Liquid-liquid phase separation is essential for reovirus viroplasm formation and immune evasion.

IF 4 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2024-08-28 DOI:10.1128/jvi.01028-24
Libo He, Qian Wang, Xuyang Wang, Fang Zhou, Cheng Yang, Yongming Li, Lanjie Liao, Zuoyan Zhu, Fei Ke, Yaping Wang
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Abstract

Grass carp reovirus (GCRV) is the most virulent pathogen in the genus Aquareovirus, belonging to the family Spinareoviridae. Members of the Spinareoviridae family are known to replicate and assemble in cytoplasmic inclusion bodies termed viroplasms; however, the detailed mechanism underlying GCRV viroplasm formation and its specific roles in virus infection remains largely unknown. Here, we demonstrate that GCRV viroplasms form through liquid-liquid phase separation (LLPS) of the nonstructural protein NS80 and elucidate the specific role of LLPS during reovirus infection and immune evasion. We observe that viroplasms coalesce within the cytoplasm of GCRV-infected cells. Immunofluorescence and transmission electron microscopy indicate that GCRV viroplasms are membraneless structures. Live-cell imaging and fluorescence recovery after photobleaching assay reveal that GCRV viroplasms exhibit liquid-like properties and are highly dynamic structures undergoing fusion and fission. Furthermore, by using a reagent to inhibit the LLPS process and constructing an NS80 mutant defective in LLPS, we confirm that the liquid-like properties of viroplasms are essential for recruiting viral dsRNA, viral RdRp, and viral proteins to participate in viral genome replication and virion assembly, as well as for sequestering host antiviral factors for immune evasion. Collectively, our findings provide detailed insights into reovirus viroplasm formation and reveal the specific functions of LLPS during virus infection and immune evasion, identifying potential targets for the prevention and control of this virus.

Importance: Grass carp reovirus (GCRV) poses a significant threat to the aquaculture industry, particularly in China, where grass carp is a vital commercial fish species. However, detailed information regarding how GCRV viroplasms form and their specific roles in GCRV infection remains largely unknown. We discovered that GCRV viroplasms exhibit liquid-like properties and are formed through a physico-chemical biological phenomenon known as liquid-liquid phase separation (LLPS), primarily driven by the nonstructural protein NS80. Furthermore, we confirmed that the liquid-like properties of viroplasms are essential for virus replication, assembly, and immune evasion. Our study not only contributes to a deeper understanding of GCRV infection but also sheds light on broader aspects of viroplasm biology. Given that viroplasms are a universal feature of reovirus infection, inhibiting LLPS and then blocking viroplasms formation may serve as a potential pan-reovirus inhibition strategy.

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液-液相分离对再病毒病毒质的形成和免疫逃避至关重要。
草鱼再病毒(GCRV)是水生病毒属(Spinareoviridae)中毒性最强的病原体。已知 Spinareoviridae 科的成员可在细胞质包涵体(称为病毒浆)中复制和组装;然而,GCRV 病毒浆形成的详细机制及其在病毒感染中的具体作用在很大程度上仍不为人所知。在本文中,我们证明了 GCRV 病毒浆液体是通过非结构蛋白 NS80 的液-液相分离(LLPS)形成的,并阐明了 LLPS 在再病毒感染和免疫逃避过程中的特殊作用。我们观察到病毒原体在受 GCRV 感染的细胞的胞浆内凝聚。免疫荧光和透射电子显微镜表明,GCRV 病毒的病毒体是无膜结构。活细胞成像和光漂白后荧光恢复分析表明,GCRV 病毒的胞浆具有类似液体的特性,是一种高度动态的结构,正在发生融合和分裂。此外,通过使用抑制 LLPS 过程的试剂和构建 LLPS 缺陷的 NS80 突变体,我们证实了病毒浆膜的液态特性对于招募病毒 dsRNA、病毒 RdRp 和病毒蛋白参与病毒基因组复制和病毒组装,以及封存宿主抗病毒因子以逃避免疫至关重要。总之,我们的研究结果详细揭示了再病毒病毒质的形成,并揭示了LLPS在病毒感染和免疫逃避过程中的特殊功能,为该病毒的防控找到了潜在靶标:草鱼再病毒(GCRV)对水产养殖业构成重大威胁,尤其是在中国,因为草鱼是中国重要的商品鱼种。然而,有关 GCRV 病毒复制体如何形成及其在 GCRV 感染中的具体作用的详细信息仍不为人知。我们发现,GCRV 病毒浆膜具有类似液体的特性,是通过一种称为液-液相分离(LLPS)的物理化学生物现象形成的,主要由非结构蛋白 NS80 驱动。此外,我们还证实了病毒浆膜的液态特性对于病毒的复制、组装和免疫逃避至关重要。我们的研究不仅有助于加深对 GCRV 感染的理解,还揭示了病毒浆体生物学的更广泛方面。鉴于病毒浆膜是再病毒感染的一个普遍特征,抑制 LLPS 然后阻断病毒浆膜的形成可能是一种潜在的泛病毒抑制策略。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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