Abstract

Various fungi have the ability to colonize surfaces and to form biofilms. Fungal biofilm-associated infections are frequently refractory to targeted treatment because of resistance to antifungal drugs. One fungus that frequently colonises the respiratory tract of cystic fibrosis (CF) patients is the opportunistic black yeast–like fungus Exophiala dermatitidis. We investigated the biofilm-forming ability of E. dermatitidis and its susceptibility to various antiinfective agents and natural compounds. We tested 58 E. dermatitidis isolates with a biofilm assay based on crystal violet staining. In addition, we used three isolates to examine the antibiofilm activity of voriconazole, micafungin, colistin, farnesol, and the plant derivatives 1,2,3,4,6-penta-O-galloyl-b-D-glucopyranose (PGG) and epigallocatechin-3-gallate (EGCG) with an XTT reduction assay. We analysed the effect of the agents on cell to surface adhesion, biofilm formation, and the mature biofilm. The biofilms were also investigated by confocal laser scan microscopy. We found that E. dermatitidis builds biofilm in a strain-specific manner. Invasive E. dermatitidis isolates form most biomass in biofilm. The antiinfective agents and the natural compounds exhibited poor antibiofilm activity. The greatest impact of the compounds was detected when they were added prior cell adhesion. These findings suggest that prevention may be more effective than treatment of biofilm-associated E. dermatitidis infections.

Highlights

  • An investigation of the biofilm behavior of 137 environmental and 7 clinical E. dermatitidis isolates, detected the ability of E. dermatitidis to form biofilm in 15% of environmental isolates and 29% of clinical isolates[12]

  • The crystal violet (CV)-based assay showed that E. dermatitidis was able to form biofilm

  • A total of 36% of the tested E. dermatitidis isolates formed biofilms with a biomass equal to or higher than the biomass of the biofilms formed by C. albicans (Figs 1, 2 and 3)

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Summary

Introduction

An investigation of the biofilm behavior of 137 environmental and 7 clinical E. dermatitidis isolates, detected the ability of E. dermatitidis to form biofilm in 15% of environmental isolates and 29% of clinical isolates[12]. We tested the antibiofilm activity of several antiinfective agents, the quorum-sensing molecule (QSM) farnesol, and two natural compounds with antibiofilm activity

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