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Digital PCR Applications in the SARS-CoV-2/COVID-19 Era: a Roadmap for Future Outbreaks.
Nyaruaba, Raphael; Mwaliko, Caroline; Dobnik, David; Neuzil, Pavel; Amoth, Patrick; Mwau, Matilu; Yu, Junping; Yang, Hang; Wei, Hongping.
  • Nyaruaba R; Key Laboratory of Special Pathogens and Biosafety, Center for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, Hubei, China.
  • Mwaliko C; International College, University of Chinese Academy of Sciences, Beijing, China.
  • Dobnik D; Sino-Africa Joint Research Center, Chinese Academy of Sciences, Wuhan, China.
  • Neuzil P; International College, University of Chinese Academy of Sciences, Beijing, China.
  • Amoth P; Sino-Africa Joint Research Center, Chinese Academy of Sciences, Wuhan, China.
  • Mwau M; CAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China.
  • Yu J; Department of Biotechnology and Systems Biology, National Institute of Biologygrid.419523.8, Ljubljana, Slovenia.
  • Yang H; Northwestern Polytechnical University, Xi'an, Shaanxi, China.
  • Wei H; Ministry of Health, Government of Kenya, Nairobi, Kenya.
Clin Microbiol Rev ; 35(3): e0016821, 2022 09 21.
Article in English | MEDLINE | ID: covidwho-1731254
ABSTRACT
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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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Clin Microbiol Rev Journal subject: Microbiology Year: 2022 Document Type: Article Affiliation country: Cmr.00168-21

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Clin Microbiol Rev Journal subject: Microbiology Year: 2022 Document Type: Article Affiliation country: Cmr.00168-21