Target site modifications and efflux phenotype in clinical isolates of Streptococcus pneumoniae from Hong Kong with reduced susceptibility to fluoroquinolones
Pl. Ho et al., Target site modifications and efflux phenotype in clinical isolates of Streptococcus pneumoniae from Hong Kong with reduced susceptibility to fluoroquinolones, J ANTIMICRO, 47(5), 2001, pp. 655-658
Ciprofloxacin-susceptible (n = 7) and -resistant (MIC greater than or equal
to 4 mg/L) (n = 15) clinical isolates of Streptococcus pneumoniae from div
erse sources in Hong Kong were studied for target site modifications and ef
flux phenotype, Reserpine-inhibited efflux of ciprofloxacin and/or levoflox
acin was common in both susceptible and non-susceptible isolates. The ParC
substitutions K137N and/or S79F or Y were associated with increased ciprofl
oxacin MICs, The GyrA substitution S81F was only found in isolates with ful
l resistance to ciprofloxacin (MIC greater than or equal to 16 mg/L) and le
vofloxacin (MIC greater than or equal to 8 mg/L). Among clinical isolates o
f S. pneumoniae, accumulation of target site mutations in strains with an e
fflux mechanism was associated with increasing MICs of fluoroquinolones.