福氏呐格勒氏菌的 72-kda 蛋白在滋养体粘附到 balb/c 小鼠鼻腔上皮细胞的过程中起着重要作用。

IF 1 4区 医学 Q4 PARASITOLOGY
B Flores-Suárez, P Bonilla-Lemus, S Rojas-Hernández, L L Terrazas-Valdés, M M Carrasco-Yépez
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引用次数: 0

摘要

鲍勒氏原虫(Naegleria fowleri)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、粘附在鼻粘膜上、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,N. fowleri 与宿主细胞的粘附是细胞致病和疾病进展过程中的一个重要因素。然而,病原体与鼻腔上皮细胞粘附的相关因素尚未确定。本研究的目的是确定 N. fowleri 表面的一种蛋白质,这种蛋白质可作为 PAM 模型中小鼠鼻腔上皮细胞的粘附素。研究人员使用重叠法和 Western 印迹法分析了 N. fowleri 提取物蛋白与 BALB/c 小鼠鼻上皮细胞之间的相互作用。一条 72 kDa 的 N. fowleri 带与上皮细胞蛋白直接相互作用,这条多肽带被纯化并通过质谱分析。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 Hsp70 相匹配的肽段。此外,经 2D-SDS-PAGE 分解的 N. fowleri 提取物显示,72 千兆位点与小鼠上皮细胞的蛋白质相互作用,其中包括质谱分析中获得的分子量和 pH 值理论数据的特征。免疫荧光试验表明,该蛋白位于滋养体表面,在体外或体内阿米巴粘附试验中发挥重要作用,这表明该蛋白在福氏阿米巴痢疾杆菌入侵和迁移至大脑并引起原发性阿米巴脑膜脑炎的过程中起到了重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE 72-KDA PROTEIN OF NAEGLERIA FOWLERI PLAYS AN IMPORTANT ROLE IN THE ADHESION OF TROPHOZOITES TO BALB/C MICE NASAL EPITHELIUM.

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.

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来源期刊
Journal of Parasitology
Journal of Parasitology 医学-寄生虫学
CiteScore
2.10
自引率
7.70%
发文量
60
审稿时长
2 months
期刊介绍: The Journal of Parasitology is the official peer-reviewed journal of the American Society of Parasitologists (ASP). The journal publishes original research covering helminths, protozoa, and other parasitic organisms and serves scientific professionals in microbiology, immunology, veterinary science, pathology, and public health. Journal content includes original research articles, brief research notes, announcements of the Society, and book reviews. Articles are subdivided by topic for ease of reference and range from behavior and pathogenesis to systematics and epidemiology. The journal is published continuously online with one full volume printed at the end of each year.
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