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Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) rapidly replaced Delta (B.1.617.2) to become dominant in England. Our study assessed differences in transmission between Omicron and Delta using two independent data sources and methods. Omicron and Delta ca...

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Autores principales: Allen, Hester, Tessier, Elise, Turner, Charlie, Anderson, Charlotte, Blomquist, Paula, Simons, David, Løchen, Alessandra, Jarvis, Christopher I., Groves, Natalie, Capelastegui, Fernando, Flannagan, Joe, Zaidi, Asad, Chen, Cong, Rawlinson, Christopher, Hughes, Gareth J., Chudasama, Dimple, Nash, Sophie, Thelwall, Simon, Lopez-Bernal, Jamie, Dabrera, Gavin, Charlett, André, Kall, Meaghan, Lamagni, Theresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10125873/
https://www.ncbi.nlm.nih.gov/pubmed/36938806
http://dx.doi.org/10.1017/S0950268823000420
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author Allen, Hester
Tessier, Elise
Turner, Charlie
Anderson, Charlotte
Blomquist, Paula
Simons, David
Løchen, Alessandra
Jarvis, Christopher I.
Groves, Natalie
Capelastegui, Fernando
Flannagan, Joe
Zaidi, Asad
Chen, Cong
Rawlinson, Christopher
Hughes, Gareth J.
Chudasama, Dimple
Nash, Sophie
Thelwall, Simon
Lopez-Bernal, Jamie
Dabrera, Gavin
Charlett, André
Kall, Meaghan
Lamagni, Theresa
author_facet Allen, Hester
Tessier, Elise
Turner, Charlie
Anderson, Charlotte
Blomquist, Paula
Simons, David
Løchen, Alessandra
Jarvis, Christopher I.
Groves, Natalie
Capelastegui, Fernando
Flannagan, Joe
Zaidi, Asad
Chen, Cong
Rawlinson, Christopher
Hughes, Gareth J.
Chudasama, Dimple
Nash, Sophie
Thelwall, Simon
Lopez-Bernal, Jamie
Dabrera, Gavin
Charlett, André
Kall, Meaghan
Lamagni, Theresa
author_sort Allen, Hester
collection PubMed
description The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) rapidly replaced Delta (B.1.617.2) to become dominant in England. Our study assessed differences in transmission between Omicron and Delta using two independent data sources and methods. Omicron and Delta cases were identified through genomic sequencing, genotyping and S-gene target failure in England from 5–11 December 2021. Secondary attack rates for named contacts were calculated in household and non-household settings using contact tracing data, while household clustering was identified using national surveillance data. Logistic regression models were applied to control for factors associated with transmission for both methods. For contact tracing data, higher secondary attack rates for Omicron vs. Delta were identified in households (15.0% vs. 10.8%) and non-households (8.2% vs. 3.7%). For both variants, in household settings, onward transmission was reduced from cases and named contacts who had three doses of vaccine compared to two, but this effect was less pronounced for Omicron (adjusted risk ratio, aRR 0.78 and 0.88) than Delta (aRR 0.62 and 0.68). In non-household settings, a similar reduction was observed only in contacts who had three doses vs. two doses for both Delta (aRR 0.51) and Omicron (aRR 0.76). For national surveillance data, the risk of household clustering, was increased 3.5-fold for Omicron compared to Delta (aRR 3.54 (3.29–3.81)). Our study identified increased risk of onward transmission of Omicron, consistent with its successful global displacement of Delta. We identified a reduced effectiveness of vaccination in lowering risk of transmission, a likely contributor for the rapid propagation of Omicron.
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spelling pubmed-101258732023-04-25 Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England Allen, Hester Tessier, Elise Turner, Charlie Anderson, Charlotte Blomquist, Paula Simons, David Løchen, Alessandra Jarvis, Christopher I. Groves, Natalie Capelastegui, Fernando Flannagan, Joe Zaidi, Asad Chen, Cong Rawlinson, Christopher Hughes, Gareth J. Chudasama, Dimple Nash, Sophie Thelwall, Simon Lopez-Bernal, Jamie Dabrera, Gavin Charlett, André Kall, Meaghan Lamagni, Theresa Epidemiol Infect Original Paper The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) rapidly replaced Delta (B.1.617.2) to become dominant in England. Our study assessed differences in transmission between Omicron and Delta using two independent data sources and methods. Omicron and Delta cases were identified through genomic sequencing, genotyping and S-gene target failure in England from 5–11 December 2021. Secondary attack rates for named contacts were calculated in household and non-household settings using contact tracing data, while household clustering was identified using national surveillance data. Logistic regression models were applied to control for factors associated with transmission for both methods. For contact tracing data, higher secondary attack rates for Omicron vs. Delta were identified in households (15.0% vs. 10.8%) and non-households (8.2% vs. 3.7%). For both variants, in household settings, onward transmission was reduced from cases and named contacts who had three doses of vaccine compared to two, but this effect was less pronounced for Omicron (adjusted risk ratio, aRR 0.78 and 0.88) than Delta (aRR 0.62 and 0.68). In non-household settings, a similar reduction was observed only in contacts who had three doses vs. two doses for both Delta (aRR 0.51) and Omicron (aRR 0.76). For national surveillance data, the risk of household clustering, was increased 3.5-fold for Omicron compared to Delta (aRR 3.54 (3.29–3.81)). Our study identified increased risk of onward transmission of Omicron, consistent with its successful global displacement of Delta. We identified a reduced effectiveness of vaccination in lowering risk of transmission, a likely contributor for the rapid propagation of Omicron. Cambridge University Press 2023-03-20 /pmc/articles/PMC10125873/ /pubmed/36938806 http://dx.doi.org/10.1017/S0950268823000420 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Paper
Allen, Hester
Tessier, Elise
Turner, Charlie
Anderson, Charlotte
Blomquist, Paula
Simons, David
Løchen, Alessandra
Jarvis, Christopher I.
Groves, Natalie
Capelastegui, Fernando
Flannagan, Joe
Zaidi, Asad
Chen, Cong
Rawlinson, Christopher
Hughes, Gareth J.
Chudasama, Dimple
Nash, Sophie
Thelwall, Simon
Lopez-Bernal, Jamie
Dabrera, Gavin
Charlett, André
Kall, Meaghan
Lamagni, Theresa
Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England
title Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England
title_full Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England
title_fullStr Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England
title_full_unstemmed Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England
title_short Comparative transmission of SARS-CoV-2 Omicron (B.1.1.529) and Delta (B.1.617.2) variants and the impact of vaccination: national cohort study, England
title_sort comparative transmission of sars-cov-2 omicron (b.1.1.529) and delta (b.1.617.2) variants and the impact of vaccination: national cohort study, england
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10125873/
https://www.ncbi.nlm.nih.gov/pubmed/36938806
http://dx.doi.org/10.1017/S0950268823000420
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