Synthesis and in vitro antifungal activity of isoniazid-derived hydrazones against Coccidioides posadasii

Abstract

Coccidioidomycosis is a potentially severe infection caused by dimorphic fungi Coccidioides immitis and Coccidioides posadasii . Although guidelines are well established, refractory disease is a matter of concern in the clinical management of coccidioidomycosis. In the present study three isoniazid-derived hydra- zones N 0 -[( E )-1-(4-methoxyphenyl)ethylidene]pyridine-4-carbohydrazide, N 0 -[( E )-1-(4-methylphenyl) ethylidene]pyridine-4-carbohydrazide, and N 0 -[( E )-1-(phenyl)ethylidene]pyridine-4-carbohydrazide were synthesized and evaluated for antifungal activity against C. posadasii . Susceptibility assays were performed by macrodilution testing. Interactions between the hydrazones and amphotericin B or itra- conazole were evaluated by the checkerboard method. We also investigated the impairment of such compounds on cell ergosterol and membrane integrity. The synthesized molecules were able to inhibit C. posadasii in vitro with MIC values that ranged from 25 to 400 m g/mL. Drug interactions between synthesized molecules and amphotericin B proved synergistic for the majority of tested isolates; regarding itraconazole, synergism was observed only when strains were tested against N 0 -[( E )-1-(phenyl) ethylidene]pyridine-4-carbohydrazide. Reduction of cellular ergosterol was observed when strains were challenged with the hydrazones alone or combined with antifungals. Only N 0 -[( E )-1-(4-methylphenyl) ethylidene]pyridine-4-carbohydrazide altered membrane permeability of C. posadasii cells. Isoniazid- derived hydrazones were able to inhibit C. posadasii cells causing reduction of ergosterol content and alterations in the permeability of cell membrane. This study con fi rms the antifungal potential of hydrazones against pathogenic fungi