首页 | 本学科首页   官方微博 | 高级检索  
     

基于免疫磁分离的三重荧光定量PCR检测食品中沙门氏菌、志贺氏菌和金黄色葡萄球菌
引用本文:马凯,李宝明,白羽,陈尔凝,刘杰,武会娟,高丽娟. 基于免疫磁分离的三重荧光定量PCR检测食品中沙门氏菌、志贺氏菌和金黄色葡萄球菌[J]. 微生物学通报, 2014, 41(11): 2369-2377
作者姓名:马凯  李宝明  白羽  陈尔凝  刘杰  武会娟  高丽娟
作者单位:北京市理化分析测试中心 北京 100089;北京市理化分析测试中心 北京 100089;北京市理化分析测试中心 北京 100089;北京市理化分析测试中心 北京 100089;北京市理化分析测试中心 北京 100089;北京市理化分析测试中心 北京 100089;北京市理化分析测试中心 北京 100089
基金项目:北京市科技新星项目(No. 2008B31)
摘    要:【目的】开发一种同时对食品中沙门氏菌、志贺氏菌和金黄色葡萄球菌快速、灵敏、准确的检测方法。【方法】利用特异性免疫磁球,在37°C条件下从250 m L猪肉增菌液体系中边富集边循环捕获目标菌。快速提取DNA后,利用特异性的引物与探针,对3种食源性致病菌进行三重荧光定量PCR检测。【结果】针对沙门氏菌、志贺氏菌和金黄色葡萄球菌的检测限分别达到2.0、6.8和9.6 CFU/g。方法总体灵敏度、特异性和准确度达到99.2%、100%及99.5%。对151份实际样品进行检测,与国标(GB/T 4789.4-2010、GB 4789.5-2012和GB/T4789.10-2010)方法的检测结果相比,金黄色葡萄球菌有一例阴性偏差。【结论】开发的基于免疫磁分离的三重荧光定量PCR方法,能够在8 h内完成对食品中3种致病菌检测,并且灵敏度高、特异性好、检测准确,可以作为快速应对此类食品安全突发事件的检测手段。

关 键 词:免疫磁分离  多重荧光定量PCR  沙门氏菌  志贺氏菌  金黄色葡萄球菌

Rapid and simultaneous detection of Salmonella, Shigella, and Staphylococcus aureus in food using a multiplex RT-PCR assay based on immunomagnetic separation
MA Kai,LI Bao-Ming,BAI Yu,CHEN Er-Ning,LIU Jie,WU Hui-Juan and GAO Li-Juan. Rapid and simultaneous detection of Salmonella, Shigella, and Staphylococcus aureus in food using a multiplex RT-PCR assay based on immunomagnetic separation[J]. Microbiology China, 2014, 41(11): 2369-2377
Authors:MA Kai  LI Bao-Ming  BAI Yu  CHEN Er-Ning  LIU Jie  WU Hui-Juan  GAO Li-Juan
Affiliation:Beijing Centre for Physical and Chemical Analysis, Beijing 100089, China;Beijing Centre for Physical and Chemical Analysis, Beijing 100089, China;Beijing Centre for Physical and Chemical Analysis, Beijing 100089, China;Beijing Centre for Physical and Chemical Analysis, Beijing 100089, China;Beijing Centre for Physical and Chemical Analysis, Beijing 100089, China;Beijing Centre for Physical and Chemical Analysis, Beijing 100089, China;Beijing Centre for Physical and Chemical Analysis, Beijing 100089, China
Abstract:[Objective] This study aimed to develop a rapid and simultaneous detection method for Salmonella, Shigella, and Staphylococcus (S.) aureus in food. [Methods] Magnetic beads coated with speci?c antibodies were used to capture target pathogens from 250 mL at 37 °C. After quick DNA extraction, multiplex RT-PCR was applied to detect the target pathogens with three sets of specific primers and probes. [Results] The limit of detections of immunomagnetic separation (IMS)-multiplex real-time PCR (RT-PCR) method were 2.0 CFU/g for Salmonella, 6.8 CFU/g for shigella and 9.6 CFU/g for S. aureus. The sensitivity, specificity, and accuracy of this method were 99.2%, 100%, and 99.5%, respectively. One hundred fifty-one samples were tested using the IMS-multiplex RT-PCR and GB methods, and only one negetive deviation was detected. [Conclusion] The IMS-multiplex RT-PCR method with high sensitivity, specificity and accuracy could enable the simultaneous detection of Salmonella, Shigella, and S. aureus in food within 8 h and offers the opportunity for a quick response in an emergency when these bacteria are detected.
Keywords:Immunomagnetic separation   Multiplex real-time PCR   Salmonella   Shigella   Staphylococcus aureus
本文献已被 CNKI 等数据库收录!
点击此处可从《微生物学通报》浏览原始摘要信息
点击此处可从《微生物学通报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号