Chan Hiu Tat, Keung Marco H T, Nguyen Ivy, Ip Ellen L O, Chew Su M, Siler Danielle, Saville Marion, Hawkes David
VCS Pathology, Australian Centre for the Prevention of Cervical Cancer, 265 Faraday Street, Carlton South, VIC 3053, Australia.
Department of Physiology, Anatomy and Microbiology, La Trobe University, Bundoora, VIC 3086, Australia.
J Clin Virol Plus. 2022 Aug;2(3):100079. doi: 10.1016/j.jcvp.2022.100079. Epub 2022 Apr 30.
To examine the comparative stochasticity profile of six commercial SARS-CoV-2 nucleic acid amplification tests (NAATs) and how this may affect retesting paradigms.
Commercial quality control (QC) material was serially diluted in viral transport media to create a panel covering 10-10,000 copies/ml. The panel was tested across six commercial NAATs. A subset of high cycle threshold results was retested on a rapid PCR assay to simulate retesting protocols commonly used to discriminate false positives.
Performance beyond the LOD differed among assays, with three types of stochasticity profiles observed. The ability of the rapid PCR assay to reproduce a true weak positive specimen was restricted to its own stochastic performance at the corresponding viral concentration.
Stochastic performance of various NAATs overlap across low viral concentrations and affect retesting outcomes. Relying on retesting alone to discriminate false positives risk missing true positives even when a more sensitive assay is deployed for confirmatory testing.
研究六种商用严重急性呼吸综合征冠状病毒2(SARS-CoV-2)核酸扩增检测(NAATs)的比较随机特性,以及这可能如何影响重新检测模式。
将商业质量控制(QC)材料在病毒运输介质中进行系列稀释,以创建一个覆盖10 - 10,000拷贝/毫升的样本组。该样本组在六种商用NAATs上进行检测。对一部分高循环阈值结果在快速聚合酶链反应(PCR)检测中进行重新检测,以模拟常用于鉴别假阳性的重新检测方案。
检测限以上的性能在不同检测方法之间存在差异,观察到三种类型的随机特性。快速PCR检测重现真正弱阳性样本的能力仅限于其在相应病毒浓度下自身的随机性能。
各种NAATs的随机性能在低病毒浓度范围内重叠,并影响重新检测结果。即使采用更灵敏的检测方法进行确证检测,仅依靠重新检测来鉴别假阳性也有遗漏真阳性的风险。