bioRxivBiochemistry
Impact of fluoroquinolones and aminoglycosides on P. aeruginosa virulence factor production and cytotoxicity
D. M. Foulkes, K. McLean, M. Sloniecka, D. Byrne, A. S. Haneef, C. Winstanley, N. Berry, D. Fernig, S. B. Kaye
Abstract
Infection from the opportunistic pathogen Pseudomonas aeruginosa is one of leading causes of disability and mortality worldwide and the world health organisation has listed it with the highest priority for the need of new antimicrobial therapies. P. aeruginosa strains responsible for the poorest clinical outcomes express either ExoS or ExoU, which are injected into target host cells via the type III secretion system (T3SS). ExoS is a bifunctional cytotoxin that promotes intracellular survival of invasive P. aeruginosa by preventing targeting of the bacteria to acidified intracellular compartments and lysosomal degradation. ExoU is a potent phospholipase which causes rapid destruction of host cell plasma membranes, leading to acute tissue damage and bacterial dissemination. Fluoroquinolones are usually employed as a first line of therapy as they have been shown to be more active against P. aeruginosa in vitro than other antimicrobial classes. However, their overuse over the past decade has caused alarming rates of antibiotic resistance to emerge. In certain clinical situations, aminoglycosides have been shown to be more effective then fluoroquinolones, despite their reduced potency towards P. aeruginosa in vitro. In this study, we evaluated the effects of fluoroquinolones (moxifloxacin and ciprofloxacin) and aminoglycosides (tobramycin and gentamycin) on T3SS expression and toxicity, in corneal epithelial cell infection models. We discovered tobramycin disrupted T3SS expression and inhibited both ExoS and ExoU mediated cytotoxicity, protecting infected HCE-T cells even at concentrations below the minimal inhibitory concentrations (MIC). Fluoroquinolones moxifloxacin and ciprofloxacin, however, upregulated the T3SS and in particular did not subvert the cytotoxic effects of ExoS and ExoU.
- organism: bacteria (other)
- research focus: host-pathogen & immune response
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Evaluation of ExoU inhibitors in a Pseudomonas aeruginosa scratch infection assay
D. M. Foulkes, K. McLean, … S. B. Kaye·bioRxiv·Jun 24, 2020
- Intracellular replication of Pseudomonas aeruginosa in epithelial cells requires suppression of the caspase-4 inflammasome
A. R. Kroken, K. A. Klein, … S. M. J. Fleiszig·bioRxiv·Feb 13, 2023
- Type III secretion system of Pseudomonas aeruginosa affects mucin gene expression via NF-κB and AKT signaling in human carcinoma epithelial cells and a pneumonia mouse model
Ji-Won Park, In-Sik Shin, … Kyung-Seop Ahn·bioRxiv·Oct 12, 2018
- Pseudomonas aeruginosa enhances the efficacy of norfloxacin against Staphylococcus aureus biofilms
G. Orazi, F. Jean-Pierre, G. O'Toole·bioRxiv·Mar 26, 2020
- A phospholipase assay screen identifies synergistic inhibitors of the P. aeruginosa toxin ExoU
D. M. Foulkes, K. McLean, … S. B. Kaye·bioRxiv·Feb 21, 2022
- Pseudomonas aeruginosa Exotoxin A is not essential for corneal disease severity or bacterial survival
James D Begando, Michaela Ellen Marshall, … Eric M. Pearlman·Infection and ImmunityPeer-reviewed·Jul 22, 2026