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Rapid evolution of SARS-CoV-2 challenges human defenses
The race between pathogens and their hosts is a major evolutionary driver, where both reshuffle their genomes to overcome and reorganize the defenses for infection, respectively. Evolutionary theory helps formulate predictions on the future evolutionary dynamics of SARS-CoV-2, which can be monitored...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017738/ https://www.ncbi.nlm.nih.gov/pubmed/35440671 http://dx.doi.org/10.1038/s41598-022-10097-z |
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author | Duarte, Carlos M. Ketcheson, David I. Eguíluz, Víctor M. Agustí, Susana Fernández-Gracia, Juan Jamil, Tahira Laiolo, Elisa Gojobori, Takashi Alam, Intikhab |
author_facet | Duarte, Carlos M. Ketcheson, David I. Eguíluz, Víctor M. Agustí, Susana Fernández-Gracia, Juan Jamil, Tahira Laiolo, Elisa Gojobori, Takashi Alam, Intikhab |
author_sort | Duarte, Carlos M. |
collection | PubMed |
description | The race between pathogens and their hosts is a major evolutionary driver, where both reshuffle their genomes to overcome and reorganize the defenses for infection, respectively. Evolutionary theory helps formulate predictions on the future evolutionary dynamics of SARS-CoV-2, which can be monitored through unprecedented real-time tracking of SARS-CoV-2 population genomics at the global scale. Here we quantify the accelerating evolution of SARS-CoV-2 by tracking the SARS-CoV-2 mutation globally, with a focus on the Receptor Binding Domain (RBD) of the spike protein determining infection success. We estimate that the > 820 million people that had been infected by October 5, 2021, produced up to 10(21) copies of the virus, with 12 new effective RBD variants appearing, on average, daily. Doubling of the number of RBD variants every 89 days, followed by selection of the most infective variants challenges our defenses and calls for a shift to anticipatory, rather than reactive tactics involving collaborative global sequencing and vaccination. |
format | Online Article Text |
id | pubmed-9017738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90177382022-04-20 Rapid evolution of SARS-CoV-2 challenges human defenses Duarte, Carlos M. Ketcheson, David I. Eguíluz, Víctor M. Agustí, Susana Fernández-Gracia, Juan Jamil, Tahira Laiolo, Elisa Gojobori, Takashi Alam, Intikhab Sci Rep Article The race between pathogens and their hosts is a major evolutionary driver, where both reshuffle their genomes to overcome and reorganize the defenses for infection, respectively. Evolutionary theory helps formulate predictions on the future evolutionary dynamics of SARS-CoV-2, which can be monitored through unprecedented real-time tracking of SARS-CoV-2 population genomics at the global scale. Here we quantify the accelerating evolution of SARS-CoV-2 by tracking the SARS-CoV-2 mutation globally, with a focus on the Receptor Binding Domain (RBD) of the spike protein determining infection success. We estimate that the > 820 million people that had been infected by October 5, 2021, produced up to 10(21) copies of the virus, with 12 new effective RBD variants appearing, on average, daily. Doubling of the number of RBD variants every 89 days, followed by selection of the most infective variants challenges our defenses and calls for a shift to anticipatory, rather than reactive tactics involving collaborative global sequencing and vaccination. Nature Publishing Group UK 2022-04-19 /pmc/articles/PMC9017738/ /pubmed/35440671 http://dx.doi.org/10.1038/s41598-022-10097-z Text en © The Author(s) 2022 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 Duarte, Carlos M. Ketcheson, David I. Eguíluz, Víctor M. Agustí, Susana Fernández-Gracia, Juan Jamil, Tahira Laiolo, Elisa Gojobori, Takashi Alam, Intikhab Rapid evolution of SARS-CoV-2 challenges human defenses |
title | Rapid evolution of SARS-CoV-2 challenges human defenses |
title_full | Rapid evolution of SARS-CoV-2 challenges human defenses |
title_fullStr | Rapid evolution of SARS-CoV-2 challenges human defenses |
title_full_unstemmed | Rapid evolution of SARS-CoV-2 challenges human defenses |
title_short | Rapid evolution of SARS-CoV-2 challenges human defenses |
title_sort | rapid evolution of sars-cov-2 challenges human defenses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017738/ https://www.ncbi.nlm.nih.gov/pubmed/35440671 http://dx.doi.org/10.1038/s41598-022-10097-z |
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