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作 者:刘子勇[1] 高继业[1] 唐妤[1] 丁孟建[1] 李继祥[1]
机构地区:[1]西南大学荣昌校区,重庆402460
出 处:《畜禽业》2010年第2期22-23,共2页Livestock and Poultry Industry
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.
分 类 号:S858.31[农业科学—临床兽医学]
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