Ćudić Emina, Surmann Kristin, Panasia Gianna, Hammer Elke, Hunke Sabine
FB 5 Microbiology, Department of Biology/Chemistry, University Osnabrück, Barbarastraße 11, 49076, Osnabrück, Germany.
Department of Biology, Institute of Molecular Microbiology and Biotechnology, Universität Münster, Corrensstraße 3, 48149, Münster, Germany.
BMC Microbiol. 2017 Sep 18;17(1):197. doi: 10.1186/s12866-017-1100-9.
The aminoglycoside antibiotic gentamicin was supposed to induce a crosstalk between the Cpx- and the Arc-two-component systems (TCS). Here, we investigated the physical interaction of the respective TCS components and compared the results with their respective gene expression and protein abundance. The findings were interpreted in relation to the global proteome profile upon gentamicin treatment.
We observed specific interaction between CpxA and ArcA upon treatment with the aminoglycoside gentamicin using Membrane-Strep-tagged protein interaction experiments (mSPINE). This interaction was neither accompanied by detectable phosphorylation of ArcA nor by activation of the Arc system via CpxA. Furthermore, no changes in absolute amounts of the Cpx- and Arc-TCS could be determined with the sensitive single reaction monitoring (SRM) in presence of gentamicin. Nevertheless, upon applying shotgun mass spectrometry analysis after treatment with gentamicin, we observed a reduction of ArcA ~ P-dependent protein synthesis and a significant Cpx-dependent alteration in the global proteome profile of E. coli.
This study points to the importance of the Cpx-TCS within the complex regulatory network in the E. coli response to aminoglycoside-caused stress.
氨基糖苷类抗生素庆大霉素被认为可诱导Cpx双组分系统(TCS)和Arc双组分系统之间发生串扰。在此,我们研究了各自TCS组分的物理相互作用,并将结果与其各自的基因表达和蛋白质丰度进行了比较。这些发现是根据庆大霉素处理后的全局蛋白质组概况来解释的。
我们使用膜链霉亲和标签蛋白相互作用实验(mSPINE)观察到,在用氨基糖苷类庆大霉素处理后,CpxA和ArcA之间存在特异性相互作用。这种相互作用既未伴随ArcA可检测到的磷酸化,也未伴随通过CpxA对Arc系统的激活。此外,在存在庆大霉素的情况下,使用灵敏的单反应监测(SRM)无法确定Cpx-TCS和Arc-TCS的绝对量变化。然而,在用庆大霉素处理后进行鸟枪法质谱分析时,我们观察到ArcA~P依赖性蛋白质合成减少,并且大肠杆菌的全局蛋白质组概况出现了显著的Cpx依赖性改变。
本研究指出了Cpx-TCS在大肠杆菌对氨基糖苷类引起的应激反应的复杂调控网络中的重要性。