(C) PAO1 is bactericidal to AH133. Two sets of wells containing

ASM+ were inoculated with AH133 and incubated for 8 h. PAO1/pMP7605 was added to one set of wells and incubation of both sets was continued for 56 h. At the specified time points, the gelatinous mass was obtained and the CFU/ml of each species was determined using selective media (Methods). White bars: AH133 CFU/ml in single culture; green bars, CFU/ml of AH133 in the co-culture; red bars, CFU/ml of PAO1/pMP7605 from the co-culture. Values represent see more the means of at least three independent experiments ± SEM. This observed phenomenon could be due to the dispersion of the AH133 BLS or a bactericidal effect of PAO1 on AH133. Therefore, at each time point, the gelatinous masses containing AH133 alone or AH133 plus PAO1 were vortexed, serially diluted, and the CFU/ml determined. Aliquots of each dilution were spotted on Pseudomonas isolation agar for P. aeruginosa and mannitol salt agar for S. aureus. At all tested time points, the CFU/ml of the single selleck products AH133 biofilm was similar (about 1 x 107) (Figure 11C, white bars). However, the CFU/ml of AH133 within the mixed BLS was visibly reduced 8 h after addition of PAO1 and significantly reduced at 40 and 56 h, with no CFU of AH133 recovered 56 h post addition of PAO1 (Figure 11C, green bars). In contrast, the CFU/ml of

PAO1/pMP7605 within the mixed BLS dropped between 8 and 16 h post biofilm initiation but did not change significantly after 16 h (Figure 11C, red bars). These results suggest that PAO1 exerts a bactericidal effect, and that the development of the P. aeruginosa BLS in the co-culture proceeded at the expense of the S. aureus BLS. Discussion CF sputum is a highly viscous secretion in which PAO1 grows readily. PAO1 forms conventional biofilms on abiotic surfaces [13, 19, 35], but it develops macrocolonies, tight aggregates consisting of numerous

microcolonies, in ASM and the CF lung [16, 21]. While PAO1 formed a typical flat undifferentiated biofilm that completely MycoClean Mycoplasma Removal Kit covered the substratum with a homogenous distribution of the biovolume in a continuous flow-through system, it grew almost exclusively as discrete microcolonies that eventually formed a mature biofilm on a mucin-covered glass surface [19]. Based on these results, Landry et al. suggested that mucin interacts with specific PAO1 adhesins thereby immobilizing the Verteporfin molecular weight bacteria onto the glass surface [19]. In our analysis, the observed BLS developed exclusively within the gelatinous mass formed by ASM+ and not on the surface of the well (Figure 1). It is likely that through the initial interaction of these putative adhesins, individual PAO1 bacteria adhere to the mucin glycoprotein forming the nuclei of the microcolonies and leaving no bacteria to adhere to the plastic surface.