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- Publisher Website: 10.1038/s41467-023-37468-y
- Scopus: eid_2-s2.0-85151317010
- PMID: 37002233
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Article: 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 |
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Authors | |
Issue Date | 2023 |
Citation | Nature Communications, 2023, v. 14, n. 1, article no. 1793 How to Cite? |
Abstract | 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. |
Persistent Identifier | http://hdl.handle.net/10722/345317 |
DC Field | Value | Language |
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dc.contributor.author | Gu, Haogao | - |
dc.contributor.author | Quadeer, Ahmed Abdul | - |
dc.contributor.author | Krishnan, Pavithra | - |
dc.contributor.author | Ng, Daisy Y.M. | - |
dc.contributor.author | Chang, Lydia D.J. | - |
dc.contributor.author | Liu, Gigi Y.Z. | - |
dc.contributor.author | Cheng, Samuel M.S. | - |
dc.contributor.author | Lam, Tommy T.Y. | - |
dc.contributor.author | Peiris, Malik | - |
dc.contributor.author | McKay, Matthew R. | - |
dc.contributor.author | Poon, Leo L.M. | - |
dc.date.accessioned | 2024-08-15T09:26:35Z | - |
dc.date.available | 2024-08-15T09:26:35Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | Nature Communications, 2023, v. 14, n. 1, article no. 1793 | - |
dc.identifier.uri | http://hdl.handle.net/10722/345317 | - |
dc.description.abstract | 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. | - |
dc.language | eng | - |
dc.relation.ispartof | Nature Communications | - |
dc.title | Within-host genetic diversity of SARS-CoV-2 lineages in unvaccinated and vaccinated individuals | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1038/s41467-023-37468-y | - |
dc.identifier.pmid | 37002233 | - |
dc.identifier.scopus | eid_2-s2.0-85151317010 | - |
dc.identifier.volume | 14 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | article no. 1793 | - |
dc.identifier.epage | article no. 1793 | - |
dc.identifier.eissn | 2041-1723 | - |