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Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load

New lineages of SARS-CoV-2 are of potential concern due to higher transmissibility, risk of severe outcomes, and/or escape from neutralizing antibodies. Lineage B.1.1.7 (the Alpha variant) became dominant in early 2021, but the association between transmissibility and risk factors, such as age of pr...

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Autores principales: Lyngse, Frederik Plesner, Mølbak, Kåre, Skov, Robert Leo, Christiansen, Lasse Engbo, Mortensen, Laust Hvas, Albertsen, Mads, Møller, Camilla Holten, Krause, Tyra Grove, Rasmussen, Morten, Michaelsen, Thomas Yssing, Voldstedlund, Marianne, Fonager, Jannik, Steenhard, Nina, Kirkeby, Carsten Thure
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8669007/
https://www.ncbi.nlm.nih.gov/pubmed/34903718
http://dx.doi.org/10.1038/s41467-021-27202-x
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author Lyngse, Frederik Plesner
Mølbak, Kåre
Skov, Robert Leo
Christiansen, Lasse Engbo
Mortensen, Laust Hvas
Albertsen, Mads
Møller, Camilla Holten
Krause, Tyra Grove
Rasmussen, Morten
Michaelsen, Thomas Yssing
Voldstedlund, Marianne
Fonager, Jannik
Steenhard, Nina
Kirkeby, Carsten Thure
author_facet Lyngse, Frederik Plesner
Mølbak, Kåre
Skov, Robert Leo
Christiansen, Lasse Engbo
Mortensen, Laust Hvas
Albertsen, Mads
Møller, Camilla Holten
Krause, Tyra Grove
Rasmussen, Morten
Michaelsen, Thomas Yssing
Voldstedlund, Marianne
Fonager, Jannik
Steenhard, Nina
Kirkeby, Carsten Thure
author_sort Lyngse, Frederik Plesner
collection PubMed
description New lineages of SARS-CoV-2 are of potential concern due to higher transmissibility, risk of severe outcomes, and/or escape from neutralizing antibodies. Lineage B.1.1.7 (the Alpha variant) became dominant in early 2021, but the association between transmissibility and risk factors, such as age of primary case and viral load remains poorly understood. Here, we used comprehensive administrative data from Denmark, comprising the full population (January 11 to February 7, 2021), to estimate household transmissibility. This study included 5,241 households with primary cases; 808 were infected with lineage B.1.1.7 and 4,433 with other lineages. Here, we report an attack rate of 38% in households with a primary case infected with B.1.1.7 and 27% in households with other lineages. Primary cases infected with B.1.1.7 had an increased transmissibility of 1.5–1.7 times that of primary cases infected with other lineages. The increased transmissibility of B.1.1.7 was multiplicative across age and viral load.
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spelling pubmed-86690072022-01-04 Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load Lyngse, Frederik Plesner Mølbak, Kåre Skov, Robert Leo Christiansen, Lasse Engbo Mortensen, Laust Hvas Albertsen, Mads Møller, Camilla Holten Krause, Tyra Grove Rasmussen, Morten Michaelsen, Thomas Yssing Voldstedlund, Marianne Fonager, Jannik Steenhard, Nina Kirkeby, Carsten Thure Nat Commun Article New lineages of SARS-CoV-2 are of potential concern due to higher transmissibility, risk of severe outcomes, and/or escape from neutralizing antibodies. Lineage B.1.1.7 (the Alpha variant) became dominant in early 2021, but the association between transmissibility and risk factors, such as age of primary case and viral load remains poorly understood. Here, we used comprehensive administrative data from Denmark, comprising the full population (January 11 to February 7, 2021), to estimate household transmissibility. This study included 5,241 households with primary cases; 808 were infected with lineage B.1.1.7 and 4,433 with other lineages. Here, we report an attack rate of 38% in households with a primary case infected with B.1.1.7 and 27% in households with other lineages. Primary cases infected with B.1.1.7 had an increased transmissibility of 1.5–1.7 times that of primary cases infected with other lineages. The increased transmissibility of B.1.1.7 was multiplicative across age and viral load. Nature Publishing Group UK 2021-12-13 /pmc/articles/PMC8669007/ /pubmed/34903718 http://dx.doi.org/10.1038/s41467-021-27202-x Text en © The Author(s) 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 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
Lyngse, Frederik Plesner
Mølbak, Kåre
Skov, Robert Leo
Christiansen, Lasse Engbo
Mortensen, Laust Hvas
Albertsen, Mads
Møller, Camilla Holten
Krause, Tyra Grove
Rasmussen, Morten
Michaelsen, Thomas Yssing
Voldstedlund, Marianne
Fonager, Jannik
Steenhard, Nina
Kirkeby, Carsten Thure
Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load
title Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load
title_full Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load
title_fullStr Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load
title_full_unstemmed Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load
title_short Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load
title_sort increased transmissibility of sars-cov-2 lineage b.1.1.7 by age and viral load
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8669007/
https://www.ncbi.nlm.nih.gov/pubmed/34903718
http://dx.doi.org/10.1038/s41467-021-27202-x
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