Antimicrobial activities of YycG histidine kinase inhibitors against Staphylococcus epidermidis biofilms

Z Qin, Bao le ri Lee, Lei Yang, J Zhang, X Yang, D Qu, H Jiang, Søren Molin

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    Staphylococcus epidermidis has become a significant pathogen causing infections due to biofilm formation on surfaces of indwelling medical devices. Biofilm-associated bacteria exhibit enhanced resistance to many conventional antibiotics. It is therefore, important to design novel antimicrobial reagents targeting S. epidermidis biofilms. In a static chamber system, the bactericidal effect of two leading compounds active as YycG inhibitors was assessed on biofilm cells by confocal laser scanning microscopy combined with viability staining. In young biofilms (6-h-old), the two compounds killed the majority ofthe embedded cells at concentrations of 100 mu M and 25 mu M, respectively. In mature biofilms (24-h-old), one compound was still effectively killing biofilm cells, whereas the other compound mainly killed cells located at the bottom of the biofilm. In contrast, vancomycin was found to stimulate biofilm development at the M13C (8 mu g mL(-1)). Even at a high concentration (128 mu g mL(-1)), vancomycin exhibited poor killing on cells embedded in biofilms. The two compounds exhibited faster and more effective killing of S. epidermidis planktonic cells than vancomycin at the early stage of exposure (6 h). The data suggest that the new inhibitors can serve as potential agents against S. epidermidis biofilms when added alone or in concert with other antimicrobial agents.
    Original languageEnglish
    JournalF E M S Microbiology Letters
    Volume273
    Issue number2
    Pages (from-to)149-56
    ISSN0378-1097
    DOIs
    Publication statusPublished - 2007

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