Where the infection is isolated rather than the specific species correlates with adherence strength, whereas biofilm density remains static in clinically isolated Candida and arthroconidial yeasts

Author:

ElGindi Mei1,Al-Baghdadi Rula1,Jackman Alex B.2,Antonyan Angelina S.2,McMahon Diana L.2,Taj-Aldeen Saad J.34,Finkel Jonathan S.12

Affiliation:

1. Department of Biological Sciences, Carnegie Mellon University, Education City, PO Box 24866, Doha, Qatar.

2. Department of Biology, College of Engineering and Science, University of Detroit Mercy, 4001 W McNichols Road, Detroit, MI 48221-3038, USA.

3. University of Babylon, Hilla, Iraq.

4. Microbiology Division, Department of Laboratory Medicine and Pathology, Mycology Unit, Hamad Medical Corporation, Doha, Qatar.

Abstract

To colonize and infect the host, arthroconidial yeasts must avoid being killed by the host’s defenses. The formation of biofilms on implanted devices allows fungi to avoid host responses and to disseminate into the host. To better study the mechanisms of infection by arthroconidial yeasts, adherence and biofilm formation were assayed using patient samples collected over 10 years. In clinical samples, adherence varies within species, but the relative adherence is constant for those samples isolated from the same infection site. Herein we document, for the first time, in-vitro biofilm formation by Trichosporon dohaense, T. ovoides, T. japonicum, T. coremiiforme, Cutaneotrichosporon mucoides, Cutaneotrichosporon cutaneum, Galactomyces candidus, and Magnusiomyces capitatus on clinically relevant catheter material. Analysis of biofilm biomass assays indicated that biofilm mass changes less than 2-fold, regardless of the species. Our results support the hypothesis that most pathogenic fungi can form biofilms, and that biofilm formation is a source of systemic infections.

Publisher

Canadian Science Publishing

Subject

Genetics,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Immunology,Microbiology

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