PRRSV evades innate immune cGAS-STING antiviral function via its Nsp5 to deter STING translocation and activation

文献类型： 外文期刊

第一作者： Xu, Yulin

作者： Xu, Yulin;Xin, Qihang;Yu, Jiang;Zhang, Yuyu;Wu, Jiaqiang;Xu, Yulin;Chi, Chenglin;Zhang, Pingping;Zheng, Wangli;Jiang, Sen;Zheng, Wanglong;Chen, Nanhua;Zhu, Jianzhong;Xu, Yulin;Chi, Chenglin;Zhang, Pingping;Zheng, Wangli;Jiang, Sen;Zheng, Wanglong;Chen, Nanhua;Zhu, Jianzhong;Xu, Yulin;Chi, Chenglin;Zhang, Pingping;Zheng, Wangli;Jiang, Sen;Zheng, Wanglong;Chen, Nanhua;Zhu, Jianzhong;Xu, Yulin;Chi, Chenglin;Zhang, Pingping;Zheng, Wangli;Jiang, Sen;Zheng, Wanglong;Chen, Nanhua;Zhu, Jianzhong

作者机构：

关键词： PRRSV; Nsp5; STING; immune evasion

期刊名称：VIRULENCE （ 影响因子：5.4； 五年影响因子：5.7 ）

ISSN： 2150-5594

年卷期： 2025 年 16 卷 1 期

页码：

收录情况： SCI

摘要： Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) is an important pathogen that seriously endangers pig breeding, causing significant economic losses to the global swine industry. Our previous study found that the DNA sensing innate cGAS-STING signaling pathway plays an important role in inducing interferon (IFN) upon PRRSV infection and inhibition of PRRSV replication. However, the mechanism underlying immune evasion by PRRSV remains unclear. In the current study, we found that PRRSV non-structural protein 5 (Nsp5) strongly inhibits the cGAS-STING-IFN antiviral response. Furthermore, we found that Nsp5 interacts with STING, blocking STING transport from the ER to the Golgi apparatus and interfering with STING recruitment of TBK1/IKK epsilon/IRF3. Finally, we demonstrated that the Nsp5 36-47 and 58-67 amino acid regions are critical for inhibiting STING activity and PRRSV replication. This study describes a novel mechanism by which PRRSV suppresses the host innate antiviral response and has implications for our understanding of PRRSV pathogenesis.

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