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Abstract

Vol.56 No.1 January 2008

Antibacterial activity of gemifloxacin against clinical isolates

Mayumi Aminaka1), Kyoko Kuwahara1,2), Akio Kitamura2), Masato Higashide3), Shigeki Misawa4), Shigemi Kondo5), Intetsu Kobayashi6), Ken Kikuchi1) and Keiichi Hiramatsu1,2)

1)Department of Infection Control Science, Postgraduate Course, Juntendo University, 2-1-1 Hongo, Bunkyo-ku, Tokyo, Japan
2)Department of Bacteriology, Juntendo University School of Medicine
3)Department of Bacteriology, Koto-Biken Medical Laboratories
4)Clinical Laboratory, Juntendo University Hospital
5)Department of Laboratory Medicine, Juntendo University School of Medicine
6)Chemotherapy Division, Mitsubishi Kagaku Bio-Clinical Laboratories, Inc.

Abstract

In vitro antibacterial activity of gemifloxacin, a new fluoro quinolone agent, and other drugs was determined against clinical isolates in 2005 Japan and clinical isolates of levofloxacin-resistant Streptococcus pneumoniae after 2003.
Gemifloxacin MIC90 was 0.031 μg/mL, higher than other fluoro quinolone agents. Gemifloxacin activity is good in levofloxacin-resistant S. pneumoniae because gemifloxacin MIC90 of levofloxacin-resistant Streptococcus pneumoniae was 0.5 μg/mL, higher than other fluoro quinolone agents. Gemifloxacin MIC90 against Haemophilus influenzae was 0.015 μg/mL. Gemifloxacin MIC90 against ampicillin-resistant β-lactamase negative Haemophilus influenzae (BLNAR) was 0.063 μg/mL. Gemifloxacin MIC90 against methicillin-resistant Staphylococcus aureus was low the same as for other fluoro quinolone agents. Gemifloxacin activity was shown in Moraxella (Branhamella) catarrhalis, Klebsiella pneumoniae, and Pseudomonas aeruginosa similar to other fluoro-quinolone agents. Our results suggest that gemifloxacin effective clinical respiratory organ infectious disease treatment.

Key word

gemifloxacin, respiratory quinolone, Streptococcus pneumoniae, BLNAR (beta-lactamase nonproducing ampicillin resistant)

Received

July 20, 2007

Accepted

November 16, 2007

Jpn. J. Chemother. 56 (1): 16-20, 2008