Tumor suppressor p53 inhibits porcine epidemic diarrhea virus infection via interferon-mediated antiviral immunity

被引:20
作者
Hao, Zhichao [1 ]
Fu, Fang [1 ]
Cao, Liyan [1 ]
Guo, Longjun [1 ]
Liu, Jianbo [1 ]
Xue, Mei [1 ]
Feng, Li [1 ]
机构
[1] Chinese Acad Agr Sci, Harbin Vet Res Inst, State Key Lab Vet Biotechnol, Div Swine Infect Dis, 678 Haping Rd, Harbin 150069, Heilongjiang, Peoples R China
基金
中国博士后科学基金;
关键词
Tumor suppressor p53; Porcine epidemic diarrhea virus; Interferon pathway; Viral infection; PAPAIN-LIKE PROTEASE; CELL-CYCLE ARREST; NUCLEOCAPSID PROTEIN; ACTIVATION; INNATE; APOPTOSIS; RESPONSES; DYNAMICS; DEATH;
D O I
10.1016/j.molimm.2019.02.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p53 is a tumor suppressor gene that can be activated in many contexts, such as DNA damage or stressful conditions. p53 has also been shown to be important for responses to certain viral infections. Porcine epidemic diarrhea virus (PEDV) is a major enteric pathogen of the coronavirus family that causes extensive mortality among piglets. The involvement of p53 during PEDV infection has not previously been investigated. In this study, we detected p53 upregulation in response to PEDV infection. Treatment with a p53 specific activator or p53 overexpression markedly decreased viral replication, and we showed that there was more viral progeny produced in p53 knock-out cells than in p53 wild-type cells. Finally, we demonstrated that inhibition of viral infection by p53 was mediated via p53-dependent IFN signaling, leading to IFN-stimulated response element (ISRE) activation, as well as the upregulation of IFN-stimulated genes (ISGs) and IFN-beta released from infected cells. These findings demonstrate that p53 suppresses PEDV infection, offering a novel therapeutic strategy for combatting this deadly disease in piglets.
引用
收藏
页码:68 / 74
页数:7
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