Axler-DiPerte Grace L, Hinchliffe Stewart J, Wren Brendan W, Darwin Andrew J
Department of Microbiology, New York University School of Medicine, New York, New York 10016, USA.
J Bacteriol. 2009 Jan;191(2):514-24. doi: 10.1128/JB.01305-08. Epub 2008 Nov 14.
The Yersinia enterocolitica YtxR protein is a LysR-type transcriptional regulator that induces expression of the ytxAB locus, which encodes a putative ADP-ribosylating toxin. The ytxR and ytxAB genes are not closely linked in the Y. enterocolitica chromosome, and whereas ytxR is present in all sequenced Yersinia spp., the ytxAB locus is not. These observations suggested that there might be other YtxR-regulon members besides ytxAB and prompted us to investigate coregulated genes and gene products by using transcriptional and proteomic approaches. Microarray and reverse transcription-PCR analysis showed that YtxR strongly activates expression of the yts2 locus, which encodes a putative type 2 secretion system, as well as several uncharacterized genes predicted to encode extracytoplasmic proteins. Strikingly, we also discovered that under Ysc-Yop type 3 secretion system-inducing conditions, YtxR prevented the appearance of Yop proteins in the culture supernatant. Microarray and lacZ operon fusion analysis showed that this was due to specific repression of ysc-yop gene expression. YtxR was also able to repress VirF-dependent Phi(yopE-lacZ) and Phi(yopH-lacZ) expression in a strain lacking the virulence plasmid, which suggested a direct repression mechanism. This was supported by DNase I footprinting, which showed that YtxR interacted with the yopE and yopH control regions. Therefore, YtxR is a newly identified regulator of the ysc-yop genes that can act as an overriding off switch for this critical virulence system.
小肠结肠炎耶尔森菌的YtxR蛋白是一种LysR型转录调节因子,可诱导ytxAB基因座的表达,该基因座编码一种假定的ADP核糖基化毒素。ytxR和ytxAB基因在小肠结肠炎耶尔森菌染色体上并非紧密相连,虽然ytxR存在于所有已测序的耶尔森菌属中,但ytxAB基因座并非如此。这些观察结果表明,除了ytxAB之外,可能还有其他YtxR调控子成员,这促使我们通过转录组学和蛋白质组学方法研究共调控的基因和基因产物。微阵列和逆转录PCR分析表明,YtxR强烈激活yts2基因座的表达,该基因座编码一种假定的2型分泌系统,以及几个预测编码胞外蛋白的未表征基因。令人惊讶的是,我们还发现,在Ysc-Yop 3型分泌系统诱导条件下,YtxR可阻止培养上清液中出现Yop蛋白。微阵列和lacZ操纵子融合分析表明,这是由于对ysc-yop基因表达的特异性抑制。YtxR还能够在缺乏毒力质粒的菌株中抑制VirF依赖性的Phi(yopE-lacZ)和Phi(yopH-lacZ)表达,这提示了一种直接的抑制机制。DNase I足迹分析支持了这一点,该分析表明YtxR与yopE和yopH调控区域相互作用。因此,YtxR是一种新鉴定的ysc-yop基因调节因子,可作为这个关键毒力系统的一个主要关闭开关。