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Published on: February 14, 2018
Novel Antifungal Activity for the Lectin Scytovirin: Inhibition of Cryptococcus neoformans and Cryptococcus gattii
Tyler H Jones1, Erin E McClelland2, Hana McFeeters1
1Department of Chemistry, University of Alabama in Huntsville, HuntsvilleAL, USA.
Abstract:
Pathogenic cryptococci are encapsulated yeast that can cause severe meningoencephalitis. Existing therapeutic options are dated and there is a growing need for new alternative antifungal agents for these fungi. Here we report novel inhibition of pathogenic cryptococci by the antimicrobial lectin Scytovirin. Inhibition was most potent against Cryptococcus neoformans var neoformans and C. gattii, with MFC values of 500 nM. Scytovirin binding was localized to the cell wall and shown to affect capsule size and release. No effect was observed on melanization or with cells grown in the presence the cell wall stressor Congo red. Synergy with existing antifungals was indicated, most strongly for amphotericin B. Overall, Scytovirin serves as a much needed new avenue for anticryptococcal development.
Insights
Novel antimicrobial lectin Scytovirin effectively inhibits pathogenic Cryptococcus yeast, including Cryptococcus neoformans and C. gattii. This lectin shows potential as a new antifungal agent, offering a promising alternative to outdated therapies.
Area of Science:
- Mycology and Infectious Diseases
- Antimicrobial Drug Discovery
Background:
- Pathogenic cryptococci, encapsulated yeasts, cause severe meningoencephalitis.
- Current antifungal therapies are limited, necessitating novel treatment strategies.
- There is a critical need for new anticryptococcal agents.
Purpose of the Study:
- To investigate the anticryptococcal activity of the antimicrobial lectin Scytovirin.
- To evaluate Scytovirin's potential as a novel antifungal therapeutic agent.
Main Methods:
- Minimum Fungicidal Concentration (MFC) assays were performed against Cryptococcus strains.
- Scytovirin's binding site and effects on cryptococcal cell morphology were analyzed.
- Synergistic effects with existing antifungals were assessed.
Main Results:
- Scytovirin demonstrated potent inhibition against Cryptococcus neoformans and C. gattii (MFC: 500 nM).
- Scytovirin localized to the cell wall, impacting capsule size and release.
- Synergy was observed with amphotericin B, suggesting combination therapy potential.
Conclusions:
- Scytovirin exhibits significant anticryptococcal activity.
- This lectin represents a promising new candidate for anticryptococcal drug development.
- Further research into Scytovirin as an antifungal is warranted.
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Fungal Group Zygomycota
Fungal Phylum Microsporidia

