When biofilms grown in iron supplemented media were treated with cobalt as well as phage in combination, a negligible amount of biofilm formation consisting of mostly of red and yellow regions was seen on day 3 [Figure 5(d)] as well as on day 7 [Figure 5(d´)] when compared

with 3rd and 7th day biofilms treated with cobalt as shown in [Figure 5(b) and Figure 5(b´)] respectively or phage alone [Figure 5(c) and Figure 5(c´)]. Figure 5 K. pneumoniae B5055 biofilm developed on coverslip (a/ a´) 3/ 7 day biofilm grown in 10  μM FeCl 3 supplemented media (b/ b´) 3/ 7 day biofilm grown in 10  μM FeCl 3  + 500  μM cobalt salt supplemented media SHP099 mouse (c /c´) 3/ 7 day biofilm grown in 10  μM FeCl 3 supplemented media followed by treatment with phage KPO1K2 (d/ d´) 3/ 7 day biofilm grown in 10  μM FeCl 3   +  500  μM cobalt salt supplemented media followed by treatment with phage KPO1K2. Discussion Biofilms are recalcitrant to antibiotics as their higher concentrations are needed to eradicate bacterial cells in this mode of growth. Attempts have been made in the past to evolve alternate strategies to destroy biofilms. Since bacteria, both in planktonic and biofilm mode require iron for their growth [14] hence, iron chelating agents

have been reported to inhibit biofilm growth. Hancock et al. [15] have reported that since Zn (II) and Co (II) have a higher than iron affinity for the master controller protein of iron uptake i.e. ‘Fur’ thus they reduce biofilm formation by infectious www.selleckchem.com/products/epz-5676.html E. coli. In this study, a significant reduction (p < 0.05) was observed in the growth of younger biofilms (1–3 day old) when 500 μM CoSO4 and 10 μM FeCl3 supplemented media was used. This might be because of the elevated levels of metals which could enough interfere with normal iron regulation by shutdown of Fur-controlled iron uptake systems like enterobactin, ferric dicitrate, aerobactin as well as additional downstream effects on putative adhesion factors

TSA HDAC solubility dmso involved in biofilm establishment thereby resulting in deleterious effect on biofilm formation [2, 22] as well as pathogenicity of the organism. No previous reports are available involving the use of phage and iron antagonizing molecules in combination on biofilm kinetics. Thus, we studied the efficacy of depolymerase producing phage (KPO1K2) in eradicating the biofilms of K. pneumoniae B5055 grown in minimal media supplemented with 500 μM CoSO4 and iron. A complete eradication of the younger biofilms (upto 2 day old) given combination treatment was observed. This was possibly due to the degradation of exopolysaccharide matrix encompassing the biofilm structure by the phage encoded depolymerase [7, 17] which facilitated the process of bacterial growth inhibition by phage as well as CoSO4.