Differences among means were determined using Fisher’s protected LSD test at P=0.05. All the experiments described were based on the interaction between bacterial cells and the glass surface of the MFCs; however, similar PCI-32765 chemical structure observations were made on polydimethylsilioxane surfaces (not shown). Differences were evident among the wild types and TFP mutants in their ability to adhere to glass as soon as cells were introduced into the MFCs. While M6 and W1 cells attached immediately to the surface, the respective TFP mutants failed to do so (Fig. 1). Blocking medium flow at the main channel for up to 90 min resulted in the accumulation of TFP mutant cells in the field of view. However, when medium flow was resumed (0.25 μL min−1),

all TFP mutants (all M6-M and the majority of M6-T and W1-A cells) were immediately displaced. In contrast to M6-M cells, which, under flow, were unable to adhere to the channel surface regardless of the incubation time, M6-T and W1-A cells showed sporadic attachment after 24 h of incubation. Interestingly, the hyperpiliated M6-T cells attached to the surface not only as solitary cells but also as small clusters of about 5–15 cells (Fig. 2). No apparent differences

were observed between M6 and M6-flg, as both effectively attached to the surfaces (not shown). Adhesion force evaluation assays were conducted to compare the strength of attachment among wild types and mutants. This assay was not performed with mutant M6-M, due to its inability to attach to the surface under tested Selleckchem Lumacaftor conditions. Gradually increasing the flow rate from 0.25 to 16 μL min−1 did not reveal substantial differences between

strains M6 and M6-T in attachment ability. However, following the application of flow rates of 32 and 64 μL min−1, the majority (84%) of the M6-T cells Coproporphyrinogen III oxidase were displaced from the surface (Fig. 2; Supporting Information, Movie S1). Under these conditions, only 37% of the M6 cells were displaced from the surface, and the differences between these strains were significant (P=0.05) (Fig. 2b). Accordingly, wild-type M6 showed a significantly (P=0.01) higher adhesion force (174.8 pN) than M6-T (104.4 pN) (Fig. 2b). For a qualitative assessment of the strength of attachment, the flow rate was increased to 100 μL min−1, equivalent to a drag force of 380 pN (De la Fuente et al., 2007b) for 1 min. Here too, the majority of M6 cells that withstood the previous rate of 64 μL min−1 remained attached to the surface. No significant differences were observed between M6 and M6-flg in adhesion assays (Fig. 2b). Wild-type W1, which, in contrast to strain M6, does not produce polar flagella (Table 1), showed a behavior similar to that of M6, with an average of 49% of the initial cells being displaced from the surface at the end of the assays (not shown). On the other hand, the majority of W1-A cells were quickly removed from the surface following the application of a flow rate of 8 μL min−1.