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Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19

The ongoing outbreak of coronavirus disease COVID-19 is significantly implicated by global heterogeneity in the genome organization of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The causative agents of global heterogeneity in the whole genome of SARS-CoV-2 are not well characteriz...

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Autores principales: Khattak, Saadullah, Rauf, Mohd Ahmar, Zaman, Qamar, Ali, Yasir, Fatima, Shabeen, Muhammad, Pir, Li, Tao, Khan, Hamza Ali, Khan, Azhar Abbas, Ngowi, Ebenezeri Erasto, Wu, Dong-Dong, Ji, Xin-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233742/
https://www.ncbi.nlm.nih.gov/pubmed/34207362
http://dx.doi.org/10.3390/biom11060912
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author Khattak, Saadullah
Rauf, Mohd Ahmar
Zaman, Qamar
Ali, Yasir
Fatima, Shabeen
Muhammad, Pir
Li, Tao
Khan, Hamza Ali
Khan, Azhar Abbas
Ngowi, Ebenezeri Erasto
Wu, Dong-Dong
Ji, Xin-Ying
author_facet Khattak, Saadullah
Rauf, Mohd Ahmar
Zaman, Qamar
Ali, Yasir
Fatima, Shabeen
Muhammad, Pir
Li, Tao
Khan, Hamza Ali
Khan, Azhar Abbas
Ngowi, Ebenezeri Erasto
Wu, Dong-Dong
Ji, Xin-Ying
author_sort Khattak, Saadullah
collection PubMed
description The ongoing outbreak of coronavirus disease COVID-19 is significantly implicated by global heterogeneity in the genome organization of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The causative agents of global heterogeneity in the whole genome of SARS-CoV-2 are not well characterized due to the lack of comparative study of a large enough sample size from around the globe to reduce the standard deviation to the acceptable margin of error. To better understand the SARS-CoV-2 genome architecture, we have performed a comprehensive analysis of codon usage bias of sixty (60) strains to get a snapshot of its global heterogeneity. Our study shows a relatively low codon usage bias in the SARS-CoV-2 viral genome globally, with nearly all the over-preferred codons’ A.U. ended. We concluded that the SARS-CoV-2 genome is primarily shaped by mutation pressure; however, marginal selection pressure cannot be overlooked. Within the A/U rich virus genomes of SARS-CoV-2, the standard deviation in G.C. (42.91% ± 5.84%) and the GC3 value (30.14% ± 6.93%) points towards global heterogeneity of the virus. Several SARS-CoV-2 viral strains were originated from different viral lineages at the exact geographic location also supports this fact. Taking all together, these findings suggest that the general root ancestry of the global genomes are different with different genome’s level adaptation to host. This research may provide new insights into the codon patterns, host adaptation, and global heterogeneity of SARS-CoV-2.
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spelling pubmed-82337422021-06-27 Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19 Khattak, Saadullah Rauf, Mohd Ahmar Zaman, Qamar Ali, Yasir Fatima, Shabeen Muhammad, Pir Li, Tao Khan, Hamza Ali Khan, Azhar Abbas Ngowi, Ebenezeri Erasto Wu, Dong-Dong Ji, Xin-Ying Biomolecules Article The ongoing outbreak of coronavirus disease COVID-19 is significantly implicated by global heterogeneity in the genome organization of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The causative agents of global heterogeneity in the whole genome of SARS-CoV-2 are not well characterized due to the lack of comparative study of a large enough sample size from around the globe to reduce the standard deviation to the acceptable margin of error. To better understand the SARS-CoV-2 genome architecture, we have performed a comprehensive analysis of codon usage bias of sixty (60) strains to get a snapshot of its global heterogeneity. Our study shows a relatively low codon usage bias in the SARS-CoV-2 viral genome globally, with nearly all the over-preferred codons’ A.U. ended. We concluded that the SARS-CoV-2 genome is primarily shaped by mutation pressure; however, marginal selection pressure cannot be overlooked. Within the A/U rich virus genomes of SARS-CoV-2, the standard deviation in G.C. (42.91% ± 5.84%) and the GC3 value (30.14% ± 6.93%) points towards global heterogeneity of the virus. Several SARS-CoV-2 viral strains were originated from different viral lineages at the exact geographic location also supports this fact. Taking all together, these findings suggest that the general root ancestry of the global genomes are different with different genome’s level adaptation to host. This research may provide new insights into the codon patterns, host adaptation, and global heterogeneity of SARS-CoV-2. MDPI 2021-06-18 /pmc/articles/PMC8233742/ /pubmed/34207362 http://dx.doi.org/10.3390/biom11060912 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Khattak, Saadullah
Rauf, Mohd Ahmar
Zaman, Qamar
Ali, Yasir
Fatima, Shabeen
Muhammad, Pir
Li, Tao
Khan, Hamza Ali
Khan, Azhar Abbas
Ngowi, Ebenezeri Erasto
Wu, Dong-Dong
Ji, Xin-Ying
Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19
title Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19
title_full Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19
title_fullStr Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19
title_full_unstemmed Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19
title_short Genome-Wide Analysis of Codon Usage Patterns of SARS-CoV-2 Virus Reveals Global Heterogeneity of COVID-19
title_sort genome-wide analysis of codon usage patterns of sars-cov-2 virus reveals global heterogeneity of covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233742/
https://www.ncbi.nlm.nih.gov/pubmed/34207362
http://dx.doi.org/10.3390/biom11060912
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