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Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), a novel evolutionary divergent RNA virus, is responsible for the present devastating COVID-19 pandemic. To explore the genomic signatures, we comprehensively analyzed 2,492 complete and/or near-complete genome sequences of SARS-CoV-2 stra...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438523/ https://www.ncbi.nlm.nih.gov/pubmed/32814791 http://dx.doi.org/10.1038/s41598-020-70812-6 |
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author | Islam, M. Rafiul Hoque, M. Nazmul Rahman, M. Shaminur Alam, A. S. M. Rubayet Ul Akther, Masuda Puspo, J. Akter Akter, Salma Sultana, Munawar Crandall, Keith A. Hossain, M. Anwar |
author_facet | Islam, M. Rafiul Hoque, M. Nazmul Rahman, M. Shaminur Alam, A. S. M. Rubayet Ul Akther, Masuda Puspo, J. Akter Akter, Salma Sultana, Munawar Crandall, Keith A. Hossain, M. Anwar |
author_sort | Islam, M. Rafiul |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), a novel evolutionary divergent RNA virus, is responsible for the present devastating COVID-19 pandemic. To explore the genomic signatures, we comprehensively analyzed 2,492 complete and/or near-complete genome sequences of SARS-CoV-2 strains reported from across the globe to the GISAID database up to 30 March 2020. Genome-wide annotations revealed 1,516 nucleotide-level variations at different positions throughout the entire genome of SARS-CoV-2. Moreover, nucleotide (nt) deletion analysis found twelve deletion sites throughout the genome other than previously reported deletions at coding sequence of the ORF8 (open reading frame), spike, and ORF7a proteins, specifically in polyprotein ORF1ab (n = 9), ORF10 (n = 1), and 3´-UTR (n = 2). Evidence from the systematic gene-level mutational and protein profile analyses revealed a large number of amino acid (aa) substitutions (n = 744), demonstrating the viral proteins heterogeneous. Notably, residues of receptor-binding domain (RBD) showing crucial interactions with angiotensin-converting enzyme 2 (ACE2) and cross-reacting neutralizing antibody were found to be conserved among the analyzed virus strains, except for replacement of lysine with arginine at 378th position of the cryptic epitope of a Shanghai isolate, hCoV-19/Shanghai/SH0007/2020 (EPI_ISL_416320). Furthermore, our results of the preliminary epidemiological data on SARS-CoV-2 infections revealed that frequency of aa mutations were relatively higher in the SARS-CoV-2 genome sequences of Europe (43.07%) followed by Asia (38.09%), and North America (29.64%) while case fatality rates remained higher in the European temperate countries, such as Italy, Spain, Netherlands, France, England and Belgium. Thus, the present method of genome annotation employed at this early pandemic stage could be a promising tool for monitoring and tracking the continuously evolving pandemic situation, the associated genetic variants, and their implications for the development of effective control and prophylaxis strategies. |
format | Online Article Text |
id | pubmed-7438523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74385232020-08-21 Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity Islam, M. Rafiul Hoque, M. Nazmul Rahman, M. Shaminur Alam, A. S. M. Rubayet Ul Akther, Masuda Puspo, J. Akter Akter, Salma Sultana, Munawar Crandall, Keith A. Hossain, M. Anwar Sci Rep Article Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), a novel evolutionary divergent RNA virus, is responsible for the present devastating COVID-19 pandemic. To explore the genomic signatures, we comprehensively analyzed 2,492 complete and/or near-complete genome sequences of SARS-CoV-2 strains reported from across the globe to the GISAID database up to 30 March 2020. Genome-wide annotations revealed 1,516 nucleotide-level variations at different positions throughout the entire genome of SARS-CoV-2. Moreover, nucleotide (nt) deletion analysis found twelve deletion sites throughout the genome other than previously reported deletions at coding sequence of the ORF8 (open reading frame), spike, and ORF7a proteins, specifically in polyprotein ORF1ab (n = 9), ORF10 (n = 1), and 3´-UTR (n = 2). Evidence from the systematic gene-level mutational and protein profile analyses revealed a large number of amino acid (aa) substitutions (n = 744), demonstrating the viral proteins heterogeneous. Notably, residues of receptor-binding domain (RBD) showing crucial interactions with angiotensin-converting enzyme 2 (ACE2) and cross-reacting neutralizing antibody were found to be conserved among the analyzed virus strains, except for replacement of lysine with arginine at 378th position of the cryptic epitope of a Shanghai isolate, hCoV-19/Shanghai/SH0007/2020 (EPI_ISL_416320). Furthermore, our results of the preliminary epidemiological data on SARS-CoV-2 infections revealed that frequency of aa mutations were relatively higher in the SARS-CoV-2 genome sequences of Europe (43.07%) followed by Asia (38.09%), and North America (29.64%) while case fatality rates remained higher in the European temperate countries, such as Italy, Spain, Netherlands, France, England and Belgium. Thus, the present method of genome annotation employed at this early pandemic stage could be a promising tool for monitoring and tracking the continuously evolving pandemic situation, the associated genetic variants, and their implications for the development of effective control and prophylaxis strategies. Nature Publishing Group UK 2020-08-19 /pmc/articles/PMC7438523/ /pubmed/32814791 http://dx.doi.org/10.1038/s41598-020-70812-6 Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Islam, M. Rafiul Hoque, M. Nazmul Rahman, M. Shaminur Alam, A. S. M. Rubayet Ul Akther, Masuda Puspo, J. Akter Akter, Salma Sultana, Munawar Crandall, Keith A. Hossain, M. Anwar Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity |
title | Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity |
title_full | Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity |
title_fullStr | Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity |
title_full_unstemmed | Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity |
title_short | Genome-wide analysis of SARS-CoV-2 virus strains circulating worldwide implicates heterogeneity |
title_sort | genome-wide analysis of sars-cov-2 virus strains circulating worldwide implicates heterogeneity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438523/ https://www.ncbi.nlm.nih.gov/pubmed/32814791 http://dx.doi.org/10.1038/s41598-020-70812-6 |
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