aeruginosa than in S. aureus, as suggested by median biofilm amounts produced (0.162 vs 0.109, www.selleckchem.com/products/sb273005.html respectively; p < 0.01) (data not shown). To determine if AMPs could be prophylactically used to prevent biofilm formation, we tested the effect of AMPs and Tobramycin at sub-inhibitory concentrations (1/2x, 1/4x, and 1/8xMIC) against biofilm
formation (Figure 2). Tobramycin at 1/2x and 1/4xMIC caused a BKM120 order significantly higher reduction in biofilm-forming ability of S. maltophilia and S. aureus, in comparison with the three AMPs. This effect was more relevant with S. aureus, being observed also at 1/8xMIC. Tobramycin showed to be more effective than BMAP-27 against P. aeruginosa at concentrations equal to 1/4x and 1/8xMIC. The activity
of Tobramycin in reducing biofilm formation was not related to drug susceptibility (data not shown). Among AMPs, BMAP-28 and P19(9/B) at 1/2xMIC were significantly more active compared to BMAP-27, and BMAP-28 at 1/4xMIC was significantly more active than other AMPs against S. aureus. Figure 2 Effect of AMPs at sub-inhibitory concentrations against biofilm formation www.selleckchem.com/products/lee011.html by CF strains. BMAP-27 (white bars), BMAP-28 (light gray bars), P19(9/B) (dark gray bars), and Tobramycin (black bars) were tested at 1/2x, 1/4x, and 1/8xMIC against biofilm formation by P. aeruginosa (n = 24, 24, 25, and 17, for BMAP-27, BMAP-28, P19(9/B) and Tobramycin, respectively), S. maltophilia Glutamate dehydrogenase (n = 14, 14, 27, and 5, for BMAP-27, BMAP-28, P19(9/B) and Tobramycin, respectively), and S. aureus (n = 11, 11, 8, and 3, for BMAP-27, BMAP-28, P19(9/B) and Tobramycin, respectively) CF strains. Prevention of biofilm formation was plotted as percentage of strains whose ability in forming biofilm was significantly decreased (of at least 25%) compared to controls (not exposed),
as analyzed by a crystal violet staining assay.* p < 0.05; ** p < 0.0001, Fisher’s exact test. We further evaluated AMPs as potential therapeutics for CF by testing their efficacy against preformed biofilms. To this, BMAP-27, BMAP-28, P19(9/B), and Tobramycin at 1xMIC and at bactericidal concentrations (5x, and 10xMIC) were assayed against preformed (24 h) biofilms by six representative P. aeruginosa strains selected for high biofilm formation ability (Figure 3). Figure 3 Activity of AMPs at bactericidal concentrations against preformed P. aeruginosa biofilms. BMAP-27, BMAP-28, P19(9/B), and Tobramycin were tested at 1x (white bars), 5x (gray bars), and 10xMIC (black bars) against preformed biofilm by 6 P. aeruginosa CF strains. Results are expressed as percentage of biofilm’ viability compared to control (not exposed, 100% viability). ** p < 0.0001, Fisher’s exact test. The activity of AMPs and Tobramycin against preformed biofilms resulted to be similar in 5 out of 6 strains tested, causing a highly significant reduction of biofilm viability compared to the controls (biofilm not exposed; p < 0.