This study aimed to establish a real-time fluorescence loop-mediated isothermal amplification(RF-LAMP)assay to detect Yersinia enterocolitica(Y.enterocolitica).The products were identified by restriction digestion followed by electrophoresis and the results indicated that the amplification was correct.The performance of the assay was evaluated with respect to specificity and sensitivity, and the detection limit of artificially contaminated chicken was tested.Among the strains tested,Y.enterocolitica strain was identified as positive, the other non-Y. enterocolitica strains were negative. The sensitivity for Y. enterocolitica was 61 CFU/mL in pure cultures. The detection limit for artificially contaminated chicken was 46 CFU/g. This method has high specificity and sensitivity and allowed real-time monitoring, which was useful to realize rapid detection of Y.enterocolitica.%本研究建立实时荧光环介导等温扩增技术检测小肠结肠炎耶尔森氏菌的方法,扩增产物经电泳和酶切鉴定,表明扩增结果正确.本研究验证该方法特异性,对灵敏度和人工污染鸡肉的检出限进行测定.结果表明小肠结肠炎耶尔森氏菌株呈阳性结果,非小肠结肠炎耶尔森氏菌株均呈阴性结果.该方法检测纯菌的灵敏度为61 CFU/mL,人工污染鸡肉的检出限为46 CFU/g.该方法特异性强、灵敏度高、可实时检测小肠结肠炎耶尔森氏菌,能够实现对小肠结肠炎耶尔森氏菌的快速检测.
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