Department of Biology, University 'Roma Tre', Viale G. Marconi 446-00146 Rome, Italy.
Environ Microbiol. 2010 Jun;12(6):1630-42. doi: 10.1111/j.1462-2920.2010.02210.x. Epub 2010 Apr 5.
In the Gram-negative pathogen Pseudomonas aeruginosa, the alternative sigma factor PvdS acts as a key regulator of the response to iron starvation. PvdS also controls P. aeruginosa virulence, as it drives the expression of a large set of genes primarily implicated in biogenesis and transport of the pyoverdine siderophore and synthesis of extracellular factors, such as protease PrpL and exotoxin A. Besides the ferric uptake regulatory protein Fur, which shuts off pvdS transcription under iron-replete conditions, no additional regulatory factor(s) controlling the pvdS promoter activity have been characterized so far. Here, we used the promoter region of pvdS as bait to tentatively capture, by DNA-protein affinity purification, P. aeruginosa proteins that are able to bind specifically to the pvdS promoter. This led to the identification and functional characterization of the LysR-like transcription factor CysB as a novel regulator of pvdS transcription. The CysB protein directly binds to the pvdS promoter in vitro and acts as a positive regulator of PvdS expression in vivo. The absence of a functional CysB protein results in about 50% reduction of expression of PvdS-dependent virulence phenotypes. Given the role of CysB as master regulator of sulfur metabolism, our findings establish a novel molecular link between the iron and sulfur regulons in P. aeruginosa.
在革兰氏阴性病原体铜绿假单胞菌中,替代 sigma 因子 PvdS 作为对缺铁应激反应的关键调节剂。PvdS 还控制铜绿假单胞菌的毒力,因为它驱动一大组基因的表达,这些基因主要与铁载体绿脓菌素的生物发生和运输以及细胞外因子(如蛋白酶 PrpL 和外毒素 A)的合成有关。除了铁摄取调节蛋白 Fur 外,Fur 在铁充足的条件下关闭 pvdS 转录,迄今为止,尚未鉴定出控制 pvdS 启动子活性的其他调节因子。在这里,我们使用 pvdS 的启动子区域作为诱饵,通过 DNA-蛋白质亲和纯化,暂时捕获能够与 pvdS 启动子特异性结合的铜绿假单胞菌蛋白。这导致鉴定和功能表征 LysR 样转录因子 CysB 作为 pvdS 转录的新型调节剂。CysB 蛋白在体外直接结合到 pvdS 启动子上,并作为体内 PvdS 表达的正调节剂。缺乏功能的 CysB 蛋白会导致依赖于 PvdS 的毒力表型的表达减少约 50%。鉴于 CysB 作为硫代谢主调节因子的作用,我们的发现确立了铜绿假单胞菌中铁和硫调节子之间的新分子联系。