Clinical evaluation of the Procleix SARS-CoV-2 assay, a sensitive, high-throughput test that runs on an automated system

Diagn Microbiol Infect Dis. 2022 Jan;102(1):115560. doi: 10.1016/j.diagmicrobio.2021.115560. Epub 2021 Sep 25.

Abstract

Testing is crucial in controlling COVID-19. The Procleix® SARS-CoV-2 assay, a transcription-mediated amplification nucleic acid test that runs on an automated system, was evaluated using inactivated virus and clinical samples. The sensitivity of the assay was assessed using heat-inactivated SARS-CoV-2 and compared to 3 other tests. Clinical validation utilized 2 sets of samples: (1) Nasal, nasopharyngeal and oropharyngeal samples (n = 963) from asymptomatic individuals, and (2) nasopharyngeal samples from symptomatic patients: 100 positive and 100 negative by RT-PCR. The Procleix assay had greater sensitivity (3-fold to 100-fold) than the comparators and had high specificity (100%) in asymptomatic subjects. In symptomatic patients, the Procleix assay detected 100% of PCR-positives and found 24 positives in the initial PCR-negatives. Eighteen of these were confirmed positive and 6 were inconclusive. These studies showed that the Procleix SARS-CoV-2 assay was a sensitive and specific tool for detecting COVID-19.

Keywords: COVID-19; Nucleic acid test (NAT); Transcription-Mediated Amplification (TMA).

MeSH terms

  • Automation*
  • COVID-19 / diagnosis*
  • COVID-19 / virology*
  • COVID-19 Testing / methods*
  • High-Throughput Screening Assays
  • Humans
  • Molecular Diagnostic Techniques
  • Nucleic Acid Amplification Techniques
  • Retrospective Studies
  • SARS-CoV-2 / isolation & purification*
  • Sensitivity and Specificity