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Proteases of Sporothrix schenckii: Cytopathological effects on a host-cell model
Myrna Sabanero López1, Lérida L Flores Villavicencio1, Karla Soto Arredondo1
1Departamento de Biología, División de Ciencias Naturales y Exactas, Campus Guanajuato, Universidad de Guanajuato, Noria Alta S/N, Col. Noria Alta, Guanajuato, Guanajuato 36000, Mexico.
Background:
Sporotrichosis is a fungal infection caused by the Sporothrix schenckii complex. The adhesion of the fungus to the host tissue has been considered the key step in the colonization and invasion, but little is known about the early events in the host-parasite interaction.
Aims:
To evaluate the proteolytic activity of S. schenckii on epithelial cells.
Methods:
The proteolytic system (at pH 5 and 7) was evaluated using azocoll and zymograms. The host-parasite interaction and epithelial cell response were also analyzed by examining the microfilament cytoskeleton using phalloidin-FITC and transmission electron microscopy. Finally, the metabolic activity was determined using an XTT assay.
Results:
The zymograms showed that S. schenckii yeast cells possess high intracellular and extracellular proteolytic activities (Mr≥200, 116, 97, and 70kDa) that are pH dependent and are inhibited by PMSF and E64, which act on serine and cysteine-type proteases. During the epithelial cell-protease interaction, the cells showed alterations in the microfilament distribution, as well as in the plasma membrane structure. Moreover, the metabolic activity of the epithelial cells decreased 60% without a protease inhibitor.
Conclusions:
Our data demonstrate the complexity of the cellular responses during the infection process. This process is somehow counteracted by the action of proteases inhibitors. Furthermore, the results provide critical information for understanding the nature of host-fungus interactions and for searching a new effective antifungal therapy, which includes protease inhibitors.
Insights
Sporothrix schenckii exhibits significant proteolytic activity, damaging epithelial cells and their structure. Protease inhibitors show promise in counteracting these fungal infection effects.
Area of Science:
- Medical Mycology
- Host-Pathogen Interaction
- Biochemistry
Background:
- Sporotrichosis is a fungal infection caused by Sporothrix schenckii.
- Early host-parasite interactions, particularly fungal adhesion, are crucial but poorly understood.
Purpose of the Study:
- To investigate the proteolytic activity of Sporothrix schenckii on host epithelial cells.
- To analyze the impact of fungal proteases on host cell structure and metabolism.
Main Methods:
- Proteolytic activity assessed using azocoll and zymograms at different pH levels.
- Host-parasite interactions visualized via microfilament cytoskeleton staining (phalloidin-FITC) and transmission electron microscopy.
- Epithelial cell metabolic activity measured using an XTT assay.
Main Results:
- Sporothrix schenckii yeast cells display high intracellular and extracellular proteolytic activity (Mr≥200, 116, 97, 70kDa), dependent on pH and inhibited by PMSF and E64 (serine/cysteine proteases).
- Interaction with proteases caused significant alterations in epithelial cell microfilament distribution and plasma membrane structure.
- Epithelial cell metabolic activity decreased by 60% in the absence of protease inhibitors.
Conclusions:
- Fungal proteases play a complex role in Sporotrichosis pathogenesis by altering host cell integrity and function.
- Protease inhibitors can counteract the detrimental effects of fungal proteases, suggesting a potential therapeutic strategy.
- Understanding these host-fungus interactions is vital for developing novel antifungal therapies targeting protease activity.
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