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The mechanisms that regulate Vibrio parahaemolyticus virulence gene expression differ between pathotypes

机译:调节致病性副溶血弧菌毒力基因表达的机制不同

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摘要

Most Vibrio parahaemolyticus isolates found in marine environments are non-pathogenic; however, certain lineages have acquired genomic pathogenicity islands (PAIs) that enable these isolates to cause human illness. The V. parahaemolyticus PAI contains one or both of two toxins: thermostable direct haemolysin (TDH) or TDH-related haemolysin (TRH) and type III secretion system 2 (T3SS2). Recently, a few V. parahaemolyticus isolates that do not have this PAI were obtained from clinical samples, and there has been interest in determining whether these isolates possess novel virulence factors. In this investigation, we have selected four V. parahaemolyticus isolates: a canonical pathogenic strain containing TDH, TRH and T3SS2; two strains from clinical cases which do not contain a PAI; and an environmental isolate which also does not contain a PAI. For each isolate, we analyzed differential gene expression after crude bile exposure. Several enteric bacterial pathogens are known to use bile as a signal to enhance virulence gene expression. We have shown that in the tdh-positive trh-positive pathotype gene virulence gene expression was not up-regulated in response to crude bile, strongly indicating that the current dogma of virulence gene regulation in V. parahaemolyticus needs to be revisited and separately investigated for each pathotype. In addition, we have created a list of genes of interest that were up-regulated in the non-canonical pathotypes which may contribute to virulence in these isolates.
机译:在海洋环境中发现的大多数副溶血性弧菌分离株是非致病性的。但是,某些谱系已经获得了使这些分离物引起人类疾病的基因组致病岛(PAI)。副溶血性弧菌PAI包含两种毒素中的一种或两种:热稳定的直接溶血素(TDH)或TDH相关的溶血素(TRH)和III型分泌系统2(T3SS2)。最近,从临床样品中获得了一些没有这种PAI的副溶血性弧菌分离株,人们对确定这些分离株是否具有新的毒力因子感兴趣。在这项调查中,我们选择了四种副溶血性弧菌:一种含有TDH,TRH和T3SS2的典型病原菌;另一种是TDH。来自临床病例的两种菌株不含PAI;和不含PAI的环境隔离物。对于每个分离物,我们分析了粗制胆汁暴露后的差异基因表达。已知几种肠细菌病原体使用胆汁作为增强毒力基因表达的信号。我们已经显示,在tdh阳性trh阳性致病型基因中,毒力基因表达未响应粗胆汁而上调,这强烈表明需要重新研究溶血弧菌中毒力基因调控的当前教条,并单独研究每个病态。此外,我们已经创建了在非典型病原体中上调的目标基因列表,这些基因可能会导致这些分离株的致病性。

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