Department of Chemistry and Biochemistry, University of Bern, Bern, Switzerland.
Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.
PLoS Pathog. 2021 May 21;17(5):e1009603. doi: 10.1371/journal.ppat.1009603. eCollection 2021 May.
The positive-sense, single-stranded RNA alphaviruses pose a potential epidemic threat. Understanding the complex interactions between the viral and the host cell proteins is crucial for elucidating the mechanisms underlying successful virus replication strategies and for developing specific antiviral interventions. Here we present the first comprehensive protein-protein interaction map between the proteins of Semliki Forest Virus (SFV), a mosquito-borne member of the alphaviruses, and host cell proteins. Among the many identified cellular interactors of SFV proteins, the enrichment of factors involved in translation and nonsense-mediated mRNA decay (NMD) was striking, reflecting the virus' hijacking of the translation machinery and indicating viral countermeasures for escaping NMD by inhibiting NMD at later time points during the infectious cycle. In addition to observing a general inhibition of NMD about 4 hours post infection, we also demonstrate that transient expression of the SFV capsid protein is sufficient to inhibit NMD in cells, suggesting that the massive production of capsid protein during the SFV reproduction cycle is responsible for NMD inhibition.
正链单链 RNA 阿尔巴病毒构成了潜在的流行威胁。了解病毒和宿主细胞蛋白之间的复杂相互作用对于阐明成功的病毒复制策略的机制以及开发特定的抗病毒干预措施至关重要。在这里,我们展示了塞姆利基森林病毒(SFV)蛋白与宿主细胞蛋白之间的第一个全面的蛋白质-蛋白质相互作用图谱。在鉴定出的 SFV 蛋白的许多细胞相互作用因子中,参与翻译和无意义介导的 mRNA 降解(NMD)的因子的富集非常明显,这反映了病毒对翻译机制的劫持,并表明病毒通过在感染周期的后期抑制 NMD 来逃避 NMD 的对策。除了观察到感染后约 4 小时 NMD 的普遍抑制外,我们还证明 SFV 衣壳蛋白的瞬时表达足以抑制细胞中的 NMD,这表明 SFV 复制周期中大量产生衣壳蛋白是导致 NMD 抑制的原因。