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Analysis of the mutation dynamics of SARS-CoV-2 reveals the spread history and emergence of RBD mutant with lower ACE2 binding affinity
YONG JIA; Gangxu Shen; Stephanie Nguyen; Yujuan Zhang; Keng-Shiang Huang; Hsing-Ying Ho; Wei-Shio Hor; Chih-Hui Yang; John B Bruning; Chengdao Li; Wei-Lung Wang.
Afiliação
  • YONG JIA; Murdoch University
  • Gangxu Shen; I-Shou University;National Changhua University of Education
  • Stephanie Nguyen; Institute of Photonics and Advanced Sensing (IPAS), School of Biological Sciences, University of Adelaide, Adelaide 5005, Australia
  • Yujuan Zhang; Murdoch University
  • Keng-Shiang Huang; I-Shou University
  • Hsing-Ying Ho; Guo-Yuan Clinic, Taichung, Taiwan
  • Wei-Shio Hor; TOPO Pharmaceutical Co., Ltd, Taichung, Taiwan
  • Chih-Hui Yang; I-Shou University
  • John B Bruning; Institute of Photonics and Advanced Sensing (IPAS), School of Biological Sciences, University of Adelaide, Adelaide 5005, Australia
  • Chengdao Li; Murdoch University; Department of Primary Industry and Regional Development, Government of Western Australia, South Perth, WA, 6155, Australia
  • Wei-Lung Wang; National Changhua University of Education
Preprint em Inglês | bioRxiv | ID: ppbiorxiv-034942
ABSTRACT
Monitoring the mutation dynamics of SARS-CoV-2 is critical for the development of effective approaches to contain the pathogen. By analyzing 106 SARS-CoV-2 and 39 SARS genome sequences, we provided direct genetic evidence that SARS-CoV-2 has a much lower mutation rate than SARS. Minimum Evolution phylogeny analysis revealed the putative original status of SARS-CoV-2 and the early-stage spread history. The discrepant phylogenies for the spike protein and its receptor binding domain proved a previously reported structural rearrangement prior to the emergence of SARS-CoV-2. Despite that we found the spike glycoprotein of SARS-CoV-2 is particularly more conserved, we identified a receptor binding domain mutation that leads to weaker ACE2 binding capability based on in silico simulation, which concerns a SARS-CoV-2 sample collected on 27th January 2020 from India. This represents the first report of a significant SARS-CoV-2 mutant, and requires attention from researchers working on vaccine development around the world. HighlightsO_LIBased on the currently available genome sequence data, we provided direct genetic evidence that the SARS-COV-2 genome has a much lower mutation rate and genetic diversity than SARS during the 2002-2003 outbreak. C_LIO_LIThe spike (S) protein encoding gene of SARS-COV-2 is found relatively more conserved than other protein-encoding genes, which is a good indication for the ongoing antiviral drug and vaccine development. C_LIO_LIMinimum Evolution phylogeny analysis revealed the putative original status of SARS-CoV-2 and the early-stage spread history. C_LIO_LIWe confirmed a previously reported rearrangement in the S protein arrangement of SARS-COV-2, and propose that this rearrangement should have occurred between human SARS-CoV and a bat SARS-CoV, at a time point much earlier before SARS-COV-2 transmission to human. C_LIO_LIWe provided first evidence that a mutated SARS-COV-2 with reduced human ACE2 receptor binding affinity have emerged in India based on a sample collected on 27th January 2020. C_LI
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: bioRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico Idioma: Inglês Ano de publicação: 2020 Tipo de documento: Preprint
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