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In-vitro activity of tigecycline against clinical isolates of Acinetobacter baumannii in Taiwan

  • Jien Wei Liu
  • , Lih Shinn Wang
  • , Yu Jen Cheng
  • , Gwo Jong Hsu
  • , Po Liang Lu
  • , Yung Ching Liu
  • , Chih Ming Chen
  • , Chun Ming Lee
  • , Wu Sun
  • , Tsrang Neng Jang
  • , Ping Cherng Chiang
  • , Yin Ching Chuang
  • , Hsiu Chen Lin
  • , Zhi Yuan Shi
  • , Hsiang Chi Kung
  • , Cheng Hua Huang*
  • , Shih Ming Tsao
  • , Chin Te Lu
  • , Chun Hsing Liao
  • , Po Ren Hsueh
  • *Corresponding author for this work
  • Chang Gung University
  • Buddhist Tzu-Chi General Hospital Taiwan
  • Changhua Christian Hospital
  • Chia-Yi Christian Hospital
  • Kaohsiung Medical University
  • Veterans General Hospital-Kaohsiung Taiwan
  • Tungs' Taichung MetroHarbor Hospital
  • Mackay Memorial Hospital Taiwan
  • Pao-Chien Hospital
  • Shin Kong Wu Ho-Su Memorial Hospital
  • Chang Gung Memorial Hospital
  • Chi-Mei Medical Center
  • Taipei Medical University
  • Veterans General Hospital-Taichung Taiwan
  • National Taiwan University
  • Cathay General Hospital Taiwan
  • Chung Shan Medical University
  • Lotung Poh-Ai Hospital
  • Far Eastern Memorial Hospital

Research output: Contribution to journalJournal Article peer-review

17 Scopus citations

Abstract

We performed susceptibility testing using the microdilution method to determine the in-vitro activity of tigecycline against 393 Acinetobacter baumannii clinical isolates collected in 2006 from 19 hospitals in Taiwan. Significant proportions of the isolates were resistant to imipenem (44%), ciprofloxacin (75%), amikacin (69%), sulbactam (34%) and all four antibiotics (22%), and susceptibility to tigecycline among these different resistant phenotypes of A. baumannii varied from 71% to 82%. The minimum inhibitory concentration (MIC) of tigecycline ranged from 0.6 to 16 μg/mL (MIC50 2 μg/mL; MIC90 4 μg/mL). The cumulative curve of tigecycline MICs showed that when the MIC cut-offs were set at 2 μg/mL and 4 μg/mL, 80.9% and 93.1% of the isolates were susceptible, respectively. As tigecycline will be used in the future for infections caused by multidrug-resistant A. baumannii because of limited antibiotic choice, and as resistance to tigecycline in A. baumannii isolates may develop following antibiotic exposure, continuous monitoring of the susceptibility of A. baumannii isolates to tigecycline is warranted.

Original languageEnglish
Pages (from-to)S188-S191
JournalInternational Journal of Antimicrobial Agents
Volume32
Issue numberSUPPL. 3
DOIs
StatePublished - 11 2008
Externally publishedYes

Keywords

  • Acinetobacter baumannii
  • Antibacterial drug resistance
  • Taiwan
  • Tigecycline

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