期刊文献+

食品接触材料中3种致病菌的多重荧光PCR检测 被引量:5

Multiplex Real-Time PCR Assays for Detection of Three Pathogenic Bacteria in Food Contact Material
下载PDF
导出
摘要 建立并优化食品接触材料中金黄色葡萄球菌、沙门氏菌和副溶血性弧菌3种致病菌的多重实时荧光聚合酶链式反应(polymerase chain reaction,PCR)检测方法,评价此方法的特异性和灵敏度,并模拟阳性样品进行检测。结果显示,该方法特异性良好,检测灵敏度均能达到10~3 CFU/mL,为食品接触材料的微生物检测提供技术保障。 Multiplex real-time polymerase chain reaction(PCR)assays were established and optimized for detection of Staphylococcus aureus,Salmonella and Vibrio parahaemolyticus in food contact materials.The specificity and sensitivity of this method was evaluated and the simulated positive samples are tested.The results showed that this method showed good specificity and the sensitivity could achieve to 103 CFU/mL,which provided technical support for detection of pathogenic bacteria in food contact material.
作者 柯振华 张雅薇 陈筱婷 林碧莲 孟鹏 高宇 戴明 KE Zhen-hua;ZHANG Ya-wei;CHEN Xiao-ting;LIN Bi-lian;MENG Peng;GAO Yu;DAI Ming(National Centre for Quality Supervision and Testing of Processed Food(Fuzhou),Fujian Inspection and Research Institute for Product Quality,Fuzhou 350000,Fujian,China)
出处 《食品研究与开发》 CAS 北大核心 2018年第23期134-141,共8页 Food Research and Development
基金 福建省质量技术监督局科技项目(FJQI2016010)
关键词 多重实时荧光聚合酶链式反应(PCR) 金黄色葡萄球菌 沙门氏菌 副溶血性弧菌 食品接触材料 multiplex real-time polymerase chain reaction(PCR) Staphylococcus aureus Salmonella Vibrio parahaemolyticus food contact material
  • 相关文献

参考文献6

二级参考文献68

  • 1杨洋,张伟,袁耀武,钟晓英,马雯.PCR检测乳品中金黄色葡萄球菌[J].中国农业科学,2006,39(5):990-996. 被引量:38
  • 2中华人民共和国卫生部.GB47894-2010食品安全国家标准食品微生物学检验沙门氏菌检验[S].北京:中国标准出版社,2010.
  • 3毛雪丹,胡俊峰,刘秀梅.2003-2007年中国1060起细菌性食源性疾病流行病学特征分析[J].中国食品卫生杂志,2010,22(3):224-228.
  • 4BALABAN N, RASOOLY A. Staphylococcal enterotoxins[J]. Interna- tional Journal of Food Microbiology, 2000, 61(1): 1-10.
  • 5KOTZEKIDOU P. Survey of Listeria monocytogenes, Salmonella spp. and Escherichia coli O157:H7 in raw ingredients and ready-to-eat products by commercial real-time PCR kits[J]. Food Microbiology, 2013, 35(2): 86-91.
  • 6YANG K, JENKINS D M, SU W W. Rapid concentration of bacteria using submicron magnetic anion exchangers for improving PCR- based multiplex pathogen detection [J]. Journal of Microbiological Methods, 2011, 86(1): 69-77.
  • 7KIM J, DEMEKE T, CLEAR R M, et al. Simultaneous detection by PCR of Escherichia coli, Listeria monocytogenes and Salmonella ty- phimurium in artificially inoculated wheat grain [J]. International Journal of Food Microbiology, 2006, 111(1): 21-25.
  • 8ELIZAQUIVEL P, GABALDON J A, AZNAR R. Quantification of Salmonella spp., Listeria monocytogenes and Escherichia coli O157: H7 in non-spiked food products and evaluation of real-time PCR as a diagnostic tool in routine food analysis[J]. Food Control, 2011, 22(2): 158-164.
  • 9FUSCO V, QUERO G M, MOREA M, et al. Rapid and reliable identi- fication of Staphylococcus aureus harbouring the enterotoxin gene cluster (egc) and quantitative detection in raw milk by real time PCR [J]. International Journal of Food Microbiology, 201 l, 144 (3): 528- 537.
  • 10PENNACCHIA C, ERCOLINI D, VILLANI F. Development of a Re- M-Time PCR assay for the specific detection of Brochothrix thermo- sphacta in fresh and spoiled raw meat[J]. International Journal of Food Microbiology, 2009, 134(3): 230-236.

共引文献49

同被引文献62

引证文献5

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部