BioAider: An efficient tool for viral genome analysis and its application in tracing SARS-CoV-2 transmission. (December 2020)

• Record Type: Journal Article
• Authors: Zhou, Zhi-Jian; Qiu, Ye; Pu, Ying; Huang, Xun; Ge, Xing-Yi
• Is Part Of: Sustainable cities and society. Volume 63(2020)
• Publication Date: 2020-12
• Subjects: BioAider -- SARS-CoV-2 -- COVID-19 -- Sustainable development -- Mutant hotspots -- SR-rich region; Sustainable urban development -- Periodicals; Sustainable buildings -- Periodicals; Urban ecology (Sociology) -- Periodicals; 307.76
• DOI: 10.1016/j.scs.2020.102466
• Languages: English
• ISSNs: 2210-6707

Abstract

Highlights: BioAider is an efficient tool for high-throughput analysis of viral genomes. BioAider monitors viral variation that facilitates epidemic control of COVID-19. 14 substitution hotspots in SARS-CoV-2 genome indicates viral polymorphism. NSP13-Y541C was found to be a crucial substitution key viral replication. The unique SSRX repeats on N protein suggests the animal origin of SARS-CoV-2. Abstract: 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.