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Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses
Three highly pathogenic human coronaviruses can cause severe acute respiratory syndrome (SARS-CoV, SARS-CoV-2 and MERS-CoV). Although phylogenetic analyses have indicated ancient origin of human coronaviruses from animal relatives, their evolutionary history remains to be established. Using phylogen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718587/ https://www.ncbi.nlm.nih.gov/pubmed/33290786 http://dx.doi.org/10.1016/j.jviromet.2020.114032 |
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author | Chen, Zigui Boon, Siaw S. Wang, Maggie H. Chan, Renee W.Y. Chan, Paul K.S. |
author_facet | Chen, Zigui Boon, Siaw S. Wang, Maggie H. Chan, Renee W.Y. Chan, Paul K.S. |
author_sort | Chen, Zigui |
collection | PubMed |
description | Three highly pathogenic human coronaviruses can cause severe acute respiratory syndrome (SARS-CoV, SARS-CoV-2 and MERS-CoV). Although phylogenetic analyses have indicated ancient origin of human coronaviruses from animal relatives, their evolutionary history remains to be established. Using phylogenetics and “high order genomic structures” including trimer spectrums, codon usage and dinucleotide suppression, we observed distinct clustering of all human coronaviruses that formed phylogenetic clades with their closest animal relatives, indicating they have encompassed long evolutionary histories within specific ecological niches before jumping species barrier to infect humans. The close relationships between SARS-CoV and SARS-CoV-2 imply similar evolutionary origin. However, a lower Effective Codon Number (ENC) pattern and CpG dinucleotide suppression in SARS-CoV-2 genomes compared to SARS-CoV and MERS-CoV may imply a better host fitness, and thus their success in sustaining a pandemic. Characterization of coronavirus heterogeneity via complementary approaches enriches our understanding on the evolution and virus-host interaction of these emerging human pathogens while the underlying mechanistic basis in pathogenicity warrants further investigation. |
format | Online Article Text |
id | pubmed-7718587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77185872020-12-07 Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses Chen, Zigui Boon, Siaw S. Wang, Maggie H. Chan, Renee W.Y. Chan, Paul K.S. J Virol Methods Article Three highly pathogenic human coronaviruses can cause severe acute respiratory syndrome (SARS-CoV, SARS-CoV-2 and MERS-CoV). Although phylogenetic analyses have indicated ancient origin of human coronaviruses from animal relatives, their evolutionary history remains to be established. Using phylogenetics and “high order genomic structures” including trimer spectrums, codon usage and dinucleotide suppression, we observed distinct clustering of all human coronaviruses that formed phylogenetic clades with their closest animal relatives, indicating they have encompassed long evolutionary histories within specific ecological niches before jumping species barrier to infect humans. The close relationships between SARS-CoV and SARS-CoV-2 imply similar evolutionary origin. However, a lower Effective Codon Number (ENC) pattern and CpG dinucleotide suppression in SARS-CoV-2 genomes compared to SARS-CoV and MERS-CoV may imply a better host fitness, and thus their success in sustaining a pandemic. Characterization of coronavirus heterogeneity via complementary approaches enriches our understanding on the evolution and virus-host interaction of these emerging human pathogens while the underlying mechanistic basis in pathogenicity warrants further investigation. Elsevier B.V. 2021-03 2020-12-05 /pmc/articles/PMC7718587/ /pubmed/33290786 http://dx.doi.org/10.1016/j.jviromet.2020.114032 Text en © 2020 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Chen, Zigui Boon, Siaw S. Wang, Maggie H. Chan, Renee W.Y. Chan, Paul K.S. Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses |
title | Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses |
title_full | Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses |
title_fullStr | Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses |
title_full_unstemmed | Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses |
title_short | Genomic and evolutionary comparison between SARS-CoV-2 and other human coronaviruses |
title_sort | genomic and evolutionary comparison between sars-cov-2 and other human coronaviruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718587/ https://www.ncbi.nlm.nih.gov/pubmed/33290786 http://dx.doi.org/10.1016/j.jviromet.2020.114032 |
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