Laboratorio de Microbiología Molecular, Departamento de Ciencias Biológicas, Facultad de Ciencias Biológicas, Universidad Andres Bello, Santiago, Chile.
DOE Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, USA.
Microbiology (Reading). 2013 Oct;159(Pt 10):2049-2057. doi: 10.1099/mic.0.066787-0. Epub 2013 Aug 5.
In response to antibiotics, bacteria activate regulatory systems that control the expression of genes that participate in detoxifying these compounds, like multidrug efflux systems. We previously demonstrated that the BaeSR two-component system from Salmonella enterica serovar Typhimurium (S. Typhimurium) participates in the detection of ciprofloxacin, a bactericidal antibiotic, and in the positive regulation of mdtA, an efflux pump implicated in antibiotic resistance. In the present work, we provide further evidence for a role of the S. Typhimurium BaeSR two-component system in response to ciprofloxacin treatment and show that it regulates sodA expression. We demonstrate that, in the absence of BaeSR, the transcript levels of sodA and the activity of its gene product are lower. Using electrophoretic mobility shift assays and transcriptional fusions, we demonstrate that BaeR regulates sodA by a direct interaction with the promoter region.
针对抗生素,细菌激活调节系统来控制参与解毒这些化合物的基因的表达,如多药外排系统。我们之前证明,来自鼠伤寒沙门氏菌(S. Typhimurium)的 BaeSR 双组分系统参与环丙沙星(一种杀菌抗生素)的检测,以及与抗生素耐药性相关的外排泵 mdtA 的正调控。在本工作中,我们进一步证明了 S. Typhimurium BaeSR 双组分系统在应对环丙沙星处理中的作用,并表明它调节 sodA 的表达。我们证明,在没有 BaeSR 的情况下,sodA 的转录水平和其基因产物的活性较低。通过电泳迁移率变动分析和转录融合实验,我们证明 BaeR 通过与启动子区域的直接相互作用来调节 sodA。