Haemagglutinin mutations responsible for the binding of H5N1 influenza A viruses to human-type receptors

• Published in: Nature Vol. 444; no. 7117; pp. 378 - 382
• Main Authors: Yamada, Shinya, Suzuki, Yasuo, Suzuki, Takashi, Le, Mai Q., Nidom, Chairul A., Sakai-Tagawa, Yuko, Muramoto, Yukiko, Ito, Mutsumi, Kiso, Maki, Horimoto, Taisuke, Shinya, Kyoko, Sawada, Toshihiko, Kiso, Makoto, Usui, Taiichi, Murata, Takeomi, Lin, Yipu, Hay, Alan, Haire, Lesley F., Stevens, David J., Russell, Rupert J., Gamblin, Steven J., Skehel, John J., Kawaoka, Yoshihiro
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 16.11.2006; Nature Publishing; Nature Publishing Group
• Subjects: Amino acids; Animal viral diseases; Animals; Aquatic birds; Avian flu; Binding sites; Biological and medical sciences; Cell Line; Cellular biology; Chickens; Crystal structure; Crystallography, X-Ray; Dogs; Fundamental and applied biological sciences. Psychology; Genetics; Hemagglutinin Glycoproteins, Influenza Virus - chemistry; Hemagglutinin Glycoproteins, Influenza Virus - genetics; Hemagglutinin Glycoproteins, Influenza Virus - metabolism; Human viral diseases; Humanities and Social Sciences; Humans; Infectious diseases; Influenza A Virus, H5N1 Subtype - chemistry; Influenza A Virus, H5N1 Subtype - genetics; Influenza A Virus, H5N1 Subtype - metabolism; Lethal effects; letter; Medical sciences; Microbiology; multidisciplinary; Mutation; Mutation - genetics; Pandemics; Poultry; Receptors, Virus - chemistry; Receptors, Virus - metabolism; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains; Saccharides; Science; Science (multidisciplinary); Viral diseases; Viral diseases of the respiratory system and ent viral diseases; Virology; Human; Hemagglutinin; Host specificity; Orthomyxoviridae; Binding site; Molecular marker; Infection; Virus; Avian influenza; Influenzavirus A(H5N1); Vertebrata; Biological fixation; Influenzavirus A; Avian influenzavirus; Viral disease; Replication; Chicken; Mutation; Aves; Aminoacid sequence; Biological receptor
• ISSN: 0028-0836; 1476-4687; 1476-4687; 1476-4679
• DOI: 10.1038/nature05264

Pandemic potential The fact that the H5N1 bird flu virus circulating in Asia, Europe and Africa is unable to attach to human-type cell receptors has helped to prevent it from causing a worldwide epidemic of a human variant of the disease. Now a study of H5N1 isolates from some of the few humans that have been infected (from Vietnam and Thailand) has identified two mutations in a viral haemagglutinin that allow it to bind to both human and avian receptors. These mutations might be of use as molecular markers for assessing the pandemic potential of H5N1 field isolates. H5N1 influenza A viruses have spread to numerous countries in Asia, Europe and Africa, infecting not only large numbers of poultry, but also an increasing number of humans, often with lethal effects 1 , 2 . Human and avian influenza A viruses differ in their recognition of host cell receptors: the former preferentially recognize receptors with saccharides terminating in sialic acid-α2,6-galactose (SAα2,6Gal), whereas the latter prefer those ending in SAα2,3Gal (refs 3–6 ). A conversion from SAα2,3Gal to SAα2,6Gal recognition is thought to be one of the changes that must occur before avian influenza viruses can replicate efficiently in humans and acquire the potential to cause a pandemic. By identifying mutations in the receptor-binding haemagglutinin (HA) molecule that would enable avian H5N1 viruses to recognize human-type host cell receptors, it may be possible to predict (and thus to increase preparedness for) the emergence of pandemic viruses. Here we show that some H5N1 viruses isolated from humans can bind to both human and avian receptors, in contrast to those isolated from chickens and ducks, which recognize the avian receptors exclusively. Mutations at positions 182 and 192 independently convert the HAs of H5N1 viruses known to recognize the avian receptor to ones that recognize the human receptor. Analysis of the crystal structure of the HA from an H5N1 virus used in our genetic experiments shows that the locations of these amino acids in the HA molecule are compatible with an effect on receptor binding. The amino acid changes that we identify might serve as molecular markers for assessing the pandemic potential of H5N1 field isolates.