Institute of Experimental Virology, TWINCORE Centre for Experimental and Clinical Infection Research, a Joint Venture Between the Hannover Medical School (MHH) and the Helmholtz Centre for Infection Research (HZI), Hannover, Germany.
Vitalant Research Institute, San Francisco, CA, USA.
Life Sci Alliance. 2021 Jun 2;4(7). doi: 10.26508/lsa.202000909. Print 2021 Jul.
Interferon-induced transmembrane (IFITM) proteins restrict membrane fusion and virion internalization of several enveloped viruses. The role of IFITM proteins during alphaviral infection of human cells and viral counteraction strategies are insufficiently understood. Here, we characterized the impact of human IFITMs on the entry and spread of chikungunya virus and Mayaro virus and provide first evidence for a CHIKV-mediated antagonism of IFITMs. IFITM1, 2, and 3 restricted infection at the level of alphavirus glycoprotein-mediated entry, both in the context of direct infection and cell-to-cell transmission. Relocalization of normally endosomal IFITM3 to the plasma membrane resulted in loss of antiviral activity. rs12252-C, a naturally occurring variant of that may associate with severe influenza in humans, restricted CHIKV, MAYV, and influenza A virus infection as efficiently as wild-type Antivirally active IFITM variants displayed reduced cell surface levels in CHIKV-infected cells involving a posttranscriptional process mediated by one or several nonstructural protein(s) of CHIKV. Finally, IFITM3-imposed reduction of specific infectivity of nascent particles provides a rationale for the necessity of a virus-encoded counteraction strategy against this restriction factor.
干扰素诱导跨膜(IFITM)蛋白限制了几种包膜病毒的膜融合和病毒粒子内化。IFITM 蛋白在人细胞中感染甲病毒和病毒对抗策略中的作用尚未充分了解。在这里,我们研究了人 IFITM 蛋白对基孔肯雅病毒和马亚罗病毒感染的影响,并首次提供了 CHIKV 介导的 IFITM 拮抗作用的证据。IFITM1、2 和 3 在甲型病毒糖蛋白介导的进入水平上限制了感染,无论是在直接感染还是细胞间传播的情况下。通常定位于内体的 IFITM3 向质膜的重新定位导致抗病毒活性丧失。rs12252-C 是一种天然存在的变体,可能与人流感的严重程度有关,它像野生型 IFITM 一样有效地限制了 CHIKV、MAYV 和甲型流感病毒感染。具有抗病毒活性的 IFITM 变体在感染 CHIKV 的细胞中显示出降低的细胞表面水平,这涉及一个由 CHIKV 的一个或几个非结构蛋白介导的转录后过程。最后,新形成的颗粒的特异性感染性降低是 IFITM3 强加的对这种限制因素的必要性的病毒编码对抗策略的依据。