[Study investigating the activity of several fluoroquinolones against Pseudomonas aeruginosa using the mutant

Elia Sirvent1, Montserrat Ruiz, Juan C Rodríguez

  • 1Servicio de Microbiología, Hospital General Universitario de Elche, Universidad Miguel Hernández, Alicante, España.

Abstract

Insights

Ciprofloxacin and levofloxacin showed the lowest mutant prevention concentration (MPC) against Pseudomonas aeruginosa. Even with persistent susceptibility, reduced activity was noted in patients with prior fluoroquinolone exposure, warranting careful drug selection.

Area of Science:

  • Microbiology
  • Pharmacology
  • Infectious Diseases

Background:

  • Pseudomonas aeruginosa is a common cause of nosocomial infections.
  • Fluoroquinolones are widely used antibiotics, but resistance is a growing concern.

Purpose of the Study:

  • To compare the mutant prevention concentration (MPC) of five fluoroquinolones against Pseudomonas aeruginosa.
  • To evaluate the impact of prior fluoroquinolone treatment on drug activity.

Main Methods:

  • Determined MPC values for ciprofloxacin, levofloxacin, moxifloxacin, gatifloxacin, and ofloxacin.
  • Utilized a high inoculum (10(10) cfu/mL) on Mueller-Hinton agar.
  • Classified isolates based on previous fluoroquinolone exposure.

Main Results:

  • Ciprofloxacin exhibited the lowest MPC, followed by levofloxacin.
  • All tested fluoroquinolones showed reduced activity against strains from previously treated patients, despite maintaining susceptibility by CLSI criteria.

Conclusions:

  • While Pseudomonas aeruginosa may remain susceptible by standard criteria, reduced fluoroquinolone activity is observed in patients with prior exposure.
  • Clinical suitability of fluoroquinolones in severe infections with a history of fluoroquinolone use requires careful consideration.