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水杨醛酰肼化合物对大肠杆菌O157:H7Ⅲ型分泌作用的表征

Characterization of the effects of salicylidene acylhydrazide compounds on type III secretion in Escherichia coli O157:H7.

作者信息

Tree Jai J, Wang Dai, McInally Carol, Mahajan Arvind, Layton Abigail, Houghton Irene, Elofsson Mikael, Stevens Mark P, Gally David L, Roe Andrew J

机构信息

Zoonotic and Animal Pathogens Research Laboratory, Immunity and Infection Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, 49 Little France Crescent, Edinburgh EH16 4SB, United Kingdom.

出版信息

Infect Immun. 2009 Oct;77(10):4209-20. doi: 10.1128/IAI.00562-09. Epub 2009 Jul 27.

Abstract

Recent work has highlighted a number of compounds that target bacterial virulence by affecting gene regulation. In this work, we show that small-molecule inhibitors affect the expression of the type III secretion system (T3SS) of Escherichia coli O157:H7 in liquid culture and when this bacterium is attached to bovine epithelial cells. Inhibition of T3SS expression resulted in a reduction in the capacity of the bacteria to form attaching and effacing lesions. Our results show that there is marked variation in the abilities of four structurally related compounds to inhibit the T3SS of a panel of isolates. Using transcriptomics, we performed a comprehensive analysis of the conserved and inhibitor-specific transcriptional responses to these four compounds. These analyses of gene expression show that numerous virulence genes, located on horizontally acquired DNA elements, are affected by the compounds, but the number of genes significantly affected varied markedly for the different compounds. Overall, we highlight the importance of assessing the effect of such "antivirulence" agents on a range of isolates and discuss the possible mechanisms which may lead to the coordinate downregulation of horizontally acquired virulence genes.

摘要

近期的研究工作突出了一些通过影响基因调控来靶向细菌毒力的化合物。在本研究中,我们表明小分子抑制剂在液体培养中以及当大肠杆菌O157:H7附着于牛上皮细胞时,会影响其三型分泌系统(T3SS)的表达。T3SS表达的抑制导致细菌形成紧密黏附并抹平损伤的能力降低。我们的结果表明,四种结构相关的化合物抑制一组分离株的T3SS的能力存在显著差异。利用转录组学,我们对这四种化合物的保守和抑制剂特异性转录反应进行了全面分析。这些基因表达分析表明,位于水平获得的DNA元件上的众多毒力基因受到这些化合物的影响,但不同化合物显著影响的基因数量差异明显。总体而言,我们强调评估此类“抗毒力”药物对一系列分离株的影响的重要性,并讨论可能导致水平获得的毒力基因协同下调的潜在机制。

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