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Autor(en) / Beteiligte
Titel
Boeravinone B, A Novel Dual Inhibitor of NorA Bacterial Efflux Pump of Staphylococcus aureus and Human P -Glycoprotein, Reduces the Biofilm Formation and Intracellular Invasion of Bacteria
Ist Teil von
  • Frontiers in microbiology, 2017-10, Vol.8, p.1868-1868
Ort / Verlag
Switzerland: Frontiers Media S.A
Erscheinungsjahr
2017
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • This study elucidated the role of boeravinone B, a NorA multidrug efflux pump inhibitor, in biofilm inhibition. The effects of boeravinone B plus ciprofloxacin, a NorA substrate, were evaluated in NorA-overexpressing, wild-type, and knocked-out (SA-1199B, SA-1199, and SA-K1758, respectively). The mechanism of action was confirmed using the ethidium bromide accumulation and efflux assay. The role of boeravinone B as a human -glycoprotein ( -gp) inhibitor was examined in the LS-180 (colon cancer) cell line. Moreover, its role in the inhibition of biofilm formation and intracellular invasion of in macrophages was studied. Boeravinone B reduced the minimum inhibitory concentration (MIC) of ciprofloxacin against and its methicillin-resistant strains; the effect was stronger in SA-1199B. Furthermore, time-kill kinetics revealed that boeravinone B plus ciprofloxacin, at subinhibitory concentration (0.25 × MIC), is as equipotent as that at the MIC level. This combination also had a reduced mutation prevention concentration. Boeravinone B reduced the efflux of ethidium bromide and increased the accumulation, thus strengthening the role as a NorA inhibitor. Biofilm formation was reduced by four-eightfold of the minimal biofilm inhibitory concentration of ciprofloxacin, effectively preventing bacterial entry into macrophages. Boeravinone B effectively inhibited -gp with half maximal inhibitory concentration (IC ) of 64.85 μM. The study concluded that boeravinone B not only inhibits the NorA-mediated efflux of fluoroquinolones but also considerably inhibits the biofilm formation of Its -gp inhibition activity demonstrates its potential as a bioavailability and bioefficacy enhancer.
Sprache
Englisch
Identifikatoren
ISSN: 1664-302X
eISSN: 1664-302X
DOI: 10.3389/fmicb.2017.01868
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_cbeae651956941dc88fa1cd60875d17b

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