Center for Functional Genomics, University at Albany, Rensselaer, New York, USA.
Department of Biomedical Sciences, School of Public Health, University at Albany, Rensselaer, New York, USA.
J Biomol Tech. 2021 Sep;32(3):148-157. doi: 10.7171/jbt.21-3203-010.
Here we present an inexpensive, rapid, and robust reverse-transcription loop-mediated isothermal amplification (RT-LAMP)-based severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) detection method that is easily scalable, enabling point-of-care facilities and clinical labs to determine results from patients' saliva directly in 30 minutes for less than $2 per reaction. The method uses a novel combination of widely available reagents that can be prepared in bulk, plated, and frozen and remain stable until samples are received. This innovation dramatically reduces preparation time, enabling high-throughput automation and testing with time to results (including setup) in less than 1 hour for 96 patient samples simultaneously when using a 384-well format. By using a dual reporter (phenol red pH indicator for end-point detection and SYTO-9 fluorescent dye for real time), the assay also provides internal validation of results and redundancy in the event of an instrument malfunction.
在这里,我们提出了一种廉价、快速且稳健的逆转录环介导等温扩增(RT-LAMP)检测方法,可直接对患者的唾液样本进行现场即时检测,30 分钟内即可出结果,每个反应的成本不到 2 美元。该方法使用了一种新颖的组合试剂,可大量制备、划线、冷冻,在收到样本之前保持稳定。这种创新极大地减少了准备时间,可实现高通量自动化,并在使用 384 孔格式时,将 96 个患者样本的结果(包括设置)时间缩短至 1 小时以内。该检测方法还使用了双报告基因(终点检测用苯酚红 pH 指示剂和实时检测用 SYTO-9 荧光染料),为结果提供了内部验证,并在仪器发生故障时提供了冗余性。