Department of Integrative Structural and Computational Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Science. 2013 Dec 6;342(6163):1230-5. doi: 10.1126/science.1243761.
The 2013 outbreak of avian-origin H7N9 influenza in eastern China has raised concerns about its ability to transmit in the human population. The hemagglutinin glycoprotein of most human H7N9 viruses carries Leu(226), a residue linked to adaptation of H2N2 and H3N2 pandemic viruses to human receptors. However, glycan array analysis of the H7 hemagglutinin reveals negligible binding to humanlike α2-6-linked receptors and strong preference for a subset of avian-like α2-3-linked glycans recognized by all avian H7 viruses. Crystal structures of H7N9 hemagglutinin and six hemagglutinin-glycan complexes have elucidated the structural basis for preferential recognition of avian-like receptors. These findings suggest that the current human H7N9 viruses are poorly adapted for efficient human-to-human transmission.
2013 年中国东部地区发生的禽流感 H7N9 疫情引起了人们对其在人群中传播能力的关注。大多数人感染 H7N9 病毒的血凝素糖蛋白携带亮氨酸(226),这种残基与 H2N2 和 H3N2 大流行病毒适应人类受体有关。然而,对 H7 血凝素的糖基阵列分析显示,其对类似人类的α2-6 连接受体的结合作用可忽略不计,而对所有禽源 H7 病毒识别的一组特定的禽源α2-3 连接糖具有强烈的偏好性。H7N9 血凝素和六个血凝素-糖复合物的晶体结构阐明了对禽源受体优先识别的结构基础。这些发现表明,目前的人感染 H7N9 病毒不太适应于高效的人际传播。