Enterohemorrhagic Escherichia coli (EHEC) O157:H7 is an important food-borne pathogen responsible for disease outbreaks worldwide. In order to colonize the human gastrointestinal (GI) tract and cause disease, EHEC must be able to sense the host environment and promote expression of virulence genes essential for adherence. Ethanolamine (EA) is an important metabolite for EHEC in the GI tract, and EA is also a signal that EHEC uses to activate virulence traits. Here, we report that EA influenced EHEC adherence to epithelial cells and fimbrial gene expression. Quantitative reverse transcriptase PCR indicated that EA promoted the transcription of the genes in characterized and putative fimbrial operons. Moreover, putative fimbrial structures were produced by EHEC cells grown with EA but not in medium lacking EA. Additionally, we defined two previously uncharacterized EA-regulated fimbrial operons, loc10 and loc11. We also tested whether choline or serine, both of which are also components of cell membranes, activated fimbrial gene expression. In addition to EA, choline activated fimbrial gene expression in EHEC. These findings describe for the first time the transcription of several putative fimbrial loci in EHEC. Importantly, the biologically relevant molecules EA and choline, which are abundant in the GI tract, promoted expression of these fimbriae.
Bacterial pathogens interact directly with mammalian hosts by expressing adhesive structures, or fimbriae, on the outer surfaces of their cells. Fimbriae typically mediate the earliest stages of host colonization and are especially critical for enteric bacteria to successfully colonize the gastrointestinal (GI) tract in order to avoid displacement by the continuous flow of intestinal contents (1, 2). Enterohemorrhagic Escherichia coli (EHEC) O157:H7 is a food-borne pathogen that causes bloody diarrhea and hemolyticuremic syndrome worldwide (3). The first step in EHEC pathogenesis involves adherence to the intestinal epithelium and subsequent intimate attachment and formation of attachingand-effacing (AE) lesions on epithelial cells (2). The locus of enterocyte effacement (LEE) pathogenicity island carries most of the genes required for AE lesion formation and intimate attachment to host cells (4). However, factors encoded by genes outside the LEE may also play important roles in EHEC adherence to epithelial cells, especially during the initial stages of EHEC infection (5). The EHEC genome carries 14 to 16 fimbrial loci (6, 7), suggesting that fimbriae are an important component of EHEC's virulence repertoire. However, very little is known about the roles of EHEC fimbriae in colonization of the mammalian GI tract or EHEC's tropism for the large intestine. This is due, at least in part, to the lack of understanding of environmental cues that promote expression of these fimbriae in vitro (2,8,9). Ethanolamine (EA) is an important metabolite for EHEC in the GI tract (10), as well as a cue that EHEC uses to recognize the host environment and modulate expression of virulence...