JAC Advance Access published online on September 1, 2003
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkg424
© 2003 by The British Society for Antimicrobial Chemotherapy
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Original article
1 Molecular Diagnostics and Typing Unit, Department of Microbiology,
University Hospital, Queens Medical Centre, Nottingham NG7 2UH,
UK
* Corresponding author. E-mail: Kevin.Towner{at}mail.qmcuh-tr.trent.nhs.uk.
Objectives. To compare the in
vitro activity of moxifloxacin and ciprofloxacin against 226
nosocomial isolates of Acinetobacter baumannii from
44 hospitals in the UK. Methods: MICs of ciprofloxacin and moxifloxacin
were determined by Etest. PCR analysis was used to detect chromosomal
mutations in the gyrA and parC genes.
Isolates resistant to ciprofloxacin and susceptible to moxifloxacin
were examined for the ability to generate spontaneous moxifloxacin-resistant
isolates. Results: Of 226 isolates, 49.1% were
resistant to ciprofloxacin and 39.4% were moxifloxacin-resistant according
to BSAC criteria. Approximately 20% of isolates resistant
to ciprofloxacin remained susceptible to moxifloxacin. A GyrA mutation
at Ser-83 was found in all ciprofloxacin-resistant isolates. Single
mutations in both the gyrA and parC genes
at codons Ser-83 and Ser-80, respectively, were found in ciprofloxacin-
and moxifloxacin-resistant isolates. Isolates that were ciprofloxacin-resistant
but moxifloxacin-susceptible generated spontaneous moxifloxacin-resistant
mutants when grown on medium containing up to 8x their initial
MIC. However, these mutants were not stable and none displayed high-level
moxifloxacin resistance. Conclusions: Moxifloxacin retained in
vitro activity against some ciprofloxacin-resistant clinical A. baumannii isolates. Mutations in both gyrA and parC were necessary for resistance to moxifloxacin
in most isolates of A. baumannii.
Keywords: Acinetobacter, fluoroquinolones, gyrA, parC, resistant
Frequencies and mechanisms of resistance to moxifloxacin
in nosocomial isolates of Acinetobacter baumannii
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