Emergence of mammalian species-infectious and -pathogenic avian influenza H6N5 virus with no evidence of adaptation

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Emergence of mammalian species-infectious and -pathogenic avian influenza H6N5 virus with no evidence of adaptation
Jeong Hyun Nam; E H Kim; Dae Sub Song; Y K Choi; Jeong-Ki Kim; Haryoung Poo
Bibliographic Citation
Journal of Virology, vol. 85, no. 24, pp. 13271-13277
Publication Year
The migratory waterfowl of the world are considered to be the natural reservoir of influenza A viruses. Of the 16 hemagglutinin subtypes of avian influenza viruses, the H6 subtype is commonly perpetuated in its natural hosts and is of concern due to its potential to be a precursor of highly pathogenic influenza viruses by reassortment. During routine influenza surveillance, we isolated an unconventional H6N5 subtype of avian influenza virus. Experimental infection of mice revealed that this isolate replicated efficiently in the lungs, subsequently spread systemically, and caused lethality. The isolate also productively infected ferrets, with direct evidence of contact transmission, but no disease or transmission was seen in pigs. Although the isolate possessed the conserved receptor-binding site sequences of avian influenza viruses, it exhibited relatively low replication efficiencies in ducks and chickens. Our genetic and molecular analyses of the isolate revealed that its PB1 sequence showed the highest evolutionary relationship to those of highly pathogenic H5N1 avian influenza viruses and that its PA protein had an isoleucine residue at position 97 (a representative virulence marker). Further studies will be required to examine why our isolate has the virologic characteristics of mammalian influenza viruses but the archetypal receptor binding profiles of avian influenza viruses, as well as to determine whether its potential virulence markers (PB1 analogous to those of H5N1 viruses or isoleucine residue at position 97 within PA) could render it highly pathogenic in mice.
Amer Soc Microb
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Division of Research on National Challenges > Infectious Disease Research Center > 1. Journal Articles
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