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Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2
To trace the evolution of coronaviruses and reveal the possible origin of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes the coronavirus disease 2019 (COVID-19), we collected and thoroughly analyzed 29,452 publicly available coronavirus genomes, including 26,312 genom...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728743/ https://www.ncbi.nlm.nih.gov/pubmed/33303849 http://dx.doi.org/10.1038/s41598-020-78703-6 |
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author | Zhu, Zhenglin Meng, Kaiwen Meng, Geng |
author_facet | Zhu, Zhenglin Meng, Kaiwen Meng, Geng |
author_sort | Zhu, Zhenglin |
collection | PubMed |
description | To trace the evolution of coronaviruses and reveal the possible origin of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes the coronavirus disease 2019 (COVID-19), we collected and thoroughly analyzed 29,452 publicly available coronavirus genomes, including 26,312 genomes of SARS-CoV-2 strains. We observed coronavirus recombination events among different hosts including 3 independent recombination events with statistical significance between some isolates from humans, bats and pangolins. Consistent with previous records, we also detected putative recombination between strains similar or related to Bat-CoV-RaTG13 and Pangolin-CoV-2019. The putative recombination region is located inside the receptor-binding domain (RBD) of the spike glycoprotein (S protein), which may represent the origin of SARS-CoV-2. Population genetic analyses provide estimates suggesting that the putative introduced genetic sequence within the RBD is undergoing directional evolution. This may result in the adaptation of the virus to hosts. Unsurprisingly, we found that the putative recombination region in S protein was highly diverse among strains from bats. Bats harbor numerous coronavirus subclades that frequently participate in recombination events with human coronavirus. Therefore, bats may provide a pool of genetic diversity for the origin of SARS-CoV-2. |
format | Online Article Text |
id | pubmed-7728743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77287432020-12-14 Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2 Zhu, Zhenglin Meng, Kaiwen Meng, Geng Sci Rep Article To trace the evolution of coronaviruses and reveal the possible origin of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes the coronavirus disease 2019 (COVID-19), we collected and thoroughly analyzed 29,452 publicly available coronavirus genomes, including 26,312 genomes of SARS-CoV-2 strains. We observed coronavirus recombination events among different hosts including 3 independent recombination events with statistical significance between some isolates from humans, bats and pangolins. Consistent with previous records, we also detected putative recombination between strains similar or related to Bat-CoV-RaTG13 and Pangolin-CoV-2019. The putative recombination region is located inside the receptor-binding domain (RBD) of the spike glycoprotein (S protein), which may represent the origin of SARS-CoV-2. Population genetic analyses provide estimates suggesting that the putative introduced genetic sequence within the RBD is undergoing directional evolution. This may result in the adaptation of the virus to hosts. Unsurprisingly, we found that the putative recombination region in S protein was highly diverse among strains from bats. Bats harbor numerous coronavirus subclades that frequently participate in recombination events with human coronavirus. Therefore, bats may provide a pool of genetic diversity for the origin of SARS-CoV-2. Nature Publishing Group UK 2020-12-10 /pmc/articles/PMC7728743/ /pubmed/33303849 http://dx.doi.org/10.1038/s41598-020-78703-6 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhu, Zhenglin Meng, Kaiwen Meng, Geng Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2 |
title | Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2 |
title_full | Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2 |
title_fullStr | Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2 |
title_full_unstemmed | Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2 |
title_short | Genomic recombination events may reveal the evolution of coronavirus and the origin of SARS-CoV-2 |
title_sort | genomic recombination events may reveal the evolution of coronavirus and the origin of sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728743/ https://www.ncbi.nlm.nih.gov/pubmed/33303849 http://dx.doi.org/10.1038/s41598-020-78703-6 |
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