Ferri Gabriel, Edreira Martin M
CONICET-Universidad de Buenos Aires, IQUIBICEN, Ciudad de Buenos Aires, Argentina.
Laboratorio de Biología Molecular de Trypanosoma, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos, Ciudad de Buenos Aires, Argentina.
Front Cell Infect Microbiol. 2021 Mar 5;11:634793. doi: 10.3389/fcimb.2021.634793. eCollection 2021.
has a complex life cycle involving four developmental stages namely, epimastigotes, metacyclic trypomastigotes, amastigotes and bloodstream trypomastigotes. Although trypomastigotes are the infective forms, extracellular amastigotes have also shown the ability to invade host cells. Both stages can invade a broad spectrum of host tissues, in fact, almost any nucleated cell can be the target of infection. To add complexity, the parasite presents high genetic variability with differential characteristics such as infectivity. In this review, we address the several strategies has developed to subvert the host cell signaling machinery in order to gain access to the host cell cytoplasm. Special attention is made to the numerous parasite/host protein interactions and to the set of signaling cascades activated during the formation of a parasite-containing vesicle, the parasitophorous vacuole, from which the parasite escapes to the cytosol, where differentiation and replication take place.
其具有复杂的生命周期,包括四个发育阶段,即前鞭毛体、循环后期锥鞭毛体、无鞭毛体和血液内锥鞭毛体。虽然锥鞭毛体是感染形式,但细胞外无鞭毛体也显示出侵入宿主细胞的能力。这两个阶段都可以侵入广泛的宿主组织,实际上,几乎任何有核细胞都可能成为感染目标。更复杂的是,该寄生虫具有高度的遗传变异性,具有诸如感染性等不同特征。在本综述中,我们阐述了其为颠覆宿主细胞信号传导机制以进入宿主细胞胞质而开发的几种策略。特别关注了众多的寄生虫/宿主蛋白相互作用以及在形成含寄生虫囊泡(即寄生泡)过程中激活的一系列信号级联反应,寄生虫从该寄生泡逃逸到胞质溶胶中进行分化和复制。