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Rapid electrochemical detection of coronavirus SARS-CoV-2

Coronavirus disease 2019 (COVID-19) is a highly contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Diagnosis of COVID-19 depends on quantitative reverse transcription PCR (qRT-PCR), which is time-consuming and requires expensive instrumentation. Here, we repor...

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Autores principales: Chaibun, Thanyarat, Puenpa, Jiratchaya, Ngamdee, Tatchanun, Boonapatcharoen, Nimaradee, Athamanolap, Pornpat, O’Mullane, Anthony Peter, Vongpunsawad, Sompong, Poovorawan, Yong, Lee, Su Yin, Lertanantawong, Benchaporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864991/
https://www.ncbi.nlm.nih.gov/pubmed/33547323
http://dx.doi.org/10.1038/s41467-021-21121-7
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author Chaibun, Thanyarat
Puenpa, Jiratchaya
Ngamdee, Tatchanun
Boonapatcharoen, Nimaradee
Athamanolap, Pornpat
O’Mullane, Anthony Peter
Vongpunsawad, Sompong
Poovorawan, Yong
Lee, Su Yin
Lertanantawong, Benchaporn
author_facet Chaibun, Thanyarat
Puenpa, Jiratchaya
Ngamdee, Tatchanun
Boonapatcharoen, Nimaradee
Athamanolap, Pornpat
O’Mullane, Anthony Peter
Vongpunsawad, Sompong
Poovorawan, Yong
Lee, Su Yin
Lertanantawong, Benchaporn
author_sort Chaibun, Thanyarat
collection PubMed
description Coronavirus disease 2019 (COVID-19) is a highly contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Diagnosis of COVID-19 depends on quantitative reverse transcription PCR (qRT-PCR), which is time-consuming and requires expensive instrumentation. Here, we report an ultrasensitive electrochemical biosensor based on isothermal rolling circle amplification (RCA) for rapid detection of SARS-CoV-2. The assay involves the hybridization of the RCA amplicons with probes that were functionalized with redox active labels that are detectable by an electrochemical biosensor. The one-step sandwich hybridization assay could detect as low as 1 copy/μL of N and S genes, in less than 2 h. Sensor evaluation with 106 clinical samples, including 41 SARS-CoV-2 positive and 9 samples positive for other respiratory viruses, gave a 100% concordance result with qRT-PCR, with complete correlation between the biosensor current signals and quantitation cycle (Cq) values. In summary, this biosensor could be used as an on-site, real-time diagnostic test for COVID-19.
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spelling pubmed-78649912021-02-16 Rapid electrochemical detection of coronavirus SARS-CoV-2 Chaibun, Thanyarat Puenpa, Jiratchaya Ngamdee, Tatchanun Boonapatcharoen, Nimaradee Athamanolap, Pornpat O’Mullane, Anthony Peter Vongpunsawad, Sompong Poovorawan, Yong Lee, Su Yin Lertanantawong, Benchaporn Nat Commun Article Coronavirus disease 2019 (COVID-19) is a highly contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Diagnosis of COVID-19 depends on quantitative reverse transcription PCR (qRT-PCR), which is time-consuming and requires expensive instrumentation. Here, we report an ultrasensitive electrochemical biosensor based on isothermal rolling circle amplification (RCA) for rapid detection of SARS-CoV-2. The assay involves the hybridization of the RCA amplicons with probes that were functionalized with redox active labels that are detectable by an electrochemical biosensor. The one-step sandwich hybridization assay could detect as low as 1 copy/μL of N and S genes, in less than 2 h. Sensor evaluation with 106 clinical samples, including 41 SARS-CoV-2 positive and 9 samples positive for other respiratory viruses, gave a 100% concordance result with qRT-PCR, with complete correlation between the biosensor current signals and quantitation cycle (Cq) values. In summary, this biosensor could be used as an on-site, real-time diagnostic test for COVID-19. Nature Publishing Group UK 2021-02-05 /pmc/articles/PMC7864991/ /pubmed/33547323 http://dx.doi.org/10.1038/s41467-021-21121-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chaibun, Thanyarat
Puenpa, Jiratchaya
Ngamdee, Tatchanun
Boonapatcharoen, Nimaradee
Athamanolap, Pornpat
O’Mullane, Anthony Peter
Vongpunsawad, Sompong
Poovorawan, Yong
Lee, Su Yin
Lertanantawong, Benchaporn
Rapid electrochemical detection of coronavirus SARS-CoV-2
title Rapid electrochemical detection of coronavirus SARS-CoV-2
title_full Rapid electrochemical detection of coronavirus SARS-CoV-2
title_fullStr Rapid electrochemical detection of coronavirus SARS-CoV-2
title_full_unstemmed Rapid electrochemical detection of coronavirus SARS-CoV-2
title_short Rapid electrochemical detection of coronavirus SARS-CoV-2
title_sort rapid electrochemical detection of coronavirus sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864991/
https://www.ncbi.nlm.nih.gov/pubmed/33547323
http://dx.doi.org/10.1038/s41467-021-21121-7
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