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Transcriptional Profile during Deoxycholate-Induced Sporulation in a Clostridium perfringens Isolate Causing Foodborne Illness

机译:产气荚膜梭菌分离株中脱氧胆酸盐诱导的孢子形成过程中的转录特征

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Clostridium perfringens type A is a common source of foodborne illness (FBI) in humans. Vegetative cells sporulate in the small intestinal tract and produce the major pathogenic factor C. perfringens enterotoxin. Although sporulation plays a critical role in the pathogenesis of FBI, the mechanisms inducing sporulation remain unclear. Bile salts were shown previously to induce sporulation, and we confirmed deoxycholate (DCA)-induced sporulation in C. perfringens strain NCTC8239 cocultured with human intestinal epithelial Caco-2 cells. In the present study, we performed transcriptome analyses of strain NCTC8239 in order to elucidate the mechanism underlying DCA-induced sporulation. Of the 2,761 genes analyzed, 333 were up- or downregulated during DCA-induced sporulation and included genes for cell division, nutrient metabolism, signal transduction, and defense mechanisms. In contrast, the virulence-associated transcriptional regulators (the VirR/VirS system, the agr system, codY , and abrB ) were not activated by DCA. DCA markedly increased the expression of signaling molecules controlled by Spo0A, the master regulator of the sporulation process, whereas the expression of spo0A itself was not altered in the presence or absence of DCA. The phosphorylation of Spo0A was enhanced in the presence of DCA. Collectively, these results demonstrated that DCA induced sporulation, at least partially, by facilitating the phosphorylation of Spo0A and activating Spo0A-regulated genes in strain NCTC8239 while altering the expression of various genes.IMPORTANCE Disease caused by Clostridium perfringens type A consistently ranks among the most common bacterial foodborne illnesses in humans in developed countries. The sporulation of C. perfringens in the small intestinal tract is a key event for its pathogenesis, but the factors and underlying mechanisms by which C. perfringens sporulates in vivo currently remain unclear. Bile salts, major components of bile, which is secreted from the liver for the emulsification of lipids, were shown to induce sporulation. However, the mechanisms underlying bile salt-induced sporulation have not yet been clarified. In the present study, we demonstrate that deoxycholate (one of the bile salts) induces sporulation by facilitating the phosphorylation of Spo0A and activating Spo0A-regulated genes using a transcriptome analysis. Thus, this study enhances our understanding of the mechanisms underlying sporulation, particularly that of bile salt-induced sporulation, in C. perfringens .
机译:A型产气荚膜梭菌是人类常见的食源性疾病(FBI)来源。营养细胞在小肠形成孢子,并产生主要致病因子产气荚膜梭菌肠毒素。尽管孢子形成在FBI的发病机理中起着至关重要的作用,但诱导孢子形成的机制仍不清楚。胆汁盐先前已显示出诱导孢子形成的作用,并且我们证实了脱氧胆酸盐(DCA)在与人肠上皮Caco-2细胞共培养的产气荚膜梭菌菌株NCTC8239中诱导的孢子形成。在本研究中,我们进行了菌株NCTC8239的转录组分析,以阐明DCA诱导孢子形成的机制。在分析的2,761个基因中,有333个在DCA诱导的孢子形成过程中被上调或下调,其中包括用于细胞分裂,营养代谢,信号转导和防御机制的基因。相反,与毒力相关的转录调节因子(VirR / VirS系统,agr系统,codY和abrB)没有被DCA激活。 DCA显着增加了孢子形成过程的主要调控因子Spo0A控制的信号分子的表达,而在DCA存在或不存在的情况下,spo0A本身的表达均未改变。在DCA的存在下Spo0A的磷酸化增强。总的来说,这些结果表明DCA通过促进Spo0A的磷酸化和激活菌株NCTC8239中Spo0A调控的基因,同时改变了各种基因的表达,至少部分地诱导了孢子形成。发达国家人类常见的细菌性食源性疾病。产气荚膜梭菌在小肠中的孢子形成是其发病机理的关键事件,但是目前尚不清楚产气荚膜梭菌在体内形成孢子的因素和潜在机制。胆汁的主要成分胆汁盐(胆汁盐)是从肝脏分泌出来的,用于乳化脂质,已显示出引起孢子形成的作用。但是,胆汁盐诱导的孢子形成的机制尚未阐明。在本研究中,我们证明脱氧胆酸盐(胆汁盐之一)通过促进Spo0A的磷酸化和使用转录组分析激活Spo0A调控的基因来诱导孢子形成。因此,本研究增强了我们对产气荚膜梭菌孢子形成机制的理解,尤其是胆盐诱导的孢子形成的机制。

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