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Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2
The COVID-19 pandemic has spread worldwide, and rapid detection of the SARS-CoV-2 virus is crucial for infection surveillance and epidemic control. This study developed a centrifugal microfluidics-based multiplex reverse transcription recombinase polymerase amplification (RT-RPA) assay for endpoint...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941069/ https://www.ncbi.nlm.nih.gov/pubmed/36845031 http://dx.doi.org/10.1016/j.isci.2023.106245 |
_version_ | 1784891205135368192 |
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author | Li, Ruoxu Su, Ning Ren, Xiaodong Sun, Xiange Li, Wenman Li, Yuwei Li, Jin Chen, Chen Wang, Hong Lu, Weiping Deng, Shaoli Huang, Qing |
author_facet | Li, Ruoxu Su, Ning Ren, Xiaodong Sun, Xiange Li, Wenman Li, Yuwei Li, Jin Chen, Chen Wang, Hong Lu, Weiping Deng, Shaoli Huang, Qing |
author_sort | Li, Ruoxu |
collection | PubMed |
description | The COVID-19 pandemic has spread worldwide, and rapid detection of the SARS-CoV-2 virus is crucial for infection surveillance and epidemic control. This study developed a centrifugal microfluidics-based multiplex reverse transcription recombinase polymerase amplification (RT-RPA) assay for endpoint fluorescence detection of the E, N, and ORF1ab genes of SARS-CoV-2. The microscope slide-shaped microfluidic chip could simultaneously accomplish three target genes and one reference human gene (i.e., ACTB) RT-RPA reactions in 30 min, and the sensitivity was 40 RNA copies/reaction for the E gene, 20 RNA copies/reaction for the N gene, and 10 RNA copies/reaction for the ORF1ab gene. The chip demonstrated high specificity, reproducibility, and repeatability. Chip performance was also evaluated using real clinical samples. Thus, this rapid, accurate, on-site, and multiplexed nucleic acid test microfluidic chip would significantly contribute to detecting patients with COVID-19 in low-resource settings and point-of-care testing (POCT) and, in the future, could be used to detect emerging new variants of SARS-CoV-2. |
format | Online Article Text |
id | pubmed-9941069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99410692023-02-21 Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2 Li, Ruoxu Su, Ning Ren, Xiaodong Sun, Xiange Li, Wenman Li, Yuwei Li, Jin Chen, Chen Wang, Hong Lu, Weiping Deng, Shaoli Huang, Qing iScience Article The COVID-19 pandemic has spread worldwide, and rapid detection of the SARS-CoV-2 virus is crucial for infection surveillance and epidemic control. This study developed a centrifugal microfluidics-based multiplex reverse transcription recombinase polymerase amplification (RT-RPA) assay for endpoint fluorescence detection of the E, N, and ORF1ab genes of SARS-CoV-2. The microscope slide-shaped microfluidic chip could simultaneously accomplish three target genes and one reference human gene (i.e., ACTB) RT-RPA reactions in 30 min, and the sensitivity was 40 RNA copies/reaction for the E gene, 20 RNA copies/reaction for the N gene, and 10 RNA copies/reaction for the ORF1ab gene. The chip demonstrated high specificity, reproducibility, and repeatability. Chip performance was also evaluated using real clinical samples. Thus, this rapid, accurate, on-site, and multiplexed nucleic acid test microfluidic chip would significantly contribute to detecting patients with COVID-19 in low-resource settings and point-of-care testing (POCT) and, in the future, could be used to detect emerging new variants of SARS-CoV-2. Elsevier 2023-02-21 /pmc/articles/PMC9941069/ /pubmed/36845031 http://dx.doi.org/10.1016/j.isci.2023.106245 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Li, Ruoxu Su, Ning Ren, Xiaodong Sun, Xiange Li, Wenman Li, Yuwei Li, Jin Chen, Chen Wang, Hong Lu, Weiping Deng, Shaoli Huang, Qing Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2 |
title | Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2 |
title_full | Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2 |
title_fullStr | Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2 |
title_full_unstemmed | Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2 |
title_short | Centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of SARS-CoV-2 |
title_sort | centrifugal microfluidic-based multiplex recombinase polymerase amplification assay for rapid detection of sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941069/ https://www.ncbi.nlm.nih.gov/pubmed/36845031 http://dx.doi.org/10.1016/j.isci.2023.106245 |
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