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通过冷冻电子显微镜在2.8埃分辨率下确定的感染性盖塔病毒结构。

Structure of infective Getah virus at 2.8 Å resolution determined by cryo-electron microscopy.

作者信息

Wang Aojie, Zhou Feng, Liu Congcong, Gao Dongsheng, Qi Ruxi, Yin Yiheng, Liu Sheng, Gao Yuanzhu, Fu Lutang, Xia Yinhe, Xu Yawei, Wang Chuanqing, Liu Zheng

机构信息

Cryo-electron Microscopy Center, Southern University of Science and Technology, Shenzhen, Guangdong, China.

College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, Henan, China.

出版信息

Cell Discov. 2022 Feb 11;8(1):12. doi: 10.1038/s41421-022-00374-6.

Abstract

Getah virus (GETV), a member of the genus alphavirus, is a mosquito-borne pathogen that can cause pyrexia and reproductive losses in animals. Although antibodies to GETV have been found in over 10% of healthy people, there are no reports of clinical symptoms associated with GETV. The biological and pathological properties of GETV are largely unknown and antiviral or vaccine treatments against GETV are still unavailable due to a lack of knowledge of the structure of the GETV virion. Here, we present the structure of infective GETV at a resolution of 2.8 Å with the atomic models of the capsid protein and the envelope glycoproteins E1 and E2. We have identified numerous glycosylation and S-acylation sites in E1 and E2. The surface-exposed glycans indicate a possible impact on viral immune evasion and host cell invasion. The S-acylation sites might be involved in stabilizing the transmembrane assembly of E1 and E2. In addition, a cholesterol and a phospholipid molecule are observed in a transmembrane hydrophobic pocket, together with two more cholesterols surrounding the pocket. The cholesterol and phospholipid stabilize the hydrophobic pocket in the viral envelope membrane. The structural information will assist structure-based antiviral and vaccine screening, design, and optimization.

摘要

盖塔病毒(GETV)是甲病毒属的成员,是一种蚊媒病原体,可导致动物发热和繁殖损失。尽管在超过10%的健康人中发现了针对GETV的抗体,但尚无与GETV相关的临床症状报告。GETV的生物学和病理学特性在很大程度上尚不清楚,由于对GETV病毒粒子结构缺乏了解,针对GETV的抗病毒或疫苗治疗仍然无法实现。在这里,我们展示了分辨率为2.8 Å的感染性GETV的结构,以及衣壳蛋白和包膜糖蛋白E1和E2的原子模型。我们在E1和E2中鉴定出了许多糖基化和S-酰化位点。表面暴露的聚糖表明可能对病毒免疫逃逸和宿主细胞入侵有影响。S-酰化位点可能参与稳定E1和E2的跨膜组装。此外,在一个跨膜疏水口袋中观察到一个胆固醇和一个磷脂分子,口袋周围还有另外两个胆固醇。胆固醇和磷脂稳定了病毒包膜膜中的疏水口袋。这些结构信息将有助于基于结构的抗病毒和疫苗筛选、设计及优化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f638/8837773/8b3ba0407675/41421_2022_374_Fig1_HTML.jpg

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