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Published in: Virology Journal 1/2021

Open Access 01-12-2021 | SARS-CoV-2 | Short report

Excellent option for mass testing during the SARS-CoV-2 pandemic: painless self-collection and direct RT-qPCR

Authors: Eva Kriegova, Regina Fillerova, Milan Raska, Jirina Manakova, Martin Dihel, Ondrej Janca, Pavel Sauer, Martina Klimkova, Petra Strakova, Petr Kvapil

Published in: Virology Journal | Issue 1/2021

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Abstract

The early identification of asymptomatic yet infectious cases is vital to curb the 2019 coronavirus (COVID-19) pandemic and to control the disease in the post-pandemic era. In this paper, we propose a fast, inexpensive and high-throughput approach using painless nasal-swab self-collection followed by direct RT-qPCR for the sensitive PCR detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This approach was validated in a large prospective cohort study of 1038 subjects, analysed simultaneously using (1) nasopharyngeal swabs obtained with the assistance of healthcare personnel and analysed by classic two-step RT-qPCR on RNA isolates and (2) nasal swabs obtained by self-collection and analysed with direct RT-qPCR. Of these subjects, 28.6% tested positive for SARS-CoV-2 using nasopharyngeal swab sampling. Our direct RT-qPCR approach for self-collected nasal swabs performed well with results similar to those of the two-step RT-qPCR on RNA isolates, achieving 0.99 positive and 0.98 negative predictive values (cycle threshold [Ct] < 37). Our research also reports on grey-zone viraemia, including samples with near-cut-off Ct values (Ct ≥ 37). In all investigated subjects (n = 20) with grey-zone viraemia, the ultra-small viral load disappeared within hours or days with no symptoms. Overall, this study underscores the importance of painless nasal-swab self-collection and direct RT-qPCR for mass testing during the SARS-CoV-2 pandemic and in the post-pandemic era.
Literature
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go back to reference FDA U.S., 2020. Policy for coronavirus disease-2019 tests during the public health emergency (Revised). Immediately in Effect Guidance for Clinical Laboratories, Commercial Manufacturers, and Food and Drug Administration Staff. https://www.fda.gov/media/135659/download. Accessed 16 March 2021. FDA U.S., 2020. Policy for coronavirus disease-2019 tests during the public health emergency (Revised). Immediately in Effect Guidance for Clinical Laboratories, Commercial Manufacturers, and Food and Drug Administration Staff. https://​www.​fda.​gov/​media/​135659/​download. Accessed 16 March 2021.
Metadata
Title
Excellent option for mass testing during the SARS-CoV-2 pandemic: painless self-collection and direct RT-qPCR
Authors
Eva Kriegova
Regina Fillerova
Milan Raska
Jirina Manakova
Martin Dihel
Ondrej Janca
Pavel Sauer
Martina Klimkova
Petra Strakova
Petr Kvapil
Publication date
01-12-2021
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2021
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/s12985-021-01567-3

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