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柯萨奇病毒 B3 的 3A 蛋白作为病毒 RNA 干扰的抑制剂。

The 3A protein of coxsackievirus B3 acts as a viral suppressor of RNA interference.

机构信息

Joint Laboratory of Infectious Diseases and Health, Wuhan Institute of Virology and Wuhan Jinyintan Hospital, CAS, Wuhan, Hubei, PR China.

State Key Laboratory of Virology, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences (CAS), Wuhan, Hubei 430071, PR China.

出版信息

J Gen Virol. 2020 Oct;101(10):1069-1078. doi: 10.1099/jgv.0.001434. Epub 2020 Jul 13.

Abstract

RNA interference (RNAi) is a potent antiviral defence mechanism in eukaryotes, and numerous viruses have been found to encode viral suppressors of RNAi (VSRs). Coxsackievirus B3 (CVB3) belongs to the genus in the family , and has been reported to be a major causative pathogen for viral myocarditis. Despite the importance of CVB3, it is unclear whether CVB3 can also encode proteins that suppress RNAi. Here, we showed that the CVB3 nonstructural protein 3A suppressed RNAi triggered by either small hairpin RNAs (shRNAs) or small interfering RNAs (siRNAs) in mammalian cells. We further uncovered that CVB3 3A interacted directly with double-stranded RNAs (dsRNAs) and siRNAs . Through mutational analysis, we found that the VSR activity of CVB3 3A was significantly reduced by mutations of D24A/L25A/L26A, Y37A/C38A and R60A in conserved residues. In addition, the 3A protein encoded by coxsackievirus B5 (CVB5), another member of , also showed VSR activity. Taken together, our findings showed that CVB3 3A has VSR activity, thereby providing insights into the pathogenesis of CVB3 and other enteroviruses.

摘要

RNA 干扰 (RNAi) 是真核生物中一种有效的抗病毒防御机制,许多病毒被发现编码 RNAi 的病毒抑制因子 (VSRs)。柯萨奇病毒 B3 (CVB3) 属于 科 属,已被报道是病毒性心肌炎的主要病原体。尽管 CVB3 很重要,但目前尚不清楚 CVB3 是否也能编码抑制 RNAi 的蛋白质。在这里,我们表明 CVB3 的非结构蛋白 3A 可在哺乳动物细胞中抑制由小发夹 RNA (shRNAs) 或小干扰 RNA (siRNAs) 引发的 RNAi。我们进一步发现 CVB3 3A 可直接与双链 RNA (dsRNAs) 和 siRNAs 相互作用。通过突变分析,我们发现 CVB3 3A 的 VSR 活性在保守残基 D24A/L25A/L26A、Y37A/C38A 和 R60A 的突变后显著降低。此外, 科 的另一种成员柯萨奇病毒 B5 (CVB5) 编码的 3A 蛋白也表现出 VSR 活性。总之,我们的发现表明 CVB3 3A 具有 VSR 活性,从而为 CVB3 和其他肠道病毒的发病机制提供了新的见解。

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