State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, Hubei, China.
State Key Laboratory of Virology, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan, Hubei, China.
J Virol. 2020 Jan 17;94(3). doi: 10.1128/JVI.01233-19.
RNA interference (RNAi) is a conserved antiviral immune defense in eukaryotes, and numerous viruses have been found to encode viral suppressors of RNAi (VSRs) to counteract antiviral RNAi. Alphaviruses are a large group of positive-stranded RNA viruses that maintain their transmission and life cycles in both mosquitoes and mammals. However, there is little knowledge about how alphaviruses antagonize RNAi in both host organisms. In this study, we identified that Semliki Forest virus (SFV) capsid protein can efficiently suppress RNAi in both insect and mammalian cells by sequestrating double-stranded RNA and small interfering RNA. More importantly, when the VSR activity of SFV capsid was inactivated by reverse genetics, the resulting VSR-deficient SFV mutant showed severe replication defects in mammalian cells, which could be rescued by blocking the RNAi pathway. Besides, capsid protein of Sindbis virus also inhibited RNAi in cells. Together, our findings show that SFV uses capsid protein as VSR to antagonize RNAi in infected mammalian cells, and this mechanism is probably used by other alphaviruses, which shed new light on the knowledge of SFV and alphavirus. Alphaviruses are a genus of positive-stranded RNA viruses and include numerous important human pathogens, such as Chikungunya virus, Ross River virus, Western equine encephalitis virus, etc., which create the emerging and reemerging public health threat worldwide. RNA interference (RNAi) is one of the most important antiviral mechanisms in plants and insects. Accumulating evidence has provided strong support for the existence of antiviral RNAi in mammals. In response to antiviral RNAi, viruses have evolved to encode viral suppressors of RNAi (VSRs) to antagonize the RNAi pathway. It is unclear whether alphaviruses encode VSRs that can suppress antiviral RNAi during their infection in mammals. In this study, we first uncovered that capsid protein encoded by Semliki Forest virus (SFV), a prototypic alphavirus, had a potent VSR activity that can antagonize antiviral RNAi in the context of SFV infection in mammalian cells, and this mechanism is probably used by other alphaviruses.
RNA 干扰 (RNAi) 是真核生物中一种保守的抗病毒免疫防御机制,大量病毒被发现编码病毒 RNAi 抑制剂 (VSRs) 以对抗抗病毒 RNAi。甲病毒是一大组正链 RNA 病毒,在蚊子和哺乳动物中维持其传播和生命周期。然而,关于甲病毒如何在两种宿主生物中拮抗 RNAi 的知识知之甚少。在这项研究中,我们发现 Semliki Forest 病毒 (SFV) 衣壳蛋白可以通过隔离双链 RNA 和小干扰 RNA 有效地抑制昆虫和哺乳动物细胞中的 RNAi。更重要的是,当 SFV 衣壳的 VSR 活性通过反向遗传学失活时,由此产生的 VSR 缺陷 SFV 突变体在哺乳动物细胞中表现出严重的复制缺陷,这可以通过阻断 RNAi 途径来挽救。此外,辛德毕斯病毒的衣壳蛋白也能抑制细胞中的 RNAi。总之,我们的研究结果表明,SFV 利用衣壳蛋白作为 VSR 来拮抗感染的哺乳动物细胞中的 RNAi,并且这种机制可能被其他甲病毒使用,这为 SFV 和甲病毒的知识提供了新的视角。甲病毒是正链 RNA 病毒的一个属,包括许多重要的人类病原体,如基孔肯雅病毒、罗斯河病毒、西方马脑炎病毒等,这些病毒在全球范围内造成了新出现和重新出现的公共卫生威胁。RNA 干扰 (RNAi) 是植物和昆虫中最重要的抗病毒机制之一。越来越多的证据为哺乳动物中存在抗病毒 RNAi 提供了强有力的支持。针对抗病毒 RNAi,病毒已经进化出编码病毒 RNAi 抑制剂 (VSRs) 的能力,以拮抗 RNAi 途径。目前尚不清楚甲病毒在感染哺乳动物时是否编码能够抑制抗病毒 RNAi 的 VSRs。在这项研究中,我们首先发现,Semliki Forest 病毒 (SFV) 衣壳蛋白编码的蛋白具有很强的 VSR 活性,能够拮抗 SFV 感染哺乳动物细胞中的抗病毒 RNAi,而且这种机制可能被其他甲病毒使用。