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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8669007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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