INRAE, ISP, Université de Tours, Nouzilly, France.
INRAE, AgroParisTech, Université Paris Saclay, Jouy-en-Josas, France.
Virulence. 2023 Dec;14(1):2158663. doi: 10.1080/21505594.2022.2158663.
is the only bacterium able to enter a host cell by the two known mechanisms: trigger and zipper. The trigger mechanism relies on the injection of bacterial effectors into the host cell through the type III secretion system 1. In the zipper mechanism, mediated by the invasins Rck and PagN, the bacterium takes advantage of a cellular receptor for invasion. This study describes the transcriptomic reprogramming of the IEC-6 intestinal epithelial cell line to Typhimurium strains that invaded cells by a trigger, a zipper, or both mechanisms. Using . Typhimurium strains invalidated for one or other entry mechanism, we have shown that IEC-6 cells could support both entries. Comparison of the gene expression profiles of exposed cells showed that irrespective of the mechanism used for entry, the transcriptomic reprogramming of the cell was nearly the same. On the other hand, when gene expression was compared between cells unexposed or exposed to the bacterium, the transcriptomic reprogramming of exposed cells was significantly different. It is particularly interesting to note the modulation of expression of numerous target genes of the aryl hydrocarbon receptor showing that this transcription factor was activated by . Typhimurium infection. Numerous genes associated with the extracellular matrix were also modified. This was confirmed at the protein level by western-blotting showing a dramatic modification in some extracellular matrix proteins. Analysis of a selected set of modulated genes showed that the expression of the majority of these genes was modulated during the intracellular life of . Typhimurium.
触发和拉链。触发机制依赖于通过 III 型分泌系统将细菌效应器注入宿主细胞 1。在拉链机制中,Rck 和 PagN 介导,细菌利用细胞入侵受体。本研究描述了 IEC-6 肠上皮细胞系对触发、拉链或两种机制入侵细胞的转录组重编程。使用一种或另一种进入机制无效的 菌株,我们已经表明 IEC-6 细胞可以支持两种进入。暴露细胞的基因表达谱比较表明,无论进入机制如何,细胞的转录组重编程几乎相同。另一方面,当比较未暴露或暴露于细菌的细胞之间的基因表达时,暴露细胞的转录组重编程差异显著。值得注意的是,许多芳烃受体靶基因的表达受到调节,表明该转录因子被 感染激活。与细胞外基质相关的许多基因也被修饰。这通过蛋白质印迹在蛋白质水平上得到证实,显示某些细胞外基质蛋白的表达发生了显著变化。对一组选定的调节基因进行分析表明,这些基因的大多数在 体内生活期间表达发生了调节。