Receptor Binding Properties of the Influenza Virus Hemagglutinin as a Determinant of Host Range

被引:65
|
作者
Xiong, Xiaoli [1 ]
McCauley, John W. [1 ]
Steinhauer, David A. [2 ]
机构
[1] Natl Inst Med Res, MRC, Div Virol, London NW7 1AA, England
[2] Emory Univ, Sch Med, O Wayne Rollins Res Ctr, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
基金
英国医学研究理事会;
关键词
SIALIDASE FUSION PROTEIN; AMINO-ACID SUBSTITUTIONS; X-RAY CRYSTALLOGRAPHY; A VIRUS; RESPIRATORY-DROPLET; IN-VITRO; KINDS; NEURAMINIDASE ACTIVITIES; SUBSTRATE-SPECIFICITY; SHOTGUN GLYCOMICS;
D O I
10.1007/82_2014_423
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Host cell attachment by influenza A viruses is mediated by the hemagglutinin glycoprotein (HA), and the recognition of specific types of sialic acid-containing glycan receptors constitutes one of the major determinants of viral host range and transmission properties. Structural studies have elucidated some of the viral determinants involved in receptor recognition of avian-like and human-like receptors for various subtypes of influenza A viruses, and these provide clues relating to the mechanisms by which viruses evolve to adapt to human hosts. We discuss structural aspects of receptor binding by influenza HA, as well as the biological implications of functional interplay involving HA binding, NA sialidase functions, the effects of antigenic drift, and the inhibitory properties of natural glycans present on mucosal surfaces.
引用
收藏
页码:63 / 91
页数:29
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