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Effects of BBR combined with FCZ on autophagy in C. albicans (A) Mean fluorescence intensity of MDC-stained C. albicans after 24 h of drug treatment (excitation/ emission wavelength: 335/512 nm). (B) Fluorescence microscopic images of MDC-stained C. albicans . At least five microscopic fields were observed at 200× magnification; scale bar = 150 μm. (C) TEM images of C. albicans after 24 h of drug intervention (3000×). N, nucleus; PM, plasma membrane; CW, cell wall; ER, endoplasmic reticulum; Ld, lipid droplet; Vac, vacuole; Ab, autophagic body; As: autophagosome; scale bar = 500 nm. (D) TEM images showing vacuole fragmentation induced by high-dose combination treatment. (E) Fluorescence microscopic images of C-DCFDA-stained C. albicans after 24 h of drug treatment. White arrows indicate the diffusely distributed fluorescent signals. At least five microscopic fields were observed at 400 × magnification; scale bar = 20 μm. (F) Percentage of C-DCFDA-positive cells. (G) Changes in cell viability of C. albicans affected by the autophagy inhibitor 3-MA assessed via the XTT reduction assay. (H) Changes in cell viability of C. albicans affected by the autophagy activator RAPA assessed via the XTT reduction assay.

Journal: Frontiers in Microbiology

Article Title: Berberine-fluconazole synergy against drug-resistant Candida albicans : association with disruption of the Ire1-mediated UPR pathway

doi: 10.3389/fmicb.2026.1965937

Figure Lengend Snippet: Effects of BBR combined with FCZ on autophagy in C. albicans (A) Mean fluorescence intensity of MDC-stained C. albicans after 24 h of drug treatment (excitation/ emission wavelength: 335/512 nm). (B) Fluorescence microscopic images of MDC-stained C. albicans . At least five microscopic fields were observed at 200× magnification; scale bar = 150 μm. (C) TEM images of C. albicans after 24 h of drug intervention (3000×). N, nucleus; PM, plasma membrane; CW, cell wall; ER, endoplasmic reticulum; Ld, lipid droplet; Vac, vacuole; Ab, autophagic body; As: autophagosome; scale bar = 500 nm. (D) TEM images showing vacuole fragmentation induced by high-dose combination treatment. (E) Fluorescence microscopic images of C-DCFDA-stained C. albicans after 24 h of drug treatment. White arrows indicate the diffusely distributed fluorescent signals. At least five microscopic fields were observed at 400 × magnification; scale bar = 20 μm. (F) Percentage of C-DCFDA-positive cells. (G) Changes in cell viability of C. albicans affected by the autophagy inhibitor 3-MA assessed via the XTT reduction assay. (H) Changes in cell viability of C. albicans affected by the autophagy activator RAPA assessed via the XTT reduction assay.

Article Snippet: Staining was conducted using an MDC Autophagy Staining Kit (Beyotime, Shanghai, China).

Techniques: Fluorescence, Staining, Clinical Proteomics, Membrane