Herold Sylvia, Paton James C, Srimanote Potjanee, Paton Adrienne W
Research Centre for Infectious Diseases, School of Molecular and Biomedical Science, University of Adelaide, South Australia, 5005, Australia.
Microbiology (Reading). 2009 Nov;155(Pt 11):3554-3563. doi: 10.1099/mic.0.029454-0. Epub 2009 Aug 14.
Shiga-toxigenic Escherichia coli (STEC) colonizing the bowel are exposed to a variety of short-chain fatty acids (SCFAs), including acetate, propionate and butyrate, produced by gut microflora. However, the total concentrations and relative amounts of SCFAs in the lumen vary with intestinal niche. Here we report that conditions simulating SCFA concentrations present in the human gut trigger expression of the iha gene, which encodes an adherence-conferring outer-membrane protein of pathogenic E. coli. We show that growth under conditions simulating colonic, but not ileal, SCFA concentrations increases iha expression in three tested STEC strains, with the strongest expression detected in LEE-negative STEC O113:H21 strain 98NK2. Expression of iha is known to be subject to Fur-mediated iron repression in O157:H7 STEC, and the same occurs in 98NK2. However, exogenous iron did not repress iha expression in the presence of colonic SCFAs in either 98NK2 or the O157:H7 strain EDL933. Moreover, exposure to the iron chelator 2,2'-dipyridyl caused no further enhancement of iha expression over that induced by colonic SCFAs. These findings indicate that SCFAs regulate iha expression in STEC independently of iron. Increased expression of iha under colonic but not ileal SCFA conditions possibly may contribute to preferential colonization of the human colon by STEC.
定殖于肠道的产志贺毒素大肠杆菌(STEC)会接触到肠道微生物群产生的多种短链脂肪酸(SCFA),包括乙酸盐、丙酸盐和丁酸盐。然而,肠腔内SCFA的总浓度和相对含量会因肠道微环境而异。在此,我们报告,模拟人类肠道中存在的SCFA浓度的条件会触发iha基因的表达,该基因编码致病性大肠杆菌的一种赋予黏附能力的外膜蛋白。我们发现,在模拟结肠而非回肠SCFA浓度的条件下生长,会增加三种受试STEC菌株中的iha表达,在LEE阴性的STEC O113:H21菌株98NK2中检测到的表达最强。已知在O157:H7 STEC中,iha的表达受Fur介导的铁抑制,98NK2中也是如此。然而,在98NK2或O157:H7菌株EDL933中,在存在结肠SCFA的情况下,外源性铁并未抑制iha的表达。此外,与结肠SCFA诱导的iha表达相比,暴露于铁螯合剂2,2'-联吡啶并不会进一步增强iha的表达。这些发现表明,SCFA在STEC中独立于铁调节iha的表达。在结肠而非回肠SCFA条件下iha表达的增加可能有助于STEC在人类结肠中的优先定殖。