Tang Na, Yuan Shenghao, Luo Yuxuan, Wang An-Jun, Sun Kang, Liu Ning-Ning, Tao Ke
State Key Lab of Metal Matrix Composites, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.
State Key Laboratory of Oncogenes and Related Genes, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
ACS Omega. 2023 Jan 17;8(4):4357-4368. doi: 10.1021/acsomega.2c07740. eCollection 2023 Jan 31.
Biofilm formation is a critical event in the pathogenesis and virulence of fungal infections caused by , giving rise to about a 1000-fold increase in the resistance to antifungal agents. Although photodynamic treatment (PDT) has been excellently implicated in bacterial infections, studies on its potential against fungal infection through the clearance of fungal biofilm formation remain at its infancy stage. Here, we have designed photodynamic nanoparticles with different sizes, modifications, and the ability of generating reactive oxygen species (ROS) to examine their effects on inhibiting biofilm formation and destructing mature biofilms of . We found that the nanoparticles modified with oligo-chitosan exhibited a better binding efficiency for planktonic cells, leading to stronger inhibitory efficacy of the filamentation and the early-stage biofilm formation. However, for mature biofilms, the nanoparticles with the smallest size (∼15 nm) showed the fastest penetration speed and a pronounced destructing effect albeit conferring the lowest ROS-producing capability. The inhibitory effect of photodynamic nanoparticles was dependent on the disruption of fungal quorum sensing (QS) by the upregulation of QS molecules, farnesol and tyrosol, mediated through the upregulation of ARO 8 and DPP 3 expression. Our findings provide a powerful strategy of nanoparticulate PDT to combat fungal infections through the inhibition of both hyphal and biofilm formation by disrupting QS.
生物膜形成是由[具体真菌名称未给出]引起的真菌感染发病机制和毒力中的关键事件,会使对抗真菌药物的耐药性增加约1000倍。尽管光动力疗法(PDT)在细菌感染方面已得到充分研究,但关于其通过清除真菌生物膜形成来对抗真菌感染的潜力的研究仍处于起步阶段。在此,我们设计了具有不同尺寸、修饰和产生活性氧(ROS)能力的光动力纳米颗粒,以研究它们对抑制[具体真菌名称未给出]生物膜形成和破坏成熟生物膜的影响。我们发现,用低聚壳聚糖修饰的纳米颗粒对浮游细胞表现出更好的结合效率,从而对丝状化和早期生物膜形成具有更强的抑制效果。然而,对于成熟生物膜,尺寸最小(约15纳米)的纳米颗粒尽管产生活性氧的能力最低,但显示出最快的穿透速度和显著的破坏作用。光动力纳米颗粒的抑制作用取决于通过上调ARO 8和DPP 3表达介导的群体感应(QS)分子法尼醇和酪醇的上调对真菌群体感应(QS)的破坏。我们的研究结果提供了一种强大的纳米颗粒光动力疗法策略,通过破坏群体感应来抑制菌丝和生物膜形成,从而对抗真菌感染。