S. Esposito et al., Activity of moxifloxacin and twelve other antimicrobial agents against 216clinical isolates of Streptococcus pneumoniae, CHEMOTHERA, 47(2), 2001, pp. 90-96
Background: An increased incidence of macrolide resistance in penicillin-re
sistant Streptococcus pneumoniae has been described. Methods: With this in
mind, 216 S. pneumoniae isolates were evaluated for their in vitro suscepti
bility to a new fluoroquinolone, moxifloxacin, which was compared with peni
cillin, amoxicillin, cefuroxime, cefotaxime, ceftriaxone, erythromycin, cla
rithromycin, ciprofloxacin, sparfloxacin, ofloxacin, vancomycin and teicopl
anin. A broth microdilution assay was performed in cation-adjusted Mueller-
Hinton broth with 5% (v/v) lysed horse blood according to NCCLS guidelines.
Results: Erythromycin resistance was observed in all the 22 penicillin-res
istant S. pneumoniae (10.1%). All the penicillin-susceptible S. pneumoniae
were susceptible to cephalosporins, whereas all the penicillin-resistant on
es showed resistance to cefuroxime and only intermediate susceptibility to
cefotaxime and ceftriaxone. The 216 tested strains were inhibited by sparfl
oxacin and moxifloxacin at concentrations of 0.12-0.5 mg/l and 0.06-0.25 mg
/l, respectively, regardless of whether the strain was penicillin and/or er
ythromycin resistant. Seven penicillin-resistant strains displayed resistan
ce to ofloxacin. All isolates were susceptible to vancomycin; teicoplanin M
IC values ranged from 0.03 to 0.12 mg/l. The excellent in vitro activity of
moxifloxacin against S. pneumoniae was not affected by penicillin and/or m
acrolides. Conclusion: Moxifloxacin appears to be a promising choice for th
e treatment of pneumococcal infections, including situations where therapeu
tic choices are limited due to penicillin and macrolide resistance. Copyrig
ht (C) 2001 S. Karger AG, Basel.