Discovery of multidrug efflux pump inhibitors with a novel chemical scaffold

Adam T. Green, Mohammad Moniruzzaman, Connor J. Cooper, John K. Walker, Jeremy C. Smith, Jerry M. Parks, Helen I. Zgurskaya

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36 Scopus citations

Abstract

Multidrug efflux is a major contributor to antibiotic resistance in Gram-negative bacterial pathogens. Inhibition of multidrug efflux pumps is a promising approach for reviving the efficacy of existing antibiotics. Previously, inhibitors targeting both the efflux transporter AcrB and the membrane fusion protein AcrA in the Escherichia coli AcrAB-TolC efflux pump were identified. Here we use existing physicochemical property guidelines to generate a filtered library of compounds for computational docking. We then experimentally test the top candidate coumpounds using in vitro binding assays and in vivo potentiation assays in bacterial strains with controllable permeability barriers. We thus identify a new class of inhibitors of E. coli AcrAB-TolC. Six molecules with a shared scaffold were found to potentiate the antimicrobial activity of erythromycin and novobiocin in hyperporinated E. coli cells. Importantly, these six molecules were also active in wild-type strains of both Acinetobacter baumannii and Klebsiella pneumoniae, potentiating the activity of erythromycin and novobiocin up to 8-fold.

Original languageEnglish
Article number129546
JournalBiochimica et Biophysica Acta - General Subjects
Volume1864
Issue number6
DOIs
StatePublished - Jun 2020

Funding

This work was supported by National Institutes of Health Grant AI052293 to HIZ. C.J.C. was supported by a National Science Foundation Graduate Research Fellowship under Grant No. 2017219379 . SPR experiments were carried out using a Biacore T200 instrument at the Oklahoma Medical Research Foundation Biacore Facility , which is funded by Shared Instrumentation Grant S10 OD025014 . This work used resources of the Compute and Data Environment for Science ( CADES ) at Oak Ridge National Laboratory , which is managed by UT-Battelle for the U.S. Department of Energy under contract no. DE-AC05-00OR22725 . We thank Illia S. Afanasiev for help with measuring MICs and MPCs. This work was supported by National Institutes of Health Grant AI052293 to HIZ. C.J.C. was supported by a National Science Foundation Graduate Research Fellowship under Grant No. 2017219379. SPR experiments were carried out using a Biacore T200 instrument at the Oklahoma Medical Research Foundation Biacore Facility, which is funded by Shared Instrumentation Grant S10 OD025014. This work used resources of the Compute and Data Environment for Science (CADES) at Oak Ridge National Laboratory, which is managed by UT-Battelle for the U.S. Department of Energy under contract no. DE-AC05-00OR22725. We thank Illia S. Afanasiev for help with measuring MICs and MPCs.

FundersFunder number
MICS
MPCs
UT-Battelle
National Science Foundation2017219379
National Institutes of Health
U.S. Department of EnergyDE-AC05-00OR22725
NIH Office of the DirectorS10OD025014
National Institute of Allergy and Infectious DiseasesR01AI052293
Oak Ridge National Laboratory
Oklahoma Medical Research FoundationS10 OD025014

    Keywords

    • Docking
    • Gram-negative
    • Minimum inhibitory concentration
    • Permeability
    • Resistance nodulation division
    • Substrate

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