Virulence-Affecting Amino Acid Changes in the PA Protein of H7N9 Influenza A Viruses

Author:

Yamayoshi Seiya1,Yamada Shinya1,Fukuyama Satoshi2,Murakami Shin3,Zhao Dongming2,Uraki Ryuta1,Watanabe Tokiko2,Tomita Yuriko2,Macken Catherine4,Neumann Gabriele5,Kawaoka Yoshihiro1235

Affiliation:

1. Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan

2. ERATO Infection-Induced Host Responses Project, Japan Science and Technology Agency, Saitama, Japan

3. Department of Special Pathogens, International Research Center for Infectious Diseases, Institute of Medical Science, University of Tokyo, Minato-ku, Tokyo, Japan

4. Theoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico, USA

5. Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin—Madison, Madison, Wisconsin, USA

Abstract

ABSTRACT 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.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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