Biofilm production of Aspergillus fumigatus on bronchial epithelia cells

M. Seidler, S. Salvenmoser, F. M. Mueller (Heidelberg, Germany)

Source: Annual Congress 2008 - Mechanisms of respiratory infections: interaction between the pathogen and the host
Session: Mechanisms of respiratory infections: interaction between the pathogen and the host
Session type: Thematic Poster Session
Number: 2288
Disease area: Airway diseases, Respiratory infections

Congress or journal article abstract

Abstract

Introduction: A. fumigatus is a frequent colonizer in patients with asthma and chronic lung diseases (e.g. cystic fibrosis). The aim of this study was to investigate the ability of A. fumigatus to form a biofilm-like matrix in vitro on human bronchial epithelia cells.
Methods: A. fumigatus ATCC #9197 was incubated on 16HBE and CFBE41o- in MEM at different pH, concentrations of FBS, temperature, production time and different flow conditions. Dry weight measurement and antifungal drug susceptibility testing was performed. Scanning electron microscopy (SEM) and confocal scanning laser microscopy (CSLM) images were analyzed.
Result: The dry weight of the produced biofilm exceeded 7.4 mg on 16HBE and 7.7 mg on CFBE41o- cells after 72h of biofilm production. There was no significant difference in dry weight increase between the cell lines. All antifungal drugs were weakened or displayed resistance (>8µg/ml) against Aspergillus embedded in biofilm. The SEM pictures displayed a network of hyphal structures and matrix at 48h. Characteristic flow channels were observed at 72h. CSLM images displayed attached conidia on the cells after 4h, conidia and hyphal structures after 24h and matrix formations after 72h. A-Alexafluor dyed polysaccharides of the cell wall and of the ECM in the biofilm. Three dimensional constructs of the CSLM pictures displayed biofilm on 16HBE and proofed viability of the cells after 48h co-incubation. Differences in biofilm production between 16HBE and CFBE41o- were not significant.
Conclusions: A. fumigatus is able to form a biofilm structure in vitro on bronchial epithelia cells. Potential clinical implications of A. fumigatus biofilm formation in vivo require further investigations.


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Citations should be made in the following way:
M. Seidler, S. Salvenmoser, F. M. Mueller (Heidelberg, Germany). Biofilm production of Aspergillus fumigatus on bronchial epithelia cells. Eur Respir J 2008; 32: Suppl. 52, 2288

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