Emergence of quinolone-resistant, topoisomerase-mutant Brucella after treatment with fluoroquinolones in a macrophage experimental infection model

• Published in: Enfermedades infecciosas y microbiologia clinica Vol. 33; no. 4; pp. 248 - 252
• Main Authors: Rodríguez Tarazona, Elisa, García Rodríguez, José Ángel, Muñoz Bellido, Juan Luis
• Format: Journal Article
• Language: English
• Published: Spain Elsevier España 01.04.2015
• Subjects: Amino Acid Sequence; Animals; Anti-Bacterial Agents - pharmacology; Bacterial Proteins - genetics; Brucella; Brucella melitensis - drug effects; Brucella melitensis - enzymology; Brucella melitensis - genetics; Cell Line; DNA Gyrase - genetics; DNA, Bacterial - genetics; Dogs; Fluoroquinolonas; Fluoroquinolone; Fluoroquinolones - pharmacology; GyrA; Infección experimental en macrófagos; Infectious Disease; Macrophage experimental infection; Macrophages, Peritoneal - microbiology; Microbial Sensitivity Tests; Mutation; Sequence Alignment; Fluoroquinolone; GyrA; Fluoroquinolonas; Infección experimental en macrófagos; Macrophage experimental infection; Brucella
• ISSN: 0213-005X; 1578-1852
• DOI: 10.1016/j.eimc.2014.03.010

Abstract Aim of the study To determine the activity of fluoroquinolones (FQ) and the selection of FQ-resistant mutants in a macrophage experimental infection model (MEIM). Material and methods Canine macrophages were inoculated with Brucella melitensis ATCC 23457 (WT), achieving intracellular counts of around 105 CFU/mL. Cell cultures were incubated in the presence of ciprofloxacin (CIP), levofloxacin (LEV), moxifloxacin (MOX), and doxycycline (DOX). After cell lysis, surviving microorganisms were plated for count purposes, and plated onto antibiotics-containing media for mutant selection. Topoisomerases mutations were detected by PCR and sequencing. Results Bacterial counts after cell lysis were 14.3% (CIP), 65.3% (LEV), and 75% (MOX) lower compared to the control. Quinolone-resistant mutants emerged in cell cultures containing CIP and LEV with a frequency of around 0.5 × 10−3 . All mutants showed an Ala87Val change in GyrA. Mutants had FQs MICs around 10 × WT. The ability of these mutants for infecting new macrophages and the intracellular lysis after antibiotic exposure did not change significantly. No 2nd step FQ-resistant mutants were selected from 1st step mutants. Conclusions Intracellular activity of FQs is low against WT and gyrA-mutant Brucella . FQs easily select gyrA mutants in MEIM. The ability of mutants for infecting new macrophages remains unchanged. In this MEIM, 2nd step mutants do not emerge.