European Journal of Clinical Microbiology and Infectious Diseases

, Volume 22, Issue 11, pp 656–662

Meropenem Prevents Levofloxacin-Induced Resistance in Penicillin-Resistant Pneumococci and Acts Synergistically with Levofloxacin in Experimental Meningitis


    • Department of Internal MedicineInselspital
  • M. Cottagnoud
    • Department of Internal MedicineSpital Bern-Ziegler
  • F. Acosta
    • Department of Internal MedicineSpital Bern-Ziegler
  • L. Flatz
    • Department of Internal MedicineSpital Bern-Ziegler
  • F. Kühn
    • Department of Internal MedicineSpital Bern-Ziegler
  • A. Stucki
    • Department of Internal MedicineInselspital
  • J. Entenza
    • Department of Infectious DiseasesCHUV

DOI: 10.1007/s10096-003-1016-1

Cite this article as:
Cottagnoud, P., Cottagnoud, M., Acosta, F. et al. Eur J Clin Microbiol Infect Dis (2003) 22: 656. doi:10.1007/s10096-003-1016-1


The aim of the present study was to investigate the potential synergy between meropenem and levofloxacin in vitro and in experimental meningitis and to determine the effect of meropenem on levofloxacin-induced resistance in vitro. Meropenem increased the efficacy of levofloxacin against the penicillin-resistant pneumococcal strain KR4 in time-killing assays in vitro and acted synergistically against a second penicillin-resistant strain WB4. In the checkerboard, only an additive effect (FIC indices: 1.0) was observed for both strains. In cycling experiments in vitro, levofloxacin alone led to a 64-fold increase in the MIC for both strains after 12 cycles. Addition of meropenem in sub-MIC concentrations (0.25×MIC) completely inhibited the selection of levofloxacin-resistant mutants in WB4 after 12 cycles. In KR4, the addition of meropenem led to just a twofold increase in the MIC for levofloxacin after 12 cycles. Mutations detected in the genes encoding for topoisomerase IV (parC) and gyrase (gyrA) confirmed the levofloxacin-induced resistance in both strains. Addition of meropenem was able to completely suppress levofloxacin-induced mutations in WB4 and led to only one mutation in parE in KR4. In experimental meningitis, meropenem, given in two doses (2×125 mg/kg), produced a good bactericidal activity (−0.45 Δlog10 cfu/ml·h) comparable to one dose (1×10 mg/kg) of levofloxacin (−0.44 Δlog10 cfu/ml·h) against the penicillin-resistant strain WB4. Meropenem combined with levofloxacin acted synergistically (−0.93 Δlog10 cfu/ml·h), sterilizing the CSF of all rabbits.

Copyright information

© Springer-Verlag 2003