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PMID: 16468984 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

The role of proton motive force in expression of the Staphylococcus aureus cid and lrg operons.

Molecular microbiology ·Vol. 59 ·No. 5 ·2006-03-00 ·Pages 1395-404

Patton TG, Yang SJ, Bayles KW

Abstract

The Staphylococcus aureus cidABC and lrgAB operons have been shown to play a key role in the regulation of murein hydrolase activity and cell death in a manner thought to be analogous to bacteriophage-encoded holins and anti-holins respectively. Because of these functions, it has been proposed that the regulation of these operons is tightly controlled and responsive to key metabolic signals. The current study revealed the presence of two overlapping regulatory pathways controlling cidABC and lrgAB expression, one dependent on acetic acid and the other dependent on proton motive force (PMF). The latter pathway was analysed using agents that affect various aspects of the PMF. Gramicidin and carbonyl cyanide m-chlorophenylhydrazone (CCCP), antimicrobial agents that dissipate the DeltapH and membrane potential (DeltaPsi), both enhanced lrgAB expression. Restoration of the PMF by incubation of the bacteria in the presence of glucose restored lrgAB expression back to the uninduced state. In addition, valinomycin, which specifically collapses the DeltaPsi, also induced lrgAB expression. In contrast, nigericin, which dissipates the DeltapH component of the PMF, was found to have a minimal effect on DeltaPsi and lrgAB transcription. Finally, the DeltaPsi-inducible expression of lrgAB was shown to be dependent on the previously characterized LytSR two-component regulatory system that is involved in the regulation of autolysis. The results of this study support a model in which the LytSR regulatory system responds to a collapse in DeltaPsi by inducing the transcription of the lrgAB operon.

MeSH Terms
Acids/pharmacology Anti-Infective Agents/pharmacology Bacterial Proteins/drug effects,genetics,metabolism Carbonyl Cyanide m-Chlorophenyl Hydrazone/pharmacology Gene Expression Regulation, Bacterial/drug effects Gramicidin/pharmacology Membrane Potentials/drug effects Nigericin/pharmacology Operon Proton-Motive Force/genetics Staphylococcus aureus/drug effects,genetics Transcription Factors/drug effects Transcription, Genetic Valinomycin/pharmacology
Chemicals
Acids Anti-Infective Agents Bacterial Proteins LytR protein, Staphylococcus aureus LytS protein, Staphylococcus aureus Transcription Factors Gramicidin Valinomycin Carbonyl Cyanide m-Chlorophenyl Hydrazone Nigericin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Patton Toni G
Department of Microbiology, Molecular Biology and Biochemistry, University of Idaho, Moscow, 83844-3052, USA.
Yang Soo-Jin
Bayles Kenneth W
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
2006-03-00
Pages
1395-404
Language
English
Region
England
NLM ID
8712028
Subset
IM
Grants
NCRR NIH HHS · P20RR15587 · United States
NIAID NIH HHS · R01AI038901 · United States
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