Department of Academic-Industrial Partnerships Promotion, Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
Department of Academic-Industrial Partnerships Promotion, Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo 162-8655, Japan.
Diagn Microbiol Infect Dis. 2024 Jul;109(3):116297. doi: 10.1016/j.diagmicrobio.2024.116297. Epub 2024 Apr 4.
The LAMPdirect Genelyzer KIT allows for the detection of SARS-CoV-2 RNA in saliva samples with a loop-mediated isothermal amplification (LAMP) method and generates results within 20 min. It has been approved by the Pharmaceuticals and Medical Devices Agency in Japan. In this study, the performance of the LAMPdirect Genelyzer KIT was compared with that of the RT-qPCR reference method using 50 nasopharyngeal swabs and 100 saliva samples. In addition, we evaluated the applicability of an alternative reverse transcriptase and the effects of an inactivation buffer. The total agreement rates were 80.0 % and 82.0 % for nasopharyngeal and saliva samples, respectively. When considering samples at the detection limit (50 copies/reaction) that increases the chance of transmission between humans, the total agreement rates were 100% and 94.1% for nasopharyngeal and saliva samples, respectively. The LAMP method is simple, fast, and inexpensive, making it useful for small medical institutions or rural areas.
LAMPdirect Genelyzer KIT 采用环介导等温扩增(LAMP)方法,可检测唾液样本中的 SARS-CoV-2 RNA,20 分钟内即可获得结果。该试剂盒已获得日本药品和医疗器械管理局的批准。本研究比较了 LAMPdirect Genelyzer KIT 与 RT-qPCR 参考方法在 50 份鼻咽拭子和 100 份唾液样本中的性能。此外,我们评估了替代逆转录酶的适用性和失活缓冲液的影响。鼻咽拭子和唾液样本的总符合率分别为 80.0%和 82.0%。当考虑到在人与人之间传播几率增加的检测限(50 拷贝/反应)样本时,鼻咽拭子和唾液样本的总符合率分别为 100%和 94.1%。LAMP 方法简单、快速、廉价,适用于小型医疗机构或农村地区。