γ-mangostin from Garcinia mangostana (L.) exerts the antifungal activity against Cryptococcus neoformans by inhibiting ribosome biogenesis.

The pericarp of Garcinia mangostana (L.) has been traditionally used in Southeast Asia and South China to alleviate diarrhea, regulate gastrointestinal functions, and promote wound healing. It is rich in xanthones, which exhibit significant antimicrobial activity. However, current research on the an...

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Publicado en:Journal of Ethnopharmacology Vol. 358
Autores principales: Li, Xiancai, Chen, Shaohua, Wu, Yaodan, Liu, Fen, Jumai, Aikebaier, Zhu, Baojun, Xiong, Binghong, Qiu, Sheng-Xiang
Formato: research Journal Article
Publicado: Elsevier B.V. Mar2026
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Mar2026
      vid: 358
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      pub: Elsevier B.V.
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        190465806
        10.1016/j.jep.2025.120986
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        atl: γ-mangostin from Garcinia mangostana (L.) exerts the antifungal activity against Cryptococcus neoformans by inhibiting ribosome biogenesis.
      aug:
        au:
          Li, Xiancai
          Chen, Shaohua
          Wu, Yaodan
          Liu, Fen
          Jumai, Aikebaier
          Zhu, Baojun
          Xiong, Binghong
          Qiu, Sheng-Xiang
        affil: Horticulture Research Center, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, 510650, China
      sug:
        subj:
          Cryptococcosis Drug Therapy
          Plant Extracts Pharmacodynamics
          Heterocyclic Compounds Therapeutic Use
          Heterocyclic Compounds Pharmacodynamics
          Antifungal Agents Pharmacodynamics
          Antifungal Agents Analysis
          RNA Drug Effects
          Human
          Descriptive Statistics
          Antifungal Agents Metabolism
          Biofilms Drug Effects
          Phytochemicals
          Microbial Culture and Sensitivity Tests
          RNA Metabolism
          Fluconazole Administration and Dosage
          Signal Transduction
          Amphotericin B Administration and Dosage
      ab: The pericarp of Garcinia mangostana (L.) has been traditionally used in Southeast Asia and South China to alleviate diarrhea, regulate gastrointestinal functions, and promote wound healing. It is rich in xanthones, which exhibit significant antimicrobial activity. However, current research on the antimicrobial properties of mangosteen pericarp has primarily concentrated on the antibacterial effects of the xanthone compound α-mangostin, while studies on the antifungal activities of xanthones remain relatively limited. The current study aimed to extract pure compounds from mangosteen pericarp and conducted antifungal activity screening against Cryptococcus neoformans , along with an analysis of the antifungal potential and related mechanisms of action of the most potent antifungal compound. The chemical constituents of G. mangostana pericarp were isolated and identified by phytochemical study and spectroscopic data. The antifungal potential of γ-mangostin was analyzed through minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) tests, structure-activity relationship (SAR) analysis, growth curves, time-kill curves, electron microscopy, biofilm eradication and capsule formation inhibition capacity, as well as a Caenorhabditis elegans infection model treatment. Its antifungal mechanism was investigated via transcriptomic and metabolomic analyses, along with corresponding validation experiments. A total of 33 monomeric compounds were isolated from the mangosteen pericarp extract, primarily xanthone derivatives. Among them, γ-mangostin exhibited the strongest antifungal activity, with MIC and MFC values of 4 μM and 16 μM, respectively. Growth curve, time-kill kinetics, and electron microscopy experiments demonstrated that γ-mangostin exerted significant and sustained antifungal effects within 24 h. At a concentration of 4 μM, γ-mangostin significantly eradicated biofilms and inhibited capsule formation. In a C. elegans infection model, 4 μM γ-mangostin showed notable therapeutic efficacy. Furthermore, γ-mangostin displayed hemolytic activity comparable to the commercial antibiotics fluconazole and amphotericin B at concentrations up to 64 μM, with no adverse effects on nematode lifespan. Transcriptomic and metabolomic analyses revealed that γ-mangostin suppressed the ribosome biogenesis signaling pathway. qPCR analysis indicated that γ-mangostin downregulated key genes (NMD3 , NOB1 , NAT10 , and NHP2) in the ribosome biogenesis pathway. Protein content assays further confirmed that γ-mangostin significantly reduced protein accumulation in C. neoformans. γ-mangostin holds potential application value in the treatment of infections caused by C. neoformans. [Display omitted]
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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