Microtubules and actin cytoskeleton of potentially pathogenic basidiomycetous yeast as targets for antifungals
Language English Country Switzerland Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19521073
DOI
10.1159/000224655
PII: 000224655
Knihovny.cz E-resources
- MeSH
- Antifungal Agents pharmacology MeSH
- Basidiomycota cytology drug effects MeSH
- Bridged Bicyclo Compounds, Heterocyclic pharmacology MeSH
- Cytochalasins pharmacology MeSH
- Cytokinesis drug effects MeSH
- Yeasts cytology drug effects MeSH
- Actin Cytoskeleton drug effects MeSH
- Microtubules drug effects MeSH
- Tubulin Modulators pharmacology MeSH
- Paclitaxel pharmacology MeSH
- Spores, Fungal drug effects MeSH
- Thiabendazole pharmacology MeSH
- Thiazolidines pharmacology MeSH
- Vinblastine pharmacology MeSH
- Vincristine pharmacology MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antifungal Agents MeSH
- Bridged Bicyclo Compounds, Heterocyclic MeSH
- Cytochalasins MeSH
- latrunculin A MeSH Browser
- Tubulin Modulators MeSH
- Paclitaxel MeSH
- Thiabendazole MeSH
- Thiazolidines MeSH
- Vinblastine MeSH
- Vincristine MeSH
BACKGROUND: The cytoskeleton was investigated as a potential target for the inhibition of cell division in Fellomyces fuzhouensis CBS 8243 related to Cryptococcus neoformans. METHODS: Vincristine, vinblastine, paclitaxel, methyl benzimidazole-2-yl carbamate (BCM), thiabendazole, cytochalasins A, B and D and latrunculin A were added to yeast extract peptone dextrose medium containing cells, investigated by phase contrast and fluorescence microscopy, counted in a Burker chamber and absorbance was measured. RESULTS: Vincristine, vinblastine, paclitaxel, cytochalasins A, B and D transiently blocked proliferation. BCM disrupted microtubules and inhibited mitosis, but F-actin patches and cables persisted and neck-less conidia appeared without stalks. Latrunculin disrupted F-actin, cells became spherical, and stalks and necks degenerated; microtubules persisted, but mitosis, cytokinesis and conidiogenesis were blocked. The combined application of latrunculin and BCM disrupted F-actin and microtubules, and inhibited cells became spherical and did not divide. CONCLUSIONS: Microtubules and F-actin are effective targets for permanent inhibition of nuclear and cell division and conidiogenesis by BCM and latrunculin A.
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