Jin Yunyun, Ouyang Muzi, Yu Ting, Zhuang Jiaxin, Wang Wenhao, Liu Xue, Duan Fangfang, Guo Deyin, Peng Xiaoxue, Pan Ji-An
The Center for Infection and Immunity Study and Molecular Cancer Research Center, School of Medicine, Sun Yat-sen University, Shenzhen, China.
Front Microbiol. 2022 Jun 1;13:907422. doi: 10.3389/fmicb.2022.907422. eCollection 2022.
Understanding the process of replication and transcription of SARS-CoV-2 is essential for antiviral strategy development. The replicase polyprotein is indispensable for viral replication. However, whether all nsps derived from the replicase polyprotein of SARS-CoV-2 are indispensable is not fully understood. In this study, we utilized the SARS-CoV-2 replicon as the system to investigate the role of each nsp in viral replication. We found that except for nsp16, all the nsp deletions drastically impair the replication of the replicon, and nsp14 could recover the replication deficiency caused by its deletion in the viral replicon. Due to the unsuccessful expressions of nsp1, nsp3, and nsp16, we could not draw a conclusion about their -rescue functions. Our study provided a new angle to understand the role of each nsp in viral replication and transcription, helping the evaluation of nsps as the target for antiviral drug development.
了解严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的复制和转录过程对于抗病毒策略的开发至关重要。复制酶多聚蛋白对于病毒复制不可或缺。然而,源自SARS-CoV-2复制酶多聚蛋白的所有非结构蛋白(nsps)是否都不可或缺尚未完全明确。在本研究中,我们利用SARS-CoV-2复制子作为系统来研究每个nsp在病毒复制中的作用。我们发现,除了nsp16外,所有nsp的缺失都严重损害了复制子的复制,并且nsp14可以恢复其在病毒复制子中缺失所导致的复制缺陷。由于nsp1、nsp3和nsp16未能成功表达,我们无法得出关于它们拯救功能的结论。我们的研究为理解每个nsp在病毒复制和转录中的作用提供了一个新视角,有助于评估nsps作为抗病毒药物开发靶点的可能性。