Zhang Xiujuan, Xiong Yingli, Zhang Jie, Shao Ting, Chen Songbiao, Miao Bichen, Wang Zhenyu, Du Qian, Huang Yong, Tong Dewen
College of Veterinary Medicine, Northwest A&F University, Yangling 712100, China.
Viruses. 2019 Dec 20;12(1):15. doi: 10.3390/v12010015.
Autophagy plays important roles in the infection and pathogenesis of many viruses, yet the regulatory roles of autophagy in the process of porcine parvovirus (PPV) infection remain unclear. Herein, we show that PPV infection induces autophagy in porcine placental trophoblasts (PTCs). Induction of autophagy by rapamycin (RAPA) inhibited the occurrence of apoptotic cell death, yet promoted viral replication in PPV-infected cells; inhibition of autophagy by 3-MA or ATG5 knockdown increased cellular apoptosis and reduced PPV replication. Interestingly, we found that in the presence of caspase-inhibitor zVAD-fmk, PPV induces non-apoptotic cell death that was characterized by lysosomal damage and associated with autophagy. Induction of complete autophagy flux by RAPA markedly promoted PPV replication compared with incomplete autophagy induced by RAPA plus bafilomycin (RAPA/BAF) in the early phase of PPV infection (24 h.p.i.). Meanwhile, induction of complete autophagy with RAPA increased lysosomal damage and non-apoptotic cell death in the later phase of PPV infection. Therefore, our data suggest that autophagy can enhance PPV replication and promote the occurrence of lysosomal-damage-associated non-apoptotic cell death in PPV-infected porcine placental trophoblasts.
自噬在许多病毒的感染和发病机制中发挥着重要作用,然而自噬在猪细小病毒(PPV)感染过程中的调控作用仍不清楚。在此,我们表明PPV感染可诱导猪胎盘滋养层细胞(PTCs)发生自噬。雷帕霉素(RAPA)诱导自噬可抑制凋亡性细胞死亡的发生,但促进PPV感染细胞中的病毒复制;3-甲基腺嘌呤(3-MA)或自噬相关蛋白5(ATG5)敲低抑制自噬可增加细胞凋亡并减少PPV复制。有趣的是,我们发现,在存在半胱天冬酶抑制剂zVAD-fmk的情况下,PPV诱导以溶酶体损伤为特征且与自噬相关的非凋亡性细胞死亡。与PPV感染早期(感染后24小时)雷帕霉素加巴弗洛霉素(RAPA/BAF)诱导的不完全自噬相比,雷帕霉素诱导的完全自噬通量显著促进了PPV复制。同时,雷帕霉素诱导的完全自噬在PPV感染后期增加了溶酶体损伤和非凋亡性细胞死亡。因此,我们的数据表明,自噬可增强PPV复制,并促进PPV感染的猪胎盘滋养层细胞中溶酶体损伤相关的非凋亡性细胞死亡的发生。