RT Journal Article
SR Electronic
T1 Optimized qRT-PCR approach for the detection of intra- and extra-cellular SARS-CoV-2 RNAs
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2020.04.20.052258
DO 10.1101/2020.04.20.052258
A1 Tuna Toptan
A1 Sebastian Hoehl
A1 Sandra Westhaus
A1 Denisa Bojkova
A1 Annemarie Berger
A1 Björn Rotter
A1 Klaus Hoffmeier
A1 Sandra Ciesek
A1 Marek Widera
YR 2020
UL http://biorxiv.org/content/early/2020/04/25/2020.04.20.052258.abstract
AB The novel coronavirus SARS-CoV-2 is the causative agent of the acute respiratory disease COVID-19 which has become a global concern due to its rapid spread. Meanwhile, increased demand in testing has led to shortage of reagents, supplies, and compromised the performance of diagnostic laboratories in many countries. Both the world health organization (WHO) and the Center for Disease Control and Prevention (CDC) recommend multi-step RT-PCR assays using multiple primer and probe pairs, which might complicate interpretation of the test results especially for borderline cases. In this study, we describe an alternative RT-PCR approach for the detection of SARS-CoV-2 RNA that can be used for the probe-based detection of clinical isolates in the diagnostics as well as in research labs using a low cost SYBR green method. For the evaluation, we used samples from patients with confirmed SARS-CoV-2 infection and performed RT-PCR assays along with successive dilutions of RNA standards to determine the limit of detection. We identified an M-gene binding primer and probe pair highly suitable for quantitative detection of SARS-CoV-2 RNA for diagnostic and research purposes.Competing Interest StatementThe authors have declared no competing interest.