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Correlative light and electron microscopy of wall formation in Eimeria nieschulzi.
Wiedmer, Stefanie; Kurth, Thomas; Buder, Ulrike; Bleischwitz, Sinja; Entzeroth, Rolf; Kurth, Michael.
Afiliação
  • Wiedmer S; Faculty of Biology, Institute of Zoology, Technische Universität Dresden, Zellescher Weg 20 B, 01217, Dresden, Germany. stefanie.wiedmer@gmx.de.
  • Kurth T; Center for Molecular and Cellular Bioengineering (CMCB), Technology Platform, Technische Universität Dresden, Fetscherstraße 105, 01307, Dresden, Germany.
  • Buder U; Faculty of Biology, Institute of Zoology, Technische Universität Dresden, Zellescher Weg 20 B, 01217, Dresden, Germany.
  • Bleischwitz S; Faculty of Biology, Institute of Zoology, Technische Universität Dresden, Zellescher Weg 20 B, 01217, Dresden, Germany.
  • Entzeroth R; Faculty of Biology, Institute of Zoology, Technische Universität Dresden, Zellescher Weg 20 B, 01217, Dresden, Germany.
  • Kurth M; Faculty of Biology, Institute of Zoology, Technische Universität Dresden, Zellescher Weg 20 B, 01217, Dresden, Germany. kurth.michael@googlemail.com.
Parasitol Res ; 119(8): 2667-2678, 2020 Aug.
Article em En | MEDLINE | ID: mdl-32627078
ABSTRACT
Coccidian parasites possess complex life cycles involving asexual proliferation followed by sexual development leading to the production of oocysts. Coccidian oocysts are persistent stages which are secreted by the feces and transmitted from host to host guaranteeing life cycle progression and disease transmission. The robust bilayered oocyst wall is formed from the contents of two organelles, the wall-forming bodies type I and II (WFBI, WFBII), located exclusively in the macrogametocyte. Eimeria nieschulzi has been used as a model parasite to study and follow gametocyte and oocyst development. In this study, the gametocyte and oocyst wall formation of E. nieschulzi was analyzed by electron microscopy and immuno-histology. A monoclonal antibody raised against the macrogametocytes of E. nieschulzi identified a tyrosine-rich glycoprotein (EnGAM82) located in WFBII. Correlative light and electron microscopy was used to examine the vesicle-specific localization and spatial distribution of GAM82-proteins during macrogametocyte maturation by this monoclonal antibody. In early and mid-stages, the GAM82-protein is ubiquitously distributed in WFBII. Few hours later, the protein is arranged in subvesicular structures. It was possible to show that the substructure of WFBII and the spatial distribution of GAM82-proteins probably represent pre-synthesized cross-linked materials prior to the inner oocyst wall formation. Dityrosine-cross-linked gametocyte proteins can also be confirmed and visualized by fluorescence microscopy (UV light, autofluorescence of WFBII).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eimeria Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Parasitol Res Assunto da revista: PARASITOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Eimeria Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Parasitol Res Assunto da revista: PARASITOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha
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