| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Previous Article | Next Article ![]()
Antimicrobial Agents and Chemotherapy, November 2006, p. 3923-3925, Vol. 50, No. 11
0066-4804/06/$08.00+0 doi:10.1128/AAC.00652-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Institute of Infectious Diseases and Public Health, Università Politecnica delle Marche-Ospedali Riuniti Ancona, Ancona, Italy
Received 30 May 2006/ Returned for modification 17 July 2006/ Accepted 18 August 2006
The in vitro activity of the cathelicidin tritrpticin was investigated against multidrug-resistant Pseudomonas aeruginosa. The isolates were susceptible to the peptide at concentrations of 0.50 to 8 mg/liter. Tritrpticin completely inhibits lipopolysaccharide procoagulant activity at a 10 µM concentration. Fractionary inhibitory concentration indexes (0.385, 0.312, and 0.458) demonstrated synergy between the peptide and ß-lactams.
Published ahead of print on 28 August 2006.
| Clin. Vaccine Immunol. | Clin. Microbiol. Rev. |
|---|---|
| J. Clin. Microbiol. | ALL ASM JOURNALS |