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A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants
The N501Y mutation in SARS-CoV-2 variants found in several strains from the UK, South Africa and Brazil has been linked to increased transmission. In order to discriminate N501Y variants quickly, a single nucleotide polymorphism (SNP) discrimination assay was designed and validated. It was then depl...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7989071/ https://www.ncbi.nlm.nih.gov/pubmed/33774075 http://dx.doi.org/10.1016/j.jviromet.2021.114143 |
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author | Sandoval Torrientes, M. Castelló Abietar, C. Boga Riveiro, J. Álvarez-Argüelles, M.E. Rojo-Alba, S. Abreu Salinas, F. Costales González, I. Pérez Martínez, Z. Martín Rodríguez, G. Gómez de Oña, J. Coto García, E. Melón García, S. |
author_facet | Sandoval Torrientes, M. Castelló Abietar, C. Boga Riveiro, J. Álvarez-Argüelles, M.E. Rojo-Alba, S. Abreu Salinas, F. Costales González, I. Pérez Martínez, Z. Martín Rodríguez, G. Gómez de Oña, J. Coto García, E. Melón García, S. |
author_sort | Sandoval Torrientes, M. |
collection | PubMed |
description | The N501Y mutation in SARS-CoV-2 variants found in several strains from the UK, South Africa and Brazil has been linked to increased transmission. In order to discriminate N501Y variants quickly, a single nucleotide polymorphism (SNP) discrimination assay was designed and validated. It was then deployed prospectively in 757 nasopharyngeal swabs. Validation of the novel variant discrimination assay corroborated the results in all validation panel samples (n = 63) through sequencing. This novel variant discrimination assay was then deployed prospectively in 757 clinical nasopharyngeal swabs during the last week of January 2021. N501Y was found in 206 (27.4 %) of the samples: 94 (28.2 %) men and 112 (26.85 %) women (p = 0.73). The patients in whom it was identified had a mean age of 47.8 ± 25.8 (0–96) years, similar to that of patients without this variant: 51.7 ± 25.9 (0–104) years (p = 0.06). 501Y variant was confirmed in 34 samples by sequence method and 501 N wild type was confirmed in 67. This method is sensitive, specific, and simple to apply in any microbiology lab. |
format | Online Article Text |
id | pubmed-7989071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79890712021-03-25 A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants Sandoval Torrientes, M. Castelló Abietar, C. Boga Riveiro, J. Álvarez-Argüelles, M.E. Rojo-Alba, S. Abreu Salinas, F. Costales González, I. Pérez Martínez, Z. Martín Rodríguez, G. Gómez de Oña, J. Coto García, E. Melón García, S. J Virol Methods Article The N501Y mutation in SARS-CoV-2 variants found in several strains from the UK, South Africa and Brazil has been linked to increased transmission. In order to discriminate N501Y variants quickly, a single nucleotide polymorphism (SNP) discrimination assay was designed and validated. It was then deployed prospectively in 757 nasopharyngeal swabs. Validation of the novel variant discrimination assay corroborated the results in all validation panel samples (n = 63) through sequencing. This novel variant discrimination assay was then deployed prospectively in 757 clinical nasopharyngeal swabs during the last week of January 2021. N501Y was found in 206 (27.4 %) of the samples: 94 (28.2 %) men and 112 (26.85 %) women (p = 0.73). The patients in whom it was identified had a mean age of 47.8 ± 25.8 (0–96) years, similar to that of patients without this variant: 51.7 ± 25.9 (0–104) years (p = 0.06). 501Y variant was confirmed in 34 samples by sequence method and 501 N wild type was confirmed in 67. This method is sensitive, specific, and simple to apply in any microbiology lab. Elsevier B.V. 2021-08 2021-03-24 /pmc/articles/PMC7989071/ /pubmed/33774075 http://dx.doi.org/10.1016/j.jviromet.2021.114143 Text en © 2021 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Sandoval Torrientes, M. Castelló Abietar, C. Boga Riveiro, J. Álvarez-Argüelles, M.E. Rojo-Alba, S. Abreu Salinas, F. Costales González, I. Pérez Martínez, Z. Martín Rodríguez, G. Gómez de Oña, J. Coto García, E. Melón García, S. A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants |
title | A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants |
title_full | A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants |
title_fullStr | A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants |
title_full_unstemmed | A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants |
title_short | A novel single nucleotide polymorphism assay for the detection of N501Y SARS-CoV-2 variants |
title_sort | novel single nucleotide polymorphism assay for the detection of n501y sars-cov-2 variants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7989071/ https://www.ncbi.nlm.nih.gov/pubmed/33774075 http://dx.doi.org/10.1016/j.jviromet.2021.114143 |
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