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Antimicrobial Agents and Chemotherapy, August 1999, p. 2000-2004, Vol. 43, No. 8
Department of
Pathology,1 Department of
Microbiology,2 and Department of
Medicine,3 Northwestern University Medical
School, Chicago, Illinois 60611
Received 16 December 1998/Returned for modification 3 March
1999/Accepted 9 June 1999
In this study, we assessed the activity of ciprofloxacin,
levofloxacin, sparfloxacin, and trovafloxacin against clinical isolates of Streptococcus pneumoniae that were resistant to the
less-recently developed fluoroquinolones by using defined amino acid
substitutions in DNA gyrase and topoisomerase IV. The molecular basis
for resistance was assessed by using mutants selected with
trovafloxacin, ciprofloxacin, and levofloxacin in vitro. This
demonstrated that the primary target of trovafloxacin in S. pneumoniae is the ParC subunit of DNA topoisomerase IV,
similar to most other fluoroquinolones. However, first-step mutants
bearing the Ser79
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Contribution of Topoisomerase IV and DNA Gyrase
Mutations in Streptococcus pneumoniae to Resistance to
Novel Fluoroquinolones
Phe/Tyr substitution in topoisomerase IV
subunit ParC were susceptible to trovafloxacin with a minimum
inhibitory concentration of 0.25 µg/ml, and mutations in the
structural genes for both topoisomerase IV subunit ParC (parC) and the DNA gyrase subunit (gyrA) were
required to achieve levels of resistance above the breakpoint. The data
also suggest that enhanced activity of trovafloxacin against
pneumococci is due to a combination of factors that may include reduced
efflux of this agent and an enhanced activity against both DNA gyrase and topoisomerase IV.
*
Corresponding author. Mailing address: Department of
Pathology, Ward Building, 6-223, 303 E. Chicago Ave., Chicago, IL
60611. Phone: (312) 503-8188. Fax: (312) 908-4137. E-mail:
evp606{at}anima.nums.nwu.edu.
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