Division of Clinical Pathology, Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, ROC.
Division of Infectious Diseases and Tropical Medicine, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, ROC.
J Microbiol Immunol Infect. 2022 Dec;55(6 Pt 1):1069-1075. doi: 10.1016/j.jmii.2021.08.003. Epub 2021 Sep 2.
BACKGROUND/PURPOSE: Mass screening for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is important to prevent the spread of coronavirus disease 2019 (COVID-19). Pooling samples can increase the number of tests processed. LabTurbo AIO 48 is an automated platform that allows ribonucleic acid extraction and sample analysis on the same instrument. We created a novel pooling assay on this platform for SARS-CoV-2 detection and demonstrated that the pooling strategy increases testing capacity without affecting accuracy and sensitivity.
Comparative limit of detection (LoD) assessment was performed on the LabTurbo AIO 48 platform and the current standard detection system based on real-time reverse transcription polymerase chain reaction (rRT-PCR) using 55 clinically positive samples. An additional 330 primary clinical samples were assessed.
Six samples pooled into one reaction tube were detected in approximately 2.5 h using the World Health Organization rRT-PCR protocol. LabTurbo AIO 48 also demonstrated a higher throughput than our reference rRT-PCR assay, with an LoD of 1000 copies/mL. The overall percentage agreement between the methods for the 330 samples was 100%.
We created a novel multi-specimen pooling assay using LabTurbo AIO 48 for the robust detection of SARS-CoV-2, allowing high-throughput results; this assay will aid in better control and prevention of COVID-19. The diagnostic assay was cost-effective and time-efficient; thus, the pooling strategy is a practical and effective method for diagnosing large quantities of specimens without compromising precision.
背景/目的:大规模筛查严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)对于预防 2019 年冠状病毒病(COVID-19)的传播至关重要。合并样本可以增加处理的测试数量。LabTurbo AIO 48 是一种自动化平台,可在同一仪器上进行核糖核酸提取和样品分析。我们在该平台上创建了一种用于 SARS-CoV-2 检测的新型合并分析方法,并证明该合并策略可在不影响准确性和敏感性的情况下增加检测能力。
使用 55 份临床阳性样本在 LabTurbo AIO 48 平台和当前基于实时逆转录聚合酶链反应(rRT-PCR)的标准检测系统上进行比较检测限(LoD)评估。另外评估了 330 份初级临床样本。
使用世界卫生组织 rRT-PCR 方案,将 6 份样本合并到一个反应管中,大约需要 2.5 小时即可检测到。LabTurbo AIO 48 还显示出比我们的参考 rRT-PCR 检测更高的通量,LoD 为 1000 拷贝/mL。对于 330 个样本,两种方法的总体百分比一致性为 100%。
我们使用 LabTurbo AIO 48 创建了一种新型的多标本合并分析方法,用于稳健检测 SARS-CoV-2,可实现高通量结果;该检测方法将有助于更好地控制和预防 COVID-19。诊断检测方法具有成本效益和时间效益;因此,该合并策略是一种实用且有效的方法,可在不影响精度的情况下诊断大量样本。