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Volume 38, Number 6, December 2005

In vitro antimicrobial effect of cefazolin and cefotaxime combined with minocycline against Vibrio cholerae non-O1 non-O139


Bo-An Su, Hung-Jen Tang, Yin-Yi Wang, Yung-Ching Liu, Wen-Chien Ko, Cheng-Yi Liu, Yin-Ching Chuang, and the Surveillance of Multicenter Antimicrobial Resistance in Taiwan (SMART) Program
Department of Medicine and Medical Research, Chi Mei Medical Center, Tainan; Department of Medicine, Kaohsiung Veterans General Hospital, Kaohsiung; Department of Medicine, National Cheng-Kung University Hospital, Tainan; and 4Taipei Veterans General Hospital, Taipei, Taiwan

Received: June 14, 2005    Revised: July 25, 2005    Accepted: August 16, 2005   

 

Corresponding author:

Yin-Ching Chuang, Chi Mei Medical Center, No. 901 Jung Hua Rd., Yung Kang City, Tainan 710, Taiwan. E-mail: chuangkenneth@hotmail.com This e-mail address is being protected from spam bots, you need JavaScript enabled to view it

 



 

Methods:

The most common clinical manifestation of Vibrio cholerae non-O1 non-O139 is gastroenteritis. This vibrion may also cause bacteremia, soft tissue infection, and other extraintestinal invasive disease, especially in immunocompromised patients. This study evaluated the current status of antimicrobial resistance in clinical isolates of V. cholerae non-O1 non-O139 in Taiwan as part of the SMART (Surveillance from Multicenter Antimicrobial Resistance in Taiwan) program. Minimal inhibitory concentrations (MICs) of 9 antimicrobial agents were determined by the agar dilution method. All of the isolates were susceptible to minocycline (MIC at which 90% of the isolates were inhibited [MIC90], 0.12 μg/mL), cefotaxime (MIC90, 0.06 μg/mL), lomefloxacin (MIC90, 0.12 μg/mL), levofloxacin (MIC90, 0.03 μg/mL), ciprofloxacin (MIC90, 0.03 μg/mL), moxifloxacin (MIC90, 0.06 μg/mL), sparfloxacin (MIC90, 0.06 μg/mL), gatifloxacin (MIC90, 0.03 μg/mL), and cefazolin (MIC90, 8 μg/mL). We conducted time-kill studies to evaluate the inhibitory activities of either cefazolin or minocycline alone or in combination against V. cholerae non-O1 non-O139 (Vc2). We also evaluated the inhibitory activity of cefazolin or cefotaxime combined with minocycline. The individual MICs of cefazolin, cefotaxime, and minocycline were 4 μg/mL, 0.0075 μg/mL, and 0.12 μg/mL, respectively, when approximately 5 × 105 colony-forming units/mL of V. cholerae non-O1 non-O139 was incubated. Bacterial growth was inhibited initially but resumed later when cefazolin, cefotaxime, or minocycline was used alone. When cefazoline or cefotaxime was combined with minocycline, V. cholerae non-O1 non-O139 was inhibited over 48 h and no regrowth was noted. We conclude that the combination of cefazolin or cefotaxime with minocycline has a synergistic inhibitory effect on V. cholerae non-O1 non-O139 in vitro.

 



 

Key words:

Combined antibiotics, microbial sensitivity tests, Vibrio cholerae non-O1, vibrio infections

 



 

J Microbiol Immunol Infect 2005;38:425-429.