孙冰清,姜 芹,张文刚,张 妤,顾 欣.基于qPCR检测金黄色葡萄球菌3种肠毒素基因的方法研究[J].食品安全质量检测学报,2020,11(9):2798-2805
基于qPCR检测金黄色葡萄球菌3种肠毒素基因的方法研究
Detection of three enterotoxin genes of Staphylococcus aureus based on qPCR
投稿时间:2020-03-15  修订日期:2020-05-09
DOI:
中文关键词:  金黄色葡萄球菌  食物中毒  肠毒素基因  荧光定量PCR
英文关键词:Staphylococcus aureus  food poisoning  enterotoxin gene  fluorescent quantitative PCR
基金项目:上海市市级农口系统青年人才成长计划项目(沪农青字(2018)第2-1号)
作者单位
孙冰清 上海市兽药饲料检测所 
姜 芹 上海市兽药饲料检测所 
张文刚 上海市兽药饲料检测所 
张 妤 上海市兽药饲料检测所 
顾 欣 上海市兽药饲料检测所 
AuthorInstitution
SUN Bing-Qing Shanghai Municipal Supervisory Institute Veterinary Drugs and Feed Staff 
JIANG Qin Shanghai Municipal Supervisory Institute Veterinary Drugs and Feed Staff 
ZHANG Wen-Gang Shanghai Municipal Supervisory Institute Veterinary Drugs and Feed Staff 
ZHANG Yu Shanghai Municipal Supervisory Institute Veterinary Drugs and Feed Staff 
GU Xin Shanghai Municipal Supervisory Institute Veterinary Drugs and Feed Staff 
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中文摘要:
      目的 建立同时检测3种可引起食物中毒金黄色葡萄球菌肠毒素sea、seb、sec基因的方法。方法 对GenBank中公布的sea、seb、sec基因序列进行分析, 针对3种肠毒素基因分别设计3对特异性引物和探针, 通过条件优化建立检测肠毒素sea、seb、sec基因的三重qPCR方法。结果 该方法可以特异性检测到sea、seb、sec基因, 而与其他病原菌或肠毒素基因无交叉反应; 对肠毒素sea、seb、sec基因的最低检测量分别为10.2、1.63、9.4 copies/μL; 组内和组间的变异系数均小于5%。结论 该方法快速灵敏、准确可靠, 为金黄色葡萄球菌肠毒素的快速检测及多重qPCR试剂盒的开发奠定基础。
英文摘要:
      Objective To establish a method for simultaneous detection of sea, seb and sec genes of three common Staphylococcus aureus enterotoxins causing food poisoning. Methods By analyzing the sea, seb and sec gene sequences published in GenBank, three pairs of specific primers and probes were designed for the three enterotoxin genes respectively, and a triple qPCR method for detecting the sea, seb and sec genes of enterotoxin was established by optimizing the conditions. Results This method could specifically detect sea, seb and sec genes without cross-reaction with other pathogens or enterotoxin genes. The minimum detection values of enterotoxin sea, seb and sec genes were 10.2, 1.63, 9.4 copies/μL, respectively. The coefficient of variation within and between groups was less than 5%. Conclusion This method is fast, sensitive, accurate and reliable, which lays a foundation for the rapid detection of Staphylococcus aureus enterotoxin and the development of multiple qPCR kits.
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