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中国中东海岸副溶血性弧菌分离株的分子分型。

Molecular typing of Vibrio parahaemolyticus isolates from the middle-east coastline of China.

机构信息

MOST-USDA Joint Research Center for Food Safety & Bor Luh Food Safety Center, School of Agriculture & Biology, Shanghai Jiao Tong University, 800 Dongchuan Rd., Shanghai 200240, China.

出版信息

Int J Food Microbiol. 2012 Feb 15;153(3):402-12. doi: 10.1016/j.ijfoodmicro.2011.12.001. Epub 2011 Dec 19.

Abstract

The occurrence of outbreaks of Vibrio parahaemolyticus gastroenteritis in China highlights the need for strain characterization and subtyping of this pathogenic species. A total of 56 epidemiologically-unrelated strains of V. parahaemolyticus were isolated from clinical samples, seafood and various environmental sites in the middle-east coastline of China from 2006 to 2008. The isolates were characterized using four molecular typing methods, including ribotyping, enterobacterial repetitive intergenic consensus sequence PCR (ERIC-PCR), pulsed-field gel electrophoresis (PFGE), and sequence analysis of the gyrB gene. Genetic profiles of cluster analysis from these molecular typing tests clearly showed that there were differences in potential pathogenicity among isolates from seafood and its environments. Genetic characterization of two isolates (F13 and QS2) that originated from seafood demonstrated that they were potentially pathogenic. Discriminatory indices of four typing methods for the 56 V. parahaemolyticus isolates were differentiated by Simpson's Index of Diversity. The discriminatory index of ERIC-PCR typing was maximal (D=0.942), while that of sequence analysis of the gyrB gene was minimal (D=0.702). The discriminatory ability was greatly enhanced (D=0.966) when ERIC-PCR was coupled with sequence analysis of the gyrB gene. These results suggest that ERIC-PCR combined with sequence analysis of gyrB gene may be a reliable, rapid typing strategy for V. parahaemolyticus strains.

摘要

在中国,副溶血性弧菌肠胃炎的爆发凸显了对该病原菌进行菌株特征描述和亚型划分的必要性。2006 年至 2008 年期间,从中国中东海岸线的临床样本、海鲜和各种环境地点中分离出了 56 株与流行病学无关的副溶血性弧菌。采用核糖体分型、肠杆菌基因间重复一致性序列 PCR(ERIC-PCR)、脉冲场凝胶电泳(PFGE)和gyrB 基因序列分析等 4 种分子分型方法对这些分离株进行了特征描述。聚类分析的遗传图谱清楚地表明,来自海鲜及其环境的分离株在潜在致病性方面存在差异。对来自海鲜的两个分离株(F13 和 QS2)的遗传特征进行分析表明,它们具有潜在的致病性。通过 Simpson 多样性指数对 56 株副溶血性弧菌分离株的 4 种分型方法的区分指数进行了区分。ERIC-PCR 分型的区分指数最大(D=0.942),而 gyrB 基因序列分析的区分指数最小(D=0.702)。当 ERIC-PCR 与 gyrB 基因序列分析相结合时,其区分能力大大增强(D=0.966)。这些结果表明,ERIC-PCR 结合 gyrB 基因序列分析可能是副溶血性弧菌菌株的一种可靠、快速的分型策略。

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