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DOI

The increasing resistance of clinical pathogens against the glycopeptide antibiotic vancomycin, a last-resort drug against infections with Gram-positive pathogens, is a major problem in the nosocomial environment. Vancomycin inhibits peptidoglycan synthesis by binding to the D-Ala-D-Ala terminal dipeptide moiety of the cell wall precursor lipid II. Plasmid-transferable resistance is conferred by modification of the terminal dipeptide into the vancomycin-insensitive variant D-Ala-D-Lac, which is produced by VanA. Here we show that exogenous D-Ala competes with D-Lac as a substrate for VanA, increasing the ratio of wildtype to mutant dipeptide, an effect that was augmented by several orders of magnitude in the absence of the D-Ala-D-Ala peptidase VanX. Liquid chromatography-mass spectrometry (LC-MS) analysis showed that high concentrations of D-Ala led to the production of a significant amount of wild-type cell wall precursors, while vanX-null mutants produced primarily wild-type precursors. This enhanced the efficacy of vancomycin in the vancomycin-resistant model organism Streptomyces coelicolor, and the susceptibility of vancomycin-resistant clinical isolates of Enterococcus faecium (VRE) increased by up to 100-fold. The enhanced vancomycin sensitivity of S. coelicolor cells correlated directly to increased binding of the antibiotic to the cell wall. Our work offers new perspectives for the treatment of diseases associated with vancomycin-resistant pathogens and for the development of drugs that target vancomycin resistance.
Original languageEnglish
Pages (from-to)4930-4939
Number of pages10
JournalAntimicrobial Agents and Chemotherapy
Volume60
Issue number8
DOI
Publication statusPublished - 2016

    Research areas

  • streptomyces-coelicolor a3(2) alanyl-d-alanine glycopeptide resistance staphylococcus-aureus enterococcus-faecalis antibiotic production molecular-basis cell-wall d-lactate bad bugs Microbiology Pharmacology & Pharmacy, national

ID: 2512045