Journal of Medicinal Chemistry · 2017 · 68 citations · 36 references
Life SciencesPharmacologyPharmacotherapyAntimicrobial PharmacotherapyAntimicrobial ResistanceDrug DiscoveryAntibacterial ResistanceAntibiotic ResistanceAntibiotic Resistance MechanismsEfflux-mediated ResistanceMultidrug ResistanceResistance In Gram-negative BacteriaAntibiotic CombinationsBacterial Multidrug ResistanceGram-negative Bacterial InfectionsIntrinsic Resistance In Gram-negative BacteriaMultidrug-resistant Gram-negative BacteriaOuter Membrane PermeabilityPseudomonas Aeruginosa ResistanceTetracycline Antibiotics
Drug efflux mechanisms interact synergistically with the outer membrane permeability barrier of Gram-negative bacteria, leading to intrinsic resistance that presents a major challenge for antibiotic drug development. Efflux pump inhibitors (EPIs) which block the efflux of antibiotics synergize antibiotics, but the clinical development of EPI/antibiotic combination therapy to treat multidrug-resistant (MDR) Gram-negative infections has been challenging. This is in part caused by the inefficiency of current EPIs to penetrate the outer membrane and resist efflux. We demonstrate that conjugation of a tobramycin (TOB) vector to EPIs like NMP, paroxetine, or DBP enhances synergy and efficacy of EPIs in combination with tetracycline antibiotics against MDR Gram-negative bacteria including Pseudomonas aeruginosa. Besides potentiating tetracycline antibiotics, TOB-EPI conjugates can also suppress resistance development to the tetracycline antibiotic minocycline, thereby providing a strategy to develop more effective adjuvants to rescue tetracycline antibiotics from resistance in MDR Gram-negative bacteria.
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