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J Mol Biol. 2008 Sep 19;381(5):1382-94. doi: 10.1016/j.jmb.2008.04.016. Epub 2008 Apr 11.

Recent avian H5N1 viruses exhibit increased propensity for acquiring human receptor specificity.

Author information

1
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA. james.stevens@cdc.hhs.gov

Abstract

Adaptation of avian influenza viruses for replication and transmission in the human host is believed to require mutations in the hemagglutinin glycoprotein (HA) which enable binding to human alpha2-6 sialosides and concomitant reduction in affinity for avian alpha2-3 linked sialosides. Here, we show by glycan microarray analyses that the two mutations responsible for such specificity changes in 1957 H2N2 and 1968 H3N2 pandemic viruses, when inserted into recombinant HAs or intact viruses of some recent avian H5N1 isolates (clade 2.2), impart such attributes. This propensity to adapt to human receptors is primarily dependent on arginine at position 193 within the receptor-binding site, as well as loss of a vicinal glycosylation site. Widespread occurrence of these susceptible H5N1 clade 2.2 influenza strains has already occurred in Europe, the Middle East, and Africa. Thus, these avian strains should be considered high-risk, because of their significantly lower threshold for acquiring human receptor specificity and, therefore, warrant increased surveillance and further study.

PMID:
18672252
PMCID:
PMC2519951
DOI:
10.1016/j.jmb.2008.04.016
[Indexed for MEDLINE]
Free PMC Article

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