摘要
目的:建立提高大样本低概率的细菌阳性检出率,降低工作强度,节约检测成本的一种检测程序。方法:采用高度特异、敏感的PCR作为样品初筛试验,结合传统方法培养、分离、鉴定。结果:342份奶粉样品,PCR检测阳性16份,阳性率为4.68%;传统方法检测阳性样品5份,阳性率为1.46%。检测耗时折算PCR法仅为传统方法的16.67%(10/60)。结论:PCR作为初筛试验,与传统方法的联合应用,为致病菌检测提供了一个新的思路,值得在大样本低概率细菌检验项目中推广应用。
Objective:A method for detecting bacteria was established to increase positive rate,decrease working strength and reduce cost. methods:Combining highly specific and sensitive PCR with traditional cultivation, isolation and identification methods. Rusults:Among 342 powdered infant formula samples, 16 positive samples (4. 68% ) were detected by PCR, and 5 positive samples ( 1.46% ) by traditional method, suggesting that the positive rate by PCR was higher than that by traditional method. Time - consuming for PCR is only 16. 67 % of the traditional one. Conclusion:The combination of PCR with traditional method presents us a new way for food - borne pathogen detection.
出处
《中国卫生检验杂志》
CAS
2009年第7期1535-1537,共3页
Chinese Journal of Health Laboratory Technology
基金
广东省科技攻关项目(2006B20501007)
关键词
PCR
阪崎肠杆菌
PCR
Enterobacter sakazakii