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在基孔肯雅病毒基因组复制和转录过程中,非结构蛋白 3(nsP3)的独特结构域(AUD)的多种作用。

Multiple roles of the non-structural protein 3 (nsP3) alphavirus unique domain (AUD) during Chikungunya virus genome replication and transcription.

机构信息

School of Molecular and Cellular Biology, Faculty of Biological Sciences and Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds, United Kingdom.

出版信息

PLoS Pathog. 2019 Jan 22;15(1):e1007239. doi: 10.1371/journal.ppat.1007239. eCollection 2019 Jan.

Abstract

Chikungunya virus (CHIKV) is a re-emerging Alphavirus causing fever, joint pain, skin rash, arthralgia, and occasionally death. Antiviral therapies and/or effective vaccines are urgently required. CHIKV biology is poorly understood, in particular the functions of the non-structural protein 3 (nsP3). Here we present the results of a mutagenic analysis of the alphavirus unique domain (AUD) of nsP3. Informed by the structure of the Sindbis virus AUD and an alignment of amino acid sequences of multiple alphaviruses, a series of mutations in the AUD were generated in a CHIKV sub-genomic replicon. This analysis revealed an essential role for the AUD in CHIKV RNA replication, with mutants exhibiting species- and cell-type specific phenotypes. To test if the AUD played a role in other stages of the virus lifecycle, the mutants were analysed in the context of infectious CHIKV. This analysis indicated that the AUD was also required for virus assembly. In particular, one mutant (P247A/V248A) exhibited a dramatic reduction in production of infectious virus. This phenotype was shown to be due to a block in transcription of the subgenomic RNA leading to reduced synthesis of the structural proteins and a concomitant reduction in virus production. This phenotype could be further explained by both a reduction in the binding of the P247A/V248A mutant nsP3 to viral genomic RNA in vivo, and the reduced affinity of the mutant AUD for the subgenomic promoter RNA in vitro. We propose that the AUD is a pleiotropic protein domain, with multiple functions during CHIKV RNA synthesis.

摘要

基孔肯雅热病毒(CHIKV)是一种重新出现的甲病毒,可引起发热、关节疼痛、皮疹、关节痛,偶尔还会导致死亡。迫切需要抗病毒疗法和/或有效的疫苗。CHIKV 的生物学特性了解甚少,特别是非结构蛋白 3(nsP3)的功能。在这里,我们介绍了对 nsP3 的丙型肝炎病毒独特域(AUD)进行诱变分析的结果。根据辛德毕斯病毒 AUD 的结构和多个甲病毒氨基酸序列的比对,在 CHIKV 亚基因组复制子中生成了 AUD 的一系列突变。该分析表明 AUD 在 CHIKV RNA 复制中起着至关重要的作用,突变体表现出种属和细胞类型特异性表型。为了测试 AUD 是否在病毒生命周期的其他阶段发挥作用,在感染性 CHIKV 的背景下分析了突变体。该分析表明 AUD 也需要病毒组装。特别是,一种突变体(P247A/V248A)的传染性病毒产量显著降低。该表型是由于亚基因组 RNA 的转录受阻导致结构蛋白的合成减少以及病毒产量相应减少所致。这种表型可以进一步解释为 P247A/V248A 突变体 nsP3 与病毒基因组 RNA 的结合减少,以及突变体 AUD 与亚基因组启动子 RNA 的亲和力降低。我们提出 AUD 是一种多功能蛋白结构域,在 CHIKV RNA 合成过程中有多种功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec1/6358111/b700ce46ebec/ppat.1007239.g001.jpg

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