摘要
目的:建立快速、特异、灵敏的PCR方法以检测生鸡肉中的肠炎沙门氏菌。方法:以肠炎沙门氏菌的sefA基因作为靶序列设计一对引物,将样品增菌后用煮沸法提取细菌基因组DNA进行检测。结果:每克生鸡肉污染3.0×10°CFU肠炎沙门氏菌,经16h增菌培养后可扩增出500bp特异性性DNA带,对28份屠宰场样品的检测结果与传统方法相符合。结论:PCR法适于生鸡肉中肠炎沙门氏菌的快速、准确检测。
Objective: To set up a detection approach of Salmonella enteritidis in raw chicken meat based on PCR. Methods: A pair of primers was designed with sefA gene of Salmonella enteritidis as target sequence for its detection. Samples Were homogenized, inoculated into buffered peptone water and grown at 37℃ for 16 hours, when the Bacterial genome was extracted. Results: A 500-bp DNA fragment was amplified from the primers. Twenty-eight samples which were collected from slaughter house were detected and the results were as same as traditional method. Conclusion: PCR technique will be applicable to examine Salmonella enteritidis in raw chicken meatquickly and accurately.
出处
《畜禽业》
2010年第2期22-23,共2页
Livestock and Poultry Industry
关键词
多聚酶链反应
生鸡肉
肠炎沙门氏菌
polymerase chain reaction
raw chicken meat
Salmonella enteritidis