高飞,曹 进,骆海鹏,任 秀,刘 娜,陈怡文,余 文,谢冠东,崔生辉.食源性致病菌快速检测方法的探索研究[J].食品安全质量检测学报,2016,7(9):3521-3524
食源性致病菌快速检测方法的探索研究
Comparative research of different detection methods of foodborne bacteria
投稿时间:2016-05-18  修订日期:2016-09-21
DOI:
中文关键词:  食源性致病菌  传统细菌培养法  荧光定量PCR检测法
英文关键词:foodborne pathogens  traditional bacterial culture method  fluorescence quantitative PCR detection
基金项目:北京市科技计划项目(D161100002116003)
作者单位
高飞 中国食品药品检定研究院 
曹 进 中国食品药品检定研究院 
骆海鹏 中国食品药品检定研究院 
任 秀 中国食品药品检定研究院 
刘 娜 中国食品药品检定研究院 
陈怡文 中国食品药品检定研究院 
余 文 中国食品药品检定研究院 
谢冠东 中国食品药品检定研究院 
崔生辉 中国食品药品检定研究院 
AuthorInstitution
GAO Fei National Institutes for Food and Drug Control 
CAO Jin National Institutes for Food and Drug Control 
LUO Hai-Peng National Institutes for Food and Drug Control 
REN Xiu National Institutes for Food and Drug Control 
LIU Na National Institutes for Food and Drug Control 
CHEN Yi-Wen National Institutes for Food and Drug Control 
YU Wen National Institutes for Food and Drug Control 
XIE Guan-Dong National Institutes for Food and Drug Control 
CUI Sheng-Hui National Institutes for Food and Drug Control 
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中文摘要:
      目的 探讨传统细菌培养法及荧光定量PCR检测两种检测方法在食源性致病菌上的检出效果。方法 对2015年采集的7类食品共600例样品采用传统细菌培养法及增菌后的增菌液荧光定量PCR检测, 对检测结果进行分析比较。结果 被检食品存在食源性致病菌污染, 600例样品共检测出35株致病菌, 食品致病菌的总检出率为5.83%, 其中副溶血性弧菌与金黄色葡萄球菌检出率最高, 达到15%。蜡样芽胞杆菌检出率较高, 达到10.00%。传统细菌培养法致病菌阳性检出率为2.67%, 荧光定量PCR检测致病菌阳性检出率为3.17%, 两种检测方法下的检出率差异没有明显差异(X2=1.882, P>0.05)。结论 检测中将传统细菌培养法同荧光定量PCR检测这两种检测方法结合起来, 不仅提高了食源性致病菌检出率, 也可缩短检测时间, 提高检出率。后续研究将继续加大样本量并覆盖更多食品种类。
英文摘要:
      Objective To discuss the detection results by using the traditional bacterial culture method and the fluorescence quantitative PCR detection method. Methods Totally 7 kinds of food overall 600 samples were collected in 2015, and analyzed by the methods of fluorescence quantitative PCR detection and traditional bacterial culture, and test results were compared and analyzed. Results The foodborne pathogenic bacteria pollution was occurred in the food, 35 strains of pathogenic bacteria were detected in 600 samples, total detection rate of food pathogenic microbe was 5.83%, and the detection rates of Vibrio parahaemolyticus and Staphylococcus aerogenes were the highest, reaching 15.00%. Meanwhile, the detection rate of Bacillus cereus was relatively high, reaching 10.00%. The positive rate of pathogenic bacteria by traditional bacterial culture method was 2.67%, by fluorescence quantitative PCR detection method was 3.17%, and there was no significant difference (X2=1.882, P>0.05) between the two kinds of detection methods. Conclusion The detection combined with the traditional bacterial culture method and the fluorescence quantitative PCR method, not only improved foodborne pathogen detection rate, but also shortened the detection time, and improved the detection sensitivity. Subsequent research will continue to focus on increasing the sample size and cover more types of food.
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