Nature CommunicationsMicrobiologyPeer-reviewed journal article
Uncovering nitroxoline activity spectrum, mode of action and resistance across Gram-negative bacteria
Elisabetta CacaceiD, Manuela TietgeniD, Meike Steinhauer, André MateusiD, Tilman G. SchultzeiD, Marina EckermanniD, Marco GalardiniiD, Vallo VarikiD, Alexandra KoumoutsiiD, Jordan J. Parzeller, Federico CoronaiD, Askarbek N OrakoviD, Michael R. KnoppiD, Amber Brauer-NikonowiD, Peer BorkiD, Célia V. RomãoiD, Michael ZimmermanniD, Peter CloetensiD, Mikhail M. SavitskiiD, Athanasios TypasiD, Stephan GöttigiD
Abstract
Nitroxoline is a bacteriostatic quinoline antibiotic, considered a metal chelator inhibiting the activity of RNA-polymerase1. Its clinical indications are limited to uncomplicated urinary tract infections (UTIs), with a clinical susceptibility breakpoint only available for Escherichia coli2. By testing > 1,000 clinical isolates, here we demonstrate a much broader activity spectrum and species-specific bactericidal activity, including multidrug-resistant Gram-negative bacteria for which therapeutic options are limited due to resistance. By combining systematic genetic and proteomic approaches with direct measurement of intracellular metals, we dissect nitroxoline perturbation of metal homeostasis and unveil additional effects on bacterial physiology. We show that nitroxoline affects outer membrane integrity, synergizing with large-scaffold antibiotics and resensitizing colistin-resistant Enterobacteriaceae in vitro and in vivo. We further characterise resistance mechanisms across E. coli, Acinetobacter baumannii and Klebsiella pneumoniae, recapitulating known E. coli resistance determinants and uncovering novel and conserved mechanisms across species, demonstrating their common effect on nitroxoline efflux.
- organism: E. coli
- organism: Arabidopsis
- assay: proteomics
- research focus: host-pathogen & immune response
- approach: experimental assay
- Citations
- 23
- FWCI
- 8.60
- Field percentile
- top 1%
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