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DWV 3C 蛋白酶揭示了昆虫 RNA 病毒中多样的催化三联体。

DWV 3C Protease Uncovers the Diverse Catalytic Triad in Insect RNA Viruses.

机构信息

Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Jiangsu Province, China.

出版信息

Microbiol Spectr. 2022 Jun 29;10(3):e0006822. doi: 10.1128/spectrum.00068-22. Epub 2022 May 16.

Abstract

Deformed wing virus (DWV) is the most prevalent Iflavirus that is infecting honey bees worldwide. However, the mechanisms of its infection and replication in host cells are poorly understood. In this study, we analyzed the structure and function of DWV 3C protease (3C), which is necessary for the cleavage of the polyprotein to synthesize mature viral proteins. Thus, it is one of the nonstructural viral proteins essential for the replication. We found that the 3Cs of DWV and picornaviruses share common enzymatic properties, including sensitivity to the same inhibitors, such as rupintrivir. The predicted structure of DWV 3C by AlphaFold2, the predicted rupintrivir binding domain, and the protease activities of mutant proteins revealed that it has a Cys-His-Asn catalytic triad. Moreover, 3Cs of other Iflaviruses and Dicistrovirus appear to contain Asn, Ser, Asp, or Glu as the third residue of the catalytic triad, suggesting diversity in insect RNA viruses. Both precursor 3C with RNA-dependent RNA polymerase and mature 3C are present in DWV-infected cells, suggesting that they may have different enzymatic properties and functions. DWV 3C is the first 3C characterized among insect RNA viruses, and our study uncovered both the common and unique characteristics among 3Cs of . Furthermore, it would be possible to use the specific inhibitors of DWV 3C to control DWV infection in honey bees in future. The number of managed honey bee (Apis mellifera) colonies has considerably declined in many developed countries in the recent years. Deformed wing virus (DWV) vectored by the mites is the major threat to honey bee colonies and health. To give insight into the mechanism of DWV replication in the host cells, we studied the structure-function relationship of 3C protease (3C), which is necessary to cleave a viral polyprotein at the specific sites to produce the mature proteins. We found that the overall structure, some inhibitors, and processing of 3C are shared between ; however, there is diversity in the catalytic triad. DWV 3C is the first viral protease characterized among insect RNA viruses and reveals the evolutionary history of 3C among . Furthermore, DWV 3C inhibitors identified in our study could also be applied to control DWV in honey bees in future.

摘要

变形翅膀病毒(DWV)是感染全球蜜蜂最普遍的 Iflavirus。然而,其在宿主细胞中的感染和复制机制尚未得到充分理解。在这项研究中,我们分析了 DWV 3C 蛋白酶(3C)的结构和功能,3C 是切割多蛋白以合成成熟病毒蛋白所必需的。因此,它是复制所必需的非结构病毒蛋白之一。我们发现,DWV 和小核糖核酸病毒的 3C 具有共同的酶促特性,包括对相同抑制剂(如鲁匹那韦)的敏感性。通过 AlphaFold2 预测的 DWV 3C 结构、预测的鲁匹那韦结合域以及突变蛋白的蛋白酶活性表明,它具有 Cys-His-Asn 催化三联体。此外,其他 Iflaviruses 和 Dicistrovirus 的 3C 似乎含有天冬酰胺、丝氨酸、天冬氨酸或谷氨酸作为催化三联体的第三个残基,这表明昆虫 RNA 病毒存在多样性。DWV 感染细胞中既有依赖 RNA 的 RNA 聚合酶的前体 3C,也有成熟的 3C,这表明它们可能具有不同的酶促特性和功能。DWV 3C 是昆虫 RNA 病毒中第一个被描述的 3C,我们的研究揭示了 3C 之间的共同和独特特征。此外,未来可能会使用 DWV 3C 的特异性抑制剂来控制蜜蜂中的 DWV 感染。近年来,许多发达国家管理的蜜蜂(Apis mellifera)蜂群数量大幅下降。由螨虫传播的变形翅膀病毒(DWV)是蜜蜂蜂群和健康的主要威胁。为了深入了解 DWV 在宿主细胞中的复制机制,我们研究了 3C 蛋白酶(3C)的结构-功能关系,3C 是在特定部位切割病毒多蛋白以产生成熟蛋白所必需的。我们发现,整体结构、一些抑制剂和 3C 的加工在之间是共享的;然而,催化三联体存在多样性。DWV 3C 是昆虫 RNA 病毒中第一个被描述的病毒蛋白酶,揭示了 3C 在之间的进化历史。此外,我们在这项研究中鉴定的 DWV 3C 抑制剂也可用于未来控制蜜蜂中的 DWV。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c1d/9241925/fcec27fca86d/spectrum.00068-22-f001.jpg

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