Loss of the cytostome-cytopharynx and endocytic ability are late events in Trypanosoma cruzi metacyclogenesis

• Published in: Journal of structural biology 2016-12, Vol.196 (3), p.319-328
• Main Authors: Vidal, Juliana C., Alcantara, Carolina de L., de Souza, Wanderley, Cunha-e-Silva, Narcisa L.
• Format: Article
• Language: English
• Subjects: Animals; Cell Membrane - chemistry; Cell Membrane - ultrastructure; Cytostome-cytopharynx; Electron Microscope Tomography; Endocytosis; Endocytosis - genetics; Humans; Metacyclogenesis; Microtubules - chemistry; Microtubules - ultrastructure; T. cruzi; Transferrin - chemistry; Transferrin - ultrastructure; Trypanosoma cruzi - chemistry; Trypanosoma cruzi - pathogenicity
• ISSN: 1047-8477; 1095-8657
• DOI: 10.1016/j.jsb.2016.07.018

Trypanosoma cruzi epimastigotes uptake nutrients by endocytosis via the cytostome-cytopharynx complex – an anterior opening (cytostome) continuous with a funnel-shaped invagination (cytopharynx) that extends to the posterior of the cell, accompanied by microtubules. During metacyclogenesis – the transformation of epimastigotes into human-infective metacyclic trypomastigotes – the cytostome-cytopharynx complex disappears, as trypomastigotes lose endocytic ability. To date, no studies have examined cytostome-cytopharynx complex disappearance in detail, or determined if endocytic activity persists during metacyclogenesis. Here, we produced 3D reconstructions of metacyclogenesis intermediates (Ia, Ib, Ic) using electron microscopy tomography and focused ion beam-scanning electron microscopy (FIB-SEM), concentrating on the cytostome-cytopharynx complex and adjacent structures, including the preoral ridge (POR). Parasite endocytic potential was examined by incubation of intermediate forms with the endocytic tracer transferrin (Tf)-Au. Ia, Ib and Ic cells were capable of internalizing Tf-Au, and had a shorter cytopharynx than that of epimastigotes, with the cytostome/POR progressively displaced towards the posterior, following the movement of the kinetoplast/flagellar pocket. While some Ic cells had a short cytopharynx with an enlarged proximal end (∼300nm in diameter, larger than that of the cytostome), other Ic cells had no cytopharynx invagination, but retained the cytopharynx microtubules, which were also present in metacyclics. We conclude that cytostome-cytopharynx disappearance and loss of endocytic ability are late events in metacyclogenesis, during which the cytostome is displaced towards the posterior, probably due to a link to the kinetoplast/flagellar pocket. Retention of the cytopharynx microtubules by metacyclics may allow prompt cytostome-cytopharynx reassembly in amastigotes, upon host cell infection.