Attenuated swine influenza vaccines and methods of making and use thereof
This disclosure provides attenuated swine influenza strains, particularly those produced via a reverse genetics approach, compositions comprising same, and methods of production and use thereof. The attenuated strains are engineered to encode HA proteins having additional glycosylation sites, relative to the HA proteins encoded by the corresponding virulent parental viruses. Advantageously, the attenuated influenza strains may be administered.
1. A non-naturally occurring attenuated swine influenza strain capable of providing a safe and effective immune response in porcine against a virulent H3N2 swine influenza or diseases caused by H3N2 swine influenza;
wherein the attenuated strain encodes an HA protein comprising at least four additional glycosylation sites, relative to its corresponding virulent parental strain;
wherein the glycosylation sites are S71N, K90N, L173T, P287T, and optionally K294T; and
wherein the locations of the Amino Acid changes are based upon the HA gene encoded by the virulent parental strain having the sequence as set forth in SEQ ID NO:18.
2. The attenuated strain of claim 1 , containing an HA gene encoding an HA protein having the polypeptide sequence as set forth in SEQ ID NO:22 or having a sequence with at least 90% homology to SEQ ID NO:22 provided the following locations have the following amino acids: 71N, 90N, 173T and 287T.
3. The attenuated strain of claim 1 , containing an HA gene encoding an HA protein having the polypeptide sequence as set forth in SEQ ID NO:22 or having a sequence with at least 90% homology to SEQ ID NO:22 provided the following locations have the following amino acids: 71N, 90N, 173T, 287T and 294T.
4. A vaccine composition, which provides a protective immune response in a porcine against a virulent H3N2 swine influenza challenge, comprising the attenuated strain of claim 1 , wherein the attenuated strain contains an HA gene encoding an HA protein having:
a. a polypeptide sequence as set forth in SEQ ID NO:22;
b. a polypeptide sequence with at least 90% homology to SEQ ID NO:22 provided the following locations have the following amino acids: 71N, 90N, 173T and 287T; or
c. a polypeptide sequence with at least 90% homology to SEQ ID NO:22 provided the following locations have the following amino acids: 71N, 90N, 173T, 287T and K294T.
5. The vaccine composition of claim 1 , further comprising a pharmaceutically or veterinary acceptable diluent or excipient.
6. The vaccine composition of claim 5 , further comprising at least one additional antigen associated with or derived from a porcine pathogen other than H3N2 swine influenza.
7. The vaccine composition of claim 6 , wherein the at least one additional antigen is capable of eliciting in a porcine an immune response against Mycoplasma hyopneumoniae (M. hyo), porcine circovirus 2 (PCV2), porcine reproductive and respiratory syndrome virus (PRRSV) or other pathogen capable of infecting and causing illness or susceptibility to illness in a porcine.
8. A method of vaccinating a porcine in need of protection against H3N2 swine influenza comprising, administering to said porcine at least one dose of the vaccine composition of claim 4 .
9. The method of claim 8 , wherein the porcine is a sow from 3 weeks to 6 weeks prefarrowing.
10. The method of claim 9 , wherein the resulting piglets have a reduced morbidity and/or mortality as compared to piglets coming from unvaccinated sows.
11. A composition comprising a plurality of vectors for producing the attenuated swine influenza strain of claim 1 , comprising a vector comprising a promoter operably linked to an H3N2 influenza virus HA cDNA, wherein the HA cDNA encodes four or five additional glycosylation sites, relative to an HA encoded by a corresponding virulent parent swine influenza strain.
12. The composition of claim 11 , wherein the additional glycosylation sites are S71N, K90N, L173T, P287T, and optionally K294T, and wherein the numbering of the amino acid changes is based upon the HA protein encoded by the virulent parental strain, having the polypeptide sequence as set forth in SEQ ID NO:18.
13. The composition of claim 12 , wherein the HA cDNA for producing attenuated influenza encodes the protein as set forth in SEQ ID NO:22 or 24.
14. The composition of claim 12 , wherein the HA cDNA encodes only 4 additional glycosylation sites, relative to the HA protein encoded by the virulent parental strain.
15. The composition of claim 12 , wherein the HA cDNA encodes only 5 additional glycosylation sites, relative to the HA protein encoded by the virulent parental strain.
16. A method of preparing an attenuated strain of swine influenza virus, wherein the attenuated strain is capable of providing a safe and effective immune response in a porcine against a virulent H3N2 influenza strain, comprising: contacting a cell with the composition of claim 12 , in an amount effective to yield infectious influenza virus, thereby preparing said attenuated strain.
17. The method of claim 16 , wherein the wherein the only additional glycosylation sites are S71N, K90N, L173T and P287T.