Saitoh Takehito, Iyoda Sunao, Yamamoto Shouji, Lu Yan, Shimuta Ken, Ohnishi Makoto, Terajima Jun, Watanabe Haruo
Department of Bacteriology, Infectious Disease Surveillance Center, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
J Bacteriol. 2008 Jul;190(14):4822-30. doi: 10.1128/JB.00231-08. Epub 2008 May 16.
The pathogenicity island termed locus of enterocyte effacement (LEE) encodes a type 3 protein secretion system, whose function is required for full virulence of enterohemorrhagic Escherichia coli (EHEC). GrlR and GrlA are LEE-encoded negative and positive regulators, respectively, for controlling transcription of the ler gene, which encodes a central activator of LEE gene expression. We previously reported that the GrlR-GrlA regulatory system controls not only the LEE genes but also flagellar gene expression in EHEC (S. Iyoda et al., J. Bacteriol. 188:5682-5692, 2006). In order to further explore virulence-related genes under the control of the GrlR-GrlA regulatory system, we characterized a grlR-deleted EHEC O157 strain, which was found to have high and low levels of expression of LEE and flagellar genes, respectively. We report here that the grlR deletion significantly induced enterohemolysin (Ehx) activity of EHEC O157 on plates containing defibrinated sheep erythrocytes. Ehx levels were not induced in the grlR grlA double mutant strain but increased markedly by overexpression of GrlA even in the ler mutant, indicating that GrlA is responsible for this regulation. Ehx of the EHEC O157 Sakai strain is encoded by the ehxCABD genes, which are carried on the large plasmid pO157. The expression of ehxC fused with FLAG tag or a promoterless lacZ gene on pO157 was significantly induced under conditions in which GrlA was overproduced. These results together suggest that GrlA acts as a positive regulator for the ehx transcription in EHEC.
被称为肠细胞脱落位点(LEE)的致病岛编码一种Ⅲ型蛋白分泌系统,其功能是肠出血性大肠杆菌(EHEC)完全致病所必需的。GrlR和GrlA分别是LEE编码的负调控因子和正调控因子,用于控制ler基因的转录,ler基因编码LEE基因表达的中心激活因子。我们之前报道过,GrlR - GrlA调控系统不仅控制EHEC中的LEE基因,还控制鞭毛基因的表达(S. Iyoda等人,《细菌学杂志》188:5682 - 5692,2006年)。为了进一步探索受GrlR - GrlA调控系统控制的毒力相关基因,我们对一株缺失grlR的EHEC O157菌株进行了表征,发现该菌株中LEE基因和鞭毛基因的表达水平分别较高和较低。我们在此报告,缺失grlR显著诱导了EHEC O157在含有去纤维羊红细胞的平板上的肠溶血素(Ehx)活性。在grlR grlA双突变菌株中未诱导出Ehx水平,但即使在ler突变体中,通过过表达GrlA也显著增加,这表明GrlA负责这种调控。EHEC O157阪崎菌株的Ehx由ehxCABD基因编码,这些基因位于大质粒pO157上。在过量产生GrlA的条件下,与FLAG标签融合的ehxC或pO157上无启动子的lacZ基因的表达被显著诱导。这些结果共同表明,GrlA在EHEC中作为ehx转录的正调控因子发挥作用。