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A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants
Molecular surveillance of the new coronavirus through new genomic sequencing technologies revealed the circulation of important variants of SARS-CoV-2. Sanger sequencing has been useful in identifying important variants of SARS-CoV-2 without the need for whole-genome sequencing. A sequencing protoco...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689870/ https://www.ncbi.nlm.nih.gov/pubmed/36359452 http://dx.doi.org/10.3390/diagnostics12112609 |
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author | Deminco, Felice Vaz, Sara N. Santana, Daniele S. Pedroso, Celia Tadeu, Jean Stoecker, Andreas Vieira, Sueli M. Netto, Eduardo Brites, Carlos |
author_facet | Deminco, Felice Vaz, Sara N. Santana, Daniele S. Pedroso, Celia Tadeu, Jean Stoecker, Andreas Vieira, Sueli M. Netto, Eduardo Brites, Carlos |
author_sort | Deminco, Felice |
collection | PubMed |
description | Molecular surveillance of the new coronavirus through new genomic sequencing technologies revealed the circulation of important variants of SARS-CoV-2. Sanger sequencing has been useful in identifying important variants of SARS-CoV-2 without the need for whole-genome sequencing. A sequencing protocol was constructed to cover a region of 1000 base pairs, from a 1120 bp product generated after a two-step RT-PCR assay in samples positive for SARS-CoV-2. Consensus sequence construction and mutation identification were performed. Of all 103 samples sequenced, 69 contained relevant variants represented by 20 BA.1, 13 delta, 22 gamma, and 14 zeta, identified between June 2020 and February 2022. All sequences found were aligned with representative sequences of the variants. Using the Sanger sequencing methodology, we were able to develop a more accessible protocol to assist viral surveillance with a more accessible platform. |
format | Online Article Text |
id | pubmed-9689870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96898702022-11-25 A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants Deminco, Felice Vaz, Sara N. Santana, Daniele S. Pedroso, Celia Tadeu, Jean Stoecker, Andreas Vieira, Sueli M. Netto, Eduardo Brites, Carlos Diagnostics (Basel) Article Molecular surveillance of the new coronavirus through new genomic sequencing technologies revealed the circulation of important variants of SARS-CoV-2. Sanger sequencing has been useful in identifying important variants of SARS-CoV-2 without the need for whole-genome sequencing. A sequencing protocol was constructed to cover a region of 1000 base pairs, from a 1120 bp product generated after a two-step RT-PCR assay in samples positive for SARS-CoV-2. Consensus sequence construction and mutation identification were performed. Of all 103 samples sequenced, 69 contained relevant variants represented by 20 BA.1, 13 delta, 22 gamma, and 14 zeta, identified between June 2020 and February 2022. All sequences found were aligned with representative sequences of the variants. Using the Sanger sequencing methodology, we were able to develop a more accessible protocol to assist viral surveillance with a more accessible platform. MDPI 2022-10-27 /pmc/articles/PMC9689870/ /pubmed/36359452 http://dx.doi.org/10.3390/diagnostics12112609 Text en © 2022 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 Deminco, Felice Vaz, Sara N. Santana, Daniele S. Pedroso, Celia Tadeu, Jean Stoecker, Andreas Vieira, Sueli M. Netto, Eduardo Brites, Carlos A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants |
title | A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants |
title_full | A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants |
title_fullStr | A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants |
title_full_unstemmed | A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants |
title_short | A Simplified Sanger Sequencing Method for Detection of Relevant SARS-CoV-2 Variants |
title_sort | simplified sanger sequencing method for detection of relevant sars-cov-2 variants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689870/ https://www.ncbi.nlm.nih.gov/pubmed/36359452 http://dx.doi.org/10.3390/diagnostics12112609 |
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