SUSCEPTIBILITY OF MELANIZED AND NONMELANIZED CRYPTOCOCCUS-NEOFORMANS TO THE MELANIN-BINDING COMPOUNDS TRIFLUOPERAZINE AND CHLOROQUINE

Citation
Yl. Wang et A. Casadevall, SUSCEPTIBILITY OF MELANIZED AND NONMELANIZED CRYPTOCOCCUS-NEOFORMANS TO THE MELANIN-BINDING COMPOUNDS TRIFLUOPERAZINE AND CHLOROQUINE, Antimicrobial agents and chemotherapy, 40(3), 1996, pp. 541-545
Citations number
23
Categorie Soggetti
Pharmacology & Pharmacy",Microbiology
ISSN journal
00664804
Volume
40
Issue
3
Year of publication
1996
Pages
541 - 545
Database
ISI
SICI code
0066-4804(1996)40:3<541:SOMANC>2.0.ZU;2-E
Abstract
Cryptococcus neoformans is an opportunistic fungal pathogen which beco mes heavily melanized in the presence of phenolic substrates such as L -dopa, Various drugs are known to bind to melanin with high affinity, including the antipsychotic agent trifluoperazine and the antimalarial agent chloroquine. We hypothesized that drugs which bind melanin may have different toxicities for melanized and nonmelanized C. neoformans cells. The effects of trifluoperazine and chloroquine or C. neoforman s were determined by measuring cell viability after exposure to these drugs, Cell viability was measured by CFU determination and flow cytom etry with propidium iodide staining. Melanized cells were more suscept ible than nonmelanized cells to the fungicidal effects of trifluoperaz ine. Chloroquine had no fungicidal effect on either melanized or nonme lanized C. neoformans under the conditions studied, Flow cytometry of trifluoperazine-treated C. neoformans cells stained with the mitochond rial stain dihydrorhodamine 123 revealed fluorescence changes consiste nt with mitochondrial damage. Our results indicate that melanized and nonmelanized C. neoformans cells can differ in susceptibility to certa in drugs and suggest that strategies which target melanin may be produ ctive for antifungal-drug discovery.