In vitro activity of tigecycline against clinical isolates of extended-spectrum beta-lactamase-producing Klebsiella pneumoniae, Serratia marcescens and Enterobacter cloacae
Yee-Huang Ku, Yin-Ching Chuang, Wen-Liang Yu
Division of Infectious Disease, Department of Internal Medicine, Chi Mei Medical Center, Liouying; Departments of Medical Research and Intensive Care Medicine, Chi-Mei Medical Center, Tainan; and Department of Medicine, Taipei Medical University, Taipei, Taiwan
Received: April 5, 2007
Revised: May 15, 2007
Accepted: June 25, 2007
Corresponding author:
Dr. Wen-Liang Yu, Department of Intensive Care Medicine, Chi-Mei Medical Center, Tainan, Taiwan. E-mail: Dr. Wen-Liang Yu
Background and purpose:
Strains of extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae have spread widely in Taiwan hospitals. In this study, we evaluated the in vitro antimicrobial activity of tigecycline against ESBL-producing Enterobacteriaceae, including Klebsiella pneumoniae, Serratia marcescens and Enterobacter cloacae.
Methods:
104 confirmed ESBL-producing bacteria were isolated from 4 hospitals in mid- and southern Taiwan between 2000 and 2006. The in vitro activity of tigecycline against these ESBL producers was tested by use of Etest strips.
Results:
The minimal tigecycline concentration at which 50% of isolates were inhibited and minimal concentration at which 90% of isolates were inhibited for ESBL-producing isolates ranged from 0.38 to 0.75 μg/mL and 0.5 to 1.5 μg/mL, respectively.
Conclusion:
Tigecycline, a new semisynthetic glycylcycline, may be considered an alternative drug of choice for patients infected with ESBL-producing bacteria.
Key words:
beta-Lactamase resistance; beta-Lactamases; Enterobacteriaceae; Microbial sensitivity tests; Minocycline
J Microbiol Immunol Infect. 2008;41:332-336.
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