内部收益率3
伪狂犬病
干扰素
病毒学
抗病毒蛋白
病毒复制
生物
蛋白质生物合成
干扰素调节因子
病毒
核糖核酸
分子生物学
基因
受体
先天免疫系统
生物化学
作者
Xiuqing Li,Mingsheng Cai,Mingyang Wang,Bowen Shi,Gangyi Yang,Jiang Wang,Bei‐Bei Chu,Sheng‐Li Ming
标识
DOI:10.1016/j.virs.2024.04.003
摘要
The pseudorabies virus (PRV) is identified as a double-helical DNA virus responsible for causing Aujeszky's disease, which results in considerable economic impacts globally. The enzyme tryptophanyl-tRNA synthetase 2 (WARS2), a mitochondrial protein involved in protein synthesis, is recognized for its broad expression and vital role in the translation process. The findings of our study showed an increase in both mRNA and protein levels of WARS2 following PRV infection in both cell cultures and animal models. Suppressing WARS2 expression via RNA interference in PK-15 cells led to a reduction in PRV infection rates, whereas enhancing WARS2 expression resulted in increased infection rates. Furthermore, the activation of WARS2 in response to PRV was found to be reliant on the cGAS/STING/TBK1/IRF3 signaling pathway and the interferon-alpha receptor-1, highlighting its regulation via the type I interferon signaling pathway. Further analysis revealed that reducing WARS2 levels hindered PRV's ability to promote protein and lipid synthesis. Our research provides novel evidence that WARS2 facilitates PRV infection through its management of protein and lipid levels, presenting new avenues for developing preventative and therapeutic measures against PRV infections.
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