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Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus

To understand SARS-CoV-2 microevolution, this study explored the genome-wide frequency, gene-wise distribution, and molecular nature of all point-mutations detected across its 71,703 RNA-genomes deposited in GISAID till 21 August 2020. Globally, nsp1/nsp2 and orf7a/orf3a were the most mutation-ridde...

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Autores principales: Roy, Chayan, Mandal, Santi M., Mondal, Suresh K., Mukherjee, Shriparna, Mapder, Tarunendu, Ghosh, Wriddhiman, Chakraborty, Ranadhir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644180/
https://www.ncbi.nlm.nih.gov/pubmed/33161087
http://dx.doi.org/10.1016/j.ygeno.2020.11.003
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author Roy, Chayan
Mandal, Santi M.
Mondal, Suresh K.
Mukherjee, Shriparna
Mapder, Tarunendu
Ghosh, Wriddhiman
Chakraborty, Ranadhir
author_facet Roy, Chayan
Mandal, Santi M.
Mondal, Suresh K.
Mukherjee, Shriparna
Mapder, Tarunendu
Ghosh, Wriddhiman
Chakraborty, Ranadhir
author_sort Roy, Chayan
collection PubMed
description To understand SARS-CoV-2 microevolution, this study explored the genome-wide frequency, gene-wise distribution, and molecular nature of all point-mutations detected across its 71,703 RNA-genomes deposited in GISAID till 21 August 2020. Globally, nsp1/nsp2 and orf7a/orf3a were the most mutation-ridden non-structural and structural genes respectively. Phylogeny of 4618 spatiotemporally-representative genomes revealed that entities belonging to the early lineages are mostly spread over Asian countries, including India, whereas the recently-derived lineages are more globally distributed. Of the total 20,163 instances of polymorphism detected across global genomes, 12,594 and 7569 involved transitions and transversions, predominated by cytidine-to-uridine and guanosine-to-uridine conversions, respectively. Positive selection of nonsynonymous mutations (dN/dS >1) in most of the structural, but not the non-structural, genes indicated that SARS-CoV-2 has already harmonized its replication/transcription machineries with the host metabolism, while it is still redefining virulence/transmissibility strategies at the molecular level. Mechanistic bases and evolutionary/pathogenicity-related implications are discussed for the predominant mutation-types.
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spelling pubmed-76441802020-11-06 Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus Roy, Chayan Mandal, Santi M. Mondal, Suresh K. Mukherjee, Shriparna Mapder, Tarunendu Ghosh, Wriddhiman Chakraborty, Ranadhir Genomics Original Article To understand SARS-CoV-2 microevolution, this study explored the genome-wide frequency, gene-wise distribution, and molecular nature of all point-mutations detected across its 71,703 RNA-genomes deposited in GISAID till 21 August 2020. Globally, nsp1/nsp2 and orf7a/orf3a were the most mutation-ridden non-structural and structural genes respectively. Phylogeny of 4618 spatiotemporally-representative genomes revealed that entities belonging to the early lineages are mostly spread over Asian countries, including India, whereas the recently-derived lineages are more globally distributed. Of the total 20,163 instances of polymorphism detected across global genomes, 12,594 and 7569 involved transitions and transversions, predominated by cytidine-to-uridine and guanosine-to-uridine conversions, respectively. Positive selection of nonsynonymous mutations (dN/dS >1) in most of the structural, but not the non-structural, genes indicated that SARS-CoV-2 has already harmonized its replication/transcription machineries with the host metabolism, while it is still redefining virulence/transmissibility strategies at the molecular level. Mechanistic bases and evolutionary/pathogenicity-related implications are discussed for the predominant mutation-types. The Authors. Published by Elsevier Inc. 2020-11 2020-11-05 /pmc/articles/PMC7644180/ /pubmed/33161087 http://dx.doi.org/10.1016/j.ygeno.2020.11.003 Text en © 2020 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Original Article
Roy, Chayan
Mandal, Santi M.
Mondal, Suresh K.
Mukherjee, Shriparna
Mapder, Tarunendu
Ghosh, Wriddhiman
Chakraborty, Ranadhir
Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus
title Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus
title_full Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus
title_fullStr Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus
title_full_unstemmed Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus
title_short Trends of mutation accumulation across global SARS-CoV-2 genomes: Implications for the evolution of the novel coronavirus
title_sort trends of mutation accumulation across global sars-cov-2 genomes: implications for the evolution of the novel coronavirus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644180/
https://www.ncbi.nlm.nih.gov/pubmed/33161087
http://dx.doi.org/10.1016/j.ygeno.2020.11.003
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