Florentino Pilar T V, Real Fernando, Orikaza Cristina M, da Cunha Julia P C, Vitorino Francisca N L, Cordero Esteban M, Sobreira Tiago J P, Mortara Renato A
Department of Microbiology, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, Brazil.
Institut Cochin, INSERM U1016, Paris, France.
Front Microbiol. 2018 Apr 10;9:693. doi: 10.3389/fmicb.2018.00693. eCollection 2018.
is the etiologic agent of Chagas' disease. It is known that amastigotes derived from trypomastigotes in the extracellular milieu are infective and . Extracellular amastigotes (EAs) have a stage-specific surface antigen called Ssp-4, a GPI-anchored glycoprotein that is secreted by the parasites. By immunoprecipitation with the Ssp-4-specific monoclonal antibodies (mAb) 2C2 and 1D9, we isolated the glycoprotein from EAs. By mass spectrometry, we identified the core protein of Ssp-4 and evaluated mRNA expression and the presence of Ssp-4 carbohydrate epitopes recognized by mAb1D9. We demonstrated that the carbohydrate epitope recognized by mAb1D9 could promote host cell invasion by EAs. Although infectious EAs express lower amounts of Ssp-4 compared with less-infectious EAs (at the mRNA and protein levels), it is the glycosylation of Ssp-4 (identified by mAb1D9 staining only in infectious strains and recognized by galectin-3 on host cells) that is the determinant of EA invasion of host cells. Furthermore, Ssp-4 is secreted by EAs, either free or associated with parasite vesicles, and can participate in host-cell interactions. The results presented here describe the possible role of a carbohydrate moiety of surface glycoproteins in host cell invasion by EA forms, highlighting the potential of these moieties as therapeutic and vaccine targets for the treatment of Chagas' disease.
是恰加斯病的病原体。已知在细胞外环境中源自锥鞭毛体的无鞭毛体具有感染性。细胞外无鞭毛体(EA)有一种阶段特异性表面抗原,称为Ssp-4,这是一种由寄生虫分泌的糖基磷脂酰肌醇锚定糖蛋白。通过用Ssp-4特异性单克隆抗体(mAb)2C2和1D9进行免疫沉淀,我们从EA中分离出了这种糖蛋白。通过质谱分析,我们鉴定了Ssp-4的核心蛋白,并评估了mRNA表达以及mAb1D9识别的Ssp-4碳水化合物表位的存在情况。我们证明,mAb1D9识别的碳水化合物表位可促进EA对宿主细胞的侵袭。尽管与感染性较低的EA相比,感染性EA在mRNA和蛋白质水平上表达的Ssp-4量较低,但Ssp-4的糖基化(仅在感染性菌株中通过mAb1D9染色鉴定,并被宿主细胞上的半乳糖凝集素-3识别)才是EA侵袭宿主细胞的决定因素。此外,Ssp-4由EA分泌,可游离存在或与寄生虫囊泡相关,并可参与宿主细胞相互作用。此处呈现的结果描述了表面糖蛋白的碳水化合物部分在EA形式侵袭宿主细胞中的可能作用,突出了这些部分作为治疗恰加斯病的治疗靶点和疫苗靶点的潜力。