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Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals

Viral and host factors can shape SARS-CoV-2 evolution. However, little is known about lineage-specific and vaccination-specific mutations that occur within individuals. Here, we analysed deep sequencing data from 2,820 SARS-CoV-2 respiratory samples with different viral lineages to describe the patt...

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Autores principales: Gu, Haogao, Quadeer, Ahmed Abdul, Krishnan, Pavithra, Ng, Daisy Y. M., Chang, Lydia D. J., Liu, Gigi Y. Z., Cheng, Samuel M. S., Lam, Tommy T. Y., Peiris, Malik, McKay, Matthew R., Poon, Leo L. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063955/
https://www.ncbi.nlm.nih.gov/pubmed/37002233
http://dx.doi.org/10.1038/s41467-023-37468-y
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author Gu, Haogao
Quadeer, Ahmed Abdul
Krishnan, Pavithra
Ng, Daisy Y. M.
Chang, Lydia D. J.
Liu, Gigi Y. Z.
Cheng, Samuel M. S.
Lam, Tommy T. Y.
Peiris, Malik
McKay, Matthew R.
Poon, Leo L. M.
author_facet Gu, Haogao
Quadeer, Ahmed Abdul
Krishnan, Pavithra
Ng, Daisy Y. M.
Chang, Lydia D. J.
Liu, Gigi Y. Z.
Cheng, Samuel M. S.
Lam, Tommy T. Y.
Peiris, Malik
McKay, Matthew R.
Poon, Leo L. M.
author_sort Gu, Haogao
collection PubMed
description Viral and host factors can shape SARS-CoV-2 evolution. However, little is known about lineage-specific and vaccination-specific mutations that occur within individuals. Here, we analysed deep sequencing data from 2,820 SARS-CoV-2 respiratory samples with different viral lineages to describe the patterns of within-host diversity under different conditions, including vaccine-breakthrough infections. In unvaccinated individuals, variant of Concern (VOC) Alpha, Delta, and Omicron respiratory samples were found to have higher within-host diversity and were under neutral to purifying selection at the full genome level compared to non-VOC SARS-CoV-2. Breakthrough infections in 2-dose or 3-dose Comirnaty and CoronaVac vaccinated individuals did not increase levels of non-synonymous mutations and did not change the direction of selection pressure. Vaccine-induced antibody or T cell responses did not appear to have significant impact on within-host SARS-CoV-2 sequence diversification. Our findings suggest that vaccination does not increase exploration of SARS-CoV-2 protein sequence space and may not facilitate emergence of viral variants.
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spelling pubmed-100639552023-03-31 Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals Gu, Haogao Quadeer, Ahmed Abdul Krishnan, Pavithra Ng, Daisy Y. M. Chang, Lydia D. J. Liu, Gigi Y. Z. Cheng, Samuel M. S. Lam, Tommy T. Y. Peiris, Malik McKay, Matthew R. Poon, Leo L. M. Nat Commun Article Viral and host factors can shape SARS-CoV-2 evolution. However, little is known about lineage-specific and vaccination-specific mutations that occur within individuals. Here, we analysed deep sequencing data from 2,820 SARS-CoV-2 respiratory samples with different viral lineages to describe the patterns of within-host diversity under different conditions, including vaccine-breakthrough infections. In unvaccinated individuals, variant of Concern (VOC) Alpha, Delta, and Omicron respiratory samples were found to have higher within-host diversity and were under neutral to purifying selection at the full genome level compared to non-VOC SARS-CoV-2. Breakthrough infections in 2-dose or 3-dose Comirnaty and CoronaVac vaccinated individuals did not increase levels of non-synonymous mutations and did not change the direction of selection pressure. Vaccine-induced antibody or T cell responses did not appear to have significant impact on within-host SARS-CoV-2 sequence diversification. Our findings suggest that vaccination does not increase exploration of SARS-CoV-2 protein sequence space and may not facilitate emergence of viral variants. Nature Publishing Group UK 2023-03-31 /pmc/articles/PMC10063955/ /pubmed/37002233 http://dx.doi.org/10.1038/s41467-023-37468-y Text en © The Author(s) 2023 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gu, Haogao
Quadeer, Ahmed Abdul
Krishnan, Pavithra
Ng, Daisy Y. M.
Chang, Lydia D. J.
Liu, Gigi Y. Z.
Cheng, Samuel M. S.
Lam, Tommy T. Y.
Peiris, Malik
McKay, Matthew R.
Poon, Leo L. M.
Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals
title Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals
title_full Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals
title_fullStr Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals
title_full_unstemmed Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals
title_short Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals
title_sort within-host genetic diversity of sars-cov-2 lineages in unvaccinated and vaccinated individuals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063955/
https://www.ncbi.nlm.nih.gov/pubmed/37002233
http://dx.doi.org/10.1038/s41467-023-37468-y
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