Porcine epidemic diarrhea virus 3CLpro causes apoptosis and collapse of mitochondrial membrane potential requiring its protease activity and signaling through MAVS
文献类型: 外文期刊
作者: Liang, Rong 1 ; Song, Haixin 1 ; Wang, Kerong 1 ; Ding, Fangyi 1 ; Xuan, Dechun 1 ; Miao, Jinfeng 2 ; Fei, Rongmei 2 ; Zhang, Jinqiu 1 ;
作者机构: 1.Jiangsu Acad Agr Sci, Inst Vet Immunol & Engn, Nanjing 210014, Peoples R China
2.Nanjing Agr Univ, Coll Vet Med, Nanjing 210095, Peoples R China
3.Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou 225009, Peoples R China
4.Jiangsu Key Lab Food Qual, Nanjing 210014, Peoples R China
5.Minist Sci & Technol, Safety State Key Lab Cultivat Base, Nanjing 210014, Peoples R China
6.Jiangsu Univ, Sch Pharm, Zhenjiang 212013, Peoples R China
关键词: PEDV; 3CLpro; Apoptosis; MAVS; Pathogenicity
期刊名称:VETERINARY MICROBIOLOGY ( 影响因子:3.246; 五年影响因子:3.565 )
ISSN: 0378-1135
年卷期: 2022 年 275 卷
页码:
收录情况: SCI
摘要: Porcine epidemic diarrhea (PED) is a highly contagious and virulent intestinal infectious disease characterized by diarrhea, vomiting and dehydration. Although PEDV-induced apoptosis has been characterized in vitro and vivo, the functional proteins related to this event and the mechanism still need further research. Here, we firstly demonstrated that PEDV epidemic strain JS2013 could trigger apoptosis in a dose-and time-dependent manner. Then, PEDV 3CLpro was further identified as a crucial inducer of PEDV-triggered apoptosis. In addition, using site-directed mutagenesis to disrupt the protease activity of 3CLpro by His41 and Cys144 mutations, we found that 3CLpro-induced apoptosis and mitochondrial damage significantly reduced, suggesting that the protease activity of 3CLpro was essential for apoptosis and mitochondrial damage. Furthermore, PEDV 3CLpro could synergistically promote MAVS-mediated apoptosis and MAVS was involved in the signaling pathway of 3CLpro- induced apoptosis, but no direct interaction between PEDV 3CLpro and MAVS was detected by immunoprecip-itation assays. Our findings provide important insights into the role of 3CLpro in the pathogenicity of PEDV.
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