Inactivation of genes TEC1 and EFG1 in Candida albicans influences extracellular matrix composition and biofilm morphology.
Beatriz Helena Dias PanarielloMarlise Inêz KleinAna Claudia PavarinaSimone DuartePublished in: Journal of oral microbiology (2017)
Background: Infections caused by Candida spp. have been associated with formation of a biofilm, i.e. a complex microstructure of cells adhering to a surface and embedded within an extracellular matrix (ECM). Methods: The ECMs of a wild-type (WT, SN425) and two Candida albicans mutant strains, Δ/Δ tec1 (CJN2330) and Δ/Δ efg1 (CJN2302), were evaluated. Colony-forming units (cfu), total biomass (mg), water-soluble polysaccharides (WSPs), alkali-soluble polysaccharides (ASPs), proteins (insoluble part of biofilms and matrix proteins), and extracellular DNA (eDNA) were quantified. Variable-pressure scanning electron microscopy and confocal scanning laser microscopy were performed. The biovolume (μm3/μm2) and maximum thickness (μm) of the biofilms were quantified using COMSTAT2. Results: ASP content was highest in WT (mean ± SD: 74.5 ± 22.0 µg), followed by Δ/Δ tec1 (44.0 ± 24.1 µg) and Δ/Δ efg1 (14.7 ± 5.0 µg). The protein correlated with ASPs (r = 0.666) and with matrix proteins (r = 0.670) in the WT strain. The population in Δ/Δ efg1 correlated with the protein (r = 0.734) and its biofilms exhibited the lowest biomass and biovolume, and maximum thickness. In Δ/Δ tec1, ASP correlated with eDNA (r = 0.678). Conclusion: ASP production may be linked to C. albicans cell filamentous morphology.
Keyphrases
- candida albicans
- extracellular matrix
- water soluble
- electron microscopy
- wild type
- optical coherence tomography
- biofilm formation
- high resolution
- single molecule
- induced apoptosis
- wastewater treatment
- protein protein
- escherichia coli
- amino acid
- white matter
- single cell
- high speed
- cell cycle arrest
- stem cells
- binding protein
- gene expression
- genome wide
- endoplasmic reticulum stress
- mesenchymal stem cells
- cell free
- high throughput
- cell therapy
- cell death
- transcription factor
- cystic fibrosis
- oxidative stress
- multiple sclerosis