Axler-Diperte Grace L, Miller Virginia L, Darwin Andrew J
Department of Microbiology, New York University School of Medicine, 550 First Avenue, New York, NY 10016, USA.
J Bacteriol. 2006 Dec;188(23):8033-43. doi: 10.1128/JB.01159-06. Epub 2006 Sep 22.
Yersinia enterocolitica causes human gastroenteritis, and many isolates have been classified as either "American" or "non-American" strains based on their geographic prevalence and virulence properties. In this study we describe identification of a transcriptional regulator that controls expression of the Y. enterocolitica ytxAB genes. The ytxAB genes have the potential to encode an ADP-ribosylating toxin with similarity to pertussis toxin. However, a ytxAB null mutation did not affect virulence in mice. Nevertheless, the ytxAB genes are conserved in many Y. enterocolitica strains. Interestingly, American and non-American strains have different ytxAB alleles encoding proteins that are only 50 to 60% identical. To obtain further insight into the ytxAB locus, we investigated whether it is regulated as part of a known or novel regulon. Transposon mutagenesis identified a LysR-like regulator, which we designated YtxR. Expression of ytxR from a nonnative promoter increased Phi(ytxA-lacZ) operon fusion expression up to 35-fold. YtxR also activated expression of its own promoter. DNase I footprinting showed that a His(6)-YtxR fusion protein directly interacted with the ytxA and ytxR control regions at similar distances upstream of their probable transcription initiation sites, identified by primer extension. Deletion analysis demonstrated that removal of the regions protected by His(6)-YtxR in vitro eliminated YtxR-dependent induction in vivo. The ytxAB locus is not present in most Yersinia species. In contrast, ytxR is conserved in multiple Yersinia species, as well as in the closely related organisms Photorhabdus luminescens and Photorhabdus asymbiotica. These observations suggest that YtxR may play a conserved role involving regulation of other genes besides ytxAB.
小肠结肠炎耶尔森菌可引起人类肠胃炎,许多分离株根据其地理分布和毒力特性被归类为“美国”或“非美国”菌株。在本研究中,我们描述了一种转录调节因子的鉴定,该调节因子控制小肠结肠炎耶尔森菌ytxAB基因的表达。ytxAB基因有可能编码一种与百日咳毒素相似的ADP核糖基化毒素。然而,ytxAB基因敲除突变并不影响小鼠的毒力。尽管如此,ytxAB基因在许多小肠结肠炎耶尔森菌菌株中是保守的。有趣的是,美国菌株和非美国菌株具有不同的ytxAB等位基因,它们编码的蛋白质只有50%至60%的同一性。为了进一步深入了解ytxAB基因座,我们研究了它是否作为已知或新的调控子的一部分受到调控。转座子诱变鉴定出一种类LysR调节因子,我们将其命名为YtxR。从非天然启动子表达的ytxR使Phi(ytxA-lacZ)操纵子融合表达增加了35倍。YtxR还激活了其自身启动子的表达。DNase I足迹分析表明,His(6)-YtxR融合蛋白在其可能的转录起始位点上游相似距离处直接与ytxA和ytxR调控区域相互作用,这是通过引物延伸鉴定的。缺失分析表明,在体外去除His(6)-YtxR保护的区域可消除体内YtxR依赖性诱导。大多数耶尔森菌属物种中不存在ytxAB基因座。相反,ytxR在多个耶尔森菌属物种以及密切相关的发光光杆状菌和共生光杆状菌中是保守的。这些观察结果表明,YtxR可能在除ytxAB之外的其他基因调控中发挥保守作用。