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食品中空肠弯曲菌荧光重组酶聚合酶扩增检测方法的建立
引用本文:兰全学,陈佳平,杨慧,杜文旗,金玉娟,甘莉萍,刘渠,刘小青. 食品中空肠弯曲菌荧光重组酶聚合酶扩增检测方法的建立[J]. 现代食品科技, 2020, 36(5): 304-309. DOI: 10.13982/j.mfst.1673-9078.2020.5.040
作者姓名:兰全学  陈佳平  杨慧  杜文旗  金玉娟  甘莉萍  刘渠  刘小青
作者单位:深圳市龙岗区疾病预防控制中心,广东深圳518172,深圳市计量质量检测研究院,广东深圳518109,深圳市龙岗区疾病预防控制中心,广东深圳518172,深圳市龙岗区疾病预防控制中心,广东深圳518172,深圳市龙岗区疾病预防控制中心,广东深圳518172,深圳市龙岗区疾病预防控制中心,广东深圳518172,深圳市龙岗区疾病预防控制中心,广东深圳518172,深圳市计量质量检测研究院,广东深圳518109
基金项目:深圳市科创委技术攻关项目(JSGG20160606144217004);广东省质量技术监督局项目(2018CZ20)
摘    要:本研究为了实现空肠弯曲菌的快速和便捷检测,建立了一种基于荧光重组酶聚合酶扩增技术(exo-RPA)快速检测空肠弯曲菌的方法。通过对空肠弯曲菌和对照菌株的exo-RPA检测来判断该方法的特异性。用梯度稀释的空肠弯曲菌作为模板进行检测来分析exo-RPA方法的灵敏度。通过对模拟污染样品检测来分析exo-RPA的应用效果。分别以exo-RPA和荧光PCR检测实际食品样品来分析二者的检测效果。空肠弯曲菌exo-RPA方法可特异检出空肠弯曲菌,检测灵敏度达到6.0×10^2CFU/m L。在模拟污染试验中,含2.5×10^1 CFU/m L空肠弯曲菌的增菌液在培养24 h后可以被exo-RPA检测出阳性信号。exo-RPA和荧光PCR对于40份样品的检测结果相同。本研究建立的空肠弯曲菌exo-RPA具有特异、灵敏和抗干扰性强的特点,方法操作简便快速,具有较好的应用前景。

关 键 词:重组酶聚合酶扩增技术  空肠弯曲菌  hipO基因
收稿时间:2019-11-23

Development of a Detection Method for Food-borne Campylobacter jejuni Based on Fluorescence Probe-based Recombinase Polymerase Amplification
LAN Quan-xue,CHEN Jia-ping,YANG hui,DU Wen-qi,JIN Yu-juan,GAN Li-ping,LIU Qu,LIU Xiao-qing. Development of a Detection Method for Food-borne Campylobacter jejuni Based on Fluorescence Probe-based Recombinase Polymerase Amplification[J]. Modern Food Science & Technology, 2020, 36(5): 304-309. DOI: 10.13982/j.mfst.1673-9078.2020.5.040
Authors:LAN Quan-xue  CHEN Jia-ping  YANG hui  DU Wen-qi  JIN Yu-juan  GAN Li-ping  LIU Qu  LIU Xiao-qing
Affiliation:(1.Shenzhen Longgang District Center for Disease Control and Prevention. Shenzhen 518172, China);(2.Shenzhen Academy of Metrology and Quality Inspection. Shenzhen 518109, China)
Abstract:In order to achieve rapid and convenient detection of Campylobacter jejuni, a rapid detection method of Campylobacter jejuni based on fluorescence probe-based recombinase polymerase amplification (exo-RPA) was developed. The specificity of the method was determined by exo-PA detection of Campylobacter jejuni and control strains. The gradient-diluted Campylobacter jejuni was used as a template to analyze the sensitivity of the exo-RPA method. The application effect of the exo-RPA method was analyzed through detecting the simulated contaminated samples.The exo-RPA and fluorescence PCR were used to test real food samples respectively, in order to analyze their detection effects. The Campylobacter jejuni exo-RPA method can specifically detect Campylobacter jejuni with a detection sensitivity of 6.0×102 CFU/mL. In the simulated contamination tests, the enrichment broth medium containing 2.5×101 CFU/mL Campylobacter jejuni was tested positive after 24 hours of culture by the exo-RPA assay. The exo-RPA and fluorescence PCR methods led to the same detection results for the 40 samples. The Campylobacter jejuni exo-RPA assay developed in this study has high specificity, sensitivity and anti-interference ability. The method is simple, convenient and rapid, with a good application prospect.
Keywords:recombinase polymerase amplification   Campylobacter jejuni   hipO gene
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