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Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis

INTRODUCTION: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a novel coronavirus causing coronavirus disease 2019 (COVID-19), has been expanding globally since late 2019. SARS-CoV-2, an RNA virus, has a genome sequence that can easily undergo mutation. Several mutated SARS-CoV-2 strai...

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Autores principales: Aoki, Akira, Mori, Yoko, Okamoto, Yoshinori, Jinno, Hideto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196315/
https://www.ncbi.nlm.nih.gov/pubmed/34154921
http://dx.doi.org/10.1016/j.jiac.2021.06.007
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author Aoki, Akira
Mori, Yoko
Okamoto, Yoshinori
Jinno, Hideto
author_facet Aoki, Akira
Mori, Yoko
Okamoto, Yoshinori
Jinno, Hideto
author_sort Aoki, Akira
collection PubMed
description INTRODUCTION: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a novel coronavirus causing coronavirus disease 2019 (COVID-19), has been expanding globally since late 2019. SARS-CoV-2, an RNA virus, has a genome sequence that can easily undergo mutation. Several mutated SARS-CoV-2 strains, including those with higher infectivity than others, have been reported. To reduce SARS-CoV-2 transmission, it is crucial to trace its infection sources. Here, we developed a simple, easy-to-use genotyping method to identify SARS-CoV-2 variants using a high-resolution melting (HRM) analysis. METHODS: We investigated five mutation sites, A23403G, G25563T, G26144T, T28144C, and G28882A, which are known strain determinants according to GISAID clades (L, S, V, G, GH, and GR). RESULTS: We first employed synthetic DNA fragments containing the five characteristic sites for HRM analysis. All sequences clearly differentiated wild-type from mutant viruses. We then confirmed that RNA fragments were suitable for HRM analysis following reverse transcription. Human saliva did not negatively affect the HRM analysis, which supports the absence of a matrix effect. CONCLUSIONS: Our results indicate that this HRM-based genotyping method can identify SARS-CoV-2 variants. This novel assay platform potentially paves the way for accurate and rapid identification of SARS-CoV-2 infection sources.
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spelling pubmed-81963152021-06-15 Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis Aoki, Akira Mori, Yoko Okamoto, Yoshinori Jinno, Hideto J Infect Chemother Original Article INTRODUCTION: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a novel coronavirus causing coronavirus disease 2019 (COVID-19), has been expanding globally since late 2019. SARS-CoV-2, an RNA virus, has a genome sequence that can easily undergo mutation. Several mutated SARS-CoV-2 strains, including those with higher infectivity than others, have been reported. To reduce SARS-CoV-2 transmission, it is crucial to trace its infection sources. Here, we developed a simple, easy-to-use genotyping method to identify SARS-CoV-2 variants using a high-resolution melting (HRM) analysis. METHODS: We investigated five mutation sites, A23403G, G25563T, G26144T, T28144C, and G28882A, which are known strain determinants according to GISAID clades (L, S, V, G, GH, and GR). RESULTS: We first employed synthetic DNA fragments containing the five characteristic sites for HRM analysis. All sequences clearly differentiated wild-type from mutant viruses. We then confirmed that RNA fragments were suitable for HRM analysis following reverse transcription. Human saliva did not negatively affect the HRM analysis, which supports the absence of a matrix effect. CONCLUSIONS: Our results indicate that this HRM-based genotyping method can identify SARS-CoV-2 variants. This novel assay platform potentially paves the way for accurate and rapid identification of SARS-CoV-2 infection sources. Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. 2021-09 2021-06-12 /pmc/articles/PMC8196315/ /pubmed/34154921 http://dx.doi.org/10.1016/j.jiac.2021.06.007 Text en © 2021 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. 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 Original Article
Aoki, Akira
Mori, Yoko
Okamoto, Yoshinori
Jinno, Hideto
Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis
title Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis
title_full Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis
title_fullStr Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis
title_full_unstemmed Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis
title_short Development of a genotyping platform for SARS-CoV-2 variants using high-resolution melting analysis
title_sort development of a genotyping platform for sars-cov-2 variants using high-resolution melting analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196315/
https://www.ncbi.nlm.nih.gov/pubmed/34154921
http://dx.doi.org/10.1016/j.jiac.2021.06.007
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