Literature DB >> 17992694

Ultrastructure of Trypanosoma cruzi revisited by atomic force microscopy.

Gustavo Miranda Rocha1, Kildare Miranda, Gilberto Weissmüller, Paulo Mascarello Bisch, Wanderley de Souza.   

Abstract

Most advances in atomic force microscopy (AFM) have been accomplished in recent years. Previous attempts to use AFM to analyze the organization of pathogenic protozoa did not significantly contribute with new structural information. In this work, we introduce a new perspective to the study of the ultrastructure of the epimastigote form of Trypanosoma cruzi by AFM. Images were compared with those obtained using field emission scanning electron microscopy of critical point dried cells and transmission electron microscopy of negative stained detergent-extracted and air-dried cells. AFM images of epimastigote forms showed a flagellum furrow separating the axoneme from the paraflagellar rod (PFR) present from the emergence of the flagellar pocket to the tip of the flagellum. At high magnification, a row of periodically organized structures, which probably correspond to the link between the axoneme, the PFR and the flagellar membrane were seen along the furrow. In the origin of the flagellum, two basal bodies were identified. Beyond the basal bodies, small periodically arranged protrusions, positioned at 400 nm from the flagellar basis were seen. This structure was formed by nine substructures distributed around the flagellar circumference and may correspond to the flagellar necklace. Altogether, our results demonstrate the importance of the application of AFM in the structural characterization of the surface components and cytoskeleton on protozoan parasites. Copyright (c) 2007 Wiley-Liss, Inc.

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Year:  2008        PMID: 17992694     DOI: 10.1002/jemt.20535

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  5 in total

1.  Structural changes of the paraflagellar rod during flagellar beating in Trypanosoma cruzi.

Authors:  Gustavo Miranda Rocha; Dirceu Esdras Teixeira; Kildare Miranda; Gilberto Weissmüller; Paulo Mascarello Bisch; Wanderley de Souza
Journal:  PLoS One       Date:  2010-06-30       Impact factor: 3.240

2.  Unlocking the secrets of multi-flagellated propulsion: drawing insights from Tritrichomonas foetus.

Authors:  Scott C Lenaghan; Stefan Nwandu-Vincent; Benjamin E Reese; Mingjun Zhang
Journal:  J R Soc Interface       Date:  2014-01-29       Impact factor: 4.118

3.  The repetitive cytoskeletal protein H49 of Trypanosoma cruzi is a calpain-like protein located at the flagellum attachment zone.

Authors:  Alexandra Galetović; Renata T Souza; Marcia R M Santos; Esteban M Cordero; Izabela M D Bastos; Jaime M Santana; Jeronimo C Ruiz; Fabio M Lima; Marjorie M Marini; Renato A Mortara; José Franco da Silveira
Journal:  PLoS One       Date:  2011-11-11       Impact factor: 3.240

4.  Sialic Acid Glycobiology Unveils Trypanosoma cruzi Trypomastigote Membrane Physiology.

Authors:  Andrés B Lantos; Giannina Carlevaro; Beatriz Araoz; Pablo Ruiz Diaz; María de Los Milagros Camara; Carlos A Buscaglia; Mariano Bossi; Hai Yu; Xi Chen; Carolyn R Bertozzi; Juan Mucci; Oscar Campetella
Journal:  PLoS Pathog       Date:  2016-04-08       Impact factor: 6.823

Review 5.  An historical perspective on how advances in microscopic imaging contributed to understanding the Leishmania Spp. and Trypanosoma cruzi host-parasite relationship.

Authors:  P T V Florentino; F Real; A Bonfim-Melo; C M Orikaza; E R Ferreira; C C Pessoa; B R Lima; G R S Sasso; R A Mortara
Journal:  Biomed Res Int       Date:  2014-04-27       Impact factor: 3.411

  5 in total

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