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Updated: Jul 17, 2026

Ultrastructural Expansion Microscopy in Three In Vitro Life Cycle Stages of Trypanosoma cruzi
Published on: May 12, 2023
Trypanosoma cruzi: attachment to perimicrovillar membrane glycoproteins of Rhodnius prolixus
C R Alves1, J M Albuquerque-Cunha, C B Mello
1Laboratório de Biologia Molecular e Doenças Endêmicas, Departamento de Bioquímica e Biologia Molecular, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, RJ, Brazil.
Abstract:
Studies were carried out to identify proteins involved in the interface of Trypanosoma cruzi with the perimicrovillar membranes (PMM) of Rhodnius prolixus. Video microscopy experiments demonstrated high level of adhesion of T. cruzi Dm 28c epimastigotes to the surface of posterior midgut cells of non-treated R. prolixus. The parasites however were unable to attach to gut cells obtained from decapitated or azadirachtin-treated insects. The influence of carbohydrates on the adhesion to insect midgut was confirmed by inhibition of parasite attachment after midgut incubation with N-acetylgalactosamine, N-acetylmannosamine, N-acetylglucosamine, D-galactose, D-mannose or sialic acid. We observed that hydrophobic proteins in the surface of epimastigotes bind to polypeptides with 47.7, 45.5, 44, 43, 40.5, 36, 31 and 13kDa from R. prolixus PMM and that pre-incubation of lectins specifically inhibited binding to 31, 40.5, 44 and 45.5kDa proteins. We suggest that glycoproteins from PMM and hydrophobic proteins from epimastigotes are important for the adhesion of the parasite to the posterior midgut cells of the vector.
Insights
Trypanosoma cruzi epimastigotes adhere to Rhodnius prolixus midgut cells via hydrophobic proteins interacting with perimicrovillar membrane glycoproteins, a process influenced by specific carbohydrates.
Area of Science:
- Parasitology
- Molecular Biology
- Vector Biology
Background:
- Trypanosoma cruzi is the causative agent of Chagas disease.
- Rhodnius prolixus is a primary vector for T. cruzi.
- Understanding parasite-vector interactions is crucial for disease control.
Purpose of the Study:
- To identify proteins mediating the adhesion of T. cruzi epimastigotes to the vector's midgut.
- To investigate the role of carbohydrates and specific proteins in this interaction.
Main Methods:
- Video microscopy to observe parasite adhesion to insect midgut cells.
- Inhibition assays using carbohydrates and lectins.
- Analysis of protein interactions between parasite and vector.
Main Results:
- T. cruzi epimastigotes showed high adhesion to non-treated R. prolixus posterior midgut cells.
- Adhesion was inhibited by specific carbohydrates (N-acetylgalactosamine, D-galactose, etc.).
- Hydrophobic epimastigote proteins bound to specific R. prolixus perimicrovillar membrane (PMM) polypeptides (e.g., 45.5, 44kDa).
Conclusions:
- Glycoproteins in the R. prolixus PMM and hydrophobic proteins on T. cruzi epimastigotes are key for parasite adhesion.
- Carbohydrate interactions play a significant role in mediating this attachment.
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