Abstract

Context: Uncaria tomentosa D.C. (Rubiaceae) has several biological activities, including activity against resistant Candida strains. The synergistic interaction with terbinafine or fluconazole can be an important alternative to overcome this resistance.Objectives: The potential synergy between a water insoluble fraction (WIF) from Uncaria tomentosa bark and the antifungals terbinafine (TRB) and fluconazole (FLZ) against non-Candida albicans resistant strains was investigated.Materials and methods: TRB and FLZ, alone and combined with WIF, were tested by the checkerboard procedure using the micro-dilution technique against seven isolates of Candida glabrata and C. krusei. The molecular interactions occurring outside the cell wall were evaluated by scanning electron microscopy, Fourier transform infrared (FT-IR) and differential scanning calorimetry (DSC) analysis.Results: The checkerboard inhibitory assay demonstrated synergy for WIF:TRB and WIF:FLZ combinations, respectively. The best synergistic cell damage was demonstrated unequivocally for the associations of WIF and TRB (1.95:4.0 μg/mL) and WIF and FLZ (1.95:8.0 μg/mL). The comparison of the FT-IR spectra of the antifungal alone, and in combination with WIF, allows recognizing clear differences in 3000, 1600, 1400, and 700–800 cm−1 bands. Additionally, modifications on TRB and FLZ thermograms were clearly noticed after their combination with WIF.Conclusions: DSC and infrared analysis demonstrated intermolecular interactions between WIF and either TRB or FLZ. Hence, quite likely the synergistic effect is related to interaction events occurring outside the cell wall between antifungal and cat’s claw proanthocyanidins. A direct action on the cell wall is suggested, without connection with the ABC efflux pump mechanism.

Highlights

  • Candida species are harmless saprophyte yeasts, a normal component of the human biota in the gastrointestinal tract and oral and vaginal mucosae

  • We investigated the antifungal activity of the insoluble fraction of polyphenols from cat’s claw bark against non-Candida albicans (NCA) species, and its synergy in combination with fluconazole and terbinafine

  • Several studies have focused on showing the antifungal activity of plant derivatives (Silva et al 2011; Ahmad et al 2013; Jun et al 2013); few have approached the impact on the cell morphology of chemical and physicochemical interactions that happen between these compounds

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Summary

Introduction

Candida species are harmless saprophyte yeasts, a normal component of the human biota in the gastrointestinal tract and oral and vaginal mucosae. These yeasts can cause superficial infections manifested as thrush and vaginitis; excepting in immunecompromised and immune-suppressed patients, for instance, to whom they can cause severe systemic infections. New emerging non-Candida albicans (NCA) species and isolates from even more become a public health challenge due to antifungal resistance. Fluconazole (FLZ) and terbinafine (TRB) belong to the main antifungal currently used in the antifungal therapy, which act in different steps of the cell membrane biosynthesis. TRB, an allylamine class antifungal, currently is indicated for the treatment of infections caused by dermatophytes. TRB has shown in vitro activity against a wide variety of Candida spp. (Ryder et al 1998), and for the oral treatment of nail candidiasis as well (Segal et al 1996)

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