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Evaluation of an Automated High-Throughput Liquid-Based RNA Extraction Platform on Pooled Nasopharyngeal or Saliva Specimens for SARS-CoV-2 RT-PCR.

Authors :
Chu AW
Yip CC
Chan WM
Ng AC
Chan DL
Siu RH
Chung CYT
Ng JP
Kittur H
Mosley GL
Poon RW
Chiu RY
To KK
Source :
Viruses [Viruses] 2021 Apr 02; Vol. 13 (4). Date of Electronic Publication: 2021 Apr 02.
Publication Year :
2021

Abstract

SARS-CoV-2 RT-PCR with pooled specimens has been implemented during the COVID-19 pandemic as a cost- and manpower-saving strategy for large-scale testing. However, there is a paucity of data on the efficiency of different nucleic acid extraction platforms on pooled specimens. This study compared a novel automated high-throughput liquid-based RNA extraction (LRE) platform (PHASIFYâ„¢) with a widely used magnetic bead-based total nucleic acid extraction (MBTE) platform (NucliSENS <superscript>®</superscript> easyMAG <superscript>®</superscript> ). A total of 60 pools of nasopharyngeal swab and 60 pools of posterior oropharyngeal saliva specimens, each consisting of 1 SARS-CoV-2 positive and 9 SARS-CoV-2 negative specimens, were included for the comparison. Real-time RT-PCR targeting the SARS-CoV-2 RdRp/Hel gene was performed, and GAPDH RT-PCR was used to detect RT-PCR inhibitors. No significant differences were observed in the Ct values and overall RT-PCR positive rates between LRE and MBTE platforms (92.5% (111/120] vs. 90% (108/120]), but there was a slightly higher positive rate for LRE (88.3% (53/60]) than MBTE (81.7% (49/60]) among pooled saliva. The automated LRE method is comparable to a standard MBTE method for the detection of SAR-CoV-2 in pooled specimens, providing a suitable alternative automated extraction platform. Furthermore, LRE may be better suited for pooled saliva specimens due to more efficient removal of RT-PCR inhibitors.

Details

Language :
English
ISSN :
1999-4915
Volume :
13
Issue :
4
Database :
MEDLINE
Journal :
Viruses
Publication Type :
Academic Journal
Accession number :
33918447
Full Text :
https://doi.org/10.3390/v13040615