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

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
Article numbere00728-23
JournalAntimicrobial Agents and Chemotherapy
Volume67
Issue number11
DOIs
StatePublished - Oct 25 2023
Externally publishedYes

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.

ASJC Scopus Subject Areas

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

Keywords

  • bacteriophages
  • ex vivo simulated endocardial vegetation models
  • infective endocarditis
  • multi-drug resistance
  • phage resistance
  • phage therapy
  • phage-antibiotic combinations
  • Pseudomonas aeruginosa
  • Bacteriophages
  • Ciprofloxacin/pharmacology
  • Humans
  • Anti-Bacterial Agents/pharmacology
  • Pseudomonas Infections/therapy

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