Hotspot Mutations in SARS-CoV-2

Since its emergence in Wuhan, China, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has spread very rapidly around the world, resulting in a global pandemic. Though the vaccination process has started, the number of COVID-affected patients is still quite large. Hence, an analysis of ho...

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Autores principales: Indrajit Saha, Nimisha Ghosh, Nikhil Sharma , Suman Nandi
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Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/6ccfbb26cbb94677a77bcbb6e9bed147
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spelling oai:doaj.org-article:6ccfbb26cbb94677a77bcbb6e9bed1472021-12-01T13:44:26ZHotspot Mutations in SARS-CoV-21664-802110.3389/fgene.2021.753440https://doaj.org/article/6ccfbb26cbb94677a77bcbb6e9bed1472021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fgene.2021.753440/fullhttps://doaj.org/toc/1664-8021Since its emergence in Wuhan, China, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has spread very rapidly around the world, resulting in a global pandemic. Though the vaccination process has started, the number of COVID-affected patients is still quite large. Hence, an analysis of hotspot mutations of the different evolving virus strains needs to be carried out. In this regard, multiple sequence alignment of 71,038 SARS-CoV-2 genomes of 98 countries over the period from January 2020 to June 2021 is performed using MAFFT followed by phylogenetic analysis in order to visualize the virus evolution. These steps resulted in the identification of hotspot mutations as deletions and substitutions in the coding regions based on entropy greater than or equal to 0.3, leading to a total of 45 unique hotspot mutations. Moreover, 10,286 Indian sequences are considered from 71,038 global SARS-CoV-2 sequences as a demonstrative example that gives 52 unique hotspot mutations. Furthermore, the evolution of the hotspot mutations along with the mutations in variants of concern is visualized, and their characteristics are discussed as well. Also, for all the non-synonymous substitutions (missense mutations), the functional consequences of amino acid changes in the respective protein structures are calculated using PolyPhen-2 and I-Mutant 2.0. In addition to this, SSIPe is used to report the binding affinity between the receptor-binding domain of Spike protein and human ACE2 protein by considering L452R, T478K, E484Q, and N501Y hotspot mutations in that region.Indrajit SahaNimisha GhoshNikhil Sharma Suman NandiFrontiers Media S.A.articleCOVID-19deletionsentropyhotspot mutationsSARS-CoV-2 genomessubstitutionGeneticsQH426-470ENFrontiers in Genetics, Vol 12 (2021)
institution DOAJ
collection DOAJ
language EN
topic COVID-19
deletions
entropy
hotspot mutations
SARS-CoV-2 genomes
substitution
Genetics
QH426-470
spellingShingle COVID-19
deletions
entropy
hotspot mutations
SARS-CoV-2 genomes
substitution
Genetics
QH426-470
Indrajit Saha
Nimisha Ghosh
Nikhil Sharma 
Suman Nandi
Hotspot Mutations in SARS-CoV-2
description Since its emergence in Wuhan, China, severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has spread very rapidly around the world, resulting in a global pandemic. Though the vaccination process has started, the number of COVID-affected patients is still quite large. Hence, an analysis of hotspot mutations of the different evolving virus strains needs to be carried out. In this regard, multiple sequence alignment of 71,038 SARS-CoV-2 genomes of 98 countries over the period from January 2020 to June 2021 is performed using MAFFT followed by phylogenetic analysis in order to visualize the virus evolution. These steps resulted in the identification of hotspot mutations as deletions and substitutions in the coding regions based on entropy greater than or equal to 0.3, leading to a total of 45 unique hotspot mutations. Moreover, 10,286 Indian sequences are considered from 71,038 global SARS-CoV-2 sequences as a demonstrative example that gives 52 unique hotspot mutations. Furthermore, the evolution of the hotspot mutations along with the mutations in variants of concern is visualized, and their characteristics are discussed as well. Also, for all the non-synonymous substitutions (missense mutations), the functional consequences of amino acid changes in the respective protein structures are calculated using PolyPhen-2 and I-Mutant 2.0. In addition to this, SSIPe is used to report the binding affinity between the receptor-binding domain of Spike protein and human ACE2 protein by considering L452R, T478K, E484Q, and N501Y hotspot mutations in that region.
format article
author Indrajit Saha
Nimisha Ghosh
Nikhil Sharma 
Suman Nandi
author_facet Indrajit Saha
Nimisha Ghosh
Nikhil Sharma 
Suman Nandi
author_sort Indrajit Saha
title Hotspot Mutations in SARS-CoV-2
title_short Hotspot Mutations in SARS-CoV-2
title_full Hotspot Mutations in SARS-CoV-2
title_fullStr Hotspot Mutations in SARS-CoV-2
title_full_unstemmed Hotspot Mutations in SARS-CoV-2
title_sort hotspot mutations in sars-cov-2
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/6ccfbb26cbb94677a77bcbb6e9bed147
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AT nimishaghosh hotspotmutationsinsarscov2
AT nikhilsharma hotspotmutationsinsarscov2
AT sumannandi hotspotmutationsinsarscov2
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