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Antimicrobial Agents and Chemotherapy, August 2009, p. 3572-3575, Vol. 53, No. 8
0066-4804/09/$08.00+0 doi:10.1128/AAC.00176-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Department of Molecular Microbiology and Immunology,1 Department of Laboratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki City 852-8501, Japan,2 Department of Infection Control and Laboratory Diagnostics, Internal Medicine, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai 980-8574, Japan3
Received 8 February 2009/ Returned for modification 19 April 2009/ Accepted 4 May 2009
We evaluated the potency of garenoxacin in selecting resistant Streptococcus pneumoniae mutants by determining its mutant prevention concentration, using strains with and without topoisomerase gene mutations, and compared its potency to that of other quinolones. Garenoxacin had a significantly greater potency against pneumococci, including strains containing topoisomerase mutations. Genetic analysis of the S. pneumoniae mutants created by garenoxacin revealed that the gyrA gene was a primary target of garenoxacin.
Published ahead of print on 18 May 2009.
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