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兔出血症病毒非结构蛋白6诱导兔肾细胞凋亡。

Rabbit Hemorrhagic Disease Virus Non-structural Protein 6 Induces Apoptosis in Rabbit Kidney Cells.

作者信息

Chen Mengmeng, Liu Xing, Hu Bo, Fan Zhiyu, Song Yanhua, Wei Houjun, Qiu Rulong, Xu Weizhong, Zhu Weifeng, Wang Fang

机构信息

Key Laboratory of Veterinary Biological Engineering and Technology, Ministry of Agriculture, National Center for Engineering Research of Veterinary Bio-products, Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Nanjing, China.

出版信息

Front Microbiol. 2019 Jan 9;9:3308. doi: 10.3389/fmicb.2018.03308. eCollection 2018.

Abstract

Rabbit hemorrhagic disease (RHD) is a highly contagious disease caused by rabbit hemorrhagic disease virus (RHDV). Previous research has shown that RHDV induces apoptosis in numerous cell types, although the molecular mechanisms underlying the apoptosis induced by RHDV are not well understood. One possible factor is non-structural protein 6 (NSP6), a 3C-like protease that plays an important role in processing viral polyprotein precursors into mature non-structural proteins. To fully establish a role for NSP6, the present study examined the effects of ectopic expression of the protein in rabbit (RK13) and human (HeLa and HepG2) cells. We found that NSP6 suppressed cell viability and promoted apoptosis in all three cell types in a dose-dependent manner. We also identified increased caspase-3, -8, and -9 activities in RK13 cell, and an increased Bax to Bcl2 mRNA ratio. Mechanistically, the ability of NSP6 to induce apoptosis was impaired by mutation of the catalytic His27 residue. Our study has shown that RHDV NSP6 can induce apoptosis in host cells and is likely an important contributor to RHDV-induced apoptosis and pathogenesis.

摘要

兔出血性疾病(RHD)是一种由兔出血性疾病病毒(RHDV)引起的高度传染性疾病。先前的研究表明,RHDV可诱导多种细胞类型发生凋亡,尽管RHDV诱导凋亡的分子机制尚未完全明确。一个可能的因素是非结构蛋白6(NSP6),它是一种3C样蛋白酶,在将病毒多蛋白前体加工成成熟的非结构蛋白过程中发挥重要作用。为了全面确定NSP6的作用,本研究检测了该蛋白在兔(RK13)和人(HeLa和HepG2)细胞中异位表达的影响。我们发现,NSP6以剂量依赖的方式抑制所有三种细胞类型的细胞活力并促进凋亡。我们还发现RK13细胞中caspase-3、-8和-9的活性增加,以及Bax与Bcl2 mRNA比值升高。从机制上讲,催化性His27残基的突变损害了NSP6诱导凋亡的能力。我们的研究表明,RHDV NSP6可诱导宿主细胞凋亡,可能是RHDV诱导凋亡和发病机制的重要促成因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36a/6333657/03a1bcf88c8e/fmicb-09-03308-g001.jpg

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