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酸应激诱导的肠出血性大肠杆菌O157 : H7毒力变化

Acid-stress-induced changes in enterohaemorrhagic Escherichia coli O157 : H7 virulence.

作者信息

House B, Kus J V, Prayitno N, Mair R, Que L, Chingcuanco F, Gannon V, Cvitkovitch D G, Barnett Foster D

机构信息

Department of Chemistry and Biology, Ryerson University, Toronto, ON M5B 2K3, Canada.

Faculty of Dentistry, University of Toronto, Toronto, ON, Canada.

出版信息

Microbiology (Reading). 2009 Sep;155(Pt 9):2907-2918. doi: 10.1099/mic.0.025171-0. Epub 2009 Jun 4.

Abstract

Enterohaemorrhagic Escherichia coli (EHEC) O157 : H7 is naturally exposed to a wide variety of stresses including gastric acid shock, and yet little is known about how this stress influences virulence. This study investigated the impact of acid stress on several critical virulence properties including survival, host adhesion, Shiga toxin production, motility and induction of host-cell apoptosis. Several acid-stress protocols with relevance for gastric passage as well as external environmental exposure were included. Acute acid stress at pH 3 preceded by acid adaptation at pH 5 significantly enhanced the adhesion of surviving organisms to epithelial cells and bacterial induction of host-cell apoptosis. Motility was also significantly increased after acute acid stress. Interestingly, neither secreted nor periplasmic levels of Shiga toxin were affected by acid shock. Pretreatment of bacteria with erythromycin eliminated the acid-induced adhesion enhancement, suggesting that de novo protein synthesis was required for the enhanced adhesion of acid-shocked organisms. DNA microarray was used to analyse the transcriptome of an EHEC O157 : H7 strain exposed to three different acid-stress treatments. Expression profiles of acid-stressed EHEC revealed significant changes in virulence factors associated with adhesion, motility and type III secretion. These results document profound changes in the virulence properties of EHEC O157 : H7 after acid stress, provide a comprehensive genetic analysis to substantiate these changes and suggest strategies that this pathogen may use during gastric passage and colonization in the human gastrointestinal tract.

摘要

肠出血性大肠杆菌(EHEC)O157 : H7自然暴露于包括胃酸冲击在内的多种应激因素中,但对于这种应激如何影响其毒力却知之甚少。本研究调查了酸应激对几种关键毒力特性的影响,包括生存能力、宿主黏附、志贺毒素产生、运动性以及宿主细胞凋亡的诱导。研究纳入了与胃内通过以及外部环境暴露相关的几种酸应激方案。在pH 5进行酸适应后,在pH 3进行急性酸应激显著增强了存活菌对上皮细胞的黏附以及细菌对宿主细胞凋亡的诱导。急性酸应激后运动性也显著增加。有趣的是,酸冲击对志贺毒素的分泌水平和周质水平均无影响。用红霉素预处理细菌消除了酸诱导的黏附增强,这表明酸冲击菌黏附增强需要从头合成蛋白质。利用DNA微阵列分析了暴露于三种不同酸应激处理的EHEC O157 : H7菌株的转录组。酸应激EHEC的表达谱显示与黏附、运动性和III型分泌相关的毒力因子有显著变化。这些结果证明了酸应激后EHEC O157 : H7毒力特性的深刻变化,提供了全面的遗传分析以证实这些变化,并提出了这种病原体在胃内通过和在人类胃肠道定植过程中可能采用的策略。

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