Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA.
Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA; Center for Vaccine Research, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Cell Rep. 2018 Dec 11;25(11):3136-3147.e5. doi: 10.1016/j.celrep.2018.11.067.
Alphaviruses are enveloped pathogens that cause arthritis and encephalitis. Here, we report a 4.4-Å cryoelectron microscopy (cryo-EM) structure of eastern equine encephalitis virus (EEEV), an alphavirus that causes fatal encephalitis in humans. Our analysis provides insights into viral entry into host cells. The envelope protein E2 showed a binding site for the cellular attachment factor heparan sulfate. The presence of a cryptic E2 glycan suggests how EEEV escapes surveillance by lectin-expressing myeloid lineage cells, which are sentinels of the immune system. A mechanism for nucleocapsid core release and disassembly upon viral entry was inferred based on pH changes and capsid dissociation from envelope proteins. The EEEV capsid structure showed a viral RNA genome binding site adjacent to a ribosome binding site for viral genome translation following genome release. Using five Fab-EEEV complexes derived from neutralizing antibodies, our investigation provides insights into EEEV host cell interactions and protective epitopes relevant to vaccine design.
甲病毒是包膜病原体,可引起关节炎和脑炎。在这里,我们报告了东方马脑炎病毒(EEEV)的 4.4Å 冷冻电镜(cryo-EM)结构,EEEV 是一种可引起人类致命脑炎的甲病毒。我们的分析提供了病毒进入宿主细胞的见解。包膜蛋白 E2 显示出与细胞附着因子硫酸乙酰肝素的结合位点。隐蔽的 E2 聚糖的存在表明 EEEV 如何逃避表达凝集素的髓样谱系细胞的监视,这些细胞是免疫系统的哨兵。根据 pH 值变化和衣壳蛋白从包膜蛋白上的解离,推断出病毒进入时核衣壳核心释放和解体的机制。EEEV 衣壳结构显示出病毒 RNA 基因组结合位点,该位点紧邻核糖体结合位点,用于基因组释放后的病毒基因组翻译。使用源自中和抗体的五个 Fab-EEEV 复合物,我们的研究提供了对 EEEV 宿主细胞相互作用和与疫苗设计相关的保护性表位的深入了解。