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铁感应 fur 调控器在环境酸化过程中控制沙门氏菌致病性岛 2 基因的表达时间和水平。

The iron-sensing fur regulator controls expression timing and levels of salmonella pathogenicity island 2 genes in the course of environmental acidification.

机构信息

Division of Microbiology, Department of Molecular Cell Biology, Samsung Biomedical Research Institute, Sungkyunkwan University School of Medicine, Suwon, South Korea.

出版信息

Infect Immun. 2014 Jun;82(6):2203-10. doi: 10.1128/IAI.01625-13. Epub 2014 Mar 18.

Abstract

In order to survive inside macrophages, Salmonella produces a series of proteins encoded by genes within Salmonella pathogenicity island 2 (SPI-2). In the present study, we report that Fur, a central regulator of iron utilization, negatively controls the expression of SPI-2 genes. Time course analysis of SPI-2 expression after the entry of Salmonella into macrophages revealed that SPI-2 genes are induced earlier and at higher levels in the absence of the Fur regulator. It was hypothesized that Fur repressed the SPI-2 expression that was activated during acidification of the phagosome. Indeed, as pH was lowered from pH 7.0 to pH 5.5, the lack of Fur enabled SPI-2 gene expression to be induced at higher pH and to be expressed at higher levels. Fur controlled SPI-2 genes via repression of the SsrB response regulator, a primary activator of SPI-2 expression. Fur repressed ssrB expression both inside macrophages and under acidic conditions, which we ascribe to the direct binding of Fur to the ssrB promoter. Our study suggests that Salmonella could employ iron inside the phagosome to precisely control the timing and levels of SPI-2 expression inside macrophages.

摘要

为了在巨噬细胞内生存,沙门氏菌产生了一系列由沙门氏菌致病岛 2(SPI-2)内基因编码的蛋白质。在本研究中,我们报告说,铁利用的中央调节剂 Fur,负调控 SPI-2 基因的表达。沙门氏菌进入巨噬细胞后 SPI-2 表达的时程分析显示,在没有 Fur 调节剂的情况下,SPI-2 基因更早且更高水平地被诱导。假设 Fur 抑制了吞噬体酸化过程中激活的 SPI-2 表达。事实上,当 pH 值从 7.0 降低到 5.5 时,缺乏 Fur 使 SPI-2 基因表达能够在更高的 pH 值下被诱导,并以更高的水平表达。Fur 通过抑制 SsrB 应答调节子来控制 SPI-2 基因的表达,SsrB 是 SPI-2 表达的主要激活子。Fur 抑制了巨噬细胞内和酸性条件下的 ssrB 表达,我们将其归因于 Fur 与 ssrB 启动子的直接结合。我们的研究表明,沙门氏菌可以在吞噬体内利用铁来精确控制 SPI-2 在巨噬细胞内的表达时间和水平。

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