抗原漂移
血凝素(流感)
病毒
抗原转移
H5N1基因结构
病毒学
生物
抗原
氨基酸
甲型流感病毒
抗原变异
表位
抗体
正粘病毒科
氨基酸取代
遗传学
基因
2019年冠状病毒病(COVID-19)
突变
医学
传染病(医学专业)
病理
疾病
作者
Björn F. Koel,David F. Burke,Theo M. Bestebroer,Stefan van der Vliet,Gerben Zondag,Gaby Vervaet,Eugene Skepner,Nicola S. Lewis,Monique I. Spronken,Colin A. Russell,Eropkin MIu,Aeron C. Hurt,Ian Barr,J.C. de Jong,Guus F. Rimmelzwaan,Albert D. M. E. Osterhaus,Ron A. M. Fouchier,Derek J. Smith
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-11-21
卷期号:342 (6161): 976-979
被引量:550
标识
DOI:10.1126/science.1244730
摘要
The molecular basis of antigenic drift was determined for the hemagglutinin (HA) of human influenza A/H3N2 virus. From 1968 to 2003, antigenic change was caused mainly by single amino acid substitutions, which occurred at only seven positions in HA immediately adjacent to the receptor binding site. Most of these substitutions were involved in antigenic change more than once. Equivalent positions were responsible for the recent antigenic changes of influenza B and A/H1N1 viruses. Substitution of a single amino acid at one of these positions substantially changed the virus-specific antibody response in infected ferrets. These findings have potentially far-reaching consequences for understanding the evolutionary mechanisms that govern influenza viruses.
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