PB2 amino acid at position 627 affects replicative efficiency, but not cell tropism, of Hong Kong H5N1 influenza A viruses in mice.

A single amino acid substitution, from glutamic acid to lysine at position 627 of the PB2 protein, converts a nonlethal H5N1 influenza A virus isolated from a human to a lethal virus in mice. In contrast to the nonlethal virus, which replicates only in respiratory organs, the lethal isolate replicates in a variety of organs, producing systemic infection. Despite a clear difference in virulence and organ tropism between the two viruses, it remains unknown whether the dissimilarity is a result of differences in cell tropism or the reduced replicative ability of the nonlethal virus in mouse cells in general. To determine how this single amino acid change affects virulence and organ tropism in mice, we investigated the growth kinetics of the two H5N1 viruses both in vitro and in vivo. The identity of the PB2 amino acid at position 627 did not appreciably affect viral replicative efficiency in chicken embryo fibroblasts and a quail cell line; however, viruses with lysine at this position instead of glutamic acid grew better in the different mouse cells tested. When the effect of this substitution was investigated in mice, all of the test viruses showed the same cell tropism, but infection by viruses containing lysine at position 627 spread more rapidly than those viruses containing glutamic acid at this position. Further analysis showed a difference in local immune responses: neutrophil infiltration in lungs infected with viruses containing lysine at position 627 persisted longer than that associated with viruses lacking a glutamic acid substitution. Our data indicate that the amino acid at position 627 of the PB2 protein determines the efficiency of viral replication in mouse (not avian) cells, but not tropism among cells in different mouse organs. The presence of lysine leads to more aggressive viral replication, overwhelming the host's defense mechanisms and resulting in high mortality rates in mice.

[1]  H. Maeda,et al.  Oxygen radicals in influenza-induced pathogenesis and treatment with pyran polymer-conjugated SOD. , 1989, Science.

[2]  Y. Guan,et al.  Neurovirulence in Mice of H5N1 Influenza Virus Genotypes Isolated from Hong Kong Poultry in 2001 , 2003, Journal of Virology.

[3]  S. de la Luna,et al.  Mutational analysis identifies functional domains in the influenza A virus PB2 polymerase subunit , 1996, Journal of virology.

[4]  R. Webster,et al.  Human influenza A H5N1 virus related to a highly pathogenic avian influenza virus , 1998, The Lancet.

[5]  Y. Honda,et al.  Fine Mapping of the Subunit Binding Sites of Influenza Virus RNA Polymerase , 2002 .

[6]  B. Wuethrich An Avian Flu Jumps to People , 2003, Science.

[7]  K. Yano,et al.  Identification of Hsp90 as a Stimulatory Host Factor Involved in Influenza Virus RNA Synthesis* , 2002, The Journal of Biological Chemistry.

[8]  J. Ortín,et al.  Identification of two separate domains in the influenza virus PB1 protein involved in the interaction with the PB2 and PA subunits: a model for the viral RNA polymerase structure. , 1996, Nucleic acids research.

[9]  Thomas Rowe,et al.  Pathogenesis of Avian Influenza A (H5N1) Viruses in Ferrets , 2002, Journal of Virology.

[10]  N. Cox,et al.  Characterization of an avian influenza A (H5N1) virus isolated from a child with a fatal respiratory illness. , 1998, Science.

[11]  Tomomasa Watanabe,et al.  Characterization and Expression of the Mx1 Gene in Wild Mouse Species , 1998, Biochemical Genetics.

[12]  H. Goto,et al.  Biological Heterogeneity, Including Systemic Replication in Mice, of H5N1 Influenza A Virus Isolates from Humans in Hong Kong , 1999, Journal of Virology.

[13]  Michael W. Shaw,et al.  Molecular Correlates of Influenza A H5N1 Virus Pathogenesis in Mice , 2000, Journal of Virology.

[14]  M. Krystal,et al.  Overexpression of the influenza virus polymerase can titrate out inhibition by the murine Mx1 protein , 1992, Journal of virology.

[15]  A. Ishihama,et al.  Molecular mapping of influenza virus RNA polymerase by site-specific antibodies. , 1999, Virology.

[16]  B. Murphy,et al.  A single amino acid in the PB2 gene of influenza A virus is a determinant of host range , 1993, Journal of virology.

[17]  P. Staeheli,et al.  Function of the mouse Mx1 protein is inhibited by overexpression of the PB2 protein of influenza virus. , 1993, Virology.

[18]  E. Fodor,et al.  Two Aromatic Residues in the PB2 Subunit of Influenza A RNA Polymerase Are Crucial for Cap Binding* , 2003, Journal of Biological Chemistry.

[19]  R. Krug,et al.  The active sites of the influenza cap‐dependent endonuclease are on different polymerase subunits , 2001, The EMBO journal.

[20]  S. van der Werf,et al.  Differential effect of nucleotide substitutions in the 3' arm of the influenza A virus vRNA promoter on transcription/replication by avian and human polymerase complexes is related to the nature of PB2 amino acid 627. , 2002, Virology.

[21]  Yoshihiro Kawaoka,et al.  Molecular Basis for High Virulence of Hong Kong H5N1 Influenza A Viruses , 2001, Science.