猪流行性腹泻病毒
生物
维罗细胞
病毒复制
病毒学
基因敲除
病毒
细胞培养
细胞生物学
遗传学
作者
Sujie Dong,Ning Kong,Wenzhen Qin,Huanjie Zhai,Xueying Zhai,Xinyu Yang,Chenqian Ye,Manqing Ye,Changlong Liu,Lingxue Yu,Hao Zheng,Tong Wu,Hai Yu,Wen Zhang,Youwen Li,Guangzhi Tong,Tongling Shan
标识
DOI:10.1016/j.vetmic.2022.109544
摘要
Autophagy-related 4B (ATG4B) is found to exert a vital function in viral replication, although the mechanism through which ATG4B activates type-I IFN signaling to hinder viral replication remains to be explained, so far. The current work revealed that ATG4B was downregulated in porcine epidemic diarrhea virus (PEDV)-infected LLC-PK1 cells. In addition, ATG4B overexpression inhibited PEDV replication in both Vero cells and LLC-PK1 cells. On the contrary, ATG4B knockdown facilitated PEDV replication. Moreover, ATG4B was observed to hinder PEDV replication by activating type-I IFN signaling. Further detailed analysis revealed that the ATG4B protein targeted and upregulated the TRAF3 protein to induce IFN expression via the TRAF3-pTBK1-pIRF3 pathway. The above data revealed a novel mechanism underlying the ATG4B-mediated viral restriction, thereby providing novel possibilities for preventing and controlling PEDV.
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