Genetic and antigenic relatedness of H3 subtype influenza A viruses isolated from avian and mammalian species

Vaccine

Volumn 26, Issue 7, 2008, Pages 966-977

  Yassine, H M ^a   Lee, C W ^a   Suarez, D L ^b   Saif, Y M ^a  

^a OHIO STATE UNIVERSITY   (United States)

^b AGRICULTURAL RESEARCH SERVICE   (United States)

Author keywords

H3N2 triple reassortants; Turkeys; Vaccine

Indexed keywords

INACTIVATED VACCINE; NUCLEOTIDE; VIRUS ANTIGEN;

ANIMAL CELL; ANTIGENICITY; ARTICLE; DUCK; FOWL; GENE SEQUENCE; HA1 GENE; HUMAN; INFLUENZA VIRUS A H3N2; MAMMAL; NONHUMAN; PHYLOGENY; PRIORITY JOURNAL; SWINE; TURKEY (BIRD); UNITED STATES; VACCINATION; VIRAL GENETICS; VIRUS GENE; VIRUS HEMAGGLUTINATION; VIRUS ISOLATION; VIRUS NEUTRALIZATION; VIRUS TYPING;

AMINO ACID SEQUENCE; ANIMALS; DUCKS; HEMAGGLUTININ GLYCOPROTEINS, INFLUENZA VIRUS; HUMANS; INFLUENZA A VIRUS; INFLUENZA A VIRUS, H3N2 SUBTYPE; INFLUENZA IN BIRDS; INFLUENZA, HUMAN; MODELS, MOLECULAR; ORTHOMYXOVIRIDAE INFECTIONS; PHYLOGENY; REASSORTANT VIRUSES; SEQUENCE ALIGNMENT; SWINE; SWINE DISEASES; TURKEYS;

EID: 39049161170     PISSN: 0264410X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vaccine.2007.11.094     Document Type: Article

References (49)

1. Knipe D.M.H.P.M. Orthomyxoviridae (2007), Lippincott Williams & Wilkins, Philadelphia pp. 1647-1740
2. Lamb R.A., and Krug R.M. Orthomyxoviradae, in: fields virology (2001), Lippincott Williams and Wilkins, Philadelphia, PA pp. 1487-1531
3. Webster R.G., Bean W.J., Gorman O.T., Chambers T.M., and Kawaoka Y. Evolution and ecology of influenza A viruses. Microbiol Rev 56 1 (1992) 152-179
4. Swayne D.E., and King D.J. Avian influenza and Newcastle disease. J Am Vet Med Assoc 222 11 (2003) 1534-1540
5. Beare A.S., and Webster R.G. Replication of avian influenza viruses in humans. Arch Virol 119 1-2 (1991) 37-42
6. Ito T. Interspecies transmission and receptor recognition of influenza A viruses. Microbiol Immunol 44 6 (2000) 423-430
7. Ito T., Couceiro J.N., Kelm S., et al. Molecular basis for the generation in pigs of influenza A viruses with pandemic potential. J Virol 72 9 (1998) 7367-7373
8. Rogers G.N., and Paulson J.C. Receptor determinants of human and animal influenza virus isolates: differences in receptor specificity of the H3 hemagglutinin based on species of origin. Virology 127 2 (1983) 361-373
9. Rogers G.N., Pritchett T.J., Lane J.L., and Paulson J.C. Differential sensitivity of human, avian, and equine influenza A viruses to a glycoprotein inhibitor of infection: selection of receptor specific variants. Virology 131 2 (1983) 394-408
10. Scholtissek C., Burger H., Kistner O., and Shortridge K.F. The nucleoprotein as a possible major factor in determining host specificity of influenza H3N2 viruses. Virology 147 2 (1985) 287-294
11. Kida H., Ito T., Yasuda J., et al. Potential for transmission of avian influenza viruses to pigs. J Gen Virol 75 Pt 9 (1994) 2183-2188
12. Olsen C.W., Carey S., Hinshaw L., and Karasin A.I. Virologic and serologic surveillance for human, swine and avian influenza virus infections among pigs in the north-central United States. Arch Virol 145 7 (2000) 1399-1419
13. Zhou N.N., Senne D.A., Landgraf J.S., et al. Genetic reassortment of avian, swine, and human influenza A viruses in American pigs. J Virol 73 10 (1999) 8851-8856
14. Karasin A.I., Schutten M.M., Cooper L.A., et al. Genetic characterization of H3N2 influenza viruses isolated from pigs in North America 1977-1999: evidence for wholly human and reassortant virus genotypes. Virus Res 68 1 (2000) 71-85
15. Webby R.J., Swenson S.L., Krauss S.L., Gerrish P.J., Goyal S.M., and Webster R.G. Evolution of swine H3N2 influenza viruses in the United States. J Virol 74 18 (2000) 8243-8251
16. Choi Y.K., Goyal S.M., and Joo H.S. Prevalence of swine influenza virus subtypes on swine farms in the United States. Arch Virol 147 6 (2002) 1209-1220
17. Suarez D.L., Woolcock P.R., Bermudez A.J., and Senne D.A. Isolation from turkey breeder hens of a reassortant H1N2 influenza virus with swine, human, and avian lineage genes. Avian Dis 46 1 (2002) 111-121
18. Tang Y., Lee C.W., Zhang Y., et al. Isolation and characterization of H3N2 influenza A virus from turkeys. Avian Dis 49 2 (2005) 207-213
19. Saif Y.M. Experimental infection of turkeys with swine influenza A virus. Proceedings of the XVI World Poultry Conference, vol. 1 (1978) 938-943
20. Mohan R., Saif Y.M., Erickson G.A., Gustafson G.A., and Easterday B.C. Serologic and epidemiologic evidence of infection in turkeys with an agent related to the swine influenza virus. Avian Dis 25 1 (1981) 11-16
21. Stone H.D. Optimization of hydrophile-lipophile balance for improved efficacy of Newcastle disease and avian influenza oil-emulsion vaccines. Avian diseases 32 1 (1988) 68-73
22. Beard C.W. A laboratory manual for the isolation and identification of avian pathotypes (1989), Kendall-Hunt publishing, Dubuque, Iowa pp.192-200
23. C.W. T.S.G.a.B. A laboratory manual for the isolation and identification of avian pathotypes, American Association of Avian Pathologists (1998), Kennett Square, PA pp. 255-266
24. Archetti I., and Horsfall Jr. F.L. Persistent antigenic variation of influenza A viruses after incomplete neutralization in ovo with heterologous immune serum. J Exp Med 92 5 (1950) 441-462
25. Spackman E., Senne D.A., Myers T.J., et al. Development of a real-time reverse transcriptase PCR assay for type A influenza virus and the avian H5 and H7 hemagglutinin subtypes. J Clin Microbiol 40 9 (2002) 3256-3260
26. Wang D., Christopher M.E., Nagata L.P., et al. Intranasal immunization with liposome-encapsulated plasmid DNA encoding influenza virus hemagglutinin elicits mucosal, cellular and humoral immune responses. J Clin Virol 31 Suppl. 1 (2004) S99-S106
27. Breathnach C.C., Clark H.J., Clark R.C., Olsen C.W., Townsend H.G., and Lunn D.P. Immunization with recombinant modified vaccinia Ankara (rMVA) constructs encoding the HA or NP gene protects ponies from equine influenza virus challenge. Vaccine 24 8 (2006) 1180-1190
28. Saha S., Yoshida S., Ohba K., et al. A fused gene of nucleoprotein (NP) and herpes simplex virus genes (VP22) induces highly protective immunity against different subtypes of influenza virus. Virology 354 1 (2006) 48-57
29. Ernst W.A., Kim H.J., Tumpey T.M., et al. Protection against H1, H5, H6 and H9 influenza A infection with liposomal matrix 2 epitope vaccines. Vaccine 24 24 (2006) 5158-5168
30. Sylte M.J., Hubby B., and Suarez D.L. Influenza neuraminidase antibodies provide partial protection for chickens against high pathogenic avian influenza infection. Vaccine (2007)
31. Wiley D.C., Wilson I.A., and Skehel J.J. Structural identification of the antibody-binding sites of Hong Kong influenza haemagglutinin and their involvement in antigenic variation. Nature 289 5796 (1981) 373-378
32. Underwood P.A. Mapping of antigenic changes in the haemagglutinin of Hong Kong influenza (H3N2) strains using a large panel of monoclonal antibodies. J Gen Virol 62 1 (1982) 153-169
33. Ha Y., Stevens D.J., Skehel J.J., and Wiley D.C. H5 avian and H9 swine influenza virus haemagglutinin structures: possible origin of influenza subtypes. EMBO J 21 5 (2002) 865-875
34. Castrucci M.R., Donatelli I., Sidoli L., Barigazzi G., Kawaoka Y., and Webster R.G. Genetic reassortment between avian and human influenza A viruses in Italian pigs. Virology 193 1 (1993) 503-506
35. Ficken M.D., Guy J.S., and Gonder E. An outbreak of influenza (H1N1) in turkey breeder hens. Avian Dis 33 2 (1989) 370-374
36. Wright S.M., Kawaoka Y., Sharp G.B., Senne D.A., and Webster R.G. Interspecies transmission and reassortment of influenza A viruses in pigs and turkeys in the United States. Am J Epidemiol 136 4 (1992) 488-497
37. Ludwig S., Haustein A., Kaleta E.F., and Scholtissek C. Recent influenza A (H1N1) infections of pigs and turkeys in northern Europe. Virology 202 1 (1994) 281-286
38. Hinshaw V.S., Webster R.G., Bean W.J., Downie J., and Senne D.A. Swine influenza-like viruses in turkeys: potential source of virus for humans?. Science 220 4593 (1983) 206-208
39. B J.B. Variants and Immunity: definitions for serological investigation. International Symposium on Foot And Mouth Disease, Variants And Immunity. vol. 8 Immunobiol, Lyon, France (1967) 1-10
40. Wilson I.A., and Cox N.J. Structural basis of immune recognition of influenza virus hemagglutinin. Annu Rev Immunol 8 (1990) 737-771
41. Wood J.M., Oxford J.S., Dunleavy U., Newman R.W., Major D., and Robertson J.S. Influenza A (H1N1) vaccine efficacy in animal models is influenced by two amino acid substitutions in the hemagglutinin molecule. Virology 171 1 (1989) 214-221
42. Newman R.W., Jennings R., Major D.L., et al. Immune response of human volunteers and animals to vaccination with egg-grown influenza A (H1N1) virus is influenced by three amino acid substitutions in the haemagglutinin molecule. Vaccine 11 4 (1993) 400-406
43. Katz J.M., and Webster R.G. Efficacy of inactivated influenza A virus (H3N2) vaccines grown in mammalian cells or embryonated eggs. J Infect Dis 160 2 (1989) 191-198
44. Kodihalli S., Justewicz D.M., Gubareva L.V., and Webster R.G. Selection of a single amino acid substitution in the hemagglutinin molecule by chicken eggs can render influenza A virus (H3) candidate vaccine ineffective. J Virol 69 8 (1995) 4888-4897
45. Lee M.S., and Chen J.S. Predicting antigenic variants of influenza A/H3N2 viruses. Emerg Infect Dis 10 8 (2004) 1385-1390
46. Rogers G.N., Paulson J.C., Daniels R.S., Skehel J.J., Wilson I.A., and Wiley D.C. Single amino acid substitutions in influenza haemagglutinin change receptor binding specificity. Nature 304 5921 (1983) 76-78
47. Vines A., Wells K., Matrosovich M., Castrucci M.R., Ito T., and Kawaoka Y. The role of influenza A virus hemagglutinin residues 226 and 228 in receptor specificity and host range restriction. J Virol 72 9 (1998) 7626-7631
48. Tumpey T.M., Maines T.R., Van Hoeven N., et al. A two-amino acid change in the hemagglutinin of the 1918 influenza virus abolishes transmission. Science 315 5812 (2007) 655-659
49. Lindstrom S., Sugita S., Endo A., et al. Evolutionary characterization of recent human H3N2 influenza A isolates from Japan and China: novel changes in the receptor binding domain. Arch Virol 141 7 (1996) 1349-1355