Chengcheng Zhang, Xiuling Wang, Jiahao Sun, Mengjiao Guo, Xiaorong Zhang, Yantao Wu
College of Veterinary Medicine, Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou University, Yangzhou, Jiangsu 225009, PR China.
College of Veterinary Medicine, Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou University, Yangzhou, Jiangsu 225009, PR China.
Virus Res. 2022 Oct 15;320:198886. doi: 10.1016/j.virusres.2022.198886. Epub 2022 Aug 7.
The classical swine fever virus (CSFV) is one of the most harmful pathogens of swine and causes considerable economic loss. Mitophagy is a selective form of autophagy that degrades damaged mitochondria by combining with lysosomes. Previous studies have been reported that CSFV infection can induce mitophagy, but which effector protein is responsible for this process remains unclear. Herein, we revealed here that the CSFV nonstructural protein 5A (NS5A) plays a critical role in inducing cellular mitophagy. Specifically, the expression of CSFV NS5A in the PK-15 cells induces membrane potential loss and mitochondrial fission, and the quantities of mitophagosomes, the expression of Parkin and PINK1 were significantly increased compared with mock cells. Intriguingly, we found that Parkin-overexpression promotes CSFV propagation. Furthermore, the expression level of reactive oxygen species (ROS) was increased by CSFV NS5A protein, while NS5A-induced mitophagy correlated with the quantity of ROS production. In summary, our results reveal a new function of NS5A in inducing cellular mitophagy and broaden our understanding of the mechanism of CSFV-induced mitophagy, which may provide a new way to develop an antiviral strategy.
经典猪瘟病毒(CSFV)是猪最有害的病原体之一,会造成相当大的经济损失。线粒体自噬是一种选择性自噬形式,通过与溶酶体结合来降解受损的线粒体。先前的研究报道CSFV感染可诱导线粒体自噬,但负责这一过程的效应蛋白尚不清楚。在此,我们揭示CSFV非结构蛋白5A(NS5A)在诱导细胞线粒体自噬中起关键作用。具体而言,CSFV NS5A在PK-15细胞中的表达诱导膜电位丧失和线粒体分裂,与对照细胞相比,线粒体自噬体的数量、Parkin和PINK1的表达显著增加。有趣的是,我们发现过表达Parkin可促进CSFV增殖。此外,CSFV NS5A蛋白可提高活性氧(ROS)的表达水平,而NS5A诱导的线粒体自噬与ROS产生量相关。总之,我们的结果揭示了NS5A在诱导细胞线粒体自噬中的新功能,拓宽了我们对CSFV诱导线粒体自噬机制的理解,这可能为开发抗病毒策略提供新途径。