Gulati Shelly, Smith David F, Cummings Richard D, Couch Robert B, Griesemer Sara B, St George Kirsten, Webster Robert G, Air Gillian M
Department of Biochemistry & Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States of America.
PLoS One. 2013 Jun 21;8(6):e66325. doi: 10.1371/journal.pone.0066325. Print 2013.
It is generally accepted that human influenza viruses bind glycans containing sialic acid linked α2-6 to the next sugar, that avian influenza viruses bind glycans containing the α2-3 linkage, and that mutations that change the binding specificity might change the host tropism. We noted that human H3N2 viruses showed dramatic differences in their binding specificity, and so we embarked on a study of representative human H3N2 influenza viruses, isolated from 1968 to 2012, that had been isolated and minimally passaged only in mammalian cells, never in eggs. The 45 viruses were grown in MDCK cells, purified, fluorescently labeled and screened on the Consortium for Functional Glycomics Glycan Array. Viruses isolated in the same season have similar binding specificity profiles but the profiles show marked year-to-year variation. None of the 610 glycans on the array (166 sialylated glycans) bound to all viruses; the closest was Neu5Acα2-6(Galβ1-4GlcNAc)3 in either a linear or biantennary form, that bound 42 of the 45 viruses. The earliest human H3N2 viruses preferentially bound short, branched sialylated glycans while recent viruses bind better to long polylactosamine chains terminating in sialic acid. Viruses isolated in 1996, 2006, 2010 and 2012 bind glycans with α2-3 linked sialic acid; for 2006, 2010 and 2012 viruses this binding was inhibited by oseltamivir, indicating binding of α2-3 sialylated glycans by neuraminidase. More significantly, oseltamivir inhibited virus entry of 2010 and 2012 viruses into MDCK cells. All of these viruses were representative of epidemic strains that spread around the world, so all could infect and transmit between humans with high efficiency. We conclude that the year-to-year variation in receptor binding specificity is a consequence of amino acid sequence changes driven by antigenic drift, and that viruses with quite different binding specificity and avidity are equally fit to infect and transmit in the human population.
人们普遍认为,人流感病毒结合含有与下一个糖以α2-6连接的唾液酸的聚糖,禽流感病毒结合含有α2-3连接的聚糖,并且改变结合特异性的突变可能会改变宿主嗜性。我们注意到人类H3N2病毒在其结合特异性上表现出显著差异,因此我们着手研究从1968年到2012年分离的代表性人类H3N2流感病毒,这些病毒仅在哺乳动物细胞中分离和进行了最少传代,从未在鸡蛋中传代。这45种病毒在MDCK细胞中培养、纯化、荧光标记,并在功能糖组学聚糖阵列联盟上进行筛选。在同一季节分离的病毒具有相似的结合特异性谱,但这些谱显示出明显的逐年变化。阵列上的610种聚糖(166种唾液酸化聚糖)中没有一种与所有病毒结合;最接近的是线性或双天线形式的Neu5Acα2-6(Galβ1-4GlcNAc)3,它与45种病毒中的42种结合。最早的人类H3N2病毒优先结合短的、分支的唾液酸化聚糖,而最近的病毒与以唾液酸结尾的长聚乳糖胺链结合得更好。1996年、2006年、2010年和2012年分离的病毒结合含有α2-3连接唾液酸的聚糖;对于2006年、2010年和2012年的病毒,这种结合被奥司他韦抑制,表明神经氨酸酶结合α2-3唾液酸化聚糖。更重要的是,奥司他韦抑制2010年和2012年病毒进入MDCK细胞。所有这些病毒都是在世界各地传播的流行毒株的代表,因此所有这些病毒都能高效地在人与人之间感染和传播。我们得出结论,受体结合特异性的逐年变化是由抗原漂移驱动的氨基酸序列变化的结果,并且具有截然不同的结合特异性和亲和力的病毒同样适合在人群中感染和传播。