Hirakawa Hidetada, Kodama Toshio, Takumi-Kobayashi Asuka, Honda Takeshi, Yamaguchi Akihito
Department of Microbiology, University of Washington, WA 98195, USA.
Department of Cell Membrane Biology, Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka 567-0047, Japan.
Microbiology (Reading). 2009 Feb;155(Pt 2):541-550. doi: 10.1099/mic.0.020420-0.
Indole is produced by tryptophanase during growth of enteric bacteria and accumulates in the culture medium. The physiological role of indole production is poorly understood. We discovered that enterohaemorrhagic Escherichia coli (EHEC) O157:H7 with a tnaA deletion has decreased secretion of EspA and EspB via the type III secretion system and as a result there is reduced formation of attaching and effacing (A/E) lesions in HeLa cells. Addition of indole restored and enhanced secretion of EspA and EspB and formation of A/E lesions by the tnaA deletion mutant EHEC. Indole addition moderately increased the promoter activity of LEE4 genes, including espA and espB, in the locus of enterocyte effacement. Thus in EHEC indole can serve to signal EspA and EspB expression and secretion and stimulate the ability of EHEC to form A/E lesions on human cells.
吲哚是肠道细菌生长过程中色氨酸酶产生的,并在培养基中积累。人们对吲哚产生的生理作用了解甚少。我们发现,缺失tnaA的肠出血性大肠杆菌(EHEC)O157:H7通过III型分泌系统减少了EspA和EspB的分泌,结果导致HeLa细胞中黏附和抹除(A/E)损伤的形成减少。添加吲哚可恢复并增强tnaA缺失突变体EHEC的EspA和EspB分泌以及A/E损伤的形成。添加吲哚适度增加了肠上皮细胞脱落位点中包括espA和espB在内的LEE4基因的启动子活性。因此,在EHEC中,吲哚可作为EspA和EspB表达及分泌的信号,并刺激EHEC在人类细胞上形成A/E损伤的能力。