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Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses
Coronavirus disease 2019 (COVID-19) is a global health concern as it continues to spread within China and beyond. The causative agent of this disease, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), belongs to the genus Betacoronavirus, which also includes severe acute respiratory synd...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223271/ https://www.ncbi.nlm.nih.gov/pubmed/32431949 http://dx.doi.org/10.1093/ve/veaa032 |
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author | Gu, Haogao Chu, Daniel K W Peiris, Malik Poon, Leo L M |
author_facet | Gu, Haogao Chu, Daniel K W Peiris, Malik Poon, Leo L M |
author_sort | Gu, Haogao |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) is a global health concern as it continues to spread within China and beyond. The causative agent of this disease, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), belongs to the genus Betacoronavirus, which also includes severe acute respiratory syndrome-related coronavirus (SARSr-CoV) and Middle East respiratory syndrome-related coronavirus (MERSr-CoV). Codon usage of viral genes are believed to be subjected to different selection pressures in different host environments. Previous studies on codon usage of influenza A viruses helped identify viral host origins and evolution trends, however, similar studies on coronaviruses are lacking. In this study, we compared the codon usage bias using global correspondence analysis (CA), within-group CA and between-group CA. We found that the bat RaTG13 virus best matched the overall codon usage pattern of SARS-CoV-2 in orf1ab, spike and nucleocapsid genes, while the pangolin P1E virus had a more similar codon usage in membrane gene. The amino acid usage pattern of SARS-CoV-2 was generally found similar to bat and human SARSr-CoVs. However, we found greater synonymous codon usage differences between SARS-CoV-2 and its phylogenetic relatives on spike and membrane genes, suggesting these two genes of SARS-CoV-2 are subjected to different evolutionary pressures. |
format | Online Article Text |
id | pubmed-7223271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72232712020-05-19 Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses Gu, Haogao Chu, Daniel K W Peiris, Malik Poon, Leo L M Virus Evol Rapid Communication Coronavirus disease 2019 (COVID-19) is a global health concern as it continues to spread within China and beyond. The causative agent of this disease, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), belongs to the genus Betacoronavirus, which also includes severe acute respiratory syndrome-related coronavirus (SARSr-CoV) and Middle East respiratory syndrome-related coronavirus (MERSr-CoV). Codon usage of viral genes are believed to be subjected to different selection pressures in different host environments. Previous studies on codon usage of influenza A viruses helped identify viral host origins and evolution trends, however, similar studies on coronaviruses are lacking. In this study, we compared the codon usage bias using global correspondence analysis (CA), within-group CA and between-group CA. We found that the bat RaTG13 virus best matched the overall codon usage pattern of SARS-CoV-2 in orf1ab, spike and nucleocapsid genes, while the pangolin P1E virus had a more similar codon usage in membrane gene. The amino acid usage pattern of SARS-CoV-2 was generally found similar to bat and human SARSr-CoVs. However, we found greater synonymous codon usage differences between SARS-CoV-2 and its phylogenetic relatives on spike and membrane genes, suggesting these two genes of SARS-CoV-2 are subjected to different evolutionary pressures. Oxford University Press 2020-05-14 /pmc/articles/PMC7223271/ /pubmed/32431949 http://dx.doi.org/10.1093/ve/veaa032 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Rapid Communication Gu, Haogao Chu, Daniel K W Peiris, Malik Poon, Leo L M Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses |
title | Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses |
title_full | Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses |
title_fullStr | Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses |
title_full_unstemmed | Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses |
title_short | Multivariate analyses of codon usage of SARS-CoV-2 and other betacoronaviruses |
title_sort | multivariate analyses of codon usage of sars-cov-2 and other betacoronaviruses |
topic | Rapid Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7223271/ https://www.ncbi.nlm.nih.gov/pubmed/32431949 http://dx.doi.org/10.1093/ve/veaa032 |
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