Pseudorabies virus manipulates mitochondrial tryptophanyl-tRNA synthetase 2 for viral replication

被引:0
|
作者
Li, Xiu-Qing [1 ,2 ,3 ]
Cai, Meng-Pan [1 ,2 ,3 ]
Wang, Ming-Yang [1 ,2 ,3 ]
Shi, Bo-Wen [7 ]
Yang, Guo-Yu [2 ,3 ,5 ]
Wang, Jiang [1 ,2 ,3 ,6 ]
Chu, Bei-Bei [1 ,2 ,3 ,4 ,5 ,6 ]
Ming, Sheng-Li [1 ,2 ,3 ]
机构
[1] Henan Agr Univ, Coll Vet Med, Zhengzhou 450046, Peoples R China
[2] Minist Agr & Rural Affairs, Key Lab Anim Biochem & Nutr, Zhengzhou 450046, Peoples R China
[3] Henan Agr Univ, Key Lab Vet Biotechnol Henan Prov, Zhengzhou 450046, Peoples R China
[4] Longhu Adv Immunizat Lab, Zhengzhou 450046, Peoples R China
[5] Henan Agr Univ, Int Joint Res Ctr Natl Anim Immunol, Zhengzhou 450046, Peoples R China
[6] Minist Educ, Key Lab Anim Pathogens & Biosafety, Zhengzhou 450046, Peoples R China
[7] Chongqing Med Univ, Sch Basic Med, Chongqing 400016, Peoples R China
关键词
Pseudorabies virus; WARS2; Innate immunity; Protein synthesis; Lipid synthesis;
D O I
10.1016/j.virs.2024.04.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
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.
引用
收藏
页码:403 / 413
页数:11
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