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Antimicrobial Agents and Chemotherapy, March 2001, p. 883-892, Vol. 45, No. 3
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.3.883-892.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Phenotypic Resistance of Staphylococcus aureus,
Selected Enterobacteriaceae, and Pseudomonas
aeruginosa after Single and Multiple In Vitro Exposures to
Ciprofloxacin, Levofloxacin, and Trovafloxacin
D. N.
Gilbert,*
S. J.
Kohlhepp,
K. A.
Slama,
G.
Grunkemeier,
G.
Lewis,
R. J.
Dworkin,
S. E.
Slaughter, and
J. E.
Leggett
Earle A. Chiles Research Institute,
Providence Portland Medical Center and the Department of Medicine,
Oregon Health Sciences University, Portland, Oregon
Received 7 March 2000/Returned for modification 27 July
2000/Accepted 19 December 2000
The phenotypic resistance of selected organisms to ciprofloxacin,
levofloxacin, and trovafloxacin was defined as a MIC of
4 µg/ml.
The dynamics of resistance were studied after single and sequential
drug exposures: clinical isolates of methicillin-susceptible and
methicillin-resistant Staphylococcus aureus (MSSA and
MRSA), Escherichia coli, Klebsiella pneumoniae,
Enterobacter cloacae, Serratia marcescens, and
Pseudomonas aeruginosa were utilized. After a single 48-h
exposure of a large inoculum to four times the initial MIC for the
organism, the frequency of selection of resistant mutants of MSSA was
greater for trovafloxacin than levofloxacin (P = 0.008); for E. cloacae, the frequency was highest for
ciprofloxacin and lowest for levofloxacin and trovafloxacin; for
S. marcescens, the frequency was highest for trovafloxacin
and lowest for ciprofloxacin (P = 0.003). The results
of serial passage experiments were analyzed both by the Kaplan-Meier
product-limited method as well as by analysis of variance of mean
inhibitory values. By both methods, MSSA and MRSA expressed mutants
resistant to ciprofloxacin after fewer passages than were required for
either levofloxacin or trovafloxacin. For the aerobic gram-negative
bacilli, two general patterns emerged. Mutants resistant to
trovafloxacin appeared sooner and reached higher mean MICs than did
mutants resistant to levofloxacin or ciprofloxacin. Mutants resistant
to ciprofloxacin appeared later and reached mean MICs lower than the
MICs of the other two drugs studied. Even though individual strain
variation occurred, the mean MICs were reproduced when the serial
passage experiment was repeated using an identical panel of E. coli isolates. In summary, the dynamic selection of
fluoroquinolone-resistant bacteria can be demonstrated in experiments
that employ serial passage of bacteria in vitro.
*
Corresponding author. Mailing address: Providence
Portland Medical Center, 5050 NE Hoyt, Suite 540, Portland, OR 97213. Phone: (503) 215-6258. Fax: (503) 215-6857. E-mail:
dagilbert{at}providence.org.
Antimicrobial Agents and Chemotherapy, March 2001, p. 883-892, Vol. 45, No. 3
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.3.883-892.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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