张焱鑫,芦 云,王新宇,岑 彦,刘海涛,王 芳,薛晓晶.实时荧光聚合酶链式反应技术与国标方法检测致病菌的应用与研究[J].食品安全质量检测学报,2020,11(6):1941-1946
实时荧光聚合酶链式反应技术与国标方法检测致病菌的应用与研究
Application and research of real-time polymerase chain reaction and national standard method for detection of pathogenic bacteria
投稿时间:2019-12-04  修订日期:2020-01-08
DOI:
中文关键词:  实时荧光聚合酶链式反应技术  国标GB 4789  致病菌  沙门氏菌  单核细胞增生李斯特氏菌  副溶血性弧菌
英文关键词:real-time polymerase chain reaction  national standard GB 4789  pathogenic bacteria  Salmonella  Listeria monocytogenes  Vibrio parahaemolyticus
基金项目:
作者单位
张焱鑫 中国检验检疫科学研究院综合检测中心 
芦 云 中国检验检疫科学研究院综合检测中心 
王新宇 中国检验检疫科学研究院综合检测中心 
岑 彦 中国检验检疫科学研究院综合检测中心 
刘海涛 中国检验检疫科学研究院综合检测中心 
王 芳 中国检验检疫科学研究院综合检测中心 
薛晓晶 中国检验检疫科学研究院综合检测中心 
AuthorInstitution
ZHANG Yan-Xin Chinese Academy of Inspection and Quarantine Comprehensive Test Center 
LU Yun Chinese Academy of Inspection and Quarantine Comprehensive Test Center 
WANG Xin-Yu Chinese Academy of Inspection and Quarantine Comprehensive Test Center 
CEN Yan Chinese Academy of Inspection and Quarantine Comprehensive Test Center 
LIU Hai-Tao Chinese Academy of Inspection and Quarantine Comprehensive Test Center 
WANG Fang Chinese Academy of Inspection and Quarantine Comprehensive Test Center 
XUE Xiao-Jing Chinese Academy of Inspection and Quarantine Comprehensive Test Center 
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中文摘要:
      目的 比较实时荧光聚合酶链式反应技术(real-time polymerase chain reaction, RT-PCR)与国标方法在食品致病菌检测中的异同。方法 应用RT-PCR法及国标GB 4789系列对采集的60件畜产品、禽产品、水产品和乳及乳制品中的沙门氏菌、金黄色葡萄球菌、单核细胞增生李斯特氏菌以及副溶血性弧菌同时进行检测。结果 除了金黄色葡萄球菌检测结果均为阴性外, 其他3种致病菌2种方法都有检出, 但RT-PCR方法的阳性率均高于国标方法。对于沙门氏菌, 国标方法阳性率为1.67%, RT-PCR方法阳性率3.33%; 单核细胞增生李斯特氏菌国标方法阳性率为7.50%, RT-PCR方法阳性率为15.00%; 副溶血性弧菌国标方法阳性率为8.33%, RT-PCR方法阳性率为11.67%。结论 在本实验条件下, RT-PCR技术的阳性检测结果多于国标GB4789系列, 并且结果可完全覆盖国标GB4789。各企业实验室甚至政府主导的食品风险监测项目可根据产品特点, 合理应用RT-PCR技术以减少人员工作量, 方便产品放行并提高工作效率。
英文摘要:
      Objective To compare the similarities and differences between real-time polymerase chain reaction (RT-PCR) and national standard methods in the detection of food pathogens. Methods Salmonella, Staphylococcus aureus, Listeria monocytogenes and Vibrio parahaemolyticus in 60 livestock products, poultry products, aquatic products and dairy and dairy products were detected simultaneously by RT-PCR and GB 4789 series. Results Except for the negative results of Staphylococcus aureus, the other three pathogenic bacteria were detected by two methods, but the positive rate of RT-PCR method was higher than that of national standard method. For Salmonella, the positive rates of GB method and RT- PCR method were 1.67% and 3.33%, respectively. For Listeria monocytogenes, the positive rates of GB method and RT- PCR method were 7.50% and 15.00%, respectively. For Vibrio parahaemolyticus, the positive rates of GB method and RT-PCR method were 8.33% and 11.67%, respectively. Conclusion Under this experimental condition, RT-PCR technology has more positive detection results than the national standard GB 4789 series, and the results can completely cover the national standard GB 4789. Enterprise laboratories and even government-led food risk monitoring projects can reasonably apply RT-PCR technology to reduce personnel workload, facilitate product release and improve work efficiency based on product characteristics.
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