Hosseinzadeh Ava, Stylianou Marios, Lopes José Pedro, Müller Daniel C, Häggman André, Holmberg Sandra, Grumaz Christian, Johansson Anders, Sohn Kai, Dieterich Christoph, Urban Constantin F
Department of Clinical Microbiology, Umeå University, Umeå, Sweden.
Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden.
Front Microbiol. 2019 Aug 20;10:1843. doi: 10.3389/fmicb.2019.01843. eCollection 2019.
Invasive mycoses remain underdiagnosed and difficult to treat. Hospitalized individuals with compromised immunity increase in number and constitute the main risk group for severe fungal infections. Current antifungal therapy is hampered by slow and insensitive diagnostics and frequent toxic side effects of standard antifungal drugs. Identification of new antifungal compounds with high efficacy and low toxicity is therefore urgently required. We investigated the antifungal activity of tempol, a cell-permeable nitroxide. To narrow down possible mode of action we used RNA-seq technology and metabolomics to probe for pathways specifically disrupted in the human fungal pathogen due to tempol administration. We found genes upregulated which are involved in iron homeostasis, mitochondrial stress, steroid synthesis, and amino acid metabolism. In an whole blood infection, tempol treatment reduced colony forming units and at the same time increased the release of pro-inflammatory cytokines, such as interleukin 8 (IL-8, monocyte chemoattractant protein-1, and macrophage migration inhibitory factor). In a systemic mouse model, tempol was partially protective with a significant reduction of fungal burden in the kidneys of infected animals during infection onset. The results obtained propose tempol as a promising new antifungal compound and open new opportunities for the future development of novel therapies.
侵袭性真菌病仍然诊断不足且难以治疗。免疫功能受损的住院患者数量不断增加,构成了严重真菌感染的主要风险群体。目前的抗真菌治疗受到诊断缓慢且不敏感以及标准抗真菌药物频繁的毒副作用的阻碍。因此,迫切需要鉴定出高效低毒的新型抗真菌化合物。我们研究了可透过细胞的氮氧化物tempol的抗真菌活性。为了缩小可能的作用模式,我们使用RNA测序技术和代谢组学来探究由于给予tempol而在人类真菌病原体中特异性破坏的途径。我们发现与铁稳态、线粒体应激、类固醇合成和氨基酸代谢相关的基因上调。在全血感染中,tempol治疗减少了菌落形成单位,同时增加了促炎细胞因子如白细胞介素8(IL-8)、单核细胞趋化蛋白-1和巨噬细胞迁移抑制因子的释放。在系统性小鼠模型中,tempol具有部分保护作用,在感染开始时感染动物肾脏中的真菌负荷显著降低。所获得的结果表明tempol是一种有前景的新型抗真菌化合物,并为新型疗法的未来发展开辟了新机遇。