4.3 Review

Regulation of virulence and antibiotic resistance in Gram-positive microbes in response to cell wall-active antibiotics

Journal

CURRENT OPINION IN INFECTIOUS DISEASES
Volume 32, Issue 3, Pages 217-222

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QCO.0000000000000542

Keywords

antibiotic; cell wall; resistance; stress response

Funding

  1. US Department of Veterans Affairs Office of Research and Development Biomedical Laboratory Research Program
  2. National Institutes of Health Centers of Biomedical Research Excellence [P20GM109007]
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [P20GM109007] Funding Source: NIH RePORTER

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Purpose of review Antibiotic stress can evoke considerable genotypic and phenotypic changes in Gram-positive bacteria. Here, we review recent studies describing altered virulence expression in response to cell wall-acting antibiotics and discuss mechanisms that coordinate regulation of the antibiotic response. Recent findings Pleiotropic effects induced by antibiotic exposure include alterations to bacterial metabolism, cell wall structure and antibiotic resistance. In addition, subinhibitory concentrations of cell wall-active (CWA) antibiotics have increasingly been shown to induce the production of exotoxins and biofilm formation that may influence virulence. Remarkably, phenotypes associated with comparable antibiotic stresses can vary considerably, emphasizing the need to better understand the response to CWA antibiotics. Recent studies support both direct antibiotic recognition and recognition of antibiotic-induced stress to the bacterial cell wall. Specifically, bacterial two-component systems, penicillin-binding protein and serine/threonine kinase-associated kinases and conserved oxidative-stress sensors each contribute to modulating the antibiotic stress response. Summary Bacterial sensory systems and global regulators coordinate signaling in response to CWA antibiotics. Regulation of the antibiotic response is complex and involves integration of signals from multiple response pathways. A better definition of the antibiotic stress response among Gram-positive pathogens may yield novel therapeutic targets to counter antibiotic resistance and virulence factor expression.

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