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. 2017 Dec;55(1):1521-1527.
doi: 10.1080/13880209.2017.1304427.

Antimicrobial activity of Buchenavia tetraphylla against Candida albicans strains isolated from vaginal secretions

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Antimicrobial activity of Buchenavia tetraphylla against Candida albicans strains isolated from vaginal secretions

José Robson Neves Cavalcanti Filho et al. Pharm Biol. 2017 Dec.

Abstract

Context: Buchenavia tetraphylla (Aubl.) RA Howard (Combretaceae: Combretoideae) is an ethnomedicinal plant with reported antifungal action.

Objective: This study evaluates the antimicrobial activity of B. tetraphylla leaf extracts against clinical isolates of Candida albicans. The morphological alterations, combinatory effects with fluconazole and the cytotoxicity of the active extract were analyzed.

Materials and methods: Extracts were obtained using different solvents (hexane: BTHE; chloroform: BTCE; ethyl acetate: BTEE; and methanol: BTME). Antimicrobial activity was determined by the broth microdilution method using nine strains of C. albicans isolated from vaginal secretions and one standard strain (UFPEDA 1007).

Results: All extracts showed anti-C. albicans activity, including against the azole-resistant strains. The MIC values ranged from 156 to 2500 μg/mL for the BTHE; 156 to 1250 μg/mL for the BTCE; 625 to 1250 μg/mL for the BTME and 625 μg/mL to 2500 μg/mL for the BTEE. BTME showed the best anti-C. albicans activity. This extract demonstrated additive/synergistic interactions with fluconazole. Scanning electron microscopy analysis suggested that the BTME interferes with the cell division and development of C. albicans. BTME showed IC50 values of 981 and 3935 μg/mL, against J774 macrophages and human erythrocytes, respectively. This extract also enhanced the production of nitric oxide by J774 macrophages.

Discussion and conclusion: Buchenavia tetraphylla methanolic extract (BTME) is a great source of antimicrobial compounds that are able to enhance the action of fluconazole against different C. albicans strains; this action seems related to inhibition of cell division.

Keywords: Antifungal agents; Caatinga biome; natural products.

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Figures

Figure 1.
Figure 1.
Combinatory effects of BTME and fluconazole against Candida albicans. non: non-interactive effect; add: additive effect; syn: synergistic effect; ant: antagonistic effect.
Figure 2.
Figure 2.
Effects of BTME on C. albicans. (a–c) Control cells; (d–f) cells treated with BTME at MIC for 12 h. (a–c) Ultrastructural aspects of untreated C. albicans culture at low (a) and high magnification (b–c) showing the presence of single and budding yeast cells with evident fragile blastoconidial septum (white arrow). (h) True hyphal structures could be also observed. Treated C. albicans culture at (d) low and (e–f) high magnifications. Note in (e) the presence of elongated cells (white asterisk) with multiple scars (white arrow). (f) Cells presenting surface depressions are indicated in white arrow.
Figure 3.
Figure 3.
Effect of BTME on nitric oxide production by J774 macrophages. *Significant differences in relation to control (p < 0.05).

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