Eating the brain - A multidisciplinary study provides new insights into the mechanisms underlying the cytopathogenicity of Naegleria fowleri.

IF 4.9 1区 医学 Q1 MICROBIOLOGY PLoS Pathogens Pub Date : 2025-03-17 eCollection Date: 2025-03-01 DOI:10.1371/journal.ppat.1012995
Ronald Malych, Filipe Folgosa, Jana Pilátová, Libor Mikeš, Vít Dohnálek, Jan Mach, Magdaléna Matějková, Vladimír Kopecký, Pavel Doležal, Robert Sutak
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Abstract

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.

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一项多学科研究为福氏奈格氏杆菌细胞致病性的机制提供了新的见解。
福氏奈格里菌是原发性阿米巴脑膜脑炎(PAM)的病原体,由于其高致死率和全球变暖可能导致发病率增加,需要加强对其的研究。本研究的目的是研究福氏奈米原虫与宿主细胞之间的相互作用,以阐明这种变形虫致病性的机制。建立了一个由人纤维肉瘤细胞组成的共培养系统,以研究接触依赖性和非接触依赖性的细胞致病性。暴露于人类细胞培养物或通过小鼠大脑传代的阿米巴原虫的蛋白质组学分析用于鉴定新的毒力因子。我们的研究结果表明,由Arp2/3和Src激酶调节的肌动蛋白动力学在变形虫摄取宿主细胞中起着相当大的作用。我们已经确定了三种有希望的候选毒力因子,即溶菌酶、胱抑素和氰菊酯,它们可能是促进福氏奈氏菌逃避宿主防御、迁移到大脑和诱导致命感染的关键。长期共培养分泌组分析显示蛋白酶分泌增加,这增强了福氏奈瑟菌的细胞致病性。拉曼显微光谱分析显示,无性变形虫和脑分离变形虫在代谢方面存在显著差异,特别是在脂质储存和利用方面。综上所述,我们的发现为福氏奈瑟菌的致病机制提供了重要的新见解,并突出了PAM治疗干预的潜在靶点。
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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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