Evolutionary dynamics of the severe acute respiratory syndrome coronavirus 2 genomes
Author:
Qian Zhaohui1, Li Pei1, Tang Xiaolu2, Lu Jian2ORCID
Affiliation:
1. NHC Key Laboratory of Systems Biology of Pathogens , Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College , Beijing , 100871 , China 2. State Key Laboratory of Protein and Plant Gene Research, Center for Bioinformatics , School of Life Sciences, Peking University , Beijing , 100176 , China
Abstract
Abstract
The coronavirus disease 2019 (COVID-19) pandemic has caused immense losses in human lives and the global economy and posed significant challenges for global public health. As severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, has evolved, thousands of single nucleotide variants (SNVs) have been identified across the viral genome. The roles of individual SNVs in the zoonotic origin, evolution, and transmission of SARS-CoV-2 have become the focus of many studies. This review summarizes recent comparative genomic analyses of SARS-CoV-2 and related coronaviruses (SC2r-CoVs) found in non-human animals, including delineation of SARS-CoV-2 lineages based on characteristic SNVs. We also discuss the current understanding of receptor-binding domain (RBD) evolution and characteristic mutations in variants of concern (VOCs) of SARS-CoV-2, as well as possible co-evolution between RBD and its receptor, angiotensin-converting enzyme 2 (ACE2). We propose that the interplay between SARS-CoV-2 and host RNA editing mechanisms might have partially resulted in the bias in nucleotide changes during SARS-CoV-2 evolution. Finally, we outline some current challenges, including difficulty in deciphering the complicated relationship between viral pathogenicity and infectivity of different variants, and monitoring transmission of SARS-CoV-2 between humans and animals as the pandemic progresses.
Publisher
Walter de Gruyter GmbH
Reference194 articles.
1. WHO. WHO coronavirus disease (COVID-19) dashboard; 2021. Available from: https://covid19.who.int/. 2. Lu, R, Zhao, X, Li, J, Niu, P, Yang, B, Wu, H, et al.. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet 2020;395:565–74. https://doi.org/10.1016/S0140-6736(20)30251-8. 3. Zhou, P, Yang, X-L, Wang, X-G, Hu, B, Zhang, L, Zhang, W, et al.. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature 2020;579:270–3. https://doi.org/10.1038/s41586-020-2012-7. 4. Ren, L-L, Wang, YM, Wu, ZQ, Xiang, ZC, Guo, L, Xu, T, et al.. Identification of a novel coronavirus causing severe pneumonia in human: a descriptive study. Chinese Med J 2020;133:1015–24. https://doi.org/10.1097/CM9.0000000000000722. 5. Wu, F, Zhao, S, Yu, B, Chen, Y-M, Wang, W, Song, Z-G, et al.. A new coronavirus associated with human respiratory disease in China. Nature 2020;579:265–9. https://doi.org/10.1038/s41586-020-2008-3.
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