Zhou Zhi-Jian, Qiu Ye, Pu Ying, Huang Xun, Ge Xing-Yi
Hunan Provincial Key Laboratory of Medical Virology, Institute of Pathogen Biology and Immunology, College of Biology, Hunan University, Changsha, China.
Department of Hospital Infection Control Center, Xiangya Hospital of Central South University, Changsha, China.
Sustain Cities Soc. 2020 Dec;63:102466. doi: 10.1016/j.scs.2020.102466. Epub 2020 Aug 28.
The novel human coronavirus (SARS-CoV-2) causes the coronavirus disease 2019 (COVID-19) pandemic worldwide. Control of COVID-19 pandemic is vital for public health and is the prerequisite to maintain social stability. However, the origin and transmission route of SARS-CoV-2 is unclear, bringing huge difficult to virus control. Monitoring viral variation and screening functional mutation sites are crucial for prevention and control of infectious diseases. In this study, we developed a user-friendly software, named BioAider, for quick sequence annotation and mutation analysis on large-scale genome-sequencing data. Herein, we detected 14 substitution hotspots within 3,240 SARS-CoV-2 genome sequences, including 3 groups of potentially linked substitution. NSP13-Y541C was crucial substitution which might affect the unwinding activity of the viral helicase. In particular, we discovered a SR-rich region of SARS-CoV-2 distinct from SARS-CoV, indicating more complex replication mechanism and unique N-M interaction of SARS-CoV-2. Interestingly, the quantity of SSRX repeat fragments in SARS-CoV-2 provided further evidence of its animal origin. Overall, we developed an efficient tool for rapid identification of viral genome mutations which could facilitate viral genomic studies. Using this tool, we have found critical clues for the transmission route of SARS-CoV-2 which would provide theoretical support for the epidemic control of pathogenic coronaviruses.
新型人类冠状病毒(SARS-CoV-2)在全球引发了2019冠状病毒病(COVID-19)大流行。控制COVID-19大流行对公共卫生至关重要,是维持社会稳定的前提条件。然而,SARS-CoV-2的起源和传播途径尚不清楚,给病毒控制带来了巨大困难。监测病毒变异并筛选功能突变位点对于传染病的预防和控制至关重要。在本研究中,我们开发了一款名为BioAider的用户友好型软件,用于对大规模基因组测序数据进行快速序列注释和突变分析。在此,我们在3240条SARS-CoV-2基因组序列中检测到14个替换热点,包括3组潜在的连锁替换。NSP13-Y541C是关键替换,可能会影响病毒解旋酶的解旋活性。特别地,我们发现了SARS-CoV-2一个不同于SARS-CoV的富含SR的区域,表明SARS-CoV-2的复制机制更复杂且具有独特的N-M相互作用。有趣的是,SARS-CoV-2中SSRX重复片段的数量为其动物起源提供了进一步证据。总体而言,我们开发了一种用于快速识别病毒基因组突变的高效工具,这有助于病毒基因组研究。使用该工具,我们发现了SARS-CoV-2传播途径的关键线索,这将为致病性冠状病毒的疫情防控提供理论支持。