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基于16S rRNA基因的食源性致病菌实时荧光定量PCR检测研究
Real-Time Quantitative PCR Detection of Food-Borne Pathogens Based on 16S rRNA Gene
【摘要】 本研究以16S rRNA基因作为靶基因,利用TaqMan探针技术建立了针对志贺氏菌(Shigella)、沙门氏菌(Salmonella)和金黄色葡萄球菌(Staphylococcus aureus)三种主要食源性致病菌的多重实时荧光定量PCR检测技术。结果表明,建立的荧光定量PCR检测体系特异性良好、灵敏度高、简便快捷,大大缩短了检测时间,在食源性致病菌快速筛查方面具有良好的应用前景。
【Abstract】 In this study,a multiplex real-time quantitative PCR detection technology for the three food-borne pathogens,Shigella,Salmonella and Staphylococcus aureus,had been established utilizing the Taq Man probe and 16 S rRNA gene as a target gene. The results indicated that the established multiplex real-time quantitative PCR detection system had good specificity and sensitivity,was simple and efficient,and greatly reduced the detection time,so it had a good prospect in the rapid screening for food-borne pathogens.
【关键词】 食源性致病菌;
16S rRNA基因;
多重实时荧光定量PCR;
TaqMan探针;
【Key words】 Food-borne pathogen; 16S rRNA gene; Multiplex real-time quantitative PCR; TaqMan probe;
【Key words】 Food-borne pathogen; 16S rRNA gene; Multiplex real-time quantitative PCR; TaqMan probe;
【基金】 山东省优秀中青年科学家科研奖励基金项目(BS2013NY012)
- 【文献出处】 山东农业科学 ,Shandong Agricultural Sciences , 编辑部邮箱 ,2017年06期
- 【分类号】O657.3;TS207.4
- 【被引频次】3
- 【下载频次】374