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Enterohemorrhagic Escherichia coli (EHEC) is the causative agent of severe diarrheal disease in humans. Cattle are the natural reservoir of EHEC, and approximately 75% of EHEC infections in humans stem from bovine products. Many common bacterial pathogens, including EHEC, rely on chemical communication systems, such as quorum sensing (QS), to regulate virulence and facilitate host colonization. EHEC uses SdiA from E. coli (SdiA EC ), an orphan LuxR-type receptor, to sense N -acyl l-homoserine lactone (AHL) QS signals produced by other members of the bovine enteric microbiome. SdiA EC regulates two phenotypes critical for colonizing cattle: acid resistance and the formation of attaching and effacing lesions. Despite the importance of SdiA EC , there is very little known about its selectivity for different AHL signals, and no chemical inhibitors that act specifically on SdiA EC have been reported. Such compounds would represent valuable tools to study the roles of QS in EHEC virulence. To identify chemical modulators of SdiA EC and delineate the structure-activity relationships (SARs) for AHL activity in this receptor, we report herein the screening of a focused library composed largely of AHLs and AHL analogues in an SdiA EC reporter assay. We describe the identity and SARs of potent modulators of SdiA EC activity, examine the promiscuity of SdiA EC , characterize the mechanism of a covalent inhibitor, and provide phenotypic assay data to support that these compounds can control SdiA EC -dependent acid resistance in E. coli . These SdiA EC modulators could be used to advance the study of LuxR-type receptor/ligand interactions, the biological roles of orphan LuxR-type receptors, and potential QS-based therapeutic approaches.

acs infectious diseases

Chemical Control of Quorum Sensing in <i>E. coli</i>: Identification of Small Molecule Modulators of SdiA and Mechanistic Characterization of a Covalent Inhibitor

Chemical Control of Quorum Sensing in E. coli: Identification of Small Molecule Modulators of SdiA and Mechanistic Characterization of a Covalent Inhibitor