Cargando…
Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis
The genome of the SARS-CoV-2 virus, the causal agent of the COVID-19 pandemic, has diverged due to multiple mutations since its emergence as a human pathogen in December 2019. Some mutations have defined several SARS-CoV-2 clades that seem to behave differently in terms of regional distribution and...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067340/ https://www.ncbi.nlm.nih.gov/pubmed/33916492 http://dx.doi.org/10.3390/genes12040531 |
_version_ | 1783682780176056320 |
---|---|
author | Diaz-Garcia, Hector Guzmán-Ortiz, Ana L. Angeles-Floriano, Tania Parra-Ortega, Israel López-Martínez, Briceida Martínez-Saucedo, Mirna Aquino-Jarquin, Guillermo Sánchez-Urbina, Rocío Quezada, Hector Granados-Riveron, Javier T. |
author_facet | Diaz-Garcia, Hector Guzmán-Ortiz, Ana L. Angeles-Floriano, Tania Parra-Ortega, Israel López-Martínez, Briceida Martínez-Saucedo, Mirna Aquino-Jarquin, Guillermo Sánchez-Urbina, Rocío Quezada, Hector Granados-Riveron, Javier T. |
author_sort | Diaz-Garcia, Hector |
collection | PubMed |
description | The genome of the SARS-CoV-2 virus, the causal agent of the COVID-19 pandemic, has diverged due to multiple mutations since its emergence as a human pathogen in December 2019. Some mutations have defined several SARS-CoV-2 clades that seem to behave differently in terms of regional distribution and other biological features. Next-generation sequencing (NGS) approaches are used to classify the sequence variants in viruses from individual human patients. However, the cost and relative scarcity of NGS equipment and expertise in developing countries prevent studies aimed to associate specific clades and variants to clinical features and outcomes in such territories. As of March 2021, the GR clade and its derivatives, including the B.1.1.7 and B.1.1.28 variants, predominate worldwide. We implemented the post-PCR small-amplicon high-resolution melting analysis to genotype SARS-CoV-2 viruses isolated from the saliva of individual patients. This procedure was able to clearly distinguish two groups of samples of SARS-CoV-2-positive samples predicted, according to their melting profiles, to contain GR and non-GR viruses. This grouping of the samples was validated by means of amplification-refractory mutation system (ARMS) assay as well as Sanger sequencing. |
format | Online Article Text |
id | pubmed-8067340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80673402021-04-25 Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis Diaz-Garcia, Hector Guzmán-Ortiz, Ana L. Angeles-Floriano, Tania Parra-Ortega, Israel López-Martínez, Briceida Martínez-Saucedo, Mirna Aquino-Jarquin, Guillermo Sánchez-Urbina, Rocío Quezada, Hector Granados-Riveron, Javier T. Genes (Basel) Article The genome of the SARS-CoV-2 virus, the causal agent of the COVID-19 pandemic, has diverged due to multiple mutations since its emergence as a human pathogen in December 2019. Some mutations have defined several SARS-CoV-2 clades that seem to behave differently in terms of regional distribution and other biological features. Next-generation sequencing (NGS) approaches are used to classify the sequence variants in viruses from individual human patients. However, the cost and relative scarcity of NGS equipment and expertise in developing countries prevent studies aimed to associate specific clades and variants to clinical features and outcomes in such territories. As of March 2021, the GR clade and its derivatives, including the B.1.1.7 and B.1.1.28 variants, predominate worldwide. We implemented the post-PCR small-amplicon high-resolution melting analysis to genotype SARS-CoV-2 viruses isolated from the saliva of individual patients. This procedure was able to clearly distinguish two groups of samples of SARS-CoV-2-positive samples predicted, according to their melting profiles, to contain GR and non-GR viruses. This grouping of the samples was validated by means of amplification-refractory mutation system (ARMS) assay as well as Sanger sequencing. MDPI 2021-04-05 /pmc/articles/PMC8067340/ /pubmed/33916492 http://dx.doi.org/10.3390/genes12040531 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 | Article Diaz-Garcia, Hector Guzmán-Ortiz, Ana L. Angeles-Floriano, Tania Parra-Ortega, Israel López-Martínez, Briceida Martínez-Saucedo, Mirna Aquino-Jarquin, Guillermo Sánchez-Urbina, Rocío Quezada, Hector Granados-Riveron, Javier T. Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis |
title | Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis |
title_full | Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis |
title_fullStr | Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis |
title_full_unstemmed | Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis |
title_short | Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis |
title_sort | genotyping of the major sars-cov-2 clade by short-amplicon high-resolution melting (sa-hrm) analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067340/ https://www.ncbi.nlm.nih.gov/pubmed/33916492 http://dx.doi.org/10.3390/genes12040531 |
work_keys_str_mv | AT diazgarciahector genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT guzmanortizanal genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT angelesflorianotania genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT parraortegaisrael genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT lopezmartinezbriceida genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT martinezsaucedomirna genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT aquinojarquinguillermo genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT sanchezurbinarocio genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT quezadahector genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis AT granadosriveronjaviert genotypingofthemajorsarscov2cladebyshortampliconhighresolutionmeltingsahrmanalysis |