Clinical LaboratoryMolecular BiologyPeer-reviewed journal article
Comparative performance of four nucleic acid amplification tests for SARS-CoV-2 virus
Qi-Zhen ZhuangiD, Zhenzhen LiiD, Chao YaniD, Fei LiiD, Yi-Yuan Ge, Yan-Hua ShaiD, Yi WangiD, Xianzhang HuangiD, Pei-Feng KeiD, Yujuan XiongiD
Abstract
Coronavirus disease 2019 (COVID-19) can be screened and diagnosed through the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by real-time reverse transcription polymerase chain reaction. SARS-CoV-2 nucleic acid amplification tests (NAATs) have been rapidly developed and quickly applied to clinical testing during the pandemic. However, studies evaluating the performance of these NAAT assays are limited. We evaluated the performance of four NAATs, which were marked by the Conformite Europeenne and widely used in China during the pandemic. Results showed that the analytical sensitivity of the four assays was significantly lower than that claimed by the NAAT manufacturers. The limit of detection (LOD) of Daan, Sansure, and Hybribio NAATs was 3000 copies/mL, whereas the LOD of Bioperfectus NAATs was 4000 copies/mL. The results of the consistency test using 46 samples showed that Daan, Sansure, and Hybribio NAATs could detect the samples with a specificity of 100% (30/30) and a sensitivity of 100% (16 /16), whereas Bioperfectus NAAT detected the samples with a specificity of 100% (30/30) and a sensitivity 81.25% (13/16). The sensitivity of Bioperfectus NAAT was lower than that of the three other NAATs; this finding was consistent with the result that Bioperfectus NAAT had a higher LOD than the three other kinds of NAATs. The four above mentioned reagents presented high specificity; however, for the detection of the samples with low virus concentration, Bioperfectus reagent had the risk of missing detection. Therefore, the LOD should be considered in the selection of SARS-CoV-2 NAATs.
- Citations
- 14
- FWCI
- 0.79
- Field percentile
- top 24%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Analytical and Clinical Comparison of Three Nucleic Acid Amplification Tests for SARS-CoV-2 Detection
E. Smith, W. Zhen, … G. J. Berry·bioRxiv·May 14, 2020
- A comparative study of isothermal nucleic acid amplification methods for SARS-CoV-2 detection at point-of-care
Diem Hong Tran, Hoang Quoc Cuong, … Hường Thị Thu Phùng·bioRxiv·May 24, 2020
- Comparison of three TaqMan Real-Time Reverse Transcription-PCR assays in detecting SARS-CoV-2
Y. Xiao, Z. Li, … J. Li·Journal of Virological MethodsPeer-reviewed·Feb 1, 2021
- Comparative study of four SARS-CoV-2 Nucleic Acid Amplification Test (NAAT) platforms demonstrates that ID NOW performance is impaired substantially by patient and specimen type.
P. R. Lephart, M. A. Bachman, … D. W. Newton·bioRxiv·Jun 4, 2020
- Design of a Novel Multiplex Real Time RT-PCR Assay for SARS-CoV-2 Detection
W. Zhen, G. J. Berry·bioRxiv·Jun 4, 2020
- Head-to-head comparison of four antigen-based rapid detection tests for the diagnosis of SARS-CoV-2 in respiratory samples
T. Weitzel, P. Legarraga, … L. Porte·bioRxiv·May 27, 2020