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Structural Profiles of SARS-CoV-2 Variants in India

India was severely affected by several waves of SARS-CoV-2 infection that occurred during April–June 2021 (second wave) and December 2021–January 2022 (third wave) and thereafter, resulting in >10 million new infections and a significant number of deaths. Global Initiative on Sharing Avian Influe...

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Autores principales: Chakraborti, Soumyananda, Gill, Jasmita, Goswami, Ritu, Kumar, Sanjeev, Chandele, Anmol, Sharma, Amit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684916/
https://www.ncbi.nlm.nih.gov/pubmed/36414797
http://dx.doi.org/10.1007/s00284-022-03094-y
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author Chakraborti, Soumyananda
Gill, Jasmita
Goswami, Ritu
Kumar, Sanjeev
Chandele, Anmol
Sharma, Amit
author_facet Chakraborti, Soumyananda
Gill, Jasmita
Goswami, Ritu
Kumar, Sanjeev
Chandele, Anmol
Sharma, Amit
author_sort Chakraborti, Soumyananda
collection PubMed
description India was severely affected by several waves of SARS-CoV-2 infection that occurred during April–June 2021 (second wave) and December 2021–January 2022 (third wave) and thereafter, resulting in >10 million new infections and a significant number of deaths. Global Initiative on Sharing Avian Influenza Data database was used to collect the sequence information of ~10,000 SARS-CoV-2 patients from India and our sequence analysis identified three variants B.1.1.7 (alpha, α), B1.617.2 (delta, Δ), B.1.1.529 (Omicron, Oo) and one Omicron sub-variant BA.2.75 as the primary drivers for SARS-CoV-2 waves in India. Structural visualization and analysis of important mutations of alpha, delta, Omicron and its sub-variants of SARS-CoV-2 Receptor-Binding Domain (RBD) was performed and our analysis clearly shows that mutations occur throughout the RBD, including the RBD surface responsible for human angiotensin-converting enzyme 2 (hACE-2) receptor-binding. A comparison between alpha, delta and omicron variants/sub-variants reveals many omicron mutations in the hACE-2 binding site and several other mutations within 5 Å of this binding region. Further, computational analysis highlights the importance of electrostatic interactions in stabilizing RBD-hACE-2-binding, especially in the omicron variant. Our analysis explores the likely role of key alpha, delta and omicron mutations on binding with hACE-2. Taken together, our study provides novel structural insights into the implications of RBD mutations in alpha, delta and omicron and its sub-variants that were responsible for India’s SARS-CoV-2 surge. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00284-022-03094-y.
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spelling pubmed-96849162022-11-28 Structural Profiles of SARS-CoV-2 Variants in India Chakraborti, Soumyananda Gill, Jasmita Goswami, Ritu Kumar, Sanjeev Chandele, Anmol Sharma, Amit Curr Microbiol Article India was severely affected by several waves of SARS-CoV-2 infection that occurred during April–June 2021 (second wave) and December 2021–January 2022 (third wave) and thereafter, resulting in >10 million new infections and a significant number of deaths. Global Initiative on Sharing Avian Influenza Data database was used to collect the sequence information of ~10,000 SARS-CoV-2 patients from India and our sequence analysis identified three variants B.1.1.7 (alpha, α), B1.617.2 (delta, Δ), B.1.1.529 (Omicron, Oo) and one Omicron sub-variant BA.2.75 as the primary drivers for SARS-CoV-2 waves in India. Structural visualization and analysis of important mutations of alpha, delta, Omicron and its sub-variants of SARS-CoV-2 Receptor-Binding Domain (RBD) was performed and our analysis clearly shows that mutations occur throughout the RBD, including the RBD surface responsible for human angiotensin-converting enzyme 2 (hACE-2) receptor-binding. A comparison between alpha, delta and omicron variants/sub-variants reveals many omicron mutations in the hACE-2 binding site and several other mutations within 5 Å of this binding region. Further, computational analysis highlights the importance of electrostatic interactions in stabilizing RBD-hACE-2-binding, especially in the omicron variant. Our analysis explores the likely role of key alpha, delta and omicron mutations on binding with hACE-2. Taken together, our study provides novel structural insights into the implications of RBD mutations in alpha, delta and omicron and its sub-variants that were responsible for India’s SARS-CoV-2 surge. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00284-022-03094-y. Springer US 2022-11-22 2023 /pmc/articles/PMC9684916/ /pubmed/36414797 http://dx.doi.org/10.1007/s00284-022-03094-y Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Chakraborti, Soumyananda
Gill, Jasmita
Goswami, Ritu
Kumar, Sanjeev
Chandele, Anmol
Sharma, Amit
Structural Profiles of SARS-CoV-2 Variants in India
title Structural Profiles of SARS-CoV-2 Variants in India
title_full Structural Profiles of SARS-CoV-2 Variants in India
title_fullStr Structural Profiles of SARS-CoV-2 Variants in India
title_full_unstemmed Structural Profiles of SARS-CoV-2 Variants in India
title_short Structural Profiles of SARS-CoV-2 Variants in India
title_sort structural profiles of sars-cov-2 variants in india
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9684916/
https://www.ncbi.nlm.nih.gov/pubmed/36414797
http://dx.doi.org/10.1007/s00284-022-03094-y
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