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Sensitive detection and quantification of SARS-CoV-2 by multiplex droplet digital RT-PCR

Authors
  • de Kock, Remco1, 2, 3
  • Baselmans, Mieke1
  • Scharnhorst, Volkher1, 2, 3
  • Deiman, Birgit1, 2, 3
  • 1 Catharina Hospital Eindhoven,
  • 2 Eindhoven University of Technology,
  • 3 Expert Center Clinical Chemistry Eindhoven, Eindhoven, The Netherlands
Type
Published Article
Journal
European Journal of Clinical Microbiology & Infectious Diseases
Publisher
Springer-Verlag
Publication Date
Oct 26, 2020
Pages
1–7
Identifiers
DOI: 10.1007/s10096-020-04076-3
PMID: 33104899
PMCID: PMC7587514
Source
PubMed Central
Keywords
License
Unknown

Abstract

The purpose of this study is to develop a one-step droplet digital RT-PCR (RT-ddPCR) multiplex assay that allows for sensitive quantification of SARS-CoV-2 RNA with respect to human-derived RNA and could be used for screening and monitoring of Covid-19 patients. A one-step RT-ddPCR multiplex assay was developed for simultaneous detection of SARS-CoV-2 E, RdRp and N viral RNA, and human Rpp30 DNA and GUSB mRNA, for internal nucleic acid (NA) extraction and RT-PCR control. Dilution series of viral RNA transcripts were prepared in water and total NA extract of Covid-19-negative patients. As reference assay, an E-GUSB duplex RT-PCR was used. GUSB mRNA detection was used to set validity criteria to assure viral RNA and RT-PCR assay quality and to enable quantification of SARS-CoV-2 RNA. In a background of at least 100 GUSB mRNA copies, 5 copies of viral RNA are reliably detectable and 10 copies viral RNA copies are reliably quantifiable. It was found that assay sensitivity of the RT-ddPCR was not affected by the total NA background while assay sensitivity of the gold standard RT-PCR assay is drastically decreased when SARS-CoV-2 copies were detected in a background of total NA extract compared with water. The present study describes a robust and sensitive one-step ddRT-PCR multiplex assay for reliable quantification of SARS-CoV-2 RNA. By determining the fractional abundance of viral RNA with respect to a human housekeeping gene, viral loads from different samples can be compared, what could be used to investigate the infectiveness and to monitor Covid-19 patients.

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