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Amino Acids in Hemagglutinin Antigenic Site B Determine Antigenic and Receptor Binding Differences between A(H3N2)v and Ancestral Seasonal H3N2 Influenza Viruses.

Xiaoquan WangNatalia A IlyushinaVladimir Y LugovtsevNicolai V BovinLaura K CouzensJin GaoRaymond P DonnellyMaryna C EichelbergerHongquan Wan
Published in: Journal of virology (2017)
Influenza A H3N2 variant [A(H3N2)v] viruses have caused hundreds of human infections in multiple states in the United States since 2009. Most cases have been children who had contact with swine in agricultural fairs. These viruses originated from human seasonal H3N2 viruses that were introduced into the U.S. swine population in the mid-1990s, but they are different from both these ancestral viruses and current circulating human seasonal H3N2 strains in terms of their antigenic characteristics as measured by hemagglutination inhibition (HI) assay. In this study, we identified amino acids in antigenic site B of the surface glycoprotein hemagglutinin (HA) that explain the antigenic difference between A(H3N2)v and the ancestral H3N2 strains. These amino acid mutations also alter binding to minor human-type glycans, suggesting that host adaptation may contribute to the selection of antigenically distinct H3N2 variants which pose a threat to public health.
Keyphrases
  • amino acid
  • endothelial cells
  • public health
  • induced pluripotent stem cells
  • escherichia coli
  • young adults
  • risk assessment
  • heavy metals
  • high throughput
  • copy number
  • transcription factor
  • human health
  • dna binding