Detection of immunogenic protein components in excretion/secretion products of Acanthamoeba T5 using polyclonal antibodies.

IF 2.5 4区 医学 Q2 PARASITOLOGY
Memorias do Instituto Oswaldo Cruz Pub Date : 2025-06-09 eCollection Date: 2025-01-01 DOI:10.1590/0074-02760240190
Lissette Retana-Moreira, Elizabeth Abrahams-Sandí, Marco Ruiz-Campos, Johan Alvarado-Ocampo, Julián Castro, Jacob Lorenzo-Morales, Giovanni Sáenz-Arce, Antonio Osuna
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引用次数: 0

Abstract

Background: Acanthamoeba is a free-living amoeba widely distributed, responsible for keratitis and granulomatous amoebic encephalitis. The presence of virulence factors in its excretion/secretion products has been demonstrated. Characterisation of these products, including the determination of immunogenic protein components using polyclonal antibodies, could be the basis for the development of new diagnostic tools and help to understand aspects related to its pathogenesis.

Objectives: To identify immunogenic protein components in Acanthamoeba conditioned medium (ACM) and extracellular vesicles (EVs) using polyclonal anti-Acanthamoeba antibodies produced in the laboratory and to evaluate the effect of these antibodies in adhesion and cytopathic effect.

Methods: Excretion/secretion products were obtained after the axenic culture of a potentially pathogenic environmental Acanthamoeba T5 isolate. The presence of immunogenic components in lysates of trophozoites, ACM and EVs was determined using polyclonal anti-Acanthamoeba antibodies produced in Wistar rats. Proteomic analyses to identify the immunogenic protein components in ACM and EVs were included. Experiments to evaluate the effect of polyclonal anti-Acanthamoeba antibodies in adhesion and cytopathic effect in vitro were also performed in Vero cells.

Findings: Protein recognition by anti-Acanthamoeba antibodies in lysates, ACM and EVs was demonstrated, and these components were identified using proteomics. Decreases in adhesion and cytopathic effect after the preincubation of trophozoites with antibodies, prior to the contact with cells, were observed.

Main conclusion: The development of polyclonal antibodies, capable of recognising proteins related to pathogenesis in ACM and EVs, and with significant effects in adhesion, provides an important tool for the search for new therapeutic and diagnostic targets in infections caused by Acanthamoeba.

棘阿米巴T5排泄/分泌产物免疫原性蛋白成分的多克隆抗体检测
背景:棘阿米巴是一种分布广泛的自由生活阿米巴原虫,可引起角膜炎和肉芽肿性阿米巴脑炎。其排泄/分泌产物中存在毒力因子已被证实。表征这些产物,包括使用多克隆抗体测定免疫原性蛋白成分,可能是开发新的诊断工具的基础,并有助于了解其发病机制的相关方面。目的:利用实验室制备的多克隆抗棘阿米巴抗体,鉴定棘阿米巴条件培养基(ACM)和细胞外囊泡(ev)中的免疫原性蛋白成分,并评价这些抗体的粘附作用和细胞病变作用。方法:对具有潜在致病性的环境棘阿米巴T5分离株进行无菌培养后获得排泄/分泌产物。利用Wistar大鼠产生的多克隆抗棘阿米巴抗体测定滋养体、ACM和ev裂解物中免疫原性成分的存在。包括蛋白质组学分析,以鉴定ACM和ev中的免疫原性蛋白质成分。同时在Vero细胞上进行了多克隆抗棘阿米巴抗体体外粘附效果和细胞病变效果的实验。结果:在裂解物、ACM和ev中,抗棘阿米巴抗体可以识别蛋白质,这些成分通过蛋白质组学进行了鉴定。在与细胞接触之前,观察到滋养体与抗体预孵育后的粘附性和细胞病变效应降低。主要结论:在棘阿米巴感染中,能够识别与ACM和EVs发病机制相关的蛋白并具有显著粘附作用的多克隆抗体的开发,为寻找新的治疗和诊断靶点提供了重要工具。
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来源期刊
CiteScore
5.00
自引率
3.60%
发文量
91
审稿时长
3-8 weeks
期刊介绍: Memórias do Instituto Oswaldo Cruz is a journal specialized in microbes & their vectors causing human infections. This means that we accept manuscripts covering multidisciplinary approaches and findings in the basic aspects of infectious diseases, e.g. basic in research in prokariotes, eukaryotes, and/or virus. Articles must clearly show what is the main question to be answered, the hypothesis raised, and the contribution given by the study. Priority is given to manuscripts reporting novel mechanisms and general findings concerning the biology of human infectious prokariotes, eukariotes or virus. Papers reporting innovative methods for diagnostics or that advance the basic research with these infectious agents are also welcome. It is important to mention what we do not publish: veterinary infectious agents research, taxonomic analysis and re-description of species, epidemiological studies or surveys or case reports and data re-analysis. Manuscripts that fall in these cases or that are considered of low priority by the journal editorial board, will be returned to the author(s) for submission to another journal.
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