期刊文献+

一起两种血清型副溶血性弧菌食物中毒的毒力基因及分子分型研究 被引量:10

Research on toxin gene and molecular genotype of Vibrio parahaemolyticus with different serotypes isolated from samples of one food poisoning
原文传递
导出
摘要 目的:对一起两种血清型副溶血性弧菌引起的食物中毒病原菌进行毒力基因及分子分型研究。方法:参照WS271-2007等标准对10名病人的肛拭进行致病菌的检测,对分离的副溶血性弧菌进行血清学试验;运用荧光定量PCR检测分离菌株的毒力基因,并用脉冲场凝胶电泳(PFGE)进行分子分型。结果:10份样本均检出O4:K8血清型副溶血性弧菌,其中5份样本同时检出O3:K6血清型副溶血性弧菌。两种血清型的副溶血性弧菌毒力基因检测均为tdh阳性、trh阴性。PFGE分型显示,同一血清型的菌株为高度相似克隆,相似度在92.9%~100%之间,同一样本不同血清型的菌株为不同克隆。结论:这是一起由O4:K8和O3:K6两种血清型副溶血性弧菌混合感染引起的食物中毒。 Objective :To analyse the toxin genes and molecular genotype of Vibrio parahaemolyticus with two kinds of serotypes isolated from samples of one food poisoning. Methods: The isolation and identification of pathogen from swab anal were conducted according to WS271 -2007 etc. Then serological test was done on the isolated Vibrio parahaemolyticus, fluorescence quantitative PCR was used to detect the toxin gene, and PFGE was used for molecular typing. Results: All the 10 samples were positive for 04 : K8 Vibrio parahaemolyticus, of which 5 samples were also positive for 03 : K6 Vibrio parahaemolyticus. Toxin gene detection of Vibrio parahaemolyticus of two serotypes were tdh positive, trh negative. PFGE typing showed that strains of the same serotype were highly similar, and the similarity was from 92.9% to 100%, while strains from the same sample of different serotypes were different clones. Conclusion: This food poisoning was caused by coinfecion with two serotypes of Vibrio parahaemolyticus: the 04:K8 serotype and the 03:K6 serotype.
出处 《中国卫生检验杂志》 北大核心 2012年第1期96-98,共3页 Chinese Journal of Health Laboratory Technology
关键词 副溶血性弧菌 血清型 毒力基因 脉冲场凝胶电泳 Vibrio parahaemolyticus Serotype Toxin gene PFGE
  • 相关文献

参考文献4

二级参考文献23

  • 1扈庆华 ,郑薇薇 ,石晓路 ,李庆阁 ,王冰 ,庄志雄 ,刘小立 ,贺连华 ,吴平芳 .双重实时PCR快速同时检测霍乱弧菌和副溶血弧菌[J].中华微生物学和免疫学杂志,2004,24(12):1004-1007. 被引量:19
  • 2蔡潭溪,蒋鲁岩,黄克和.用基于TaqMan探针的Real-time PCR技术定量检测副溶血弧菌[J].微生物学报,2005,45(4):638-642. 被引量:25
  • 3张俊彦,梅玲玲,朱敏,张严峻,潘雪霞,石雅素,郑官增.301份海水产品副溶血性弧菌定量检测分析[J].中国卫生检验杂志,2007,17(3):509-510. 被引量:49
  • 4BEJ A K, PATTERSON D P, BRASHER C W, et al. Detection of total and hemolysin-producing Vibrio parahaemolyticus in shellfish using multiplex PCR amplification of tl, tdh and trh[J].J Microbiol Methods, 1999, 36(3) : 215-225.
  • 5TADA J, OHASHI T, NISHIMURA N, et al. Detection of the thermostable direct hemolysin gene(tdh) and the thermostable direct hemolysin-related hemolysin gen (trh) of vibrio parahaemolyticus by polymerase chain reaction [ J]. Mol Cell Probes, 1992, 6: 477-487.
  • 6KIM Y B, OKUDA J, MATSUMOTO C, et al. Identification of Vibrio parahaemolyticus strains at the species level by PCR targeted to the toxR gene [J]. J Clin Mierobiol, 1999, 37(4) :1173-1177.
  • 7PARSONS M B, COOPER K L F, KUBOTA K A, et al. PulseNet USA standardized pulsed-field gel electrophoresis protocol for subtyping of Vibrio parahaemolyticus [ J ]. Foodborne Pathog Dis, 2007, 4 ( 3 ) :285-292.
  • 8KAM K M, LUEY C K Y, PARSONS M B, et al. Evaluation and validation of a PulseNet standardized pulsed-field gel eleetrophoresis protocol for subtyping Vibrio parahaemolyticus: an international muhieenter collaborative study[ J ]. J Clin Mierobiol, 2008, 46 (8) : 2766-2773.
  • 9DEPAOLA A, KAYSNER C A, BOWERS J, et al. Environmental investigations of Vibrio parahaemolyticus in oysters after outbreaks in Washington, Texas, and New York (1997 and 1998)[J]. Appl Environ Microbiol, 2000, 66 ( 11 ) : 4649-4654.
  • 10MCLAUGHLIN J B, DEPAOLA A, BOPP C A, et al. Outbreak of Vibrio parahaemolyticus gastroenteritis associated with Alaskan oysters [J]. N EnglJ Med, 2005, 353(14): 1463-1470.

共引文献43

同被引文献80

引证文献10

二级引证文献84

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