Bacitracin sensing in Bacillus subtilis.

TitleBacitracin sensing in Bacillus subtilis.
Publication TypeJournal Article
Year of Publication2008
AuthorsRietkötter, E, Hoyer, D, Mascher, T
JournalMol Microbiol
Volume68
Issue3
Pagination768-85
Date Published2008 May
ISSN1365-2958
KeywordsAdenosine Triphosphate, Anti-Bacterial Agents, ATP-Binding Cassette Transporters, Bacillus subtilis, Bacitracin, Bacterial Proteins, Biological Transport, Drug Resistance, Bacterial, Gene Expression Regulation, Bacterial, Genes, Reporter, Genetic Complementation Test, Hydrolysis, Promoter Regions, Genetic, Protein Structure, Tertiary, Sequence Deletion, Signal Transduction
Abstract

The extracellular presence of antibiotics is a common threat in microbial life. Their sensitive detection and subsequent induction of appropriate resistance mechanisms is therefore a prerequisite for survival. The bacitracin stress response network of Bacillus subtilis consists of four signal-transducing systems, the two-component systems (TCS) BceRS, YvcPQ and LiaRS, and the extracytoplasmic function (ECF) sigma factor sigma(M). Here, we investigated the mechanism of bacitracin perception and the response hierarchy within this network. The BceRS-BceAB TCS/ABC transporter module is the most sensitive and efficient bacitracin resistance determinant. The ABC transporter BceAB not only acts as a bacitracin detoxification pump, but is also crucial for bacitracin sensing, indicative of a novel mechanism of stimulus perception, conserved in Firmicutes bacteria. The Bce system seems to respond to bacitracin directly (drug sensing), whereas the LiaRS TCS and sigma(M) respond only at higher concentrations and indirectly to bacitracin action (damage sensing). The YvcPQ-YvcRS system is subject to cross-activation via the paralogous Bce system, and is therefore only indirectly induced by bacitracin. The bacitracin stress response network is optimized to respond to antibiotic gradients in a way that maximizes the gain and minimizes the costs of this stress response.

DOI10.1111/j.1365-2958.2008.06194.x
Alternate JournalMol. Microbiol.