Wang Chongyang, Wang Ting, Duan Liuyuan, Chen Hui, Hu Ruochen, Wang Xiangwei, Jia Yanqing, Chu Zhili, Liu Haijin, Wang Xinglong, Zhang Shuxia, Xiao Sa, Wang Juan, Dang Ruyi, Yang Zengqi
College of Veterinary Medicine, Northwest A&F University, Xianyang, China.
Front Microbiol. 2022 Jan 31;12:790191. doi: 10.3389/fmicb.2021.790191. eCollection 2021.
For efficient replication, viruses have developed multiple strategies to evade host antiviral innate immunity. Paramyxoviruses are a large family of enveloped RNA viruses that comprises diverse human and animal pathogens which jeopardize global public health and the economy. The accessory proteins expressed from the P gene by RNA editing or overlapping open reading frames (ORFs) are major viral immune evasion factors antagonizing type I interferon (IFN-I) production and other antiviral innate immune responses. However, the antagonistic mechanisms against antiviral innate immunity by accessory proteins differ among viruses. Here, we summarize the current understandings of immune evasion mechanisms by paramyxovirus accessory proteins, specifically how accessory proteins directly or indirectly target the adaptors in the antiviral innate immune signaling pathway to facilitate virus replication. Additionally, some cellular responses, which are also involved in viral replication, will be briefly summarized.
为了高效复制,病毒已发展出多种策略来逃避宿主抗病毒固有免疫。副粘病毒是一大类包膜RNA病毒,包含多种危害全球公共卫生和经济的人类及动物病原体。通过RNA编辑或重叠开放阅读框(ORF)从P基因表达的辅助蛋白是对抗I型干扰素(IFN-I)产生及其他抗病毒固有免疫反应的主要病毒免疫逃逸因子。然而,不同病毒的辅助蛋白对抗病毒固有免疫的机制有所不同。在此,我们总结了目前对副粘病毒辅助蛋白免疫逃逸机制的认识,特别是辅助蛋白如何直接或间接靶向抗病毒固有免疫信号通路中的衔接蛋白以促进病毒复制。此外,还将简要总结一些也参与病毒复制的细胞反应。