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. 2001 Feb;45(2):433-8.
doi: 10.1128/AAC.45.2.433-438.2001.

Mutant prevention concentrations of fluoroquinolones for clinical isolates of Streptococcus pneumoniae

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Mutant prevention concentrations of fluoroquinolones for clinical isolates of Streptococcus pneumoniae

J M Blondeau et al. Antimicrob Agents Chemother. 2001 Feb.

Abstract

The mutant prevention concentration (MPC) represents a threshold above which the selective proliferation of resistant mutants is expected to occur only rarely. A provisional MPC (MPC(pr)) was defined and measured for five fluoroquinolones with clinical isolates of Streptococcus pneumoniae. Based on their potential for restricting the selection of resistant mutants, the five fluoroquinolones, in descending order, were found to be moxifloxacin > trovafloxacin > gatifloxacin > grepafloxacin > levofloxacin. For several compounds, 90% of about 90 clinical isolates that lacked a known resistance mutation had a value of MPC(pr) that was close to or below the serum levels that could be attained with a dosing regimen recommended by the manufacturers. Since MPC(pr) overestimates MPC, these data identify moxifloxacin and gatifloxacin as good candidates for determining whether MPC(pr) can be used as a guide for choosing and eventually administering fluoroquinolones to significantly reduce the development of resistance.

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Figures

FIG. 1
FIG. 1
Distribution of S. pneumoniae isolates with respect to MPCpr. MPCpr was determined for each isolate by the agar dilution method. White areas of bars represent isolates containing parC mutations known to confer resistance; shaded regions represent isolates containing parC mutations that have not been demonstrated by genetic tests to confer quinolone resistance; solid regions represent unsequenced isolates. Dashed line is for alignment of panels. Panels: A, moxifloxacin; B, gatifloxacin; C, trovafloxacin; D, grepafloxacin; and E, levofloxacin.

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