| Literature DB >> 24371069 |
Seiya Yamayoshi1, Shinya Yamada, Satoshi Fukuyama, Shin Murakami, Dongming Zhao, Ryuta Uraki, Tokiko Watanabe, Yuriko Tomita, Catherine Macken, Gabriele Neumann, Yoshihiro Kawaoka.
Abstract
UNLABELLED: Novel avian-origin influenza A(H7N9) viruses were first reported to infect humans in March 2013. To date, 143 human cases, including 45 deaths, have been recorded. By using sequence comparisons and phylogenetic and ancestral inference analyses, we identified several distinct amino acids in the A(H7N9) polymerase PA protein, some of which may be mammalian adapting. Mutant viruses possessing some of these amino acid changes, singly or in combination, were assessed for their polymerase activities and growth kinetics in mammalian and avian cells and for their virulence in mice. We identified several mutants that were slightly more virulent in mice than the wild-type A(H7N9) virus, A/Anhui/1/2013. These mutants also exhibited increased polymerase activity in human cells but not in avian cells. Our findings indicate that the PA protein of A(H7N9) viruses has several amino acid substitutions that are attenuating in mammals. IMPORTANCE: Novel avian-origin influenza A(H7N9) viruses emerged in the spring of 2013. By using computational analyses of A(H7N9) viral sequences, we identified several amino acid changes in the polymerase PA protein, which we then assessed for their effects on viral replication in cultured cells and mice. We found that the PA proteins of A(H7N9) viruses possess several amino acid substitutions that cause attenuation in mammals.Entities:
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Year: 2013 PMID: 24371069 PMCID: PMC3957961 DOI: 10.1128/JVI.03155-13
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103