Department of Biological Engineering, College of Engineering, Konkuk University, Gwangjin-gu, Seoul, 05029, Republic of Korea.
Daegyeong Division, Safety System R&D Group, Korea Institute of Industrial Technology (KITECH), Yeongcheon-si, Gyeongsangbuk-do, 38822, Republic of Korea.
Anal Bioanal Chem. 2021 Aug;413(20):5003-5011. doi: 10.1007/s00216-021-03462-w. Epub 2021 Jun 16.
A simple and rapid polymerase chain reaction (PCR)-based lateral flow assay (LFA) was developed for multiplex detection of hygiene indicator bacteria. Specifically, new PCR primers were designed for accurately detecting Escherichia coli, coliform bacteria, and total bacteria, and the results obtained as a colorimetric signal (generated by the accumulation of gold nanoparticles at distinct test zones on flow strips) could be identified by the naked eye in <10 min after the completion of PCR. The proposed LFA system did not exhibit any cross-reactivities with 8 distinct bacterial strains and can detect down to 1 colony forming unit (CFU)/mL. Furthermore, three species of cultured bacteria (Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa) inoculated onto sterilized ham were successfully analyzed using the LFA system, which demonstrated that this system shows sufficient sensitivity and specificity for food hygiene monitoring. The speed and simplicity of this LFA make it suitable for use in the food industry as part of routine screening analysis.
一种简单快速的基于聚合酶链反应(PCR)的侧向流动检测(LFA)方法被开发出来,用于卫生指示菌的多重检测。具体来说,设计了新的 PCR 引物来准确检测大肠杆菌、大肠菌群和总菌,并且在 PCR 完成后不到 10 分钟,通过肉眼就可以识别作为比色信号(在流动条上的不同测试区积累的金纳米粒子产生)。所提出的 LFA 系统与 8 种不同的细菌菌株没有任何交叉反应性,并且可以检测到低至 1 个菌落形成单位(CFU)/mL。此外,使用 LFA 系统成功分析了接种在灭菌火腿上的三种培养细菌(大肠杆菌、肺炎克雷伯菌和铜绿假单胞菌),这表明该系统对食品卫生监测具有足够的灵敏度和特异性。该 LFA 的速度和简单性使其适合在食品工业中用作常规筛选分析的一部分。