Institute of Plant and Microbial Biology, Academia Sinica, Taipei, Taiwan.
PLoS Pathog. 2012 Sep;8(9):e1002938. doi: 10.1371/journal.ppat.1002938. Epub 2012 Sep 27.
The type VI secretion system (T6SS) is a widespread, versatile protein secretion system in pathogenic Proteobacteria. Several T6SSs are tightly regulated by various regulatory systems at multiple levels. However, the signals and/or regulatory mechanisms of many T6SSs remain unexplored. Here, we report on an acid-induced regulatory mechanism activating T6SS in Agrobacterium tumefaciens, a plant pathogenic bacterium causing crown gall disease in a wide range of plants. We monitored the secretion of the T6SS hallmark protein hemolysin-coregulated protein (Hcp) from A. tumefaciens and found that acidity is a T6SS-inducible signal. Expression analysis of the T6SS gene cluster comprising the imp and hcp operons revealed that imp expression and Hcp secretion are barely detected in A. tumefaciens grown in neutral minimal medium but are highly induced with acidic medium. Loss- and gain-of-function analysis revealed that the A. tumefaciens T6SS is positively regulated by a chvG/chvI two-component system and negatively regulated by exoR. Further epistasis analysis revealed that exoR functions upstream of the chvG sensor kinase in regulating T6SS. ChvG protein levels are greatly increased in the exoR deletion mutant and the periplasmic form of overexpressed ExoR is rapidly degraded under acidic conditions. Importantly, ExoR represses ChvG by direct physical interaction, but disruption of the physical interaction allows ChvG to activate T6SS. The phospho-mimic but not wild-type ChvI response regulator can bind to the T6SS promoter region in vitro and activate T6SS with growth in neutral minimal medium. We present the first evidence of T6SS activation by an ExoR-ChvG/ChvI cascade and propose that acidity triggers ExoR degradation, thereby derepressing ChvG/ChvI to activate T6SS in A. tumefaciens.
VI 型分泌系统(T6SS)是一种广泛存在且多功能的蛋白质分泌系统,存在于致病性变形菌中。多个 T6SS 受到多种调节系统在多个水平上的严格调节。然而,许多 T6SS 的信号和/或调节机制仍未被探索。在这里,我们报告了一种酸诱导的调节机制,该机制可激活根癌农杆菌中的 T6SS,根癌农杆菌是一种引起广泛植物发生冠瘿病的植物病原菌。我们监测了根癌农杆菌中 T6SS 标志性蛋白溶血素共调节蛋白(Hcp)的分泌,发现酸度是 T6SS 的诱导信号。对包含 imp 和 hcp 操纵子的 T6SS 基因簇的表达分析表明,在中性最小培养基中生长的根癌农杆菌中几乎检测不到 imp 表达和 Hcp 分泌,但在酸性培养基中高度诱导。缺失和功能获得分析表明,根癌农杆菌 T6SS 受 chvG/chvI 双组分系统的正调控,受 exoR 的负调控。进一步的上位性分析表明,exoR 在调节 T6SS 时位于 chvG 传感器激酶的上游。在 exoR 缺失突变体中,chvG 蛋白水平大大增加,在酸性条件下,过表达 ExoR 的周质形式迅速降解。重要的是,ExoR 通过直接物理相互作用抑制 ChvG,但破坏物理相互作用允许 ChvG 激活 T6SS。磷酸模拟但不是野生型 ChvI 反应调节蛋白可以在体外与 T6SS 启动子区域结合,并在中性最小培养基中生长时激活 T6SS。我们首次证明了 T6SS 由 ExoR-ChvG/ChvI 级联激活,并提出酸度触发 ExoR 降解,从而解除 ChvG/ChvI 的抑制作用,激活根癌农杆菌中的 T6SS。