期刊文献+

实时定量PCR法快速检测水产品中的副溶血性弧菌 被引量:7

Detection of Vibrio parahaemolyticus in seafood products by real-time quantitative PCR assay
下载PDF
导出
摘要 副溶血性弧菌是一种广泛存在于水产品中的食源性致病菌,可污染食物,引起严重的食物中毒。利用实时定量PCR方法建立一种快速检测水产品中副溶血性弧菌的方法,根据随机扩增多态性分析(RAPD)鉴定特异性片段,设计特异性引物。采用建立的实时定量PCR方法检测市售水产品20份,检出阳性食品6份,最小检测灵敏度为50 fg DNA,与传统微生物检测结果相比无显著差异。该检测方法特异性强,灵敏度高。 Vibrio parahaemolyticus is a food-borne pathogen, which can contaminate food and cause serious and acute gastroenteritis to human beings. In this study, a real-time polymerase chain reaction (PCR) assay was developed for the quantitative detection of Vibrio parahaemolyticus in aquatic products. Randomly amplified polymorphic DNA (RAPD) method was introduced to characterize species-specific DNA fragment of V. parahaemolyticus , and specific primers were designed. The proposed method was used to detect V. parahaemolyticus in 20 aquatic products on sale. It was shown that 6 samples out of 20 were carrying V. parahaemolyticus . The minimum detection sensitivity was 50 fg DNA. Compared with the methods recommended in national standard, the proposed method was swifter and more convenient to detect V. parahaemolyticus in auqatic products.
作者 陈琳 周青青 顾青 郦萍 CHEN Lin;ZHOU Qingqing;GU Qing;LI Ping(Key Laboratory for Food Microbial Technology of Zhejiang Province, Zhejiang Gongshang University, Hangzhou 310018 , China;Hangzhou Wahaha Group Co., Ltd., Hangzhou 310018 , China)
出处 《浙江农业学报》 CSCD 北大核心 2019年第5期823-828,共6页 Acta Agriculturae Zhejiangensis
基金 浙江省重大专项(2015C02039 2015C02022) 国家自然科学基金(31606449 31871775) 浙江省自然科学基金(LY16C200002 LQ18C200004)
关键词 副溶血性弧菌 随机扩增多态性分析 实时荧光定量PCR Vibrio parahaemolyticus randomly amplified polymorphic DNA real-time polymerase chain reaction
  • 相关文献

参考文献3

二级参考文献35

  • 1张美玲,周志华,赵立平.粪便样品中大肠杆菌多态性分子研究[J].微生物学通报,2005,32(2):5-9. 被引量:10
  • 2胡骑,程安春,汪铭书,刘艳丽,葛忠源,黄永成,张素辉,杨晓燕,齐雪峰,陈孝跃.16SrDNA实时荧光定量PCR检测DPV强毒感染鸭气管及消化道大肠杆菌动力学[J].四川农业大学学报,2006,24(3):331-336. 被引量:4
  • 3江树勋,吴圣静,李寿崧,饶静静,江云.PCR检测沙门氏菌invA基因的灵敏度[J].食品科技,2006,31(10):251-253. 被引量:12
  • 4王毳,闫磊,曾庆祝.沙门氏菌的检测技术与方法[J].现代食品科技,2007,23(5):82-85. 被引量:64
  • 5IZHAR U H, VIC G, ROB K, et al. Development of a Rapid Quantitative PCR Assay for Direct Detection and Quantification of Culmrable and Non-culmrable Escherichia coil from Agriculture watersheds[J].Journal of Microbiological Methods, 2007, 69: 480 - 488.
  • 6BEJ A K, STEFFAN R J, DICESARE J, et al. Detection of Coliform Bacteria in Water by Polymerase Chain Reaction and Gene Probes[J]. Applied and Environment Microbiology, 1990, 56:307 - 314.
  • 7IQBAL S, ROBINSON J, DEERE D, et al. Efficiency of the Polymerase Chain Reaction Amphfication of the Uid Gene for Detection of Escherichia coli in Contaminated Water [J]. Letters in Applied Microbiology, 1997, 24:498 - 502.
  • 8TSENT H Y, LIN C K, CHI W R. Development and Use of 16S rRNA Gene Targeted PCR Primers for the Identification of Escherichia coli Cells in Water [J]. Appfied and Environment Microbiology, 1998, 85:554 - 560.
  • 9GRANT M A, WEAGENT S D, FENG P. Glutamate Decarboxylase Genes as a Prescreening Marker for Detection of Pathogenic Escherichia coli Groups[J]. Applied and Environment Microbiology, 2001, 67:3110-3114.
  • 10HORACHOVA K, MLEJNKOVA H, MLEJNEK P. Direct Detection of Bacterial Fecal Indicators in Water Samples Using PCR [J]. Water Science and Technology, 2006, 54:135 - 140.

共引文献82

同被引文献106

引证文献7

二级引证文献28

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