生物
传染性支气管炎病毒
病毒学
STAT1
STAT蛋白
病毒复制
免疫系统
冠状病毒
病毒
微生物学
磷酸化
干扰素
车站3
细胞生物学
传染病(医学专业)
免疫学
2019年冠状病毒病(COVID-19)
病理
疾病
医学
作者
Min Wang,Shengkui Xu,Xueyan Li,Wenke Ruan
出处
期刊:Virology
[Elsevier]
日期:2024-02-01
卷期号:590: 109944-109944
标识
DOI:10.1016/j.virol.2023.109944
摘要
Avian coronavirus, known as infectious bronchitis virus (IBV), is the causative agent of infectious bronchitis (IB). Viral nonstructural proteins play important roles in viral replication and immune modulation. IBV NSP9 is a component of the RNA replication complex for viral replication. In this study, we uncovered a function of NSP9 in immune regulation. First, the host proteins that interacted with NSP9 were screened. The immune-related protein signal transducer and activator of transcription 1 (STAT1) was identified and the interaction between NSP9 and STAT1 was further confirmed. Furthermore, IBV replication was inhibited in STAT1-overexpressing cells but inversely affected in STAT1 knock-down cells. Importantly, NSP9 inhibited STAT1 phosphorylation. Finally, the expression of JAK/STAT pathway downstream genes IRF7 and ISG20 was significantly decreased in NSP9-overexpressing cells. These results showed the important role of IBV NSP9 in immunosuppression.
科研通智能强力驱动
Strongly Powered by AbleSci AI