JAC Advance Access published online on January 28, 2003
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkg121
© 2003 by The British Society for Antimicrobial Chemotherapy
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Original article
1 Division of Immunity & Infection, Medical School,
University of Birmingham, Edgbaston, Birmingham B15 2TT, UK
* Corresponding author. E-mail: m.j.gill{at}bham.ac.uk.
Received 20 September 2001
; revised 8 February 2002
; accepted 13 December 2002
We describe a mutant of Streptococcus pyogenes NCTC
8198 with a multidrug efflux phenotype. A mutant selected with ethidium
bromide showed a four-fold rise in MIC of norfloxacin, a 16-fold rise
in MIC of ethidium bromide and an eight-fold rise in MIC of acriflavine
when compared with the parent strain. The MICs were unaffected
by the efflux pump inhibitors reserpine, rescinnamine and verapamil.
The mutant's ethidium bromide MIC was reduced two-fold
by norfloxacin. Ethidium bromide accumulation after 10 min was 58% lower
in the mutant compared with the parent. This difference was not
affected by carbonyl cyanide m-chlorophenylhydrazone.
A multidrug efflux phenotype mutant of Streptococcus pyogenes
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