Synergistic wall digestion and cuproptosis against fungal infections using lywallzyme-induced self-assembly of metal-phenolic nanoflowers

Fungi are very common infectious pathogens, which may cause invasive and potentially life-threatening infections. However, the efficacy of antifungal medications remains limited. Herein, a Cu 2+ -phenolic nanoflower is designed to combat fungal infections by combining cuproptosis and cell wall diges...

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Veröffentlicht in:Nature communications 2024-10, Vol.15 (1), p.9004-18, Article 9004
Hauptverfasser: Liu, Fang, Chen, Yongcheng, Huang, Yue, Li, Yutong, Lu, Zhouyu, Han, Haijie, Song, Xiaohui, Jin, Qiao, Ji, Jian
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Sprache:eng
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Zusammenfassung:Fungi are very common infectious pathogens, which may cause invasive and potentially life-threatening infections. However, the efficacy of antifungal medications remains limited. Herein, a Cu 2+ -phenolic nanoflower is designed to combat fungal infections by combining cuproptosis and cell wall digestion. Firstly, protocatechuic acid (PA)-Cu 2+ (PC) nanopetals are prepared by coordination interaction. Lywallzyme (Lyw) is then added to induce the self-assembly of PC to form Lyw loaded PC (PCW) nanoflowers. PCW nanoflowers can effectively adhere to fungal surface and Lyw can digest fungal cell walls to facilitate Cu 2+ to penetrate into fungal interior, thereby exerting a synergistic fungicidal effect. PCW nanoflowers exhibit excellent fungicidal activity even in protein-rich and high-salt conditions, where dissociative Cu 2+ completely loses fungicidal activity. Transcriptome sequencing analysis reveals that PCW can lead to fungal cuproptosis. The in vivo fungicidal effect of PCW nanoflowers is confirmed on a murine skin fungal infection model and a murine fungal keratitis model. Fungal infections can be debilitating and life-threatening. Here, the authors report a fungicidal strategy by the combination of cell wall digestion and cuproptosis using lywallzyme-assembled copper-phenolic nanoflowers demonstrating synergistic effects in fungal infection and fungal keratitis models.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-53410-2