食品科学 ›› 2009, Vol. 30 ›› Issue (12): 233-236.doi: 10.7506/spkx1002-6630-200912053

• 分析检测 • 上一篇    下一篇

免疫捕捉通用引物PCR检测食品中沙门氏菌

张体银,黄晓蓉,郑 晶,邵碧英,黄嫦娇,陈 彬,林 杰,汤敏英   

  1. 福建出入境检验检疫局
  • 收稿日期:2008-08-20 修回日期:2008-12-18 出版日期:2009-06-15 发布日期:2010-12-29
  • 通讯作者: 张体银 E-mail:zhty5337@yahoo.com.cn
  • 基金资助:

    国家质检总局科技项目(FK2005-15)

Immunocapture-Universal Primer PCR Detection of Salmonella sp. in Foods

ZHANG Ti-yin,HUANG Xiao-rong,ZHENG Jing,SHAO Bi-ying,HUANG Chang-jiao,
CHEN Bin,LIN Jie,TANG Min-ying   

  1. (Fujian Entry-Excit Inspection and Quarantine Bureau, Fuzhou 350001, China)
  • Received:2008-08-20 Revised:2008-12-18 Online:2009-06-15 Published:2010-12-29
  • Contact: ZHANG Ti-yin, E-mail:zhty5337@yahoo.com.cn

摘要:

利用免疫吸附富集结合经典PCR 技术建立免疫捕捉通用引物PCR(IC-UPPCR)检测食品中沙门氏菌。采用细菌16S rRNA 基因保守区设计特异性引物,建立通用引物PCR 技术是可行的,该IC-UPPCR 检测沙门氏菌的灵敏度最低,能检测到2 × 102CFU/ml,检测沙门氏菌属和非沙门氏菌属标准株的特异性为100%,无假阳性和假阴性出现。结果表明该方法具有简单、快速、特异性好和敏感性高等特点,并可满足大批样品沙门氏菌筛选检测的要求,适用于食品卫生监管、商品检验检疫以及临床诊断等领域。

关键词: 免疫捕捉, 通用引物, PCR, 沙门氏菌, 食品

Abstract:

An immunocapture-universal primer polymerase chain reaction (PCR) (IC-UPPCR) method was developed by combining the floride ion-selective electrode method with classical PCR assay for detection of Salmonella sp. in food and its sensitivity and specificity were investigated. It was feasible to establish a universal primer PCR technology was by designing specific primers from conserved regions of bacterial 16S ribosomal RNA genes. The sensitivity of the IC-UPPCR to detect Salmonella sp. was 2 × 102 CFU/ml and the specificity was 100% without any false negative or positive cases. The results demonstrate that the IC-UPPCR is a simple, rapid, highly sensitive and specific method for the detection of Salmonella sp. in the foods and suitable for detection of Salmonella sp. in a large number of food samples.

Key words: immunocapture, universal primer, PCR, Salmonella sp., foods

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