MERS-CoV vaccine REFERENCE TO SEQUENCE LISTING SUBMITTED VIA EFS-WEB This application includes an electronically submitted sequence listing in .txt format. The .txt file contains a sequence listing entitled "0195924.0007_ST25.txt" created on April 14, 2021 and is 29,211 bytes in size. The sequence listing contained in this .txt file is part of the specification and is hereby incorporated by reference herein in its entirety. FIELD OF THE INVENTION The present invention relates to MERS-CoV, in particular to recombinant vesicular stomatitis viruses containing one or more MERS-CoV structural proteins, vaccines and prime-boost vaccines or immunogenic compositions against MERS-CoV. BACKGROUND OF THE INVENTION Throughout this application, various references are cited in brackets to describe more fully the state of the art to which this invention pertains. The disclosure of these references is hereby incorporated by reference into the present invention. MERS-CoV is an enveloped, single-stranded, positive-sense RNA virus, which belongs to the β-coronaviruses in the family of Coronaviridae (de Groot et al., 2013). It causes severe acute respiratory disease with symptoms of fever, cough, and shortness of breath in humans, and the fatality reaches as high as 30 to 40% (WHO, 2015). Since the known first cases of the disease in Jordan and Saudi Arabia in 2012, the disease spread to other middle-eastern countries and other parts of the world by travelers. The transmission of the MERS-CoV starts from the dromedary camels to humans, and from human to human transmission occurs through close contacts by the patient to care-takers such as hospital personnel, family members, and other people who are in close contact (Buchholz et al., 2013; Drosten et al., 2013). Considering the high fatality of the disease and the possibility of the epidemics in any parts of the world through human to human contacts, development of an efficient vaccine against MERS-CoV is needed to prevent the onset and the spread of the disease in human. The 3´ one-third of MERS-CoV genome encodes structural proteins such as spike (S) protein, envelope (E) protein, nucleocapsid protein (N), and membrane protein (M) (Fig. 1). All S, E, and M proteins reside on the virus envelope. These three structural proteins form virus-like particles when they are expressed together (Wang et al., 2017). MERS-CoV infects host cells using the spike (S) protein, which is a virus surface glycoprotein forming homotrimers (Kirchdoerfer et al., 2016). S protein is a type I membrane protein, which is cleaved into subunit 1 and subunit 2. Subunit 2 is a transmembrane region and is involved in the fusion activity of S protein to the cellular membrane (Kirchdoerfer et al., 2016; Walls et al., 2016). S protein binds to cellular receptor dipeptidyl peptidase 4 (DPP4) through the receptor binding domain in the S1 subunit (Raj et al., 2013). The receptor binding domain (RBD) (Fig.2) on the spike protein, S, contains a critical neutralizing domain (CND) which generates very effective neutralizing antibodies in vaccinated mice (Lu et al., 2014; Li, 2015; Tai et al., 2017). An ideal MERS-CoV vaccine should induce completely protective immune responses, must be safe, relatively easy to administrate, and efficient for manufacturing. There is room for an improved MERS-CoV vaccine to meet all the criteria for an ideal MERS-CoV vaccine. The Applicant has developed a system comprising a combination of vaccines that elicits a response against MERS-CoV. SUMMARY OF THE INVENTION In accordance with the present invention, a recombinant vesicular stomatitis virus (rVSV) carries at least one gene that encodes for a MERS-CoV structural protein or modifications thereof. In one embodiment of the rVSV of the present invention, the MERS-CoV structural protein or modifications thereof includes one or more of a full-length spike (S _F ) protein of MERS-CoV, a receptor binding domain (RBD) of the S _F protein, an envelope (E) protein of MERS-CoV, or a membrane (M) protein of MERS-CoV, or modifications thereof. In another embodiment of the rVSV of the present invention, the at least one gene includes a gene that encodes for the RBD having a glycoprotein signal peptide at the NH ₂ -terminus of the RBD. In one aspect, the glycoprotein signal peptide is a melittin signal peptide (msp). In another embodiment of the rVSV of the present invention, the at least one gene includes a gene that encodes for the S _F protein. In another embodiment of the rVSV of the present invention, the at least one gene includes a gene that encodes for the E protein. In another embodiment of the rVSV of the present invention, the at least one gene includes a gene that encodes for the RBD having a glycoprotein signal peptide at the NH ₂ -terminus of the RBD, a gene that encodes for the E protein and a gene that encodes for the M protein. In one aspect, the glycoprotein signal peptide is a melittin signal peptide (msp). In another embodiment of the rVSV of the present invention, the at least one gene includes a gene that encodes for the RBD having a glycoprotein signal peptide at the NH ₂ -terminus of the RBD and a gene that encodes for the E protein. In one aspect the glycoprotein signal peptide is a melittin signal peptide (msp). In another embodiment of the rVSV of the present invention, the rVSV is a replication competent rVSV of Indiana serotype(rVSV _Ind ). In another embodiment of the rVSV of the present invention, the rVSV _Ind include a mutant matrix protein gene. In another embodiment of the rVSV of the present invention, the mutant rVSV _Ind matrix protein includes a GML mutation (rVSV _Ind -GML). In another embodiment of the rVSV of the present invention, the rVSV is a replication competent rVSV of New Jersey serotype (rVSV _NJ ). In another embodiment of the rVSV of the present invention, the rVSV _NJ include a mutant matrix protein gene. In another embodiment of the rVSV of the present invention, the rVSV _NJ M protein includes a GMM mutation (rVSV _NJ -GMM) or a GMML mutation (rVSV _NJ -GMML). In another embodiment, the present invention is a MERS-CoV vaccine or immunogenic composition including a recombinant vesicular stomatitis virus (rVSV) of the present invention. In one embodiment of the MERS-CoV vaccine or immunogenic composition of the present invention, the MERS-CoV vaccine or immunogenic composition comprises the rVSV carrying the gene that encodes for the full-length spike protein of the MERS-CoV, and wherein the rVSV is rVSV _Ind -GML, rVSV _NJ -GMM or rVSV _NJ -GMML. In another embodiment of the MERS-CoV vaccine or immunogenic composition of the present invention, the MERS-CoV vaccine or immunogenic composition comprises the rVSV carrying the gene that encodes for the RBD having the glycoprotein signal peptide at the NH ₂ terminus of the RBD, and wherein the rVSV is rVSV _Ind -GML, rVSV _NJ -GMM or rVSV _NJ - GMML. In another embodiment of the MERS-CoV vaccine or immunogenic composition of the present invention, the MERS-CoV vaccine or immunogenic composition comprises the rVSV carrying the gene that encodes for the E protein of the MERS-CoV, and wherein the rVSV is rVSV _Ind -GML, rVSV _NJ -GMM or rVSV _NJ -GMML. In another embodiment of the MERS-CoV vaccine or immunogenic composition of the present invention, the MERS-CoV vaccine or immunogenic composition comprises the rVSV carrying the gene that encodes for the M protein of the MERS-CoV, and wherein the rVSV is rVSV _Ind -GML, rVSV _NJ -GMM or rVSV _NJ- GMML. In another embodiment of the MERS-CoV vaccine or immunogenic composition of the present invention, the MERS-CoV vaccine or immunogenic composition comprises the rVSV carrying the gene that encodes for the having the glycoprotein signal peptide at the NH ₂ - terminus of the RBD and the gene that encodes for the E protein, and wherein the rVSV is rVSV _Ind -GML, rVSV _NJ -GMM or rVSV _NJ -GMML. In another embodiment of the MERS-CoV vaccine or immunogenic composition of the present invention, the MERS-CoV vaccine or immunogenic composition comprises the rVSV carrying the gene that encodes for the RBD having the glycoprotein signal peptide at the NH ₂ terminus of the RBD, the gene that encodes for the E protein of the MERS-CoV and the gene that encodes for the M protein of the MERS-CoV, and wherein the rVSV is rVSV _Ind -GML, rVSV _NJ -GMM or rVSV _NJ -GMML. In another embodiment of the MERS-CoV vaccine or immunogenic composition of the present invention, the glycoprotein signal peptide is a honeybee melittin signal peptide. In another embodiment, the present invention is a prime boost immunization combination against MERS-CoV including: (a) a prime vaccine or immunogenic composition comprising a replication competent recombinant vesicular stomatitis virus (rVSV) carrying at least one gene that encodes for a MERS-CoV structural protein or a modification thereof, and (b) a booster vaccine or immunogenic composition comprising a replication competent rVSV carrying the same at least one gene. In one embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the MERS-CoV structural protein or modification thereof includes one or more of a full-length spike (S _F ) protein of MERS-CoV, a receptor binding domain (RBD) of the S _F protein, an envelope (E) protein of MERS-CoV, or a membrane (M) protein of MERS- CoV, or any modifications thereof. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the at least one gene includes a gene that encodes for the RBD having a glycoprotein signal peptide at the NH ₂ -terminus of the RBD. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the at least one gene includes a gene that encodes for the S _F protein. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the at least one gene includes a gene that encodes for the E protein. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the at least one gene includes a gene that encodes for the RBD having a glycoprotein signal peptide at the NH ₂ -terminus of the RBD, the E protein and the M protein. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the at least one gene includes a gene that encodes for the RBD having a glycoprotein signal peptide at the NH ₂ -terminus of the RBD and a gene that encodes for the E protein. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the glycoprotein signal peptide is a honeybee melittin signal peptide. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the rVSV of the prime vaccine or immunogenic composition and the rVSV of the booster vaccine or immunogenic composition are rVSV of the same serotype. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the rVSV of the prime vaccine or immunogenic composition and the rVSV of the booster vaccine or immunogenic composition are rVSV of Indiana serotype (rVSV _Ind ). In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the rVSV of the prime vaccine or immunogenic composition and the rVSV of the booster vaccine or immunogenic composition are rVSV of New Jersey serotype (rVSV _NJ ). In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the rVSV of the prime vaccine or immunogenic composition is Indiana serotype (VSVInd) and the rVSV of the booster vaccine or immunogenic composition is New Jersey serotype (VSV _NJ ). In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the rVSV of the prime vaccine or immunogenic composition is New Jersey serotype (rVSV _NJ ) and the rVSV of the booster vaccine or immunogenic composition is rVSV of Indiana serotype (rVSV _Ind ). In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the rVSV of the prime vaccine and the rVSV of the booster vaccine include a mutant matrix protein gene of the rVSV. In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, when the rVSV is rVSV _Ind , the matrix protein of the rVSV _Ind includes a GML mutation (rVSV _Ind -GML). In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, when the rVSV is rVSV _NJ , the matrix protein of the rVSV _NJ includes a GMM mutation (rVSV _NJ -GMM) or a GMML mutation (rVSV _NJ -GMML). In another embodiment of the prime boost immunization combination against MERS-CoV of the present invention, the rVSV of the prime vaccine or immunogenic composition and the rVSV of the booster vaccine or immunogenic composition include are codon optimized for expression in a human cell. In another embodiment, the present invention is a method for inducing an immune response in a mammal against MERS-CoV, comprising administering to the mammal an effective amount of a vaccine or immunogenic composition of the present invention or administering the mammal a prime boost immunization platform of the present invention. In one embodiment of the method for inducing an immune response in a mammal against MERS-CoV, the immune response includes a humoral and a cellular immune response. In another embodiment, the present invention is a use of a MERS-CoV vaccine of the present invention for the prevention or treatment of a MERS-CoV infection. In another embodiment, the present invention is a use of a combination medicament for the prevention or treatment of a MERS-CoV infection, the combination medicament comprising a prime boost immunization platform of the present invention. In another embodiment, the present invention is a use of a rVSV of the present invention in the manufacture of a vaccine or immunogenic composition for the prevention or treatment of a MERS-CoV infection. In accordance to the present invention, a recombinant receptor binding domain (RBD) of a spike protein of MERS-CoV includes or has a honeybee melittin signal peptide (msp) at the NH ₂ terminus of the RBD. In one embodiment, said recombinant RBD is encoded by a gene including SEQ ID NO: 20 or consisting essentially of SEQ ID NO: 20 or consisting of SEQ ID NO: 20. BRIEF DESCRIPTION OF THE DRAWINGS The present invention will become more fully understood from the detailed description given herein and from the accompanying drawings, which are given by way of illustration only and do not limit the intended scope of the invention. Fig.1. Illustration of a MERS CoV clone. Fig. 2. (SEQ ID NO: 17) Illustration of MERS CoV spike protein, showing the receptor binding protein. Fig.3. Illustration of the generation of an avirulent VSV _Ind with mutations in the M gene. Fig.4. Illustration of the generation of an avirulent VSV _NJ with mutations in the M gene. Fig. 5. (SEQ ID NO: 17 and 18) Cloning MERS-CoV genes (S, RBD, M, S/E and S/E/M) into rVSV _Ind -GML (G21E, M51R, L111A) and rVSV _NJ -GMM (G22E, M48R, M51R). Fig.6. Illustration of recovery of rVSV by reverse genetics (Buchholz, et al., J. Virol.73:251, 1999). Figs. 7A to 7D. Expression of MERS-CoV proteins (S, RBD, M and E) in three different cell lines (BHK-21 (a), VeroC1008 (b) and Huh-T7 C8 (c)) infected with rVSV _Ind series.7A: rVSV _Ind -GML, 2. rVSV _Ind -GMLS; 7B: 1. rVSV _Ind -GML, 2. rVSV _Ind -GML-msp-RBD; 7C: rVSV _Ind -GML, 2. rVSV _Ind -GML-M; 7D.1. rVSV _Ind -GML, 2. rVSV _Ind -GML-E. Figs.8A to 8F. Expression of MERS-CoV proteins (RBD, M and E) in BHK-21infected with rVSV _NJ -GMM series carrying the genes that encode these MERS-CoV proteins. Panels 8A, 8B, 8C, 8D, 8E and 8F represent Western blot analyses of all three proteins. Figs. 9A to 9C. Detection of MERS-CoV proteins (S, RBD, M and E) in the extracellular culture media of the three different cell lines (BHK-21 (a), VeroC1008 (b) and Huh-T7 C8 (c)) infected with rVSV _Ind series. 9A. 1. rVSV _Ind -GML, 2. rVSV _Ind -GML-S, 3, 4, and 5. rVSV _Ind -GML-mspRBD, 9B.1. rVSV _Ind -GML, 2. rVSV _Ind -GML-M, 9C.1. rVSV _Ind -GML, 2. rVSV _Ind -GLM-E. Figs.10A to 10D. Detection of MERS-CoV proteins (S, RBD, M and E) in pseudotype viral particles from three different cell lines (BHK-21, VeroC1008 and Huh-T7 C8) infected with rVSVNJ-GMM series. 10A. 1. Not infected cells, 2. rVSVInd-GML-S, 10B. 1. Not infected cells, 2. rVSVInd-GML-mspRBD, 10C. 1. Not infected cells, 2. rVSVInd-GML-M, 10D. 1. Not infected cells, 2. rVSVIND-GML-E. Figs. 11A to 11E. Electron microphotographs of sedimentable particles in the concentrated culture media from the infected BHK-21 cells.11A: electron micrograph of control cells; 11B electron micrograph of cells infected with rVSV _Ind -GML-S and corresponding Western blot; 11C: electron micrograph of cells infected with rVSV _Ind -GML-E and corresponding Western blot; 11D: electron micrograph of cells infected with rVSV _Ind -GML-M and corresponding Western blot; 11E: electron micrograph of cells infected with rVSV _Ind -GML-EM. Fig. 12. Illustration of serum antibody titration (MERS groups 1-4 and negative control group). Fig. 13. Illustration of antibody tier against MERS-CoV S1 RBD in rabbit sera for the different vaccination groups (MERS groups 1-4 and negative control group). Figs.14A to 14B. Plaque reduction in neutralization test.14A. Neutralizing ability of rabbit sera from groups vaccinated with MERS 1-4 and control (PBS) against MERS-CoV EMC/2012.14B. Positive neutralizing rabbit monoclonal antibody. DETAILED DESCRIPTION OF THE INVENTION 1. Definitions For convenience, the meaning of certain terms and phrases employed in the specification, examples, and appended claims are provided below. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The articles "a" and "an" are used herein to refer to one or more than one (i.e., to at least one) of the grammatical object of the article. The terms "animal" and “subject” as used herein includes all members of the animal kingdom including mammals, preferably humans. The term "effective amount" as used herein means an amount effective and at dosages and for periods of time necessary to achieve the desired result. “rVSV” is used to refer to a recombinant vesicular stomatitis virus. The term “Indiana”, and “IND” are used to refer to the VSV serotype Indiana (VSV _Ind ). The term “New Jersey”, and “NJ” are used to refer to the VSV serotype New Jersey (VSV _NJ ). In aspects of this invention, the VSV _NJ is Hazelhurst strain (VSV _NJ-H ) or Ogden strain (VSV _NJ-O ). “M _WT ” “M(WT)” are used to refer to VSV expressing a wild type matrix protein. “G22E” is used to refer to a mutant matrix of VSV _NJ having a glycine changed to a glutamic acid at position 22. “G21E” is used to refer to a mutant matrix protein of VSV _Ind having a glycine changed to a glutamic acid at position 21. “L110A” is used to refer to a mutant matrix protein of VSV _NJ having a leucine changed to alanine at position 110. “L111A” is used to refer to a mutant matrix protein protein of VSV _Ind having a leucine changed to alanine at position 111. “L110F” is used to refer to a mutant matrix protein of VSV _NJ having a leucine changed to phenylalanine at position 110. “L111F” is used to refer to a mutant matrix protein of VSV _Ind having a leucine changed to phenylalanine at position 111. “M51R” is used to refer to mutant matrix protein of the VSV _Ind having a methionine changed to an arginine at position 51. “M48R + M51R” or “M48R/M51R” are used to refer to a mutant matrix protein of VSV _NJ having a methionine changed to an arginine at positions 48 and 51 respectively. “rVSV _Ind (GML)” is used to refer to VSV _Ind having the combined mutation G21E, M51R and one of L111A or L111F. “rVSV _NJ (GMM)” is used to refer to a VSV _NJ having the combined mutation G22E, M48R/M51R. “rVSV _NJ (GMML)” is used to refer to a VSV _NJ having the combined mutation G22E, M48R/M51R and one of L110A or L110F. “S _F ” is a recombinant full length spike protein of MERS-CoV. “S protein” is used to refer to the S _F or partial length forms of the spike protein of MERS- CoV “S1” is a recombinant S1 region or subunit of S _F of MERS-CoV. “S2” is a recombinant S2 region or subunit of S _F of MERS-CoV. “RBD” is used to refer to the receptor binding domain of the S _F , found in S1 subunit. “Partial length of the S protein” is used to refer to one or more of S1, S2 and RBD. The term “protein” as used herein is defined as a chain of amino acid residues, usually having a defined sequence. As used herein the term protein is inclusive of the terms “peptides” and “proteins”. The terms also encompass an amino acid polymer that has been modified. 2. Overview The present invention features rVSVs, immunization platforms, immunization regimens and medicaments and kits useful for inducing an immune response in a subject and preventing or treating MERS-CoV infection in a subject, wherein said rVSVs, platforms, regimens and medicaments and useful kits comprise a rVSV that carries one or more genes that encode for one or more structural proteins of MERS-CoV, including modifications of said one or more structural proteins to form pseudotype rVSVs that trigger efficient humoral immune responses against MERS-CoV. The MERS-CoV gene can be genetically modified to encode a modified MERS-CoV structural protein that elevates glycoprotein synthesis and triggers efficient humoral immune response. In one embodiment, the MERS-CoV gene is genetically modified to produce modified structural proteins having a glycoprotein signal peptide at its N-terminus. Any glycoprotein signal peptide that allows the MERS-CoV structural protein to be glycosylated and involved in intracellular trafficking can be used, for example the honeybee melittin signal peptide. For example, a gene is genetically modified to produce RBD proteins having a honeybee melittin signal peptide (msp) at its N-terminus or to produce RBD proteins having the msp at its N-terminus, and the transmembrane domain and cytoplasmic tail of the VSV glycoprotein (Gtc) to form pseudotype VSVs that trigger efficient humoral immune responses against the RBD protein. In one embodiment, the one or more MERS-CoV structural protein is one or more of a spike (S) protein, a receptor binding domain (RBD) of the S protein, an envelope (E) protein, or a membrane (M) protein of MERS-CoV, modifications of said S, RBD, E and M proteins. The S protein of MERS-CoV can be a full-length spike (S _F ) protein or a partial length S protein. The partial length form of the S protein is one or more of S1 peptides of the S _F protein, S2 peptides of the S _F protein, the receptor binding domain of the S _F protein (RBD) or any modifications thereof. In embodiments, at least one of the S protein (S _F or partial length S protein) and the E protein are modified with a glycoprotein signal peptide, such as the honeybee melittin signal peptide (msp), at the NH2-terminus of the at least one of the S protein (S _F or partial length S protein) and the E protein, and/or the VSV G protein transmembrane domain and cystoplasmic tail (Gtc) at the COOH-terminus of the at least one of the S protein (S _F or partial length S protein) and the E protein. In one embodiment, the RBD gene is genetically modified to produce an RBD protein having a honeybee melittin signal peptide (msp) at its NH ₂ -terminus to glycosylate the RBD that trigger efficient humoral immune responses against MERS-CoV. 3. Vaccines or Immunogenic Compositions of the Invention The present invention further features vaccines or immunogenic compositions. The present invention describes MERS-CoV vaccines or immunogenic compositions including a recombinant vesicular stomatitis virus (rVSV) that carries one or more genes that encode for at least one MERS-CoV structural protein, including at least one of the S protein (full or partial length forms), the E protein, of MERS-CoV, including modifications of said S, and E proteins. The S protein can be provided as a full-length spike (S _F ) protein, a S1 subunit of the S _F protein, a S2 subunit of the S _F protein, and/or a receptor binding domain (RBD) of the S _F protein. In embodiments, the at least one of the S (S _F or partial length S protein) and E proteins are modified with a glycoprotein signal peptide such as the honeybee melittin signal peptide (msp) at its NH ₂ -terminus and/or a VSV G protein transmembrane domain and cystoplasmic tail (Gtc) at the COOH-terminus of the S (S _F or partial length S protein) and/or E protein. In embodiments, the RBD protein is modified to include a glycoprotein signal peptide, such as the honeybee melittin signal peptide (msp) at its NH ₂ - terminus to form pseudotype rVSVs that trigger efficient humoral immune responses against MERS-CoV. In embodiments, one or more genes that encode for the S (full or partial length forms), and E proteins and modifications therein are codon-optimized for expression in a human cell. The rVSV may be of Indiana serotype, New Jersey serotype or any other suitable VSV subtype. The vaccines or immunogenic compositions of this invention may be provided as a prime- boost immunization combination against MERS-CoV. The rVSV of the prime vaccine or immunogenic composition may be of the same or different serotype as the rVSV of the boost vaccine or immunogenic composition. For example, both the prime and boost vaccines or immunogenic compositions are rVSV _Ind ; or both the prime and boost vaccines or immunogenic compositions are rVSV _NJ ; or the rVSV of the prime vaccine or immunogenic composition is rVSV _Ind and the rVSV of the boost vaccine or immunogenic composition is rVSV _NJ ; or the rVSV of the prime vaccine or immunogenic composition is rVSV _NJ and the rVSV of the boost vaccine or immunogenic composition is rVSV _Ind . The vaccine or immunogenic compositions of the invention are suitable for administration to subjects in a biologically compatible form in vivo. The expression "biologically compatible form suitable for administration in vivo" as used herein means a form of the substance to be administered in which any toxic effects are outweighed by the therapeutic effects. The substances maybe administered to any animal or subject, preferably humans. The vaccines of the present invention may be provided as a lyophilized preparation. The vaccines of the present invention may also be provided as a solution that can be frozen for transportation. Additionally, the vaccines may contain suitable preservatives such as human albumin, bovine albumin, sucrose, glycerol or may be formulated without preservatives. If appropriate (i.e., no damage to the VSV in the vaccine), the vaccines may also contain suitable diluents, adjuvants and/or carriers. The dose of the vaccine may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of antibody to elicit a desired response in the individual. Dosage regime may be adjusted to provide the optimum therapeutic response. The dose of the vaccine may also be varied to provide optimum preventative dose response depending upon the circumstances. 4. Methods of Use The present invention also features methods of inducing an immune response in a subject against MERS-CoV and/or preventing or treating a MERS-CoV infection in a subject comprising administering to the subject an effective amount of a vaccine or immunogenic composition or a combination of vaccines or immunogenic compositions of the present invention. As such, in one embodiment, the present invention provides for a method for inducing an immune response in a subject to a MERS-CoV comprising the step (a) of administering to the subject an effective amount of a vaccine or immunogenic composition including a rVSV carrying one or more geneses that encode for one or more structural protein of MERS-CoV. In one embodiment, the method further comprises the step (b) of administering to the subject another vaccine or immunogenic composition comprising a rVSV carrying the same one or more genes that encode the same one or more structural proteins of MERS-CoV. The rVSV of the vaccine or immunogenic composition of step (a), the priming vaccine or immunogenic composition, may be of the same or different serotype as the rVSV of the vaccine or immunogenic composition (b), the booster vaccine or immunogenic composition. For example, both the prime and boost vaccines or immunogenic compositions are rVSV _Ind ; or both the prime and boost vaccines or immunogenic compositions are rVSV _NJ ; or the rVSV of the prime vaccine or immunogenic composition is rVSV _Ind and the rVSV of the boost vaccine or immunogenic composition is rVSV _NJ ; or the rVSV of the prime vaccine or immunogenic composition is rVSV _NJ and the rVSV of the boost vaccine or immunogenic composition is rVSV _Ind . In embodiments of the invention the methods for inducing an immune response in a mammal to a MERS-CoV and the methods for preventing or treating an infection caused by MERS- CoV may further comprise the step of (c) administering to the subject an effective amount of the vaccine or immunogenic composition of either step (a) or step (b). Step (c) may be administered to the subject more than one time over the course of inducing an immune response, preventing or treating. Advantages Advantages of the recombinant VSV-based platform technology of the present invention are first, a highly efficient prime-boost vaccination can be achieved with two antigenically distinct serotypes of rVSV vectors, because the vector immunity against the priming Indiana serotype (VSV _Ind ) will not neutralize the boosting New Jersey serotype (VSV _NJ ) vector. Thus,VSV _NJ carrying the same gene of interest as rVSV _Ind ) will provide maximum boost effects A highly efficient prime-boost vaccination can also be achieved with the same serotype of rVSV vectors (i.e., both the prime and boost are rVSV _Ind or both the prime and boost are rVSV _NJ ), because The pseudotype VSVs carrying both VSV G protein and MERS-CoV spike protein on the surface of the virion can bind to either the low-density lipoprotein receptor (LDL-R)by VSV G protein and/or the human dipeptidyl peptidase 4 (hDPP-4) receptor by the spike protein of MERS-CoV. Thus, the vector immunity against one serotype of VSV may not block the infection of the same pseudotype VSV completely. This may provide boost effects. Second, the genetically modified VSV _Ind M gene mutant (rVSV _Ind -GML) and genetically modified VSV _NJ M gene mutant (rVSV _NJ -GMM) vectors are completely safe, attenuated temperature sensitive mutants [22]. Third, rVSV _Ind -GML and rVSV _NJ -GMM vectors carrying foreign genes replicate highly efficiently. Therefore, high titer rVSV-based vaccines are relatively easy to prepare. Fourth, both rVSV _Ind -GML and rVSV _NJ -GMM vectors can accommodate a large-size foreign gene with up to 6,000 nucleotides, without decreasing the virus titer [24], and finally both serotypes of VSV have a very wide host range including humans. The above disclosure generally describes the present invention. A more complete understanding can be obtained by reference to the following specific Examples. These Examples are described solely for purposes of illustration and are not intended to limit the scope of the invention. Changes in form and substitution of equivalents are contemplated as circumstances may suggest or render expedient. Although specific terms have been employed herein, such terms are intended in a descriptive sense and not for purposes of limitation. EXAMPLES The examples are described for the purposes of illustration and are not intended to limit the scope of the invention. We have employed a genetically modified dual serotype of vesicular stomatitis virus (VSV) platform technology [22,23] to develop vaccines against MERS-CoV. We have developed MERS-CoV vaccines using temperature-sensitive avirulent rVSV _Ind - GML and rVSV _NJ -GMM as vaccine vectors (Fig.3, Fig.4) (Kim et al., 2015). MERS-CoV S, E, and M genes were cloned (Fig. 5), together or separately into the plasmids of rVSV _Ind - GML and rVSV _NJ -GMM for the generation of the attenuated rVSV vectors expressing MERS-CoV structural proteins. Co-expression of Coronavirus S, E, and M proteins form virus-like particles (VLP) (Boscarino et al., 2008; de Haan et al., 2000; Vennema et al., 1996), which are non-pathogenic and could form a proper conformation of trimeric S proteins on the VLP surface. We also cloned only receptor binding domain (RBD) (Fig.2, Fig.5, 212 amino acids) of S protein containing honeybee melittin signal peptide (21 aa, Fig. 5) at the NH ₂ - terminus of RBD (mspRBD) into the VSV vectors. Normally S proteins are secreted as a part of the MERS-CoV particles and stimulate the circulating B lymphocytes to generate neutralizing antibodies against epitopes in the RBD of S protein. However, if RBD is expressed without the signal peptide at the NH ₂ -terminus, the protein would not be secreted outside of the cells resulting in less chance of encountering with B lymphocytes. Naturally, S protein is highly glycosylated in the ER, and lack of signal peptide sequence on the RBD makes the protein non-glycosylated. Signal peptides at the amino-terminal region of the secretory proteins target the protein to the ER and Golgi network for the modification of the protein and to the cytoplasmic membrane for the secretion. Honeybee msp increases the overall expression level, glycosylation, and secretion of the protein through cytoplasmic membrane. Therefore, we added honeybee msp sequences to the NH ₂ -terminus of RBD of S protein to increase the expression of the RBD protein (Fig.5). We also included E protein and M protein as components of MERS-CoV vaccine together with full length S protein (S or S _f ) or RBD of S protein and will compare the immunogenicity and efficacy of the vaccine in the presence or absence of E and M proteins. We recovered recombinant VSVs expressing MERS-CoV genes using the VSV reverse genetics system (Fig. 6). The newly recovered viruses are rVSV _Ind -GML-S, rVSV _Ind -GML- RBD, rVSV _Ind -GML-M, rVSV _Ind -GML-E, rVSV _Ind -GML-E/M, rVSV _Ind -GML-S/E, rVSV _Ind - GML-mspRBD/E, rVSV _Ind -GML-mspRBD/E/M, rVSV _NJ -GMM-S, rVSV _NJ -GMM-mspRBD, rVSV _NJ -GMM-M, rVSV _NJ -GMM-E, rVSV _NJ -GMM-E/M, rVSV _NJ -GMM-S/E, rVSV _NJ - GMM-mspRBD/E, and rVSV _NJ -GMM-mspRBD/E/M. The recovered viruses were plaque purified three times and amplified in BHK ₂₁ cells for virus stock preparation. The intracellular expression of MERS-CoV S, E, and M proteins from the recombinant VSVs were determined by Western blot analysis using rabbit antibodies against S protein (Sino Biological Inc.), rabbit antibodies against E protein (GenScript USA Inc), and rabbit antibodies against M protein (GenScript USA Inc.). Rabbit antibodies against M and E proteins were generated in rabbits using custom-designed linear peptides located at the carboxyl-terminal region of each protein (Table 6, polyclonal antibodies against MERS-CoV Spike protein were purchased from Sino Biological Inc.). BHK ₂₁ cells were infected with MOI of 6 of each virus and the cell lysates were prepared at 6 hours post-infection. The 10µg cell lysates were loaded into the SDS-PAGE gel and MERS-CoV S, RBD, E, and M were detected by Western blot analyses. Proper sizes and good quantities of the MERS-CoV proteins were expressed from the rVSV _Ind -GML (Fig. 7) and rVSV _NJ -GMM (Fig. 8). About 210 kDa size of S protein was detected from the cells infected with rVSV _Ind -GML-S (Fig.7A), rVSV _Ind -GML-S/E (Fig.7E) and rVSV _NJ -GMM-S/E (Fig. 8E). About 30 kDa (212 aa, 23kDa) size of mspRBD was detected from the cells infected with rVSV _Ind -GML-mspRBD (Fig. 7A) and rVSV _NJ -GMM- mspRBD (Fig.8A). RBD migrated slightly slower than the actual size RBD probably because of the glycosylation of the protein. E protein was detected as a protein slightly larger than that of 7 kDa protein and showed double bands in a high concentration SDS-PAGE gel (Fig. 7B, 8E, 9B, and 9E), which we are not sure why E protein shows double bands. M protein was detected as about 24 kDa and 22 kDa protein bands when it was expressed in BHK ₂₁ cells (Fig.7A and Fig.8A). The predicted molecular mass for the M protein is 24 kDa. We are not certain why M protein was detected as 2 separate bands. The differences may come from the differences in the glycosylation or may come from the cleavage of the protein by a cellular protease. We checked the expression of M protein as well as S, RBD, and E proteins in other cell lines such as green monkey kidney cells (Vero) and human liver cells (Huh 7.5) in order to examine whether they are expressed the same as in BHK ₂₁ cells. The three different cell lines were infected separately with rVSV _Ind -GML-S, rVSV _Ind -GML-M, rVSV _Ind -GML- mspRBD, rVSV _Ind -GML-E (Fig.9). The infected cells were lysed at 6 hrs post-infection. The expression level and migration pattern in the SDS-PAGE was examined by Western blot analysis (Fig. 9). Full-length S protein was expressed as the same size in all three cell lines, although the expression level was highest in the human liver cell line, Huh7.5 (Fig.9A line c). M protein was expressed the most in Huh7.5 cells, but the migration pattern was quite different from the M proteins expressed in BHK ₂₁ cells and Vero cells (Fig. 9C). M protein expressed in BHK ₂₁ cells and Vero cells showed the same migration pattern (Fig. 9C line a and 10C line b). In Huh7.5 cells, M protein migrated as one band, but it migrated faster than the slowly migrating band of the two bands from BHK ₂₁ cells and Vero cells (Fig. 9C). It seems that the variability of the M protein expression depends on the origin of the cell lines. We are not certain why M protein shows different expression patterns in different cell lines. The mspRBD and E proteins from three different cell lines showed the same migration pattern (Fig. 9). The expression levels in the three different cell lines were the same for E protein. The mspRBD was expressed the least in Huh7.5 cells (Fig. 9). The expression of VSV proteins in 3 different cell lines did not show much of differences in the level of protein expressions and protein migration patterns in the SDS-PAGE (Fig.10). We also checked the secretion of the MERS-CoV proteins from three different cell lines infected with rVSV _Ind -GML-S, rVSV _Ind -GML-mspRBD, rVSV _Ind -GML-M, and rVSV _Ind - GML-E (Fig. 10). We wanted to examine whether adding honeybee melittin signal peptide (msp) sequence to the NH ₂ -terminus of the RBD makes it secret or not. The three different cell lines were infected with MOI of 6 and were incubated at 37°C. The culture media from the infected cells were collected at 22 hrs post-infection. The collected culture media was centrifuged at 4,000 rpm for 10 minutes to remove cell debris. The secreted extracellular proteins were concentrated by using ultrafiltration device with 5,000 molecular weight cut-off membrane (Sartorius). The concentrated proteins were detected by Western blot analysis (Fig. 10). MERS-CoV full-length S protein was not detected in the samples from all three cell lines indicating that S does not secret when it is expressed alone without other MERS-CoV proteins (Fig. 10A). On the other hand, mspRBD, which has the msp at the NH ₂ -terminus was secreted from all three different infected cell lines (Fig.10A). The mspRBD was secreted the most from BHK21 cells. Huh7.5 cells secreted the least amount of mspRBD. M protein and E protein was either non-detectable or secreted very small amount in BHK ₂₁ cells (Fig.10B and 10C) indicating that singly expressed M and E proteins do not secret from the infected cells. The concentrated culture media contains recombinant VSVs as well as the enveloped structures, which is made of MERS-CoV S, M, or E proteins. Recombinant VSV particles with randomly incorporated MERS-CoV S, E, and M proteins might be present in the concentrated culture media. In order to detect the MERS-CoV S, mspRBD, M, and E proteins, the culture media from the infected cells were collected at 22 hrs post-infection. The collected media was cleared off cell debris and was concentrated by the ultracentrifugation at 36,000 rpm for 2 hrs. MERS-CoV proteins in the pelleted material were detected by Western blot analysis using antibodies against S, M, and E proteins (Fig. 10). Very little amount of S and M protein was detected in samples from BHK ₂₁ cells and Vero cells (Fig. 10). There was no detectable amount of S and M proteins in the samples from Huh7.5 cells (Fig. 10). The mspRBD was not present in the pelleted samples from all three different cell lines, indicating that mspRBD alone did not form any sedimentable particles. E protein was detected in all three samples from the different cell lines and BHK ₂₁ cells produced the most detectable E protein in the concentrated pellet. The presence of E, M, and S protein in the pelleted samples indicated that there were VSV _Ind -GML particles incorporated with these MERS-CoV proteins or sedimented membranous structures with MERS-CoV E, M, and S proteins. The Western blot analysis using the pelleted culture media indicated that MERS-CoV S, M, and E proteins were part of the sedimentable particles such as virus-like particles (VLP) and/or pseudotyped VSV particles. Therefore, we wanted to examine the presence of such particles which resemble the MERS-CoV by electron microscopy. We infected BHK ₂₁ cells separately with MOI of 6 of rVSV _Ind -GML-S, rVSV _Ind -GML-E, rVSV _Ind -GML-M, and rVSV _Ind -GML-E/M. The culture media was collected at 22 hrs post-infection. After clearing off cell debris, the culture media was concentrated by ultracentrifugation at 36,000 rpm for 2 hrs. The pelleted material was resuspended in PBS and was fixed in 0.1% glutaraldehyde at room temperature for an hour. The fixed samples were loaded on a formvar/carbon grid and was stained with 1% posphotungstic acid (PTA). All of the samples from BHK ₂₁ cells infected with rVSV _Ind -GML with S (Fig.11B), E (Fig.11C), M (Fig.11D), or E/M (Fig.11E) contained typical MERS-CoV structures indicating that as long as one of the structural proteins are expressed, MERS-CoV like membranous structures are generated and are secreted from the infected cells (Fig. 11). The secreted VLPs of MERS-CoV structural proteins will present the antigens to B cells as well as T cells for inducing MERS-CoV protein-specific immune responses. This rVSV-MERS-CoV vaccine has been used for immune response studies. There is no currently available vaccine against MERS-CoV. Considering the high fatality of the disease, the development of an effective vaccine is required to prevent MERS. Expression of MERS-CoV E, M, and RBD(S) could generate virus-like particles (VLPs) and could induce neutralizing antibodies against MERS-CoV. We generated attenuated rVSVs of both Indiana and New Jersey serotypes expressing MERS-CoV structural proteins, RBD of Spike glycoprotein (S), Envelope protein (E), and Membrane protein (M). The rVSVs of the present invention are noncytolytic and avirulent. We examined the production of neutralization antibodies (nAb) against RBD, a receptor binding domain of Spike glycoprotein. We compared the efficiency of producing nAb by rVSV expressing RBD(S) alone or by rVSV expressing RBD(S), E, and M proteins. We checked the level of nAb against various MERS- CoV isolates. The following animal groups have been vaccinated with rVSV expressing MERS-CoV structural proteins, M, E, and RBD of S proteins. Rabbits were prime-immunized with rVSV _Ind -GML expressing MERS-CoV proteins and boos-immunized with rVSV _NJ - GMM expressing MERS-CoV proteins (Table 1). Group 1: As a negative control group, rabbits have been injected with 500µl of phosphate buffered saline Group 2: Rabbits have been injected with rVSV without MERS-CoV gene inserts. Each rabbit was prime immunized with 5X10 ⁸ pfu/500µl rVSV _Ind -GML, 3 weeks after priming, boost immunized with 5X10 ⁸ pfu/500µl rVSV _NJ -GMM. Two weeks after boost-immunization, rabbits have been euthanized for serum collection Groups 3: Each rabbit was prime immunized with 5X10 ⁸ pfu/500µl rVSV _Ind -GML MERS- CoV mspRBD(S), 3 weeks after priming, boost immunized with 5X10 ⁸ pfu/500µl rVSV _NJ - GMM MERS-CoV mspRBD(S). Two weeks after boost-immunization, rabbits have been euthanized for serum collection. Groups 4: Each rabbit were prime immunized with 5X10 ⁸ pfu/500µl rVSV _Ind -GML MERS- CoV mspRBD(S)/E, 3 weeks after priming, boost immunized with 5X10 ⁸ pfu/500µl rVSV _NJ - GMM MERS-CoV RBD(S)/E. Two weeks after boost-immunization, rabbits have been euthanized for serum collection. Group 5: Each rabbit was prime immunized with 5X10 ⁸ pfu/500µl rVSV _Ind -GML MERS- CoV RBD(S)/E/M, 3 weeks after priming, boost immunized with 5X10 ⁸ pfu/500µl rVSV _NJ - GMM)-N MERS-CoV RBD(S)/E/M. Two weeks after boost-immunization, rabbits have been euthanized for serum collection. We found rabbits immunized with 5X10 ⁸ pfu/500µl of rVSV _Ind -GML MERS-CoV mspRBD(S) followed by boost immunization with 5X10 ⁸ pfu/500µl rVSV _NJ -GMM MERS- CoV mspRBD(S) induced high levels of antibodies (Fig. 12, Fig. 13). Moreover, rabbits immunized with 5X10 ⁸ pfu/500µl rVSV _Ind -GML MERS-CoV mspRBD(S)/E followed by boost immunization with 5X10 ⁸ pfu/500µl rVSV _NJ -GMM MERS-CoV RBD(S)/E induced equally high levels of neutralizing antibodies (Fig.14). The RBD specific antibodies were generated in rabbits vaccinated with rVSV expressing RBD(S) alone, rVSV expressing RBD(S) and E, and rVSV expressing RBD(S), E, and M (Fig.12, Fig.13)). RBD specific antibodies were generated equally well in groups immunized with rVSV expressing RBD(S) alone and rVSV expressing RBD(S) and E, which was shown in the titration curve (Fig. 12, Fig.13) and in the 1/1600 diluted sera (Fig. 13). We also examined neutralizing ability of the rabbit sera from the vaccinated groups against MERS- CoV EMC/2012 (IVI, Seoul, Korea). The diluted sera were mixed with 200 pfu of MERS- CoV EMC/2012, incubated for 30 min, and the serum-virus mixture was inoculated onto Vero E6 cells. The infected plates were kept in the CO ₂ incubator for 3 days until CPE showed 100% in the cells infected with virus only. The results for our rabbit serum samples were compared to a positive neutralizing rabbit monoclonal antibody (Sino Biological, 40069- R723). The rabbit sera from vaccinations with rVSV-MERS-CoV RBD(S) and rVSV-MERS- CoV RBD(S)/E showed 100% to 50% neutralization activity against MERS-CoV EMC/2012 in the dilutions to 1/20 (Fig.14). Sera from rVSV-MERS-CoV RBD(S)/E vaccination showed better neutralization activity than the sera from rVSV-MERS-CoV RBD(S) (Fig. 14) The results indicated that although the single expression of RBD(S) could induce neutralizing antibodies against MERS-CoV, co-expression of RBD(S) and E protein induce more RBD(S) specific antibodies and neutralize the wild type MERS-CoV EMC/2012 better. We are now in position to carry out MERS-CoV challenge experiments. There has been advances made in generating small animal models for the MERS-CoV infection. Mice are not susceptible to MERS-CoV infections, however, when human dipeptidyl peptidase 4 (DPP-4), the cell surface receptor for MERS-CoV, were introduced into mouse genome as a transgene, mice became highly susceptible to MERS-CoV infection (Agrawal et al., 2015; Pascal et al., 2015). The infection in the human dipeptidyl peptidase 4 (hDPP-4) transgenic mice, hDPP-4 C57BL/C led to the replication of MERS-CoV in the lung and showed the typical symptoms of MERS-CoV infection, lethargy, rapid and shallow breathing, severe weight loss, and 40- 100% mortality. This transgenic mouse is the perfect animal model to test the efficacy of our vaccines against MERS-CoV. We will vaccinate this hDPP-4 transgenic mice with our rVSVs expressing MERS-CoV structural proteins and challenge the vaccinated mice with wild type MERS-CoV and score the clinical signs and mortality of the vaccinated and unvaccinated control mice. We have a new State-Of-The-Art BSL3 Laboratory just opened at Western University where we can carry out the challenge studies using the hDPP-4 C57BL/C transgenic mice. We will use both rVSV _Ind and rVSV _NJ . In prime-boost vaccines, the priming vaccine or immunogenic composition, are of the same or different serotype as the rVSV of the booster vaccine or immunogenic composition. For example, both the prime and boost vaccines or immunogenic compositions are rVSV _Ind ; or both the prime and boost vaccines or immunogenic compositions are rVSV _NJ ; or the rVSV of the prime vaccine or immunogenic composition are rVSV _Ind and the rVSV of the boost vaccine or immunogenic composition are rVSV _NJ ; or the rVSV of the prime vaccine or immunogenic composition are rVSV _NJ and the rVSV of the boost vaccine or immunogenic composition will be rVSV _Ind . Table 1 – Vaccination groups with various vaccines consisted of MERS-CoV RBS(S), E, and M Table 2. Neucleotide Sequence Comparison between M Genes of VSV Indiana serotype, Wild Type (SEQ ID NO: 1) and a Mutant G21E/L111A/M51R (SEQ ID NO 2)

Table 3. Amino Acid Sequence Comparison between M Proteins of VSV Indiana serotype Wild Type (SEQ ID NO: 3) and a Mutant G21E/L111A/M51R (SEQ ID NO: 4) Table 4. Nucleotide Sequence Comparison between M Genes of VSV New Jersey serotype Wild Type (SEQ ID NO: 5) and Mutants, G22E/M48R/M51R (SEQ ID NO: 6) and G22E/L110A/M48R/M51R (SEQ ID NO: 7)

Table 5. Amino Acid Sequence Comparison between M Proteins of VSV New Jersey serotype Wild Type (SEQ ID NO: 8) and Mutants, G22E/M48R/M51R (SEQ ID NO: 9) and G22E/L110A/M48R/M51R (SEQ ID NO: 10) Table 6 MERS-CoV E protein (82 aa) (SEQ ID NO:11) Peptide for antibody (14mer) against MERS-CoV E protein MERS-CoV M Protein (219 aa) (SEQ ID NO: 13) Peptides for antibody against MERS-CoV M protein (14mer) Melittin Signal Peptide Gene (SEQ ID NO: 17) IG:VSV Intergenic Junction sequence (SEQ ID NO: 18) S Full Length (S _F ) gene (SEQ ID NO: 19) References 1. de Groot RJ, Baker SC, Baric RS, Brown CS, Drosten C et al. Middle East respiratory syndrome coronavirus (MERS-CoV): announcement of the Coronavirus Study Group. J Virol 2013;87(14):7790-7792. 2. Buchholz U, Muller MA, Nitsche A, Sanewski A, Wevering N et al. Contact investigation of a case of human novel coronavirus infection treated in a German hospital, October- November 2012. Euro Surveill 2013;18(8). 3. Drosten C, Seilmaier M, Corman VM, Hartmann W, Scheible G et al. Clinical features and virological analysis of a case of Middle East respiratory syndrome coronavirus infection. Lancet Infect Dis 2013;13(9):745-751. 4. Wang C, Zheng X, Gai W, Zhao Y, Wang H et al. MERS-CoV virus-like particles produced in insect cells induce specific humoural and cellular imminity in rhesus macaques. Oncotarget 2017;8(8):12686-12694. 5. Kirchdoerfer RN, Cottrell CA, Wang N, Pallesen J, Yassine HM et al. Pre-fusion structure of a human coronavirus spike protein. Nature 2016;531(7592):118-121. 6. Walls AC, Tortorici MA, Bosch BJ, Frenz B, Rottier PJM et al. Cryo-electron microscopy structure of a coronavirus spike glycoprotein trimer. Nature 2016;531(7592):114-117. 7. Raj VS, Mou H, Smits SL, Dekkers DH, Muller MA et al. Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC. Nature 2013;495(7440):251- 254. 8. Lu L, Liu Q, Zhu Y, Chan KH, Qin L et al. Structure-based discovery of Middle East respiratory syndrome coronavirus fusion inhibitor. Nat Commun 2014;5:3067. 9. Li F. Receptor recognition mechanisms of coronaviruses: a decade of structural studies. J Virol 2015;89(4):1954-1964. 10. Tai W, Wang Y, Fett CA, Zhao G, Li F et al. Recombinant Receptor-Binding Domains of Multiple Middle East Respiratory Syndrome Coronaviruses (MERS-CoVs) Induce Cross- Neutralizing Antibodies against Divergent Human and Camel MERS-CoVs and AntibodyEscape Mutants. J Virol 2017;91(1). 11. Kim, GN, Wu, K, Hong, JP, Awamleh, Z, Kang, CY. Creation of matrix protein gene variants of two serotypes of vesicular stomatitis virus as prime-boost vaccine vectors. J. Virol 2015;(12) 89:6338-6351. 12. Agrawal AS, Garron T, Tao X, Peng BH, Wakamiya M, Chan TS, et al. Generation of a transgenic mouse model of Middle East respiratory syndrome coronavirus infection and disease. J Virol 2015;89:3659-70. 13. Pascal KE, Coleman CM, Mujica AO, Kamat V, Badithe A, Fairhurst J, et al. Pre- and postexposure efficacy of fully human antibodies against Spike protein in a novel humanized mouse model of MERS-CoV infection. Proc Natl Acad Sci USA.2015;112:8738-43. It should be understood that although the present invention has been specifically disclosed by certain aspects, embodiments, and optional features, modification, improvement and variation of such aspects, embodiments, and optional features can be resorted to by those skilled in the art, and that such modifications, improvements and variations are considered to be within the scope of this invention. The invention has been described broadly and generically herein. Each of the narrower species and subgeneric groupings falling within the generic disclosure also form part of the invention. In addition, where features or aspects of the invention are described in terms of Markush groups, those skilled in the art will recognize that the invention is also thereby described in terms of any individual member or subgroup of members of the Markush group.