Grass carp peroxiredoxin 5 and 6-mediated autophagy inhibit grass carp reovirus replication and mitigate oxidative stress

被引:3
|
作者
Wang, Qian [1 ,2 ]
Liang, Xinyu [1 ,2 ]
Wang, Hanyue [1 ,2 ]
Yang, Cheng [1 ]
Li, Yongming [1 ]
Liao, Lanjie [1 ]
Zhu, Zuoyan [1 ]
Wang, Yaping [1 ,3 ]
He, Libo [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Hydrobiol, State Key Lab Breeding Biotechnol & Sustainable Aq, Wuhan 430072, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Innovat Acad Seed Design, Beijing 100101, Peoples R China
基金
中国国家自然科学基金;
关键词
Grass carp reovirus; Peroxiredoxin; 5; 6; Reactive oxygen species (ROS); Antioxidant; Autophagy; ROS; ANTIOXIDANT; MITOCHONDRIA; EXPRESSION; EVOLUTION;
D O I
10.1016/j.fsi.2024.109419
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Peroxiredoxins (Prxs) are a family of antioxidant enzymes crucial for shielding cells against oxidative damage from reactive oxygen species (ROS). In this study, we cloned and analyzed two grass carp peroxiredoxin genes, CiPrx5 and CiPrx6. These genes exhibited ubiquitous expression across all sampled tissues, with their expression levels significantly modulated upon exposure to grass carp reovirus (GCRV). CiPrx5 was localized in the mitochondria, while CiPrx6 was uniformly distributed in the whole cells. Transfection or transformation of CiPrx5 and CiPrx6 into fish cells or E. coli significantly enhanced host resistance to H2O2 and heavy metals, leading to increased cell viability and reduced cell apoptosis rates. Furthermore, purified recombinant CiPrx5 and CiPrx6 proteins effectively protected DNA against oxidative damage. Notably, overexpression of both peroxiredoxins in fish cells effectively inhibited GCRV replication, reduced intracellular ROS levels induced by GCRV infection and H2O2 treatment, and induced autophagy. Significantly, these functions of CiPrx5 and CiPrx6 in GCRV replication and ROS mitigation were abolished upon treatment with an autophagy inhibitor. In summation, our findings suggest that grass carp Prx5 and Prx6 promote autophagy to inhibit GCRV replication, decrease intracellular ROS, and provide protection against oxidative stress.
引用
收藏
页数:13
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