Effects of lipopeptide biosurfactants on clinical strains of Malassezia furfur growth and biofilm formation.

Lipopeptide biosurfactants (LBs) are biological molecules with low toxicity that have aroused growing interest in the pharmaceutical industry. Their chemical structure confers antimicrobial and antibiofilm properties against different species. Despite their potential, few studies have demonstrated their capability against Malassezia spp., commensal yeasts which can cause dermatitis and serious infections. Thus, the aim of this study was to evaluate the antifungal activity of biosurfactants produced by new strains of Bacillus subtilis TIM10 and B. vallismortis TIM68 against M. furfur and their potential for removal and inhibition of yeast biofilms. Biosurfactants were classified as lipopeptides by FTIR, and their composition was characterized by ESI-Q-TOF/MS, showing ions for iturin, fengycin, and surfactin, with a greater abundance of surfactin. Through the broth microdilution method, both biosurfactants inhibited the growth of clinical M. furfur strains. Biosurfactant TIM10 showed greater capacity for growth inhibition, with no statistical difference compared to those obtained by the commercial antifungal fluconazole for M. furfur 153DR5 and 154DR8 strains. At minimal inhibitory concentrations (MIC-2), TIM10 and TIM68 were able to inhibit biofilm formation, especially TIM10, with an inhibition rate of approximately 90%. In addition, both biosurfactants were able to remove pre-formed biofilm. Both biosurfactants showed no toxicity against murine fibroblasts, even at concentrations above MIC-2. Our results show the effectiveness of LBs in controlling the growth and biofilm formation of M. furfur clinical strains and highlight the potential of these agents to compose new formulations for the treatment of these fungi.

An innovative bioremediation strategy using a bacterial consortium entrapped in chitosan beads.

This aim of this work was to develop a bioremediation strategy for oil-contaminated mangrove sediments using chitosan beads containing an immobilised hydrocarbonoclastic bacterial consortium. The consortium composed of 17 isolates was obtained from an enrichment culture. The isolates were identified by 16S rDNA sequencing, which revealed 12 different genera. Thirteen isolates showed resistance to chitosan and were thus able to be trapped in chitosan beads for microcosm evaluation. The data revealed that entrapped consortium grew in the microcosms until day 15, which is when the beads disintegrated and released their biomass into the sediments. Bacterial bioaugmentation within the sediments was confirmed by cell counts; additionally, the dynamics of the bacterial populations were analysed through denaturing gradient gel electrophoresis. The chitosan showed a prebiotic effect on the autochthonous bacterial communities. Therefore, chitosan beads containing selected immobilised bacteria attain two bioremediation purposes, bioaugmentation and biostimulation, and thus represent an emergent approach.