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Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein

The mortality rates due to COVID-19 have been found disproportionate globally and are currently being researched. India mortality rate with a population of 1.3 billion people is relatively lowest to other countries with high infection rates. Genetic composition of circulating isolates continues to b...

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Autores principales: Alai, Shweta, Gujar, Nidhi, Joshi, Manali, Gautam, Manish, Gairola, Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972664/
https://www.ncbi.nlm.nih.gov/pubmed/33758785
http://dx.doi.org/10.1016/j.heliyon.2021.e06564
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author Alai, Shweta
Gujar, Nidhi
Joshi, Manali
Gautam, Manish
Gairola, Sunil
author_facet Alai, Shweta
Gujar, Nidhi
Joshi, Manali
Gautam, Manish
Gairola, Sunil
author_sort Alai, Shweta
collection PubMed
description The mortality rates due to COVID-19 have been found disproportionate globally and are currently being researched. India mortality rate with a population of 1.3 billion people is relatively lowest to other countries with high infection rates. Genetic composition of circulating isolates continues to be a key determinant of virulence and pathogenesis. This study aimed to analyse the extent of divergence between genomes of Indian isolates (n = 2525 as compared to reference Wuhan-1 strain and isolates from countries showing higher fatality rates including France, Italy, Belgium, and the USA. The study also analyses the impact of key mutations on interactions with angiotensin converting enzyme 2 (ACE2) and panel of neutralizing monoclonal antibodies. Using 1,44,605 spike protein sequences, global prevalence of mutations in spike protein was observed. The study suggests that SARS-CoV-2 genomes from India share consensus with global trends with respect to D614G as most prevalent mutational event (81.66% among 2525 Indian isolates). Indian isolates did not reported prevalence of N439K mutation in receptor binding motif (RBM) as compared to global isolates (0.54%). Computational docking and molecular dynamics simulation analysis of N439K mutation with respect to ACE 2 binding and reactivity with RBM targeted antibodies viz., B38, BD23, CB6, P2B–F26 and EY6A suggests that variant have relatively higher affinity with ACE 2 receptor which may support higher infectivity. The study warrants large scale monitoring of Indian isolates as SARS-CoV-2 virus is expected to evolve and mutations may appear in unpredictable way.
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spelling pubmed-79726642021-03-19 Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein Alai, Shweta Gujar, Nidhi Joshi, Manali Gautam, Manish Gairola, Sunil Heliyon Research Article The mortality rates due to COVID-19 have been found disproportionate globally and are currently being researched. India mortality rate with a population of 1.3 billion people is relatively lowest to other countries with high infection rates. Genetic composition of circulating isolates continues to be a key determinant of virulence and pathogenesis. This study aimed to analyse the extent of divergence between genomes of Indian isolates (n = 2525 as compared to reference Wuhan-1 strain and isolates from countries showing higher fatality rates including France, Italy, Belgium, and the USA. The study also analyses the impact of key mutations on interactions with angiotensin converting enzyme 2 (ACE2) and panel of neutralizing monoclonal antibodies. Using 1,44,605 spike protein sequences, global prevalence of mutations in spike protein was observed. The study suggests that SARS-CoV-2 genomes from India share consensus with global trends with respect to D614G as most prevalent mutational event (81.66% among 2525 Indian isolates). Indian isolates did not reported prevalence of N439K mutation in receptor binding motif (RBM) as compared to global isolates (0.54%). Computational docking and molecular dynamics simulation analysis of N439K mutation with respect to ACE 2 binding and reactivity with RBM targeted antibodies viz., B38, BD23, CB6, P2B–F26 and EY6A suggests that variant have relatively higher affinity with ACE 2 receptor which may support higher infectivity. The study warrants large scale monitoring of Indian isolates as SARS-CoV-2 virus is expected to evolve and mutations may appear in unpredictable way. Elsevier 2021-03-19 /pmc/articles/PMC7972664/ /pubmed/33758785 http://dx.doi.org/10.1016/j.heliyon.2021.e06564 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Alai, Shweta
Gujar, Nidhi
Joshi, Manali
Gautam, Manish
Gairola, Sunil
Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein
title Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein
title_full Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein
title_fullStr Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein
title_full_unstemmed Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein
title_short Pan-India novel coronavirus SARS-CoV-2 genomics and global diversity analysis in spike protein
title_sort pan-india novel coronavirus sars-cov-2 genomics and global diversity analysis in spike protein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7972664/
https://www.ncbi.nlm.nih.gov/pubmed/33758785
http://dx.doi.org/10.1016/j.heliyon.2021.e06564
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