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A Multifaceted Study of Scedosporium boydii Cell Wall Changes during Germination and Identification of GPI-Anchored
Sarah Ghamrawi1, Amandine Gastebois1, Agata Zykwinska2
1L'UNAM Université, Université d'Angers, Groupe d'Etude des Interactions Hôte-Pathogène, EA 3142, Angers, France.
Abstract:
Scedosporium boydii is a pathogenic filamentous fungus that causes a wide range of human infections, notably respiratory infections in patients with cystic fibrosis. The development of new therapeutic strategies targeting S. boydii necessitates a better understanding of the physiology of this fungus and the identification of new molecular targets. In this work, we studied the conidium-to-germ tube transition using a variety of techniques including scanning and transmission electron microscopy, atomic force microscopy, two-phase partitioning, microelectrophoresis and cationized ferritin labeling, chemical force spectroscopy, lectin labeling, and nanoLC-MS/MS for cell wall GPI-anchored protein analysis. We demonstrated that the cell wall undergoes structural changes with germination accompanied with a lower hydrophobicity, electrostatic charge and binding capacity to cationized ferritin. Changes during germination also included a higher accessibility of some cell wall polysaccharides to lectins and less CH3/CH3 interactions (hydrophobic adhesion forces mainly due to glycoproteins). We also extracted and identified 20 GPI-anchored proteins from the cell wall of S. boydii, among which one was detected only in the conidial wall extract and 12 only in the mycelial wall extract. The identified sequences belonged to protein families involved in virulence in other fungi like Gelp/Gasp, Crhp, Bglp/Bgtp families and a superoxide dismutase. These results highlighted the cell wall remodeling during germination in S. boydii with the identification of a substantial number of cell wall GPI-anchored conidial or hyphal specific proteins, which provides a basis to investigate the role of these molecules in the host-pathogen interaction and fungal virulence.
Insights
Scedosporium boydii germination involves significant cell wall remodeling, altering its properties and revealing new potential drug targets. This study identifies specific GPI-anchored proteins crucial for fungal virulence.
Area of Science:
- Mycology
- Medical Mycology
- Fungal Pathogenesis
Background:
- Scedosporium boydii is a significant fungal pathogen causing diverse infections, particularly in cystic fibrosis patients.
- Understanding S. boydii physiology and identifying novel molecular targets are crucial for developing new antifungal therapies.
Purpose of the Study:
- To investigate the structural and molecular changes in the S. boydii cell wall during the conidium-to-germ tube transition.
- To identify potential molecular targets for therapeutic strategies by analyzing cell wall composition.
Main Methods:
- Utilized advanced microscopy (SEM, TEM, AFM) and biophysical techniques (two-phase partitioning, microelectrophoresis, chemical force spectroscopy).
- Analyzed cell wall properties including hydrophobicity, electrostatic charge, and lectin binding.
- Performed nanoLC-MS/MS to identify glycosylphosphatidylinositol (GPI)-anchored proteins in the cell wall.
Main Results:
- Germination induced significant cell wall alterations, including decreased hydrophobicity, lower electrostatic charge, and reduced cationized ferritin binding.
- Increased accessibility of cell wall polysaccharides to lectins and reduced hydrophobic interactions were observed during germination.
- Identified 20 GPI-anchored proteins, with several exhibiting conidial or hyphal specificity, including virulence-associated families and superoxide dismutase.
Conclusions:
- The study demonstrates extensive cell wall remodeling during S. boydii germination.
- Identification of conidial or hyphal-specific GPI-anchored proteins provides a foundation for exploring their roles in host-pathogen interactions and virulence.
- These findings offer new avenues for developing targeted antifungal therapies against S. boydii infections.
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