Rapid emergence of a PB2-E627K substitution confers a virulent phenotype to an H9N2 avian influenza virus during adoption in mice

Arch Virol. 2015 May;160(5):1267-77. doi: 10.1007/s00705-015-2383-5. Epub 2015 Mar 19.

Abstract

The worldwide circulation of H9N2 avian influenza virus in poultry, the greater than 2.3 % positive rate for anti-H9 antibodies in poultry-exposed workers, and several reports of human infection indicate that H9N2 virus is a potential threat to human health. Here, we found three mutations that conferred high virulence to H9N2 virus in mice after four passages. The PB2-E627K substitution rapidly appeared at the second passage and played a decisive role in virulence. Polymerase complexes possessing PB2-E627K displayed 16.1-fold higher viral polymerase activity when compared to the wild-type virus, which may account for enhanced virulence of this virus. The other two substitutions (HA-N313D and HA-N496S) enhanced binding to both α2,3-linked and α2,6-linked sialic acid receptors; however, the HA-N313D and N496S substitutions alone decreased the virulence of mouse-adapted virus. Furthermore, this mouse-adapted virus was still not transmissible among guinea pigs by direct contact (0/3 pairs). Our findings show that adaption in mice enhanced the viral polymerase activity and receptor-binding ability, which resulted in a virulent phenotype in mice but not a transmissible phenotype in guinea pigs, indicating that host factors play an important role in adaptive evolution of influenza in new hosts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Biological*
  • Amino Acid Substitution*
  • Animals
  • Female
  • Guinea Pigs
  • Influenza A Virus, H9N2 Subtype / genetics
  • Influenza A Virus, H9N2 Subtype / growth & development
  • Influenza A Virus, H9N2 Subtype / isolation & purification*
  • Influenza A Virus, H9N2 Subtype / physiology
  • Mice, Inbred BALB C
  • Mutation, Missense
  • Orthomyxoviridae Infections / transmission
  • Orthomyxoviridae Infections / virology*
  • RNA-Dependent RNA Polymerase / genetics*
  • RNA-Dependent RNA Polymerase / metabolism
  • Serial Passage
  • Viral Proteins / genetics*
  • Viral Proteins / metabolism
  • Virulence
  • Virus Attachment
  • Virus Replication

Substances

  • PB2 protein, Influenzavirus A
  • Viral Proteins
  • RNA-Dependent RNA Polymerase