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J Gen Virol 85 (2004), 3249-3259; DOI 10.1099/vir.0.80021-0

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© 2004 Society for General Microbiology

Homology model of the structure of influenza B virus HA1

Chang-Shung Tung, Joshua L. Goodman{dagger}, Henry Lu{ddagger} and Catherine A. Macken

Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, NM 87545, USA

Correspondence
Catherine A. Macken
cmacken{at}lanl.gov

Influenza B virus is one of two types of influenza virus that cause substantial morbidity and mortality in humans, the other being influenza A virus. The inability to provide lasting protection to humans against influenza B virus infection is due, in part, to antigenic drift of the viral surface glycoprotein, haemagglutinin (HA). Studies of the antigenicity of the HA of influenza B virus have been hampered by lack of knowledge of its structure. To address this gap, two possible models have been inferred for this structure, based on two known structures of the homologous HA of the influenza A virus (subtypes H3 and H9). Statistical, structural and functional analyses of these models suggested that they matched important details of experimental observations and did not differ from each other in any substantive way. These models were used to investigate two HA sites at which viral variants appeared to carry a selective advantage. It was found that each of these sites coevolved with nearby sites to compensate for either size or charge changes.

{dagger}Present address: Department of Biology, Indiana University, 1001 E. Third Street, Bloomington, IN 47403, USA.

{ddagger}Present address: 454 Life Science Corporation, 20 Commercial Street, Branford, CT 06405, USA.




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