Abstract

Background Dermatophytosis are fungal infections caused by keratinophilic fungi known as dermatophytes and classified in three genera: Trichophyton, Epidermophyton and Microsporum. Trichophyton rubrum is the most frequent species associated to dermatophytosis worldwide [1]. The infections caused by dermatophytes are not lethal, but are difficult to treat and uncomfortable. In the case of T. rubrum, they tend to be chronic, and although the superficial infections are more common, cases of deep infection have been reported in immunocompromised patients [2][3]. The number of antifungal drugs are still limited, and the acquired resistance for some of clinical antifungal have been shown as well as the side effects that have been promoted by them. Reasons for the challenge in development of new antifungal drugs are the similarities shared by fungal and mammalian cells and the lack of knowledge about the biology of these pathogens. Recent evidences have shown that the fatty acid sinthase (FAS) is an interesting antifungal target [4] because of marked differences between human and fungal cells. The aim of this study was to evaluate the antifungal activity of four flavonoids described as FAS inhibitors and verify the modulation of genes in the pathway of fatty acid synthesis in T. rubrum growth in presence of the most effective one as FAS inhibitor.

Highlights

  • Dermatophytosis are fungal infections caused by keratinophilic fungi known as dermatophytes and classified in three genera: Trichophyton, Epidermophyton and Microsporum

  • Quercetin showed the most effective antifungal activity with MIC of 125 μg/mL, ellagic acid presented MIC of 250 μg/mL, galangin and genistein were ineffective toward T.rubrum (MIC >1000 μg/mL)

  • The analyse of gene expression of the fatty acid synthetic pathway showed the majority of the genes were downregulated by quercetin, fluconazole and cerulenin

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Summary

Introduction

Dermatophytosis are fungal infections caused by keratinophilic fungi known as dermatophytes and classified in three genera: Trichophyton, Epidermophyton and Microsporum. Fatty acid synthesis(FAS 1p, FAS 2p subunits), acetyl-COA carboxylase 2p subunity and fatty acid transporter protein (FAT1) was analyzed by quantitative PCR using Sybr Green after 16h of incubation of strain of T.rubrum with MIC of quercetin in liquid Sabouraud medium.

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