The Journal of Experimental Medicine
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Published online 13 March 2006 doi:10.1084/jem.20051938
Rockefeller University Press, 0022-1007 $8.00
JEM, Volume 203, Number 3, 689-697
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ARTICLE

 The polymerase complex genes contribute to the high virulence of the human H5N1 influenza virus isolate A/Vietnam/1203/04

Rachelle Salomon1, John Franks1, Elena A. Govorkova1, Natalia A. Ilyushina1, Hui-Ling Yen1, Diane J. Hulse-Post1, Jennifer Humberd1, Michel Trichet1, Jerold E. Rehg2, Richard J. Webby1, Robert G. Webster1,3, and Erich Hoffmann1

1 Department of Infectious Diseases and 2 Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN 38105
3 Department of Pathology, University of Tennessee, Memphis, TN 38105

CORRESPONDENCE Robert Webster: Robert.Webster{at}stjude.org

H5N1 influenza viruses transmitted from poultry to humans in Asia cause high mortality and pose a pandemic threat. Viral genes important for cell tropism and replication efficiency must be identified to elucidate and target virulence factors. We applied reverse genetics to generate H5N1 reassortants combining genes of lethal A/Vietnam/1203/04 (VN1203), a fatal human case isolate, and nonlethal A/chicken/Vietnam/C58/04 (CH58) and tested their pathogenicity in ferrets and mice. The viruses' hemagglutinins have six amino acids differences, identical cleavage sites, and avian-like {alpha}-(2,3)–linked receptor specificity. Surprisingly, exchanging hemagglutinin and neuraminidase genes did not alter pathogenicity, but substituting CH58 polymerase genes completely attenuated VN1203 virulence and reduced viral polymerase activity. CH58's NS gene partially attenuated VN1203 in ferrets but not in mice. Our findings suggest that for high virulence in mammalian species an avian H5N1 virus with a cleavable hemagglutinin requires adaptive changes in polymerase genes to overcome the species barrier. Thus, novel antivirals targeting polymerase proteins should be developed.

Abbreviations used: a.i., after inoculation; EID, egg infectious dose; HA, hemagglutinin; MDCK, Madin-Darby canine kidney; NA, neuraminidase; RG, reverse genetics; SA, {alpha}-(2,3)–linked sialic acid.


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