Brazilian Biosciences National Laboratory, Brazilian Center for Research in Energy and Materials (CNPEM), Campinas, SP, Brazil.
Brazilian Nanotechnology National Laboratory, Brazilian Center for Research in Energy and Materials (CNPEM), Campinas, SP, Brazil.
Nat Commun. 2021 May 24;12(1):3038. doi: 10.1038/s41467-021-23400-9.
Mayaro virus (MAYV) is an emerging arbovirus of the Americas that may cause a debilitating arthritogenic disease. The biology of MAYV is not fully understood and largely inferred from related arthritogenic alphaviruses. Here, we present the structure of MAYV at 4.4 Å resolution, obtained from a preparation of mature, infective virions. MAYV presents typical alphavirus features and organization. Interactions between viral proteins that lead to particle formation are described together with a hydrophobic pocket formed between E1 and E2 spike proteins and conformational epitopes specific of MAYV. We also describe MAYV glycosylation residues in E1 and E2 that may affect MXRA8 host receptor binding, and a molecular "handshake" between MAYV spikes formed by N262 glycosylation in adjacent E2 proteins. The structure of MAYV is suggestive of structural and functional complexity among alphaviruses, which may be targeted for specificity or antiviral activity.
马亚罗病毒(MAYV)是一种新兴的美洲虫媒病毒,可能导致使人虚弱的关节炎疾病。MAYV 的生物学特性尚未完全了解,主要是从相关的关节炎甲型病毒推断出来的。在这里,我们展示了 4.4Å 分辨率的 MAYV 结构,该结构来自成熟、感染性病毒粒子的制备。MAYV 呈现出典型的甲型病毒特征和组织。描述了导致颗粒形成的病毒蛋白之间的相互作用,以及 E1 和 E2 刺突蛋白之间形成的疏水口袋和 MAYV 特有的构象表位。我们还描述了 E1 和 E2 中的 MAYV 糖基化残基,这些残基可能影响 MXRA8 宿主受体结合,以及由相邻 E2 蛋白中 N262 糖基化形成的 MAYV 刺突之间的分子“握手”。MAYV 的结构表明甲型病毒之间存在结构和功能的复杂性,这可能是特异性或抗病毒活性的靶点。