Ciprofloxacin in combination with bacteriophage cocktails against multi-drug resistant Pseudomonas aeruginosa in ex vivo simulated endocardial vegetation models

Amer El Ghali, Kyle Stamper, Ashlan J. Kunz Coyne, Dana Holger, Razieh Kebriaei, Jose Alexander, Susan M. Lehman, Michael J. Rybak

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Pseudomonas aeruginosa-associated infective endocarditis represents difficult-to-treat, deep-seated infections. Phage-antibiotic combinations have shown to eradicate multi-drug resistant (MDR) P. aeruginosa, limit the development of phage resistance, and restore antibiotic sensitivity. The objective of this study was to evaluate the activity of phage-ciprofloxacin (CIP) combinations in 4-day ex vivo simulated endocardial vegetation (SEV) models against drug-resistant P. aeruginosa isolates. Two P. aeruginosa isolates, extensively drug-resistant AR351 and MDR I0003-1, were selected for their drug resistance and sensitivity to phage. Three phages [LL-5504721-AH (LL), E2005-C (EC), and 109] and CIP were evaluated alone and in combination for their activity and influence on drug and phage resistance using 24-h time-kill analysis. The three-phage cocktail (q24h) in combination with CIP (400 mg q12h) was then tested in dynamic 4-day ex vivo SEV models, with reduction of log10 CFU∕mL compared using ANOVA with Bonferroni analysis. Compared to other combinations, CIP-LL-EC-109 demonstrated synergistic and bactericidal activity from starting CFU∕g against AR351 and I0003-1 (−Δ5.65 and 6.60 log10 CFU∕g, respectively; P < 0.001). Additionally, CIP-LL-EC-109 mitigated phage resistance, while all other therapies had a high degree of resistance to >1 phages, and all phage-containing regimens prevented CIP mean inhibitory concentration increases compared to CIP alone for both AR351 and I0003-1 at 96 h.

Original languageEnglish
JournalAntimicrobial Agents and Chemotherapy
Volume67
Issue number11
DOIs
StatePublished - Nov 2023

Bibliographical note

Publisher Copyright:
This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply.

Keywords

  • Pseudomonas aeruginosa
  • bacteriophages
  • ex vivo simulated endocardial vegetation models
  • infective endocarditis
  • multi-drug resistance
  • phage resistance
  • phage therapy
  • phage-antibiotic combinations

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

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