Affiliation:
1. Royal Perth Hospital, Perth
2. Women's and Children's Hospital, Adelaide, Australia
3. The JONES Group/JMI Laboratories, North Liberty, Iowa
Abstract
ABSTRACT
Between 1999 and 2001, 16,731 isolates from the Asia-Pacific Region were tested in the SENTRY Program for susceptibility to six fluoroquinolones including garenoxacin. Garenoxacin was four- to eightfold less active against
Enterobacteriaceae
than ciprofloxacin, although both drugs inhibited similar percentages at 1 μg/ml. Garenoxacin was more active against gram-positive species than all other fluoroquinolones except gemifloxacin. For
Staphylococcus aureus
, oxacillin resistance was high in many participating countries (Japan, 67%; Taiwan, 60%; Hong Kong, 55%; Singapore, 52%), with corresponding high levels of ciprofloxacin resistance (57 to 99%) in oxacillin-resistant
S. aureus
(ORSA). Of the ciprofloxacin-resistant ORSA isolates, the garenoxacin MIC was >4 μg/ml for only 9% of them. For
Streptococcus pneumoniae
, penicillin nonsusceptibility and macrolide resistance were high in many countries. No relationship was seen between penicillin and garenoxacin susceptibility, with all isolates being susceptible at <2 μg/ml. There was, however, a partial correlation between ciprofloxacin and garenoxacin MICs. For ciprofloxacin-resistant isolates for which garenoxacin MICs were 0.25 to 1 μg/liter, mutations in both the ParC and GyrA regions of the quinolone resistance-determining region could be demonstrated. No mutations conferring high-level resistance were detected. Garenoxacin shows useful activity against a wide range of organisms from the Asia-Pacific region. In particular, it has good activity against
S. aureus
and
S. pneumoniae
, although there is evidence that low-level resistance is present in those organisms with ciprofloxacin resistance.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference36 articles.
1. Antimicrobial Activities of BMS-284756 Compared with Those of Fluoroquinolones and β-Lactams against Gram-Positive Clinical Isolates
2. Bell, J. M., J. D. Turnidge, and R. N. Jones. 2002. Antimicrobial resistance trends in community-acquired respiratory tract pathogens in the Western Pacific Region and South Africa: report from the SENTRY antimicrobial surveillance program, (1998-1999) including an in vitro evaluation of BMS284756. Int. J. Antimicrob. Agents19:125-132.
3. Biedenbach, D. J., R. N. Jones, and M. A. Pfaller. 2001. Activity of BMS284756 against 2,681 recent clinical isolates of Haemophilus influenzae and Moraxella catarrhalis: report from the SENTRY antimicrobial surveillance program (2000) in Europe, Canada and the United States. Diagn. Microbiol. Infect. Dis.39:245-250.
4. Prevalence of a Putative Efflux Mechanism among Fluoroquinolone-Resistant Clinical Isolates of
Streptococcus pneumoniae
5. Broskey, J., K. Coleman, M. N. Gwynn, L. McCloskey, C. Traini, L. Voelker, and R. Warren. 2000. Efflux and target mutations as quinolone resistance mechanisms in clinical isolates of Streptococcus pneumoniae. J. Antimicrob. Chemother.45(Suppl. 1):95-99.
Cited by
20 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献