| Literature DB >> 33626071 |
Henrik Dimke1,2, Sanne L Larsen3, Marianne N Skov3, Hanne Larsen3, Gitte N Hartmeyer3, Jesper B Moeller4,5.
Abstract
The outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) rapidly reached pandemic levels. Sufficient testing for SARS-CoV-2 has remained essential for tracking and containing the virus. SARS-CoV-2 testing capabilities are still limited in many countries. Here, we explore the use of conventional RNA purification as an alternative to automated systems for detection of SARS-CoV-2 by RT-qPCR. 87 clinical swab specimens were extracted by conventional phenol-chloroform RNA purification and compared to commercial platforms for RNA extraction and the fully integrated Cobas®6800 diagnostic system. Our results show that the conventional RNA extraction is fully comparable to modern automated systems regarding analytical sensitivity and specificity with respect to detection of SARS-CoV-2 as evaluated by RT-qPCR. Moreover, the method is easily scalable and implemented in conventional laboratories as a low cost and suitable alternative to automated systems for the detection of SARS-CoV-2.Entities:
Year: 2021 PMID: 33626071 DOI: 10.1371/journal.pone.0247524
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240