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Antimicrobial Agents and Chemotherapy, May 2001, p. 1467-1472, Vol. 45, No. 5
Section of Infectious Diseases and Clinical
Immunology, Department of Medicine, University Hospital and Medical
Center, D-89070 Ulm, Germany
Received 16 August 2000/Returned for modification 18 November
2000/Accepted 23 February 2001
The development of fluoroquinolone resistance in Escherichia
coli may be associated with mutations in regulatory gene loci such as marRAB that lead to increased multidrug efflux,
presumably through activation of expression of the AcrAB multidrug
efflux pump. We found that multidrug-resistant (MDR) phenotypes with enhanced efflux can also be selected by fluoroquinolones from marRAB- or acrAB-inactivated E. coli K-12 strains having a single mutation in the
quinolone-resistance-determining region of gyrA. Mutant
3-AG100MKX, obtained from a mar knockout strain after
two selection steps, showed enhanced expression of acrB in
a reverse transcriptase PCR associated with insertion of
IS186 into the AcrAB repressor gene acrR. In
vitro selection experiments with acrAB knockout strains
yielded MDR mutants after a single step. Enhanced efflux in these
mutants was due to increased expression of acrEF and
associated with insertion of IS2 into the upstream region of
acrEF, presumably creating a hybrid promoter. These observations confirm the importance of efflux-associated nontarget gene
mutations and indicate that transposition of genetic elements may have
a role in the development of fluoroquinolone resistance in E. coli.
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.5.1467-1472.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Enhanced Expression of the Multidrug Efflux Pumps AcrAB and
AcrEF Associated with Insertion Element Transposition in
Escherichia coli Mutants Selected with a
Fluoroquinolone
*
Corresponding author. Mailing address: Medizinische
Universitätsklinik und Poliklinik, D-89070 Ulm, Germany. Phone:
49-731-502 4423. Fax: 49-731-502 4488. E-mail:
winfried.kern{at}medizin.uni-ulm.de.
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