Xie Jingying, Zhang Xiangbo, Chen Lei, Bi Yingjie, Idris Adi, Xu Shujuan, Li Xiangrong, Zhang Yong, Feng Ruofei
Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Biomedical Research Center, Northwest Minzu University, Lanzhou, China.
College of Veterinary Medicine, Gansu Agricultural University, Lanzhou, China.
Front Microbiol. 2021 Oct 22;12:761282. doi: 10.3389/fmicb.2021.761282. eCollection 2021.
Pseudorabies virus is a typical swine alphaherpesvirus, which can cause obvious neurological disorders and reproductive failure in pigs. It is capable of evading host antiviral immune response. However, the mechanism by which many PRV proteins assist the virus to evade innate immunity is not fully understood. This study identified PRV US3 protein as a crucial antagonistic viral factor that represses interferon beta (IFN-β) expression. A in-depth study showed that US3 protein restricted type I IFN production by targeting interferon regulatory factor 3 (IRF3), a key molecule required for type I IFN induction. Additionally, US3 protein interacted with IRF3, degraded its protein expression to block the phosphorylation of IRF3. These findings suggested a novel strategy utilized by PRV to inhibit IFN-β production and escape the host innate immunity.
伪狂犬病病毒是一种典型的猪α疱疹病毒,可导致猪出现明显的神经紊乱和繁殖障碍。它能够逃避宿主的抗病毒免疫反应。然而,许多伪狂犬病病毒蛋白协助病毒逃避先天免疫的机制尚未完全清楚。本研究确定伪狂犬病病毒US3蛋白是一种关键的拮抗病毒因子,可抑制干扰素β(IFN-β)的表达。深入研究表明,US3蛋白通过靶向干扰素调节因子3(IRF3)来限制I型干扰素的产生,IRF3是I型干扰素诱导所需的关键分子。此外,US3蛋白与IRF3相互作用,降解其蛋白表达以阻断IRF3的磷酸化。这些发现提示了伪狂犬病病毒用于抑制IFN-β产生并逃避宿主先天免疫的一种新策略。