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J Membr Biol. 2018 Feb;251(1):65-74. doi: 10.1007/s00232-018-0014-2. Epub 2018 Jan 27.

Evidence of Cross-Regulation in Two Closely Related Pyruvate-Sensing Systems in Uropathogenic Escherichia coli.

Author information

1
Department of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN, USA.
2
Division of Molecular Pathogenesis, Department of Pathology, Microbiology & Immunology, Vanderbilt University Medical Center, 1161 21st Avenue South, MCN A5225A, Nashville, TN, 37232, USA.
3
Roche Diagnostics GmbH, Nonnenwald 2, 82377, Penzberg, Germany.
4
Munich Center for Integrated Protein Science (CIPSM) at the Department of Microbiology, Ludwig-Maximilians-Universität München, Martinsried, Germany.
5
Division of Molecular Pathogenesis, Department of Pathology, Microbiology & Immunology, Vanderbilt University Medical Center, 1161 21st Avenue South, MCN A5225A, Nashville, TN, 37232, USA. maria.hadjifrangiskou@vanderbilt.edu.
6
Department of Urologic Surgery, Vanderbilt University Medical Center, Nashville, TN, USA. maria.hadjifrangiskou@vanderbilt.edu.
7
Vanderbilt Institute for Infection, Immunology & Inflammation, Nashville, TN, USA. maria.hadjifrangiskou@vanderbilt.edu.

Abstract

Two-component systems (TCSs) dictate many bacterial responses to environmental change via the activation of a membrane-embedded sensor kinase, which has molecular specificity for a cognate response regulator protein. However, although the majority of TCSs operate through seemingly strict cognate protein-protein interactions, there have been several reports of TCSs that violate this classical model of signal transduction. Our group has recently demonstrated that some of these cross-interacting TCSs function in a manner that imparts a fitness advantage to bacterial pathogens. In this study, we describe interconnectivity between the metabolite-sensing TCSs YpdA/YpdB and BtsS/BtsR in uropathogenic Escherichia coli (UPEC). The YpdA/YpdB and BtsS/BtsR TCSs have been previously reported to interact in K12 E. coli, where they alter the expression of putative transporter genes yhjX and yjiY, respectively. These target genes are both upregulated in UPEC during acute and chronic murine models of urinary tract infection, as well as in response to pyruvate and serine added to growth media in vitro. Here, we show that proper regulation of yhjX in UPEC requires the presence of all components from both of these TCSs. By utilizing plasmid-encoded luciferase reporters tracking the activity of the yhjX and yjiY promoters, we demonstrate that deletions in one TCS substantially alter transcriptional activity of the opposing system's target gene. However, unlike in K12 E. coli, single gene deletions in the YpdA/YpdB system do not alter yjiY gene expression in UPEC, suggesting that niche and lifestyle-specific pressures may be selecting for differential cross-regulation of TCSs in pathogenic and non-pathogenic E. coli.

KEYWORDS:

Cross-regulation; Escherichia coli; Pyruvate-sensing; Two-component systems

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