Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 600 S. Mathews Ave, Urbana, IL, 61801, USA.
Department of Microbiology and Immunology, Faculty of Pharmacy, Helwan University - Ain Helwan, Helwan, 11795, Egypt.
BMC Microbiol. 2019 Sep 5;19(1):211. doi: 10.1186/s12866-019-1583-7.
Salmonella enterica serovar Typhimurium is a common food-borne pathogen. S. enterica uses a type III secretion system encoded within Salmonella pathogenicity island 1 (SPI-1) to invade intestinal epithelial cells. A complex network of interacting transcription factors regulates SPI-1 gene expression. In addition, SPI-1 gene expression is coupled to flagellar gene expression. Both SPI-1 and flagellar gene expression are bistable, with co-existing populations of cells expressing and not expressing these genes. Previous work demonstrated that nutrients could be used to tune the fraction of cells expressing the flagellar genes. In the present study, we tested whether nutrients could also tune the fraction of cells expressing the SPI-1 genes through transcriptional crosstalk with the flagellar genes.
Nutrients alone were not found to induce SPI-1 gene expression. However, when the cells were also grown in the presence of acetate, the concentration of nutrients in the growth medium was able to tune the fraction of cells expressing the SPI-1 genes. During growth in nutrient-poor medium, acetate alone was unable to induce SPI-1 gene expression. These results demonstrate that acetate and nutrients synergistically activate SPI-1 gene expression. The response to acetate was governed by the BarA/SirA two-component system and the response to nutrients was governed by transcriptional crosstalk with the flagella system, specifically through the action of the flagellar regulator FliZ.
Acetate and nutrients are capable of synergistically activating SPI-1 gene expression. In addition, these signals were found to tune the fraction of cells expressing the SPI-1 genes. The governing mechanism involves transcriptional crosstalk with the flagellar gene network. Collectively, these results further our understanding of SPI-1 gene regulation and provide the basis for future studies investigating this complex regulatory mechanism.
鼠伤寒沙门氏菌是一种常见的食源性病原体。鼠伤寒沙门氏菌使用一种编码于沙门氏菌致病岛 1(SPI-1)内的 III 型分泌系统来入侵肠道上皮细胞。一个相互作用的转录因子复杂网络调节 SPI-1 基因表达。此外,SPI-1 基因表达与鞭毛基因表达偶联。SPI-1 和鞭毛基因表达均为双稳态,细胞群体中同时存在表达和不表达这些基因的细胞。先前的工作表明,营养物质可用于调节表达鞭毛基因的细胞比例。在本研究中,我们测试了营养物质是否也可以通过与鞭毛基因的转录串扰来调节表达 SPI-1 基因的细胞比例。
单独的营养物质不能诱导 SPI-1 基因表达。然而,当细胞在乙酸盐存在的情况下生长时,生长培养基中的营养物质浓度能够调节表达 SPI-1 基因的细胞比例。在营养贫乏的培养基中生长时,单独的乙酸盐不能诱导 SPI-1 基因表达。这些结果表明,乙酸盐和营养物质协同激活 SPI-1 基因表达。对乙酸盐的反应受 BarA/SirA 双组分系统调控,对营养物质的反应受与鞭毛系统的转录串扰调控,具体通过鞭毛调节因子 FliZ 的作用。
乙酸盐和营养物质能够协同激活 SPI-1 基因表达。此外,这些信号被发现能够调节表达 SPI-1 基因的细胞比例。调控机制涉及与鞭毛基因网络的转录串扰。总的来说,这些结果进一步加深了我们对 SPI-1 基因调控的理解,并为未来研究这一复杂调控机制提供了基础。