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Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal
We used whole genome sequencing to identify and analyze mutations in SARS-CoV-2 in urban settings during the deadliest wave of the COVID-19 epidemic—from March to April 2021—in Senegal. Nasopharyngeal samples testing positive for SARS-CoV-2 were sequenced on the Illumina NovaSeq 6000 sequencing syst...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302768/ https://www.ncbi.nlm.nih.gov/pubmed/37376533 http://dx.doi.org/10.3390/v15061233 |
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author | Ndiaye, Anna Julienne Selbé Beye, Mamadou Lo, Gora Kacel, Idir Sow, Aissatou Leye, Nafissatou Padane, Abdou Mboup, Aminata Diop-Ndiaye, Halimatou Sokhna, Cheikh Kane, Coumba Touré Colson, Philippe Fenollar, Florence Mboup, Souleymane Fournier, Pierre-Edouard |
author_facet | Ndiaye, Anna Julienne Selbé Beye, Mamadou Lo, Gora Kacel, Idir Sow, Aissatou Leye, Nafissatou Padane, Abdou Mboup, Aminata Diop-Ndiaye, Halimatou Sokhna, Cheikh Kane, Coumba Touré Colson, Philippe Fenollar, Florence Mboup, Souleymane Fournier, Pierre-Edouard |
author_sort | Ndiaye, Anna Julienne Selbé |
collection | PubMed |
description | We used whole genome sequencing to identify and analyze mutations in SARS-CoV-2 in urban settings during the deadliest wave of the COVID-19 epidemic—from March to April 2021—in Senegal. Nasopharyngeal samples testing positive for SARS-CoV-2 were sequenced on the Illumina NovaSeq 6000 sequencing system using the COVIDSeq protocol. A total of 291 genotypable consensus genome sequences were obtained. Phylogenetic analyses grouped the genomes into 16 distinct PANGOLIN lineages. The major lineage was B.1.1.420, despite circulation of the Alpha variant of concern (VOC). A total of 1125 different SNPs, identified relative to the Wuhan reference genome, were detected. These included 13 SNPs in non-coding regions. An average density of 37.2 SNPs per 1000 nucleotides was found, with the highest density occurring in ORF10. This analysis allowed, for the first time, the detection of a Senegalese SARS-CoV-2 strain belonging to the P.1.14 (GR/20J, Gamma V3) sublineage of the Brazilian P.1 lineage (or Gamma VOC). Overall, our results highlight substantial SARS-CoV-2 diversification in Senegal during the study period. |
format | Online Article Text |
id | pubmed-10302768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103027682023-06-29 Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal Ndiaye, Anna Julienne Selbé Beye, Mamadou Lo, Gora Kacel, Idir Sow, Aissatou Leye, Nafissatou Padane, Abdou Mboup, Aminata Diop-Ndiaye, Halimatou Sokhna, Cheikh Kane, Coumba Touré Colson, Philippe Fenollar, Florence Mboup, Souleymane Fournier, Pierre-Edouard Viruses Article We used whole genome sequencing to identify and analyze mutations in SARS-CoV-2 in urban settings during the deadliest wave of the COVID-19 epidemic—from March to April 2021—in Senegal. Nasopharyngeal samples testing positive for SARS-CoV-2 were sequenced on the Illumina NovaSeq 6000 sequencing system using the COVIDSeq protocol. A total of 291 genotypable consensus genome sequences were obtained. Phylogenetic analyses grouped the genomes into 16 distinct PANGOLIN lineages. The major lineage was B.1.1.420, despite circulation of the Alpha variant of concern (VOC). A total of 1125 different SNPs, identified relative to the Wuhan reference genome, were detected. These included 13 SNPs in non-coding regions. An average density of 37.2 SNPs per 1000 nucleotides was found, with the highest density occurring in ORF10. This analysis allowed, for the first time, the detection of a Senegalese SARS-CoV-2 strain belonging to the P.1.14 (GR/20J, Gamma V3) sublineage of the Brazilian P.1 lineage (or Gamma VOC). Overall, our results highlight substantial SARS-CoV-2 diversification in Senegal during the study period. MDPI 2023-05-24 /pmc/articles/PMC10302768/ /pubmed/37376533 http://dx.doi.org/10.3390/v15061233 Text en © 2023 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 | Article Ndiaye, Anna Julienne Selbé Beye, Mamadou Lo, Gora Kacel, Idir Sow, Aissatou Leye, Nafissatou Padane, Abdou Mboup, Aminata Diop-Ndiaye, Halimatou Sokhna, Cheikh Kane, Coumba Touré Colson, Philippe Fenollar, Florence Mboup, Souleymane Fournier, Pierre-Edouard Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal |
title | Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal |
title_full | Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal |
title_fullStr | Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal |
title_full_unstemmed | Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal |
title_short | Genomic Epidemiology of SARS-CoV-2 in Urban Settings in Senegal |
title_sort | genomic epidemiology of sars-cov-2 in urban settings in senegal |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10302768/ https://www.ncbi.nlm.nih.gov/pubmed/37376533 http://dx.doi.org/10.3390/v15061233 |
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