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A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients
Since its first detection in December 2019, more than 232 million cases of COVID-19, including 4.7 million deaths, have been reported by the WHO. The SARS-CoV-2 viral genomes have evolved rapidly worldwide, causing the emergence of new variants. This systematic review and meta-analysis was conducted...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620851/ https://www.ncbi.nlm.nih.gov/pubmed/34833100 http://dx.doi.org/10.3390/life11111224 |
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author | Yusof, Wardah Irekeola, Ahmad Adebayo Wada, Yusuf Engku Abd Rahman, Engku Nur Syafirah Ahmed, Naveed Musa, Nurfadhlina Khalid, Muhammad Fazli Rahman, Zaidah Abdul Hassan, Rosline Yusof, Nik Yusnoraini Yean Yean, Chan |
author_facet | Yusof, Wardah Irekeola, Ahmad Adebayo Wada, Yusuf Engku Abd Rahman, Engku Nur Syafirah Ahmed, Naveed Musa, Nurfadhlina Khalid, Muhammad Fazli Rahman, Zaidah Abdul Hassan, Rosline Yusof, Nik Yusnoraini Yean Yean, Chan |
author_sort | Yusof, Wardah |
collection | PubMed |
description | Since its first detection in December 2019, more than 232 million cases of COVID-19, including 4.7 million deaths, have been reported by the WHO. The SARS-CoV-2 viral genomes have evolved rapidly worldwide, causing the emergence of new variants. This systematic review and meta-analysis was conducted to provide a global mutational profile of SARS-CoV-2 from December 2019 to October 2020. The review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA), and a study protocol was lodged with PROSPERO. Data from 62 eligible studies involving 368,316 SARS-CoV-2 genomes were analyzed. The mutational data analyzed showed most studies detected mutations in the Spike protein (n = 50), Nucleocapsid phosphoprotein (n = 34), ORF1ab gene (n = 29), 5′-UTR (n = 28) and ORF3a (n = 25). Under the random-effects model, pooled prevalence of SARS-CoV-2 variants was estimated at 95.1% (95% CI; 93.3–96.4%; I(2) = 98.952%; p = 0.000) while subgroup meta-analysis by country showed majority of the studies were conducted ‘Worldwide’ (n = 10), followed by ‘Multiple countries’ (n = 6) and the USA (n = 5). The estimated prevalence indicated a need to continuously monitor the prevalence of new mutations due to their potential influence on disease severity, transmissibility and vaccine effectiveness. |
format | Online Article Text |
id | pubmed-8620851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86208512021-11-27 A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients Yusof, Wardah Irekeola, Ahmad Adebayo Wada, Yusuf Engku Abd Rahman, Engku Nur Syafirah Ahmed, Naveed Musa, Nurfadhlina Khalid, Muhammad Fazli Rahman, Zaidah Abdul Hassan, Rosline Yusof, Nik Yusnoraini Yean Yean, Chan Life (Basel) Systematic Review Since its first detection in December 2019, more than 232 million cases of COVID-19, including 4.7 million deaths, have been reported by the WHO. The SARS-CoV-2 viral genomes have evolved rapidly worldwide, causing the emergence of new variants. This systematic review and meta-analysis was conducted to provide a global mutational profile of SARS-CoV-2 from December 2019 to October 2020. The review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA), and a study protocol was lodged with PROSPERO. Data from 62 eligible studies involving 368,316 SARS-CoV-2 genomes were analyzed. The mutational data analyzed showed most studies detected mutations in the Spike protein (n = 50), Nucleocapsid phosphoprotein (n = 34), ORF1ab gene (n = 29), 5′-UTR (n = 28) and ORF3a (n = 25). Under the random-effects model, pooled prevalence of SARS-CoV-2 variants was estimated at 95.1% (95% CI; 93.3–96.4%; I(2) = 98.952%; p = 0.000) while subgroup meta-analysis by country showed majority of the studies were conducted ‘Worldwide’ (n = 10), followed by ‘Multiple countries’ (n = 6) and the USA (n = 5). The estimated prevalence indicated a need to continuously monitor the prevalence of new mutations due to their potential influence on disease severity, transmissibility and vaccine effectiveness. MDPI 2021-11-11 /pmc/articles/PMC8620851/ /pubmed/34833100 http://dx.doi.org/10.3390/life11111224 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Systematic Review Yusof, Wardah Irekeola, Ahmad Adebayo Wada, Yusuf Engku Abd Rahman, Engku Nur Syafirah Ahmed, Naveed Musa, Nurfadhlina Khalid, Muhammad Fazli Rahman, Zaidah Abdul Hassan, Rosline Yusof, Nik Yusnoraini Yean Yean, Chan A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients |
title | A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients |
title_full | A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients |
title_fullStr | A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients |
title_full_unstemmed | A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients |
title_short | A Global Mutational Profile of SARS-CoV-2: A Systematic Review and Meta-Analysis of 368,316 COVID-19 Patients |
title_sort | global mutational profile of sars-cov-2: a systematic review and meta-analysis of 368,316 covid-19 patients |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620851/ https://www.ncbi.nlm.nih.gov/pubmed/34833100 http://dx.doi.org/10.3390/life11111224 |
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