Volatile Extract (SXC): A Dual-Action Antioxidant and Antifungal Agent Targeting Pathogenicity and Vulvovaginal Candidiasis via Host Oxidative Stress Modulation and Fungal Metabolic Reprogramming.

BACKGROUND AND PURPOSE

Vulvovaginal candidiasis (VVC), caused by (), is exacerbated by oxidative stress and uncontrolled inflammation. Pathogens like generate reactive oxygen species (ROS) to enhance virulence, while host immune responses further amplify oxidative damage. This study investigates the antioxidant and antifungal properties of volatile extract (SXC), a traditional Uyghur medicinal herb, against fluconazole-resistant VVC. We hypothesize that SXC's bioactive volatiles counteract pathogen-induced oxidative stress while inhibiting fungal growth and inflammation.

METHODS

GC-MS identified SXC's major bioactive components, while broth microdilution assays determined minimum inhibitory concentrations (MICs) against bacterial/fungal pathogens, and synergistic interactions with amphotericin B (AmB) or fluconazole (FLC) were assessed via time-kill kinetics. Anti-biofilm activity was quantified using crystal violet/XTT assays, and in vitro studies evaluated SXC's effects on -induced cytotoxicity (LDH release in A431 cells) and inflammatory responses (cytokine production in LPS-stimulated RAW264.7 macrophages). A murine VVC model, employing estrogen-mediated pathogenesis and intravaginal challenge, confirmed SXC's in vivo effects. Immune modulation was assessed using ELISA and RT-qPCR targeting inflammatory and antioxidative stress mediators, while UPLC-MS was employed to profile metabolic perturbations in .

RESULTS

Gas chromatography-mass spectrometry identified 10 key volatile components contributing to SXC's activity. SXC exhibited broad-spectrum antimicrobial activity with MIC values ranging from 0.125-16 μL/mL against bacterial and fungal pathogens, including fluconazole-resistant Candida strains. Time-kill assays revealed that combinations of AmB-SXC and FLC-SXC achieved sustained synergistic bactericidal activity across all tested strains. Mechanistic studies revealed SXC's dual antifungal actions: inhibition of hyphal development and biofilm formation through downregulation of the Ras1-cAMP-Efg1 signaling pathway, and attenuation of riboflavin-mediated energy metabolism crucial for fungal proliferation. In the VVC model, SXC reduced vaginal fungal burden, alleviated clinical symptoms, and preserved vaginal epithelial integrity. Mechanistically, SXC modulated host immune responses by suppressing oxidative stress and pyroptosis through TLR4/NF-κB/NLRP3 pathway inhibition, evidenced by reduced caspase-1 activation and decreased pro-inflammatory cytokines (IL-1β, IL-6, TNF-α).

CONCLUSIONS

SXC shows promise as a broad-spectrum natural antimicrobial against fungal pathogens. It inhibited hyphal growth, adhesion, biofilm formation, and invasion in vitro, while reducing oxidative and preserving vaginal mucosal integrity in vivo. By disrupting fungal metabolic pathways and modulating host immune responses, SXC offers a novel approach to treating recurrent, drug-resistant VVC.