SUMMARY:A total of 279 isolates of Escherichia coli (n = 128) and Klebsiella pneumoniae (n = 151) were obtained from blood samples from children at the Seoul National University Children's Hospital, Seoul, Korea from 1999 to 2007. Five plasmid-mediated quinolone resistance (PMQR) genes, qnrA, qnrB, qnrS, qepA, and aac(6?)-Ib-cr, and the minimal inhibitory concentration (MIC) values for ciprofloxacin were tested for all the strains. Mutations in both gyrA and parC were analyzed in 57 representative strains. Twenty-seven strains (9.7z) had at least 1 of the 5 PMQR genes: qnrB in 20 isolates, qnrS in 1, aac(6?)-Ib-cr in 5, and both qnrB and aac(6?)-Ib-cr in 1 isolate. The overall PMQR prevalence rates tended to increase over time ( P = 0.001). The non-susceptibility rate to ciprofloxacin was 11.0z (31/279). PMQR-harboring isolates tended to have increased ciprofloxacin MIC values among both quinolone resistance-determining region (QRDR) mutation-present (P = 0.016) and QRDR mutation-absent isolates ( P º 0.001). The increasing prevalence of PMQR genes was associated with increase in quinolone use over time ( P º 0.001) and increasing frequency of non-susceptibility to ciprofloxacin ( P º 0.001).Quinolone resistance in Enterobacteriaceae has increased in line with the increased number of quinolone prescriptions being administered for the treatment of infections by multidrug-resistant Enterobacteriaceae isolates. Mutations in the quinolone resistance-determining region (QRDR) and the presence of plasmidmediated quinolone resistance (PMQR) genes contribute to quinolone resistance in complex and diverse ways (1-3). However, only limited studies have addressed the quinolone resistance of Enterobacteriaceae in pediatric isolates so far; long-term studies involving bloodstream isolates are even fewer in number (4-6).In this study, we identified PMQR genes from Escherichia coli and Klebsiella pneumoniae isolates obtained from pediatric patients with bloodstream infections. We analyzed the isolates for changes in the prevalence of the PMQR genes and also regarding whether the presence of the PMQR genes is related to the amount of quinolones prescribed and to quinolone-resistance profiles.