Department of Biological Sciences, Purdue University, 915 W. State Street, West Lafayette, IN 47907-2054, USA.
J Virol. 2010 Dec;84(24):12665-74. doi: 10.1128/JVI.00837-10. Epub 2010 Sep 29.
Echovirus 7 (EV7) belongs to the Enterovirus genus within the family Picornaviridae. Many picornaviruses use IgG-like receptors that bind in the viral canyon and are required to initiate viral uncoating during infection. However, in addition, some of the enteroviruses use an alternative or additional receptor that binds outside the canyon. Decay-accelerating factor (DAF) has been identified as a cellular receptor for EV7. The crystal structure of EV7 has been determined to 3.1-Å resolution and used to interpret the 7.2-Å-resolution cryo-electron microscopy reconstruction of EV7 complexed with DAF. Each DAF binding site on EV7 is near a 2-fold icosahedral symmetry axis, which differs from the binding site of DAF on the surface of coxsackievirus B3, indicating that there are independent evolutionary processes by which DAF was selected as a picornavirus accessory receptor. This suggests that there is an advantage for these viruses to recognize DAF during the initial process of infection.
肠病毒 7 型(EV7)属于小核糖核酸病毒科肠道病毒属。许多小核糖核酸病毒使用结合在病毒峡谷中的 IgG 样受体,这些受体在感染过程中启动病毒脱壳是必需的。然而,除此之外,一些肠道病毒还使用结合在峡谷外的替代或额外受体。衰变加速因子(DAF)已被确定为 EV7 的细胞受体。EV7 的晶体结构已被确定至 3.1-Å 分辨率,并用于解释与 DAF 结合的 EV7 的 7.2-Å 分辨率冷冻电镜重建。EV7 上的每个 DAF 结合位点都靠近 2 倍的二十面体对称轴,这与 DAF 在柯萨奇病毒 B3 表面的结合位点不同,表明 DAF 被选为小核糖核酸病毒辅助受体是独立的进化过程。这表明,在感染的初始过程中,这些病毒识别 DAF 具有优势。