Malych Ronald, Folgosa Filipe, Pilátová Jana, Mikeš Libor, Dohnálek Vít, Mach Jan, Matějková Magdaléna, Kopecký Vladimír, Doležal Pavel, Sutak Robert
Department of Parasitology, Faculty of Science, Charles University, BIOCEV, Vestec, Czech Republic.
Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal.
PLoS Pathog. 2025 Mar 17;21(3):e1012995. doi: 10.1371/journal.ppat.1012995. eCollection 2025 Mar.
Naegleria fowleri, the causative agent of primary amoebic meningoencephalitis (PAM), requires increased research attention due to its high lethality and the potential for increased incidence as a result of global warming. The aim of this study was to investigate the interactions between N. fowleri and host cells in order to elucidate the mechanisms underlying the pathogenicity of this amoeba. A co-culture system comprising human fibrosarcoma cells was established to study both contact-dependent and contact-independent cytopathogenicity. Proteomic analyses of the amoebas exposed to human cell cultures or passaged through mouse brain were used to identify novel virulence factors. Our results indicate that actin dynamics, regulated by Arp2/3 and Src kinase, play a considerable role in ingestion of host cells by amoebae. We have identified three promising candidate virulence factors, namely lysozyme, cystatin and hemerythrin, which may be critical in facilitating N. fowleri evasion of host defenses, migration to the brain and induction of a lethal infection. Long-term co-culture secretome analysis revealed an increase in protease secretion, which enhances N. fowleri cytopathogenicity. Raman microspectroscopy revealed significant metabolic differences between axenic and brain-isolated amoebae, particularly in lipid storage and utilization. Taken together, our findings provide important new insights into the pathogenic mechanisms of N. fowleri and highlight potential targets for therapeutic intervention against PAM.
福氏耐格里阿米巴是原发性阿米巴脑膜脑炎(PAM)的病原体,因其高致死率以及全球变暖可能导致发病率上升,需要更多的研究关注。本研究的目的是调查福氏耐格里阿米巴与宿主细胞之间的相互作用,以阐明这种阿米巴致病性的潜在机制。建立了包含人纤维肉瘤细胞的共培养系统,以研究接触依赖性和接触非依赖性细胞致病性。对暴露于人类细胞培养物或通过小鼠脑传代的阿米巴进行蛋白质组分析,以鉴定新的毒力因子。我们的结果表明,由Arp2/3和Src激酶调节的肌动蛋白动力学在阿米巴摄取宿主细胞中起重要作用。我们已经鉴定出三种有前景的候选毒力因子,即溶菌酶、胱抑素和蚯蚓血红蛋白,它们可能在促进福氏耐格里阿米巴逃避宿主防御、迁移到脑部以及引发致命感染方面起关键作用。长期共培养分泌组分析显示蛋白酶分泌增加,这增强了福氏耐格里阿米巴的细胞致病性。拉曼光谱分析揭示了无菌培养和从脑部分离的阿米巴之间显著的代谢差异,特别是在脂质储存和利用方面。综上所述,我们的研究结果为福氏耐格里阿米巴的致病机制提供了重要的新见解,并突出了针对PAM治疗干预的潜在靶点。