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Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020
INTRODUCTION: The SARS-CoV-2 lineages carrying the amino acid change D614G have become the dominant variants in the global COVID-19 pandemic. By June 2021, all the emerging variants of concern carried the D614G mutation. The rapid spread of the G614 mutant suggests that it may have a transmission ad...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Centre for Disease Prevention and Control (ECDC)
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662801/ https://www.ncbi.nlm.nih.gov/pubmed/34886945 http://dx.doi.org/10.2807/1560-7917.ES.2021.26.49.2002005 |
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author | Leung, Kathy Pei, Yao Leung, Gabriel M Lam, Tommy TY Wu, Joseph T |
author_facet | Leung, Kathy Pei, Yao Leung, Gabriel M Lam, Tommy TY Wu, Joseph T |
author_sort | Leung, Kathy |
collection | PubMed |
description | INTRODUCTION: The SARS-CoV-2 lineages carrying the amino acid change D614G have become the dominant variants in the global COVID-19 pandemic. By June 2021, all the emerging variants of concern carried the D614G mutation. The rapid spread of the G614 mutant suggests that it may have a transmission advantage over the D614 wildtype. AIM: Our objective was to estimate the transmission advantage of D614G by integrating phylogenetic and epidemiological analysis. METHODS: We assume that the mutation D614G was the only site of interest which characterised the two cocirculating virus strains by June 2020, but their differential transmissibility might be attributable to a combination of D614G and other mutations. We define the fitness of G614 as the ratio of the basic reproduction number of the strain with G614 to the strain with D614 and applied an epidemiological framework for fitness inference to analyse SARS-CoV-2 surveillance and sequence data. RESULTS: Using this framework, we estimated that the G614 mutant is 31% (95% credible interval: 28–34) more transmissible than the D614 wildtype. Therefore, interventions that were previously effective in containing or mitigating the D614 wildtype (e.g. in China, Vietnam and Thailand) may be less effective against the G614 mutant. CONCLUSION: Our framework can be readily integrated into current SARS-CoV-2 surveillance to monitor the emergence and fitness of mutant strains such that pandemic surveillance, disease control and development of treatment and vaccines can be adjusted dynamically. |
format | Online Article Text |
id | pubmed-8662801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | European Centre for Disease Prevention and Control (ECDC) |
record_format | MEDLINE/PubMed |
spelling | pubmed-86628012022-01-05 Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020 Leung, Kathy Pei, Yao Leung, Gabriel M Lam, Tommy TY Wu, Joseph T Euro Surveill Research INTRODUCTION: The SARS-CoV-2 lineages carrying the amino acid change D614G have become the dominant variants in the global COVID-19 pandemic. By June 2021, all the emerging variants of concern carried the D614G mutation. The rapid spread of the G614 mutant suggests that it may have a transmission advantage over the D614 wildtype. AIM: Our objective was to estimate the transmission advantage of D614G by integrating phylogenetic and epidemiological analysis. METHODS: We assume that the mutation D614G was the only site of interest which characterised the two cocirculating virus strains by June 2020, but their differential transmissibility might be attributable to a combination of D614G and other mutations. We define the fitness of G614 as the ratio of the basic reproduction number of the strain with G614 to the strain with D614 and applied an epidemiological framework for fitness inference to analyse SARS-CoV-2 surveillance and sequence data. RESULTS: Using this framework, we estimated that the G614 mutant is 31% (95% credible interval: 28–34) more transmissible than the D614 wildtype. Therefore, interventions that were previously effective in containing or mitigating the D614 wildtype (e.g. in China, Vietnam and Thailand) may be less effective against the G614 mutant. CONCLUSION: Our framework can be readily integrated into current SARS-CoV-2 surveillance to monitor the emergence and fitness of mutant strains such that pandemic surveillance, disease control and development of treatment and vaccines can be adjusted dynamically. European Centre for Disease Prevention and Control (ECDC) 2021-12-09 /pmc/articles/PMC8662801/ /pubmed/34886945 http://dx.doi.org/10.2807/1560-7917.ES.2021.26.49.2002005 Text en This article is copyright of the authors or their affiliated institutions, 2021. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) Licence. You may share and adapt the material, but must give appropriate credit to the source, provide a link to the licence, and indicate if changes were made. |
spellingShingle | Research Leung, Kathy Pei, Yao Leung, Gabriel M Lam, Tommy TY Wu, Joseph T Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020 |
title | Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020 |
title_full | Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020 |
title_fullStr | Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020 |
title_full_unstemmed | Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020 |
title_short | Estimating the transmission advantage of the D614G mutant strain of SARS-CoV-2, December 2019 to June 2020 |
title_sort | estimating the transmission advantage of the d614g mutant strain of sars-cov-2, december 2019 to june 2020 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662801/ https://www.ncbi.nlm.nih.gov/pubmed/34886945 http://dx.doi.org/10.2807/1560-7917.ES.2021.26.49.2002005 |
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