All these data implicate that AggA TISS is required for pellicle

All these data implicate that AggA TISS is required for pellicle formation, most likely at the monolayer pellicle formation stage, which appears to be different from that in SSA biofilm formation. Figure 5 Biofilm assay of MR-1 and aggA mutant. (A) Pellicle formation of MR-1, ΔaggA, ΔaggA* (aggA in-frame deletion mutant containing pBBR-AGGA). Defactinib mw (B) SSA Biofilm was assessed for the strains indicated after 16 and 24 h, respectively. Cultures were prepared as described in Methods. The averaged OD readings of four independent culture tubes were given with images of representative CV-stained tubes. Discussion and Conclusions In the microbial world, existence within surface-associated

structured multicellular communities is the prevailing lifestyle [36, 37]. The pellicles of facultative bacteria formed at the liquid-air interface can be selectively advantageous given that respiration with oxygen as the terminal electron acceptor

is the most productive. In S. oneidensis, the growth rate was promoted by better access to oxygen evidenced by that the cells grew much faster in shaking than in static cultures. Along with the observation that SSA biofilm formation of S. oneidensis was inhibited under Selleck JQEZ5 anaerobic conditions, the requirement of oxygen for pellicle formation may mainly come from its facilitation of aggregation and attachment of cells to the solid surfaces. This is consistent with previous findings that oxygen promotes autoaggregation of and sudden depletion of molecular oxygen was shown to

act as the predominant trigger for initiating detachment of individual cells from biofilms [26, 38]. We therefore propose that an oxygen gradient established in Mannose-binding protein-associated serine protease static cultures with the highest oxygen concentration at the surface resulted in a larger number of cells at the A-L interface to form pellicles, which eventually induce attachment of individual cells to the abiotic surface. To form pellicles, S. oneidensis cultures require certain divalent ions. Involvement of metals in biofilm formation either as a facilitator or an inhibitor has been well documented. In recent years, many elegant studies about the susceptibility of biofilms to metals (as an inhibitor) have been published [39–41]. Although metals as a biofilm formation facilitator have been studied for more than two decades, only a few metals (Ba(II), Mg(II), Ca(II), Fe(III), and Fe(III)) have been investigated [34, 42, 43]. In P. aeruginosa, all these metals but Ba(II) are able to protect P. aeruginosa biofilms against EDTA treatment, PI3K inhibitor review presumably by stabilizing the biofilm matrix. In addition, it has been shown that there is a positive correlation between calcium concentration and amount of biofilm accumulation [44]. While our data support previous conclusions that calcium plays an important role in stabilizing biofilms of bacteria [34, 43, 44], most of other findings are either new or surprising.

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