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The Genomic Contributions of Avian H1N1 Influenza A Viruses to the Evolution of Mammalian Strains

tetano

Editor, Senior Moderator
PLoS One. 2015 Jul 24;10(7):e0133795. doi: 10.1371/journal.pone.0133795. eCollection 2015.
[h=1]The Genomic Contributions of Avian H1N1 Influenza A Viruses to the Evolution of Mammalian Strains.[/h] Ko?er ZA[SUP]1[/SUP], Carter R[SUP]2[/SUP], Wu G[SUP]2[/SUP], Zhang J[SUP]2[/SUP], Webster RG[SUP]3[/SUP].
[h=3]Author information[/h]

[h=3]Abstract[/h] Among the influenza A viruses (IAVs) in wild aquatic birds, only H1, H2, and H3 subtypes have caused epidemics in humans. H1N1 viruses of avian origin have also caused 3 of 5 pandemics. To understand the reappearance of H1N1 in the context of pandemic emergence, we investigated whether avian H1N1 IAVs have contributed to the evolution of human, swine, and 2009 pandemic H1N1 IAVs. On the basis of phylogenetic analysis, we concluded that the polymerase gene segments (especially PB2 and PA) circulating in North American avian H1N1 IAVs have been reintroduced to swine multiple times, resulting in different lineages that led to the emergence of the 2009 pandemic H1N1 IAVs. Moreover, the similar topologies of hemagglutinin and nucleoprotein and neuraminidase and matrix gene segments suggest that each surface glycoprotein coevolved with an internal gene segment within the H1N1 subtype. The genotype of avian H1N1 IAVs of Charadriiformes origin isolated in 2009 differs from that of avian H1N1 IAVs of Anseriformes origin. When the antigenic sites in the hemagglutinin of all 31 North American avian H1N1 IAVs were considered, 60%-80% of the amino acids at the antigenic sites were identical to those in 1918 and/or 2009 pandemic H1N1 viruses. Thus, although the pathogenicity of avian H1N1 IAVs could not be inferred from the phylogeny due to the small dataset, the evolutionary process within the H1N1 IAV subtype suggests that the circulation of H1N1 IAVs in wild birds poses a continuous threat for future influenza pandemics in humans.


PMID: 26208281 [PubMed - in process] PMCID: PMC4514870 Free PMC Article
 
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