Cruz-Saavedra Lissa, Vallejo Gustavo A, Guhl Felipe, Ramírez Juan David
Grupo de Investigaciones Microbiológicas-UR (GIMUR), Departamento de Biología, Facultad de Ciencias Naturales, Universidad del Rosario, Bogota, Colombia.
Laboratorio de Investigación en Parasitología Tropical, Facultad de Ciencias, Universidad del Tolima, Ibagué, Colombia.
PeerJ. 2020 May 14;8:e8947. doi: 10.7717/peerj.8947. eCollection 2020.
is a flagellated protozoan that causes Chagas disease; it presents a complex life cycle comprising four morphological stages: epimastigote (EP), metacyclic trypomastigote (MT), cell-derived trypomastigote (CDT) and amastigote (AM). Previous transcriptomic studies on three stages (EPs, CDTs and AMs) have demonstrated differences in gene expressions among them; however, to the best of our knowledge, no studies have reported on gene expressions in MTs. Therefore, the present study compared differentially expressed genes (DEGs), and signaling pathway reconstruction in EPs, MTs, AMs and CDTs. The results revealed differences in gene expressions in the stages evaluated; these differences were greater between MTs and AMs-PTs. The signaling pathway that presented the highest number of DEGs in all the stages was associated with ribosomes protein profiles, whereas the other related pathways activated were processes related to energy metabolism from glucose, amino acid metabolism, or RNA regulation. However, the role of autophagy in the entire life cycle of and the presence of processes such as meiosis and homologous recombination in MTs (where the expressions of SPO11 and Rad51 plays a role) are crucial. These findings represent an important step towards the full understanding of the molecular basis during the life cycle of .
是一种导致恰加斯病的鞭毛虫原生动物;它呈现出一个复杂的生命周期,包括四个形态阶段:前鞭毛体(EP)、循环后期锥鞭毛虫(MT)、细胞衍生锥鞭毛虫(CDT)和无鞭毛体(AM)。先前对三个阶段(前鞭毛体、细胞衍生锥鞭毛虫和无鞭毛体)的转录组学研究已经证明了它们之间基因表达的差异;然而,据我们所知,尚无关于循环后期锥鞭毛虫基因表达的研究报道。因此,本研究比较了前鞭毛体、循环后期锥鞭毛虫、无鞭毛体和细胞衍生锥鞭毛虫中的差异表达基因(DEG)以及信号通路重建。结果揭示了所评估阶段中基因表达的差异;这些差异在循环后期锥鞭毛虫与无鞭毛体 - 前鞭毛体之间更大。在所有阶段中呈现差异表达基因数量最多的信号通路与核糖体蛋白质谱相关,而其他激活的相关通路是与葡萄糖能量代谢、氨基酸代谢或RNA调控相关的过程。然而,自噬在整个生命周期中的作用以及循环后期锥鞭毛虫中减数分裂和同源重组等过程的存在(其中SPO11和Rad51的表达起作用)至关重要。这些发现代表了朝着全面理解整个生命周期分子基础迈出的重要一步。