Laboratorio de Microbiología Ambiental. Proyecto CyMA, UIICSE, Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Tlalnepantla, C.P. 54090, Estado de México, México.
Posgrado en Ciencias Biológicas, Unidad de Posgrado, Edificio A, 1° Piso, Circuito de Posgrados, Ciudad Universitaria, Coyoacán, C.P. 04510, Distrito Federal, México.
J Parasitol. 2024 Aug 1;110(4):360-374. doi: 10.1645/22-86.
Naegleria fowleri is a protozoan that causes primary amebic meningoencephalitis (PAM). The infection occurs when the trophozoites enter the nasal cavity, adhere to the nasal mucosa, invade the epithelium, and migrate until they reach the olfactory bulb. Like other pathogens, there is evidence that the adhesion of N. fowleri to host cells is an important factor in the process of cytopathogenicity and disease progression. However, the factors involved in the adhesion of the pathogen to the cells of the nasal epithelium have not been characterized. The objective of this study was to identify a protein on the surface of N. fowleri, which could act as adhesin to the mouse nasal epithelium in the PAM model. The interaction between proteins of extracts of N. fowleri and cells of the nasal epithelium of BALB/c mice was analyzed using overlay and Western blot assays. A 72-kDa band of N. fowleri interacted directly with epithelial cell proteins, this polypeptide band was purified and analyzed by mass spectrometry. Analysis revealed that polypeptide bands of 72 kDa contained peptides that matched the membrane protein, actin 1 and 2, and Hsp70. Moreover, the N. fowleri extracts resolved in 2D-SDS-PAGE showed that 72-kDa spot interacted with proteins of mouse epithelial cells, which include characteristics of the theoretical data of molecular weight and pH obtained in the analysis by mass spectrometry. Immunofluorescence tests showed that this protein is located on the surface of trophozoites and plays an important role in the adhesion of amoeba either in vitro or in vivo assays, suggesting that this protein contributes during the N. fowleri invasion and migration to the brain, causing primary amoebic meningoencephalitis.
福氏耐格里阿米巴原虫是一种原生动物,可引起原发性阿米巴脑膜脑炎(PAM)。当滋养体进入鼻腔、黏附于鼻黏膜、侵入上皮细胞并迁移至嗅球时,就会发生感染。与其他病原体一样,有证据表明福氏耐格里阿米巴原虫黏附于宿主细胞是细胞病变和疾病进展过程中的一个重要因素。然而,尚未确定该病原体与鼻上皮细胞黏附的相关因素。本研究的目的是鉴定福氏耐格里阿米巴原虫表面的一种蛋白,该蛋白在 PAM 模型中可作为黏附素与小鼠鼻上皮细胞相互作用。采用蛋白重叠印迹和 Western blot 分析方法,研究福氏耐格里阿米巴原虫提取物与 BALB/c 小鼠鼻上皮细胞之间的相互作用。福氏耐格里阿米巴原虫的 72 kDa 蛋白带与上皮细胞蛋白直接相互作用,该多肽带被纯化并通过质谱分析进行鉴定。分析表明,72 kDa 的多肽带含有与膜蛋白、肌动蛋白 1 和 2 以及热休克蛋白 70 相匹配的肽段。此外,二维 SDS-PAGE 分离的福氏耐格里阿米巴原虫提取物显示,72 kDa 斑点与包括通过质谱分析获得的分子量和 pH 理论数据特征的小鼠上皮细胞蛋白相互作用。免疫荧光试验表明,该蛋白位于滋养体表面,在体外或体内黏附试验中均发挥重要作用,提示该蛋白在福氏耐格里阿米巴原虫入侵和向脑迁移过程中发挥作用,引起原发性阿米巴脑膜脑炎。