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Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis
Coronavirus disease 2019 (COVID‐19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), has recently posed a significant threat to global public health. The objective of this study was to develop and evaluate a rapid, expandable and sequencing‐free high‐resolution melti...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9111094/ https://www.ncbi.nlm.nih.gov/pubmed/35233932 http://dx.doi.org/10.1111/1751-7915.14027 |
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author | Sun, Liying Xiu, Leshan Zhang, Chi Xiao, Yan Li, Yamei Zhang, Lulu Ren, Lili Peng, Junping |
author_facet | Sun, Liying Xiu, Leshan Zhang, Chi Xiao, Yan Li, Yamei Zhang, Lulu Ren, Lili Peng, Junping |
author_sort | Sun, Liying |
collection | PubMed |
description | Coronavirus disease 2019 (COVID‐19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), has recently posed a significant threat to global public health. The objective of this study was to develop and evaluate a rapid, expandable and sequencing‐free high‐resolution melting (HRM) approach for the direct detection and classification of SARS‐CoV‐2. Thirty‐one common pathogens that can cause respiratory tract infections were used to evaluate the specificity of the method. Synthetic RNA with serial dilutions was utilized to determine the sensitivity of the method. Finally, the clinical performance of the method was assessed using 290 clinical samples. The one‐step multiplex HRM could accurately identify SARS‐CoV‐2 and differentiate mutations in each marker site within approximately 2 h. For each target, the limit of detection was lower than 10 copies/reaction, and no cross‐reactivity was observed among organisms within the specificity testing panel. The method showed good uniformity for SARS‐CoV‐2 detection with a consistency of 100%. Regarding the clade classification performance, the results showed good concordance compared with sequencing, with the rate of agreement being 95.1% (78/82). The one‐step multiplex HRM method is a rapid method for SARS‐CoV‐2 detection and classification. |
format | Online Article Text |
id | pubmed-9111094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91110942022-05-17 Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis Sun, Liying Xiu, Leshan Zhang, Chi Xiao, Yan Li, Yamei Zhang, Lulu Ren, Lili Peng, Junping Microb Biotechnol Research Articles Coronavirus disease 2019 (COVID‐19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), has recently posed a significant threat to global public health. The objective of this study was to develop and evaluate a rapid, expandable and sequencing‐free high‐resolution melting (HRM) approach for the direct detection and classification of SARS‐CoV‐2. Thirty‐one common pathogens that can cause respiratory tract infections were used to evaluate the specificity of the method. Synthetic RNA with serial dilutions was utilized to determine the sensitivity of the method. Finally, the clinical performance of the method was assessed using 290 clinical samples. The one‐step multiplex HRM could accurately identify SARS‐CoV‐2 and differentiate mutations in each marker site within approximately 2 h. For each target, the limit of detection was lower than 10 copies/reaction, and no cross‐reactivity was observed among organisms within the specificity testing panel. The method showed good uniformity for SARS‐CoV‐2 detection with a consistency of 100%. Regarding the clade classification performance, the results showed good concordance compared with sequencing, with the rate of agreement being 95.1% (78/82). The one‐step multiplex HRM method is a rapid method for SARS‐CoV‐2 detection and classification. John Wiley and Sons Inc. 2022-03-01 /pmc/articles/PMC9111094/ /pubmed/35233932 http://dx.doi.org/10.1111/1751-7915.14027 Text en © 2022 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Sun, Liying Xiu, Leshan Zhang, Chi Xiao, Yan Li, Yamei Zhang, Lulu Ren, Lili Peng, Junping Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis |
title | Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis |
title_full | Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis |
title_fullStr | Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis |
title_full_unstemmed | Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis |
title_short | Detection and classification of SARS‐CoV‐2 using high‐resolution melting analysis |
title_sort | detection and classification of sars‐cov‐2 using high‐resolution melting analysis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9111094/ https://www.ncbi.nlm.nih.gov/pubmed/35233932 http://dx.doi.org/10.1111/1751-7915.14027 |
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