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Zinc Oxide Nanoparticles Prime a Protective Immune Response in Galleria mellonella to Defend Against Candida albicans.
Xu, Mei-Nian; Li, Li; Pan, Wen; Zheng, Huan-Xin; Wang, Meng-Lei; Peng, Xiao-Ming; Dai, Si-Qi; Tang, Ying-Mei; Zeng, Kang; Huang, Xiao-Wen.
Afiliação
  • Xu MN; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Li L; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Pan W; Division of Infectious Diseases, Rhode Island Hospital, Warren Alpert Medical School of Brown University, Providence, RI, United States.
  • Zheng HX; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Wang ML; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Peng XM; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Dai SQ; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Tang YM; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Zeng K; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Huang XW; Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Front Microbiol ; 12: 766138, 2021.
Article em En | MEDLINE | ID: mdl-34956129
Purpose: Zinc oxide nanoparticles (ZnO-NPs) have exerted antimicrobial properties. However, there is insufficient evaluation regarding the in vivo antifungal activity of ZnO-NPs. This study aimed to investigate the efficacy and mechanism of ZnO-NPs in controlling Candida albicans in the invertebrate Galleria mellonella. Methods: Galleria mellonella larvae were injected with different doses of ZnO-NPs to determine their in vivo toxicity. Non-toxic doses of ZnO-NPs were chosen for prophylactic injection in G. mellonella followed by C. albicans infection. Then the direct in vitro antifungal effect of ZnO-NPs against C. albicans was evaluated. In addition, the mode of action of ZnO-NPs was assessed in larvae through different assays: quantification of hemocyte density, morphology observation of hemocytes, characterization of hemocyte aggregation and phagocytosis, and measurement of hemolymph phenoloxidase (PO) activity. Results: Zinc oxide nanoparticles were non-toxic to the larvae at relatively low concentrations (≤20 mg/kg). ZnO-NP pretreatment significantly prolonged the survival of C. albicans-infected larvae and decreased the fungal dissemination and burden in the C. albicans-infected larvae. This observation was more related to the activation of host defense rather than their fungicidal capacities. Specifically, ZnO-NP treatment increased hemocyte density, promoted hemocyte aggregation, enhanced hemocyte phagocytosis, and activated PO activity in larvae. Conclusion: Prophylactic treatment with lower concentrations of ZnO-NPs protects G. mellonella from C. albicans infection. The innate immune response primed by ZnO-NPs may be part of the reason for the protective effects. This study provides new evidence of the capacity of ZnO-NPs in enhancing host immunity and predicts that ZnO-NPs will be attractive for further anti-infection applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article