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Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant

BACKGROUND: Emergence of new variant of SARS-CoV-2, namely omicron, has posed a global concern because of its high rate of transmissibility and mutations in its genome. Researchers worldwide are trying to understand the evolution and emergence of such variants to understand the mutational cascade ev...

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Autores principales: Bansal, Kanika, Kumar, Sanjeet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968180/
https://www.ncbi.nlm.nih.gov/pubmed/35367284
http://dx.doi.org/10.1016/j.virusres.2022.198765
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author Bansal, Kanika
Kumar, Sanjeet
author_facet Bansal, Kanika
Kumar, Sanjeet
author_sort Bansal, Kanika
collection PubMed
description BACKGROUND: Emergence of new variant of SARS-CoV-2, namely omicron, has posed a global concern because of its high rate of transmissibility and mutations in its genome. Researchers worldwide are trying to understand the evolution and emergence of such variants to understand the mutational cascade events. METHODS: We have considered all omicron genomes (n = 302 genomes) available till 2nd December 2021 in the public repository of GISAID along with representatives of variants of concern (VOC), i.e., alpha, beta, gamma, delta, and omicron; variant of interest (VOI) mu and lambda; and variant under monitoring (VUM). Whole genome-based phylogeny and mutational analysis were performed to understand the evolution of SARS CoV-2 leading to emergence of omicron variant. RESULTS: Whole genome-based phylogeny depicted two phylogroups (PG-I and PG-II) forming variant specific clades except for gamma and VUM GH. Mutational analysis detected 18,261 mutations in the omicron variant, majority of which were non-synonymous mutations in spike (A67, T547K, D614G, H655Y, N679K, P681H, D796Y, N856K, Q954H), followed by RNA dependent RNA polymerase (rdrp) (A1892T, I189V, P314L, K38R, T492I, V57V), ORF6 (M19M) and nucleocapsid protein (RG203KR). CONCLUSION: Delta and omicron have evolutionary diverged into distinct phylogroups and do not share a common ancestry. While, omicron shares common ancestry with VOI lambda and its evolution is mainly derived by the non-synonymous mutations.
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spelling pubmed-89681802022-03-31 Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant Bansal, Kanika Kumar, Sanjeet Virus Res Article BACKGROUND: Emergence of new variant of SARS-CoV-2, namely omicron, has posed a global concern because of its high rate of transmissibility and mutations in its genome. Researchers worldwide are trying to understand the evolution and emergence of such variants to understand the mutational cascade events. METHODS: We have considered all omicron genomes (n = 302 genomes) available till 2nd December 2021 in the public repository of GISAID along with representatives of variants of concern (VOC), i.e., alpha, beta, gamma, delta, and omicron; variant of interest (VOI) mu and lambda; and variant under monitoring (VUM). Whole genome-based phylogeny and mutational analysis were performed to understand the evolution of SARS CoV-2 leading to emergence of omicron variant. RESULTS: Whole genome-based phylogeny depicted two phylogroups (PG-I and PG-II) forming variant specific clades except for gamma and VUM GH. Mutational analysis detected 18,261 mutations in the omicron variant, majority of which were non-synonymous mutations in spike (A67, T547K, D614G, H655Y, N679K, P681H, D796Y, N856K, Q954H), followed by RNA dependent RNA polymerase (rdrp) (A1892T, I189V, P314L, K38R, T492I, V57V), ORF6 (M19M) and nucleocapsid protein (RG203KR). CONCLUSION: Delta and omicron have evolutionary diverged into distinct phylogroups and do not share a common ancestry. While, omicron shares common ancestry with VOI lambda and its evolution is mainly derived by the non-synonymous mutations. Elsevier B.V. 2022-07-02 2022-03-31 /pmc/articles/PMC8968180/ /pubmed/35367284 http://dx.doi.org/10.1016/j.virusres.2022.198765 Text en © 2022 Elsevier B.V. All rights reserved. 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 Article
Bansal, Kanika
Kumar, Sanjeet
Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant
title Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant
title_full Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant
title_fullStr Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant
title_full_unstemmed Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant
title_short Mutational cascade of SARS-CoV-2 leading to evolution and emergence of omicron variant
title_sort mutational cascade of sars-cov-2 leading to evolution and emergence of omicron variant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968180/
https://www.ncbi.nlm.nih.gov/pubmed/35367284
http://dx.doi.org/10.1016/j.virusres.2022.198765
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