay media as depicted in Figure 4. EXAMPLE 5: Expression of Enterovirus D68

Vero cell adapted Enterovirus D68 antigen was checked for the expression of Enterovirus D68 VP1, VP2 proteins by Western Blot using Enterovirus D68 -VP1 and VP2 specific antibodies as shown in Figure 5. The specific antigen was separated by 12% SDS-PAGE gel followed by transfer to PVDF membrane. The blot was blocked with 1% BSA and subsequently incubated with Enterovirus D68-VP1 and VP2 specific primary antibodies (GeneTex) for 90 minutes. Soon after, the blot was washed four times with phosphate buffered saline with Tween 20 (PBST) followed by incubation with Horseradish peroxidase (HRP) conjugated secondary antibody. The signal for expression was detected using chromogenic substrate-metal enhanced DAB (Thermo Scientific).

EXAMPLE 6: Preparation and Formulation of the vaccine for immunization

The propagated and harvested EVD68 virus encoding cDNAs as in SEQ ID No. 1 was sterile filtered; the host nucleic acid was removed using nuclease treatment and concentrated by tangential flow filtration using lOOkDa filter. Subsequently, the concentrated vims was inactivated using 1/2000-1/4000 formalin for upto 3 weeks at temperature varying from 25-37°C or with BPL at 4-25°C for upto 120 hours. Formalin was neutralized by using thiosulphate. Alternatively, the virus was inactivated with 0.005% to 3% hydrogen peroxide at 25±5°C for upto 6 hours. The residual hydrogen peroxide was hydrolyzed by the addition of 10 U/ml of catalase to stop the reaction. At the end of the inactivation experiments, the inactivation was confirmed with the absence of cytopathic effect by serially passage of the inactivated virus up to thrice in Vero cells. The inactivated virus antigen is tested and confirmed for invitro antigenicity using Enterovirus 68 antigen specific VP1 antibodies. The inactivated virus was subsequently purified using gel filtration using Sepharose CL-4B followed by anion exchange chromatography using DEAE resins or by Capto Core 700 resins (GE healthcare Life Sciences). The purification was also performed by double steps/two rounds of size exclusion chromatography. The inactivated virus can be also purified using cellufine sulphate followed by anion exchange chromatography if required. The purification was also performed by mixed mode resins -CHT Type II (Biorad) alone or in combination with the resins mentioned earlier. Alternatively, the inactivation as described above was done after purification of the vims. The buffer used for the inactivated vaccine is 10-30 mM Phosphate buffer. Alternatively, Tris buffer, Histidine buffer, Sucrose phosphate Glutamate or any pharmaceutically accepted buffer was used for the formulations.

Suitable excipients that were used for the inactivated vaccine includes but not limited to stabilizers selected from sugar alcohols like glycerol, sorbitol, mannitol (Upto 20%). The formulation also includes stabilizer like Sucrose, and/or Trehalose and/or Polysorbate 40 or Polysorbate 80. The vaccine formulation includes amino acids selected from glycine, Glutamic acids, arginine or arginine hydrochloride (Upto 2%). The vaccine formulation also includes human or animal serum albumin.

The vaccine formulation includes preservatives selected from Thiomersal and 2- phenoxy ethanol. For mercury free vaccine formulation, 2-phenoxyethanol (2.5- 20mg/ml) will be used. In another embodiment, formulation is devoid of any preservatives.

Inactivated antigen is formulated with or without Alum adjuvant of concentration ranging from 100 pg to lmg; more precisely with 200-500pg of alum for immunization. Inactivated Enterovirus 68 vaccine can be formulated using other adjuvants such as emulsions like oil in a water adjuvants or water -in oil adjuvants, Toll-like receptors (TLR) ligands like monophosphoryl lipid A (MPL), flagellin either whole or truncated, adjuvant including bacterial cell components, squalene-based adjuvants like MF59 or AddaVax, montanide etc., Ribi adjuvants, CpG and non-CpG containing oligonucleotides, saponins like QS-21, Immune stimulating complexes (ISCOM), ISCOMATRIX etc, vitamins, immunomodulants including cytokines.

EXAMPLE 7: Combination vaccines

EVD68, EV71 and polio virus causes neurological symptoms and is often associated with Accute flaccid myelitis- weakness associated with spinal cord resulting in weakness in muscles and reflexes in the body. Thus, combination vaccines directed against EVD68, EV71 and polio viruses will reduce the neurological complication associated with these viruses. In one embodiment, formalin inactivated EVD68 antigen (Upto 5 micrograms) was formulated with formalin inactivated EV71 inactivated antigen (Upto 5 micrograms) in phosphate buffer (10-30mM) (1:1 ratio of antigens). The other components of the formulation include adjuvants (including but not limited to alum upto 0.9 mg/ml or MPLA or Alum and MPLA combined), sugar and/or sugar alcohols. The formulation may include amino acids like Glycine, and/or Glutamate and/or Arginine (Upto 2%). The formulation may or may not include preservatives such as Thiomersal or 2- phenoxy ethanol.

In another embodiment, formalin inactivated EVD68 antigen (upto 5 microgram of antigen) was formulated with formalin inactivated sabin type 1 polio (upto 40D antigen units) and sabin type 3 polio vaccine (upto 32 D antigen units). The combination vaccine may or may not include formalin inactivated EV71 antigen (upto 5 microgram of antigen).

EV71 vims inactivation and type 1 and type 3 polio virus inactivation was done with formalin at 36°C ±1°C for upto 14 days. In another embodiment, inactivated EVD68, EV71 and type 1 and 3 polioviruses were adsorbed separately in alum for 2-3 hours in room temperature or for upto 6 hours or for 16 hours in 4°C under stirring condition. Subsequently, the adsorbed antigens were mixed together under stirring conditions.

Alternatively, EVD68 antigen or EV71 or polio antigens were adsorbed first in alum followed by the other antigens.

Formulation was also made without adjuvant by mixing the antigens.

The tables provided below is just for illustration. The scope of possible formulations with monovalent inactivated EVD68 vaccine and combination vaccines having inactivated EVD68, inactivated EV71, inactivated sabin type 1 polio and inactivated sabin type 3 polio vaccine is not limited to the formulations mentioned in the tables. The pH of the vaccine formulations was kept in the range of 6.5 to 7.5.

Table 2: Formulation for EVD68 monovalent vaccine

Table 3: Formulation for combination vaccines

EXAMPLE 8: Vaccine Stability Stability of EVD68 antigen was tested by exposing the inactivated EVD68 antigen at 2- 8°C for upto 6 months. Alternatively, accelerated stability study was performed at 37 °C for 1 month. The inactivated antigen was found to maintain >75% stability for one month at 37°C without any stabilizers _· In presence of 10% sucrose or 10% sucrose and 10% sorbitol combination, the stability is > 90% at 37°C for 1 month. Stability at 2-8°C is more than 85% when stored for 6 months without stabilizer and more than 95% with 10% sucrose or 10% sucrose and 10% sorbitol combination (Figure 6).

Table 4: Stability study of inactivated Enterovirus D68 antigens EXAMPLE 9: Immunogenicity of vaccine antigen

The vaccine containing inactivated antigen was used to immunize mice of 6-8 weeks thrice with three weeks apart. The serum was collected before and after each immunization. ELISA was performed after coating with Enterovirus D68 specific antigen followed by blocking in 1% BSA and subsequent treatment of the ELISA plate with immunized mice serum and anti-mouse secondary antibody. It was found that Formalin inactivated antigen induces very high Enterovirus D68 specific antibody titer (upto 200,000) and is depicted in Figure 7. BPL inactivated antigen induces comparatively lesser but significant amount of Enterovirus D68 specific antibody titer (upto 20,000), as depicted in Figure 8.

Further, Enterovirus D68 specific IgGl/IG2a ratio was determined from serum collected from mice two weeks after the third immunization to detect whether the pattern of immune response is Thl or Th2 type by ELISA (Figure 9). The immune response in Balb/C mice is considered to be associated with predominantly Th2 lymphocytes if IgGl is higher than IgG2a and predominantly associated with Thl lymphocytes when IgG2a is higher than IgGl. When IgGl/ IgG2a is close to 1, it is generally considered as a balanced Thl and Th2 immune response. It has been found that unadjuvanted Beta- propiolactone (BPL) inactivated EVD68 antigen elicited high IgGl type virus specific antibody in compare to IgG2a (IgGl/IgG2a=3) indicating Th2 type immune response. Alum adjuvanted BPL inactivated EVD68 antigen elicited even higher IgGl type virus specific antibody in compare to IgG2a (IgGl/IgG2a=9.8) indicating further polarization towards Th2 type immune response. On the contrary, it has been found that unadjuvanted Formalin inactivated EVD68 antigen elicited balanced IgGl and IgG2a antibody response(IgG2a/IgGl=1.22) indicating a more balanced Thl and Th2 type immune response which got tilted little bit more towards Th2 type immune response in presence of alum as adjuvant (IgGl/IgG2a=1.67).

For neutralization titer detection, serum from EVD68 inactivated antigens vaccine (formulated with or without adjuvants) immunized mice was diluted serially and incubated with Enterovirus D68 virus for 2 hours in 1:1 ratio. The serum-virus mixture was added to the Vero cells and incubated for 2 hours. Subsequently, the cells were overlayered with 1.2% Avicel in DMEM media. The cells were fixed in 10% formalin four days post infection and stained with 0.8% crystal violet solution for plaque visualization. PRNT50 was calculated as the highest sera dilution showing 50% or more reduction in the number of plaques.

Alternatively, microneutralization assay was performed in 96 well format. In microneutralization method, 2.5 million cells per 96 well plate was plated. The serum from EVD68 inactivated antigens vaccine (formulated with or without adjuvants) immunized mice was diluted serially and incubated with Enterovirus D68 virus for 2 hours in 1:1 ratio. Subsequently, serum-virus mixture was added to the Vero cells and waited for upto 4 days to observe inhibition of cytopathic effect of Vero cells in the wells having serum-virus mixture. Neutralization titer was considered as the last dilution of the serum that inhibit 50% of cytopathic effect in compare to the wells having controls virus or negative control serum-virus mixture.

Both Formalin and BPL inactivated Enterovirus D68 antigen induces significant neutralization antibody titer in Balb/c mice.

Table 5: Neutralization titer induced by formalin and BPL inactivated Vero cell adapted Enterovirus D68 antigen.