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Antimicrobial Agents and Chemotherapy, November 2001, p. 3084-3091, Vol. 45, No. 11
0066-4804/01/$04.00+0   DOI: 10.1128/AAC.45.11.3084-3091.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Emergence of Reduced Susceptibility and Resistance to Fluoroquinolones in Escherichia coli in Taiwan and Contributions of Distinct Selective Pressures

L. Clifford McDonald,1,dagger Feng-Jui Chen,1 Hsiu-Jung Lo,1 Hsiao-Chuan Yin,1 Po-Liang Lu,2 Cheng-Hua Huang,3 Pei Chen,1 Tsai-Ling Lauderdale,1 and Monto Ho1,*

Division of Clinical Research, National Health Research Institutes,1 and Cathay General Hospital,3 Taipei, and Kaohsiung Medical University Hospital, Kaohsiung,2 Taiwan

Received 20 March 2001/Returned for modification 11 June 2001/Accepted 9 August 2001

A survey of 1,203 Escherichia coli isolates from 44 hospitals in Taiwan revealed that 136 (11.3%) isolates were resistant to fluoroquinolones and that another 261 (21.7%) isolates had reduced susceptibility. Resistance was more common in isolates responsible for hospital-acquired (mostly in intensive care units) infections (17.5%) than in other adult inpatient (11.4%; P = 0.08) and outpatient isolates (11.9%; P > 0.1). Similarly, reduced susceptibility was more common in isolates responsible for hospital-acquired infections (30.9%) than in other adult inpatient (21.0%; P = 0.04) and outpatient (21.4%; P = 0.06) isolates. Isolates from pediatric patients were less likely to be resistant (1.3 versus 12.0%; P < 0.01) but were nearly as likely to have reduced susceptibility (17.7 versus 21.9%; P > 0.1) as nonpediatric isolates. There was an inverse relationship in the proportion of isolates that were resistant versus the proportion that had reduced susceptibility among isolates from individual hospitals (R = 0.031; P < 0.05). In an analysis of isolates from two hospitals, all 9 resistant strains possessed double point mutations in gyrA and all 19 strains with reduced susceptibility strains had single point mutations; no mutations were found among fully susceptible strains. Risk factors for resistance included underlying cancer (odds ratio [OR], 83; 95% confidence interval [CI95], 7.3 to 2,241; P < 0.001), exposure to a quinolone (OR, undefined; P = 0.02), and exposure to a nonquinolone antibiotic (OR, 20; CI95, 2.2 to 482; P < 0.001); underlying cancer was the only independent risk factor (OR, 83; CI95, 8.6 to 807; P < 0.001). There were no significant associations between any of these factors and reduced susceptibility. Whereas acute and chronic quinolone use in cancer patients is a major selective pressure for resistance, other undetermined but distinct selective pressures appear to be more responsible for reduced susceptibility to fluoroquinolones in E. coli.


* Corresponding author. Mailing address: Division of Clinical Research, National Health Research Institutes, 128 Yen-Chiu-Yuan Rd. Sec. 2, Taipei 11529, Taiwan, Republic of China. Phone: 886-2-2653-4401, ext. 7120. Fax: 886-2-2789-0254. E-mail: monto{at}nhri.org.tw.

dagger Present address: Division of Infectious Diseases, University of Louisville, Louisville, Ky.


Antimicrobial Agents and Chemotherapy, November 2001, p. 3084-3091, Vol. 45, No. 11
0066-4804/01/$04.00+0   DOI: 10.1128/AAC.45.11.3084-3091.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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