Activity of clinafloxacin, compared with six other quinolones, against Acinetobacter baumannii clinical isolates
- Jordi Vila(corresponding author),
- Anna Ribera,
- Francesc Marco,
- ,
- Josep Mensa,
- Josep Chaves
- Hospital Clínic – Universitat de Barcelona,
- ,
- Parke-Davis
Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 471-477 (7 pages)Journal (Volume, Issue Number)
Journal of Antimicrobial Chemotherapy (Volume 49, Issue 3)Publication milestones
- Published - 2002
Publication status
ISSN
0305-7453Publication IDs
- Scopus: 0036125317
- PubMed: 11864947
Abstract
The in vitro activity of clinafloxacin was studied in comparison with ciprofloxacin, levofloxacin, moxifloxacin, nalidixic acid, sparfloxacin and trovafloxacin against Acinetobacter baumannii clinical isolates. Clinafloxacin showed a MIC90 of 4 mg/L, whereas the remaining quinolones showed a MIC90 equal to or higher than 16 mg/L. MIC50 determination in the presence of reserpine resulted in a two-fold decrease, except for trovafloxacin, which decreased four-fold, and for moxifloxacin and nalidixic acid, which did not change. The effect of reserpine was most pronounced among strains with a low level of resistance to quinolones. The MIC of clinafloxacin for strains with no mutation in either gyrA or parC genes ranged from 0.008 to 0.25 mg/L. In strains with a single mutation at amino acid codon Ser83 of the gyrA gene, the MIC of clinafloxacin ranged from 0.12 to 1 mg/L, whereas strains with a double mutation, one in the gyrA gene and another in the parC gene, showed a range of MIC of clinafloxacin from 1 to 8 mg/L. Therefore, clinafloxacin shows good activity against strains carrying a single mutation in the gyrA gene, and hence a second mutation is required for the microorganism to express resistance.
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