Cámara María de Los Milagros, Cánepa Gaspar E, Lantos Andrés B, Balouz Virginia, Yu Hai, Chen Xi, Campetella Oscar, Mucci Juan, Buscaglia Carlos A
Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico de Chascomús (IIB-INTECh), Universidad Nacional de San Martín (UNSAM) and Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina.
Instituto de Tecnología, Universidad Argentina de la Empresa (UADE), Buenos Aires, Argentina.
PLoS Negl Trop Dis. 2017 Aug 11;11(8):e0005856. doi: 10.1371/journal.pntd.0005856. eCollection 2017 Aug.
TSSA (Trypomastigote Small Surface Antigen) is an antigenic, adhesion molecule displayed on the surface of Trypanosoma cruzi trypomastigotes. TSSA displays substantial sequence identity to members of the TcMUC gene family, which code for the trypomastigote mucins (tGPI-mucins). In addition, TSSA bears sequence polymorphisms among parasite strains; and two TSSA variants expressed as recombinant molecules (termed TSSA-CL and TSSA-Sy) were shown to exhibit contrasting features in their host cell binding and signaling properties.
METHODS/PRINCIPLE FINDINGS: Here we used a variety of approaches to get insights into TSSA structure/function. We show that at variance with tGPI-mucins, which rely on their extensive O-glycoslylation to achieve their protective function, TSSA seems to be displayed on the trypomastigote coat as a hypo-glycosylated molecule. This has a functional correlate, as further deletion mapping experiments and cell binding assays indicated that exposition of at least two peptidic motifs is critical for the engagement of the 'adhesive' TSSA variant (TSSA-CL) with host cell surface receptor(s) prior to trypomastigote internalization. These motifs are not conserved in the 'non-adhesive' TSSA-Sy variant. We next developed transgenic lines over-expressing either TSSA variant in different parasite backgrounds. In strict accordance to recombinant protein binding data, trypomastigotes over-expressing TSSA-CL displayed improved adhesion and infectivity towards non-macrophagic cell lines as compared to those over-expressing TSSA-Sy or parental lines. These phenotypes could be specifically counteracted by exogenous addition of peptides spanning the TSSA-CL adhesion motifs. In addition, and irrespective of the TSSA variant, over-expression of this molecule leads to an enhanced trypomastigote-to-amastigote conversion, indicating a possible role of TSSA also in parasite differentiation.
CONCLUSION/SIGNIFICANCE: In this study we provided novel evidence indicating that TSSA plays an important role not only on the infectivity and differentiation of T. cruzi trypomastigotes but also on the phenotypic variability displayed by parasite strains.
锥虫小表面抗原(TSSA)是一种抗原性粘附分子,展示在克氏锥虫锥鞭毛体表面。TSSA与TcMUC基因家族成员具有高度的序列同一性,该基因家族编码锥鞭毛体粘蛋白(tGPI-粘蛋白)。此外,TSSA在不同寄生虫株之间存在序列多态性;两种作为重组分子表达的TSSA变体(称为TSSA-CL和TSSA-Sy)在宿主细胞结合和信号特性方面表现出截然不同的特征。
方法/主要发现:在此,我们使用了多种方法来深入了解TSSA的结构/功能。我们发现,与依赖广泛的O-糖基化来实现其保护功能的tGPI-粘蛋白不同,TSSA似乎以低糖基化分子的形式展示在锥鞭毛体表面。这具有功能相关性,因为进一步的缺失定位实验和细胞结合试验表明,至少两个肽基序的暴露对于“粘附性”TSSA变体(TSSA-CL)在锥鞭毛体内化之前与宿主细胞表面受体的结合至关重要。这些基序在“非粘附性”TSSA-Sy变体中并不保守。接下来,我们在不同的寄生虫背景下开发了过表达任一TSSA变体的转基因系。与过表达TSSA-Sy或亲本系的锥鞭毛体相比,严格按照重组蛋白结合数据,过表达TSSA-CL的锥鞭毛体对非巨噬细胞系表现出改善的粘附性和感染性。这些表型可以通过外源添加跨越TSSA-CL粘附基序的肽来特异性抵消。此外,无论TSSA变体如何,该分子的过表达都会导致锥鞭毛体向无鞭毛体的转化率提高,表明TSSA在寄生虫分化中也可能发挥作用。
结论/意义:在本研究中,我们提供了新的证据,表明TSSA不仅在克氏锥虫锥鞭毛体的感染性和分化中起重要作用,而且在寄生虫株所表现出的表型变异性中也起重要作用。