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Fluconazole downregulates metallothionein expression and increases copper cytotoxicity in Microsporum canis
Aumaid Uthman1, Sassan Rezaie, Michael Dockal
1Ludwig Boltzmann Institute for venero-dermatological infection, University of Vienna Medical School, Währinger Gürtel 18-20, A-1090, Vienna, Austria.
Abstract:
Azole antifungals are widely used to treat infections with dermatophyte fungi. Whereas it is well established that this class of drugs interferes with fungal ergosterol synthesis, little is known about its potential other biological effects. Here we report the isolation and structural organization of Microsporum canis metallothionein gene and demonstrate that fluconazole is able to downregulate the baseline as well as copper-induced expression of this gene. Since this effect occurred within 30 min after exposure of the fungus to fluconazole, it is unlikely that it is due to impaired ergosterol synthesis. Our additional demonstration that fluconazole enhances copper toxicity for M. canis suggests that inhibition of metallothionein expression by fluconazole is biologically relevant and may represent an important additional mode of the antifungal action of this drug. Therefore our data indicate that antifungal effects of azole derivatives might not only be due to interference with cell wall synthesis but may also affect other biological circuits within the fungal cells.