Mapping direct and indirect MarA/SoxS/Rob/RamA regulons in Salmonella Typhimurium reveals repression of csgD and biofilm formation

Author:

Middlemiss Alistair D.1,Haycocks James R. J.1,Stringer Anne M.2,Piddock Laura J. V.34,Wade Joseph T.52,Grainger David C.1

Affiliation:

1. School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK

2. Wadsworth Center, New York State Department of Health, Albany, New York, USA

3. Present address: Global Antibiotic R&D Partnership, 15 Chemin Camille-Vidart, 1202 Geneva, Switzerland

4. Institute of Microbiology and Infection, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK

5. Department of Biomedical Sciences, School of Public Health, University at Albany, Albany, New York, USA

Abstract

The closely related transcription factors MarA, SoxS, Rob and RamA control overlapping stress responses in many enteric bacteria. Furthermore, constitutive expression of such regulators is linked to clinical antibiotic resistance. In this work we have mapped the binding of MarA, SoxS, Rob and RamA across the Salmonella Typhimurium genome. In parallel, we have monitored changes in transcription start site use resulting from expression of the regulators. Together, these data allow direct and indirect gene regulatory effects to be disentangled. Promoter architecture across the regulon can also be deduced. At a phylogenetic scale, around one third of regulatory targets are conserved in most organisms encoding MarA, SoxS, Rob or RamA. We focused our attention on the control of csgD, which encodes a transcriptional activator responsible for stimulating production of curli fibres during biofilm formation. We show that expression of csgD is particularly sensitive to SoxS that binds upstream to repress transcription. This differs to the situation in Escherichia coli , where MarA regulates csgD indirectly.

Funder

Wellcome

Publisher

Microbiology Society

Subject

Microbiology

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