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The micronutrient zinc inhibits EAEC strain 042 adherence, biofilm formation, virulence gene expression, and epithelial cytokine responses benefiting the infected host

机译:微量营养素锌可抑制EAEC 042菌株的粘附,生物膜形成,毒力基因表达和上皮细胞因子反应,从而使受感染的宿主受益

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Enteroaggregative Escherichia coli (EAEC) is a major pathogen worldwide, associated with diarrheal disease in both children and adults, suggesting the need for new preventive and therapeutic treatments. We investigated the role of the micronutrient zinc in the pathogenesis of an E. coli strain associated with human disease. A variety of bacterial characteristics-growth in vitro, biofilm formation, adherence to IEC-6 epithelial cells, gene expression of putative EAEC virulence factors as well as EAEC-induced cytokine expression by HCT-8 cells-were quantified. At concentrations (≤ 0.05 mM) that did not alter EAEC growth (strain 042) but that are physiologic in serum, zinc markedly decreased the organism's ability to form biofilm (P 0.001), adhere to IEC-6 epithelial cells (P 0.01), and express putative EAEC virulence factors (aggR, aap, aatA, virK) (P 0.03). After exposure of the organism to zinc, the effect on virulence factor generation was prolonged (3 h). Further, EAEC-induced IL-8 mRNA and protein secretion by HCT-8 epithelial cells were significantly reduced by 0.05 mM zinc (P 0.03). Using an in vivo murine model of diet-induced zinc-deficiency, oral zinc supplementation (0.4 μg/mouse daily) administered after EAEC challenge (1010 CFU/mouse) significantly abrogated growth shortfalls (by 90%; P 0.01); furthermore, stool shedding was reduced (days 9-11) but tissue burden of organisms in the intestine was unchanged. These findings suggest several potential mechanisms whereby physiological levels of zinc alter pathogenetic events in the bacterium (reducing biofilm formation, adherence to epithelium, virulence factor expression) as well as the bacterium's effect on the epithelium (cytokine response to exposure to EAEC) to alter EAEC pathogenesis in vitro and in vivo. These effects may help explain and extend the benefits of zinc in childhood diarrhea and malnutrition.
机译:肠聚合性大肠杆菌(EAEC)是世界范围内的主要病原体,在儿童和成人中均与腹泻病有关,这表明需要新的预防和治疗方法。我们调查了微量营养元素锌在与人类疾病相关的大肠杆菌菌株的发病机理中的作用。量化了各种细菌特征-体外生长,生物膜形成,对IEC-6上皮细胞的粘附,假定的EAEC毒力因子的基因表达以及HCT-8细胞对EAEC诱导的细胞因子表达的影响。浓度(≤0.05 mM)不会改变EAEC的生长(042菌株),但在血清中具有生理性,锌显着降低了生物形成生物膜的能力(P <0.001),粘附于IEC-6上皮细胞(P <0.01 ),并表达推定的EAEC毒力因子(aggR,aap,aatA,virK)(P <0.03)。生物体暴露于锌后,对毒力因子产生的影响得以延长(> 3小时)。此外,0.05 mM锌显着降低了HCT-8上皮细胞EAEC诱导的IL-8 mRNA和蛋白分泌(P <0.03)。使用饮食诱导的锌缺乏的体内鼠模型,在EAEC激发后(1010 CFU /小鼠)口服锌补充剂(每天0.4μg/小鼠)可显着消除生长不足(> 90%; P <0.01);此外,粪便脱落减少了(第9-11天),但肠道中生物的组织负荷没有变化。这些发现表明,锌的生理水平可以改变细菌中的致病事件(减少生物膜形成,对上皮的粘附,毒力因子表达)以及细菌对上皮的影响(细胞因子对暴露于EAEC的反应)以改变EAEC的几种潜在机制。体内外发病机理。这些作用可能有助于解释和扩展锌在儿童腹泻和营养不良中的益处。

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