Zingg Jean-Marc, Yang Yu-Ping, Seely Spencer, Joshi Pratibha, Roshid Md Harun Or, Iribarren Latasa Fabiola, O'Connor Gregory, Alfaro Jennifer, Riquelme Eduardo, Bernales Sebastian, Dikici Emre, Deo Sapna, Daunert Sylvia
Department of Biochemistry and Molecular Biology, Miller School of Medicine, University of Miami, Miami, FL, 33136-6129, USA.
Department of Chemistry, University of Miami, Miami, FL, 33146, USA.
Asp Mol Med. 2023;1:100002. doi: 10.1016/j.amolm.2023.100002. Epub 2023 Jan 31.
Rapid on-site diagnosis of emerging pathogens is key for early identification of infected individuals and for prevention of further spreading in a population. Currently available molecular diagnostic tests are instrument-based whereas rapid antibody and antigen tests are often not sufficiently sensitive for detection in pre-symptomatic subjects. There is a need for rapid point of care molecular screening tests that can be easily adapted to emerging pathogens and are selective, sensitive, reliable in different settings around the world. We have developed a simple, rapid (<30 min), and inexpensive test for SARS-CoV-2 that is based on combination of isothermal reverse transcription recombinase polymerase amplification (RT-RPA) using modified primers and visual detection with paper-based microfluidics. Our test (CoRapID) is specific for SARS-CoV-2 (alpha to omicron variants) and does not detect other coronaviruses and pathogens by in silico and in vitro analysis. A two-step test protocol was developed with stable lyophilized reagents that reduces handling by using portable and disposable components (droppers, microapplicators/swabs, paper-strips). After optimization of assay components and conditions, we have achieved a limit of detection (LoD) of 1 copy/reaction by adding a blocking primer to the lateral flow assay. Using a set of 138 clinical samples, a sensitivity of 88.1% (P < 0.05, CI: 78.2-93.8%) and specificity of 93.9% (P < 0.05, CI: 85.4-97.6%) was determined. The lack of need for instrumentation for our CoRapID makes it an ideal on-site primary screening tool for local hospitals, doctors' offices, senior homes, workplaces, and in remote settings around the world that often do not have access to clinical laboratories.
快速现场诊断新出现的病原体是早期识别感染者以及防止病原体在人群中进一步传播的关键。目前可用的分子诊断测试基于仪器,而快速抗体和抗原测试对于在症状出现前的受试者中进行检测通常不够灵敏。需要一种快速的即时护理分子筛查测试,这种测试能够轻松适应新出现的病原体,并且在世界各地的不同环境中具有选择性、灵敏性和可靠性。我们开发了一种针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的简单、快速(<30分钟)且廉价的测试方法,该方法基于使用修饰引物的等温逆转录重组酶聚合酶扩增(RT-RPA)与基于纸的微流控视觉检测相结合。我们的测试(CoRapID)对SARS-CoV-2(从阿尔法到奥密克戎变体)具有特异性,通过计算机模拟和体外分析未检测到其他冠状病毒和病原体。我们开发了一种两步测试方案,使用稳定的冻干试剂,通过使用便携式和一次性组件(滴管、微型涂抹器/拭子、纸条)减少了操作。在优化检测组件和条件后,我们通过在侧向流动检测中添加阻断引物实现了1拷贝/反应的检测限(LoD)。使用一组138份临床样本,确定敏感性为88.1%(P<0.05,置信区间:78.2-93.8%),特异性为93.9%(P<0.05,置信区间:85.4-97.6%)。我们的CoRapID无需仪器,这使其成为当地医院、医生办公室、养老院、工作场所及世界各地偏远地区(这些地方通常无法使用临床实验室)理想的现场初步筛查工具。