Rapid detection of Salmonella based on loop-mediated isothermal amplification

被引:16
|
作者
Ou, Hongling [1 ,2 ]
Wang, Yan [2 ]
Gao, Jiayi [3 ]
Bai, Jing [2 ]
Zhang, Qiaoyun [2 ]
Shi, Lei [2 ]
Wang, Xinru [2 ]
Wang, Chengbin [1 ,4 ]
机构
[1] Med Sch Chinese PLA, Beijing, Peoples R China
[2] PLA Rocket Characterist Med Ctr, Dept Clin Lab, Beijing 100088, Peoples R China
[3] North Med Univ, Sch Med Lab, Clin Lab, Teaching & Res Dept, Zhangjiakou, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Clin Lab Med, Beijing 100029, Peoples R China
关键词
Loop-mediated isothermal amplification (LAMP); Salmonella; rapid detection; FOODBORNE PATHOGENS; SYSTEM; ENTERITIDIS;
D O I
10.21037/apm-21-1387
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Salmonella enterica is a zoonotic pathogen of substantial concern to human and animal health and is a leading cause of morbidity and mortality in people worldwide. Loop-mediated isothermal amplification (LAMP) technology is a new type of nucleic acid amplification technology, which has the characteristics of high specificity, high sensitivity, simple operation, convenience, and low cost. This study aims to establish a rapid detection method for Salmonella based on LAMP technology. Methods: Primers were designed for Salmonella's specific conservative invA gene. Through primer screening and optimization of reaction conditions, and a LAMP method for detecting Salmonella with real-time fluorescence and visual observation results was established. The sensitivity and specificity of the method were assessed, and the accuracy was evaluated through the testing of Salmonella-contaminated and non-contaminated clinical samples. Results: The optimal reaction temperature of LAMP was 60-65 degrees C, and the optimal reaction time was 25-30 minutes. The detection limits of real-time fluorescence and visual observation were both 1.4 pg/mu L. There was no cross-reactivity observed with 22 non-Salmonella species, and the specificity was 100%. Additionally, 30 samples contaminated with Salmonella, 30 samples not contaminated with Salmonella, and 8 clinical samples identified as positive by bacterial culture and microbial mass spectrometry were tested. The positive coincidence rate of the detection system was 97.4% by real-time fluorescence and 89.5% by visual observation, the negative coincidence rate was 100%, and the total coincidence rate was 98.5% and 94.1%, respectively. Conclusions: In the scene of infection, primary hospital, disaster area treatment and other scenarios, the conditions of environment, equipment and personnel was limited, therefore, the established real-time fluorescence and visual lamp method can provide a powerful means for the rapid detection of Salmonella.
引用
收藏
页码:6850 / 6858
页数:9
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