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8起副溶血性弧菌食物中毒分子流行病学特征分析 被引量:7

Molecular epidemiology traits of 8 Vibrio parahaemolyticus food poisoning incidents
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摘要 目的调查并分析镇江及周边部分地区8起副溶血性弧菌食物中毒的分子流行病学特征。方法对经API生化鉴定的40株副溶血性弧菌进行毒力基因(tdh和trh)及功能基因(toxRS/new和orf8)测定、血清学分型和脉冲场凝胶电泳(PFGE)分型。结果 tdh阳性率为85.0%(34/40),trh阳性率为5.0%(2/40),toxRS/new阳性率为50.0%(20/40),orf8阳性率为42.5%(17/40);血清型以O3∶K6为主;PFGE分型显示A^B群间相似度>80%。结论镇江及周边部分地区8起食物中毒事件中的副溶血性弧菌主要为O3∶K6大流行克隆,且具有高度同源性。 Objective To analyze the molecular epidemiology traits of Vibrio parahaemolyticu. in Zhenjiang and surrounding areas. Methods 40 Vibriu parahaemolyticus strains were collected from the samples of food poison incidents occurred in Zhenjiang and surrounding areas in 2011. Biochemical identification, tdh, trh and toxRS/new gene detection, serotyping and pulse-field gel electrophoresis (PFGE) were applied to these strains. Results The positive rate of tclh, trh, toxRS/new and orJ8 were 85.0% , 5.0% , 50. 0% and 42. 5% , respectively. The prevalent serotype was O3:K6 (32/40). The similarity of PFGE type between group A and B was more than 80%. Conclusion Strains from different regions in Zhenjiang and surrounding areas were mainly O3:K6 pandemic clone and highly homologous.
出处 《中国食品卫生杂志》 北大核心 2014年第1期9-13,共5页 Chinese Journal of Food Hygiene
基金 江苏省自然科学基金项目(BK2010350) 镇江市卫生科技重点专项项目(SH2011068)
关键词 副溶血性弧菌 血清型 O3:K6大流行克隆 脉冲场凝胶电泳 食源性致病菌 食物中毒 Vibrio parahaemolyticus serotype O3 : K6 pandemic clone pulse-field gel electrophoresis food-borne pathogens food poisoning
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参考文献14

  • 1Yeung P S M, Boor K J. Epidemiology, pathogenesis, andprevention of foodborne Vibrio parahaemolyticus infections [ J].Foodborne Pathog Dis,2004 ,1(2) :74-88.
  • 2刘秀梅,陈艳,王晓英,计融.1992~2001年食源性疾病暴发资料分析——国家食源性疾病监测网[J].卫生研究,2004,33(6):725-727. 被引量:333
  • 3刘丽萍,徐岚,何晓砚,李歆彤.镇江市区市售食品中食源性致病菌检测情况分析[J].实用预防医学,2009,16(6):1835-1837. 被引量:8
  • 4CHAO G, JIAO X, ZHOU X, et al. Serodiversity,pandemic 03 : K6clone,molecular typing,and antibiotic susceptibility of foodborne andclinical Vibrio parahaemolyticus isolates in Jiangsu,China [ J].Foodborne Pathog Dis,2009 ,6(6) :1021-1028.
  • 5TIida,A Hattori, K Tagomori, et al. A filamentous phage associatedwith recent pandemic Vibrio parahaemolyticus 03 : K6 strains [ J]. JClin Microbiol ,2000,38 :2156-2161.
  • 6Parsonss M B , Cooper K L F, Kubota K A, et al. PulseNet USAstandardized pulsed-field gel electrophoresis protocol for subtyping ofVibrio parahaemolyticus [ J]. Foodborne Pathog Dis,2007,4 (3):285-292.
  • 7Kam K M,Luey C K Y,Parsonss M B,et al. Evaluation andvalidation of a PulseNet standardized pulsed-field gel electrop-horesis protocol for subtyping Vibrio parahaemolyticus : an inter-national multicenter collaborative study [ J]. J Clin Microbiol,2008,46(8) :2766-2773.
  • 8Tenover F C , Arbeit R D, Goering R V, et al. Interpretingchromosomal DNA restriction patterns produced by pulsed-fieldgel electrophoresis: criteria for bacterial strain typing[ J]. J ClinMicrobial,1995f33(9) :2233-2239.
  • 9Taniguchi H, Hirano H, Kubomura S,et al. Comparison of the nucleo-tide sequences of the genes for the thermolabile hemolysin fromVibrio parahaemolyticus [ J]. Microb Pathogen,1986,1 (5) :425-432.
  • 10Nishibuchi M,Kaper J B. Thermostable direct hemolysin gen ofVibrio parahaemolyticus : a virulence gene acquired by a marinebacterium[ J]. Infect Immun,1995 ,63(6) :2093-2099.

二级参考文献16

  • 1齐小秋.病原生物学检验-细菌[M].卫生部病原生物学检验教材编写组,2009.369.
  • 2BEJ 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.
  • 3TADA 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.
  • 4KIM 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.
  • 5PARSONS 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.
  • 6KAM 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.
  • 7DEPAOLA 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.
  • 8MCLAUGHLIN 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.
  • 9MARSHALL S, CLARK C G, WANG G, et al. Comparison of molecular methods for typing Vibrio parahaemolytlcus [ J ]. J Clin Microbiol, 1999, 37 (8) : 2473-2478.
  • 10ZHOU H J, DIAO B W, CUI Z G, et al. Comparison of automated ribotyping and pulsed-field gel electrophoresis for subtyplng of Vibrio cholera [ J ]. Lett Appl Microbiol, 2009, 48 (6) : 726-731.

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