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Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks

The ongoing coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has led to a global public health disaster. The current gold standard for the diagnosis of infected patients is real-time reverse transcription-quantitative PCR (RT-qPCR)...

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Autores principales: Nyaruaba, Raphael, Mwaliko, Caroline, Dobnik, David, Neužil, Pavel, Amoth, Patrick, Mwau, Matilu, Yu, Junping, Yang, Hang, Wei, Hongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491181/
https://www.ncbi.nlm.nih.gov/pubmed/35258315
http://dx.doi.org/10.1128/cmr.00168-21
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author Nyaruaba, Raphael
Mwaliko, Caroline
Dobnik, David
Neužil, Pavel
Amoth, Patrick
Mwau, Matilu
Yu, Junping
Yang, Hang
Wei, Hongping
author_facet Nyaruaba, Raphael
Mwaliko, Caroline
Dobnik, David
Neužil, Pavel
Amoth, Patrick
Mwau, Matilu
Yu, Junping
Yang, Hang
Wei, Hongping
author_sort Nyaruaba, Raphael
collection PubMed
description The ongoing coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has led to a global public health disaster. The current gold standard for the diagnosis of infected patients is real-time reverse transcription-quantitative PCR (RT-qPCR). As effective as this method may be, it is subject to false-negative and -positive results, affecting its precision, especially for the detection of low viral loads in samples. In contrast, digital PCR (dPCR), the third generation of PCR, has been shown to be more effective than the gold standard, RT-qPCR, in detecting low viral loads in samples. In this review article, we selected publications to show the broad-spectrum applications of dPCR, including the development of assays and reference standards, environmental monitoring, mutation detection, and clinical diagnosis of SARS-CoV-2, while comparing it analytically to the gold standard, RT-qPCR. In summary, it is evident that the specificity, sensitivity, reproducibility, and detection limits of RT-dPCR are generally unaffected by common factors that may affect RT-qPCR. As this is the first time that dPCR is being tested in an outbreak of such a magnitude, knowledge of its applications will help chart a course for future diagnosis and monitoring of infectious disease outbreaks.
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spelling pubmed-94911812022-09-22 Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks Nyaruaba, Raphael Mwaliko, Caroline Dobnik, David Neužil, Pavel Amoth, Patrick Mwau, Matilu Yu, Junping Yang, Hang Wei, Hongping Clin Microbiol Rev Review The ongoing coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has led to a global public health disaster. The current gold standard for the diagnosis of infected patients is real-time reverse transcription-quantitative PCR (RT-qPCR). As effective as this method may be, it is subject to false-negative and -positive results, affecting its precision, especially for the detection of low viral loads in samples. In contrast, digital PCR (dPCR), the third generation of PCR, has been shown to be more effective than the gold standard, RT-qPCR, in detecting low viral loads in samples. In this review article, we selected publications to show the broad-spectrum applications of dPCR, including the development of assays and reference standards, environmental monitoring, mutation detection, and clinical diagnosis of SARS-CoV-2, while comparing it analytically to the gold standard, RT-qPCR. In summary, it is evident that the specificity, sensitivity, reproducibility, and detection limits of RT-dPCR are generally unaffected by common factors that may affect RT-qPCR. As this is the first time that dPCR is being tested in an outbreak of such a magnitude, knowledge of its applications will help chart a course for future diagnosis and monitoring of infectious disease outbreaks. American Society for Microbiology 2022-03-08 /pmc/articles/PMC9491181/ /pubmed/35258315 http://dx.doi.org/10.1128/cmr.00168-21 Text en Copyright © 2022 American Society for Microbiology. https://doi.org/10.1128/ASMCopyrightv2All Rights Reserved (https://doi.org/10.1128/ASMCopyrightv2) . https://doi.org/10.1128/ASMCopyrightv2This article is made available via the PMC Open Access Subset for unrestricted noncommercial re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Nyaruaba, Raphael
Mwaliko, Caroline
Dobnik, David
Neužil, Pavel
Amoth, Patrick
Mwau, Matilu
Yu, Junping
Yang, Hang
Wei, Hongping
Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks
title Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks
title_full Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks
title_fullStr Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks
title_full_unstemmed Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks
title_short Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks
title_sort digital pcr applications in the sars-cov-2/covid-19 era: a roadmap for future outbreaks
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491181/
https://www.ncbi.nlm.nih.gov/pubmed/35258315
http://dx.doi.org/10.1128/cmr.00168-21
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