张明明,梁美丹,黄志深,劳嘉倩,肖 剑.6类致泻大肠埃希氏菌多重PCR检测体系的建[J].食品安全质量检测学报,2019,10(14):4667-4672
6类致泻大肠埃希氏菌多重PCR检测体系的建
Establishment of multiplex PCR detection method for 6 strains of diarrheagenic Escherichia coli
投稿时间:2019-04-30  修订日期:2019-07-19
DOI:
中文关键词:  食品  致泻大肠埃希氏菌  多重PCR  毒力基因
英文关键词:food  diarrheagenic Escherichia coli  multiple PCR  virulence gene
基金项目:广东省省级科技计划项目(2017B020207004)、广东省食品药品监督管理局科技创新项目(2018YDB21)
作者单位
张明明 广州市食品检验所 
梁美丹 广州市食品检验所 
黄志深 广州市食品检验所 
劳嘉倩 广州市食品检验所 
肖 剑 广州市食品检验所 
AuthorInstitution
ZHANG Ming-Ming Guangzhou Institute for Food Inspection 
LIANG Mei-Dan Guangzhou Institute for Food Inspection 
HUANG Zhi-Shen Guangzhou Institute for Food Inspection 
LAO Jia-Qian Guangzhou Institute for Food Inspection 
XIAO Jian Guangzhou Institute for Food Inspection 
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中文摘要:
      目的 构建食源性致泻大肠埃希氏菌高效、快速、特异性强的检验方法。方法 根据6类致泻大肠埃希菌11种毒力基因引物, 采用煮沸法制备细菌基因组DNA作为模板构建致泻大肠埃希氏菌单菌多重PCR检测体系; 采用试剂盒法制备细菌基因组DNA作为模板构建6类菌十重PCR检测体系, 对2种检测体系进行优化并对其进行特异性、重复性验证。结果 构建了6类致泻大肠埃希氏菌多重PCR检测体系, 包括单菌多重PCR、6类菌十重PCR检测体系。仅6类致泻大肠埃希氏菌阳性菌株有特异性条带产生; 不同类型致泻大肠埃希氏菌菌株均检出其特异性阳性条带, 该多重PCR检测方法重复性好, 稳定性强。结论 该方法可高效快速地确定待测样是否为大肠埃希氏菌及其致病型, 为食品中致泻大肠埃希氏菌的监控、预警及爆发引起食物中毒后溯源等提供参考。
英文摘要:
      Objective To establish an effective, rapid and specific detection method for foodborne diarrheagenic Escherichia coli. Methods Based on 11 virulence gene primers of diarrheagenic E. coli, multiple PCR detection system of single type strain and decuple PCR detection system of 6 strains were constructed by using bacterial genome DNA prepared by the boiling method and kit method respectively as template. The 2 detection systems were optimized, then their specificity and repeatability were verified. Results Multiplex PCR detection systems for 6 strains of diarrheagenic E. coli were established, including multiple PCR detection system for single type strain and decuple PCR detection system for 6 strains. The specific bands were amplified only in the 6 strains of diarrheagenic E. coli. Different kinds of diarrheagenic E. coli were detected the same specific positive bands, indicating that the repeatability and stability of the multiplex PCR detection systems were good. Conclusion This method can effectively and rapidly determine whether the test samples are E.coli and their pathotype, which can provide references for the monitoring, warning and tracing of food poisoning outbreaks caused by diarrheagenic E. coli.
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