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Establishment of Larval Zebrafish as an Animal Model to Investigate Trypanosoma cruzi Motility In Vivo
Published on: September 30, 2017
[The mammalian TOR pathway is present in Trypanosoma cruzi. In silico reconstruction and possible functions]
Fabio A Digirolamo1, Mariana R Miranda, León A Bouvier
1Laboratorio de Biología Molecular de Trypanosoma cruzi, Instituto de Investigaciones Médicas Alfredo Lanari, Buenos Aires.
Abstract:
The mammalian TOR pathway ("Target Of Rapamycin") is a regulatory protein network involved in a wide range of processes including cell growth and differentiation, providing a functional switch between anabolic and catabolic cell metabolism. Trypanosoma cruzi, the etiologic agent of Chagas disease, has a complex life cycle with different morphological stages in various hosts. This life cycle implies that parasites have to deal with fluctuations in the extracellular medium that should be detected and counteracted adapting their metabolism. A candidate to be the mediator between the receptors / sensors of the environment and cellular adaptive response is the TOR pathway. In this paper we integrate the bibliographic data of the TOR pathway in trypanosomatids by in silico analysis (computer simulation of biological structures and processes) of the parasite's genome. Possible effectors and processes regulated by this metabolic pathway are also proposed. Given that the information on the mechanisms of signal transduction in trypanosomatids is scarce, we consider the model presented in this work may be a reference for future experimental work.
Insights
The Target Of Rapamycin (TOR) pathway regulates cell metabolism and growth. This study models the TOR pathway in Trypanosoma cruzi, offering insights into parasite adaptation and potential therapeutic targets for Chagas disease.
Area of Science:
- Molecular Biology
- Parasitology
- Bioinformatics
Background:
- The Target Of Rapamycin (TOR) pathway is crucial for regulating cell growth, metabolism, and adaptation in eukaryotes.
- Trypanosoma cruzi, the parasite causing Chagas disease, exhibits a complex life cycle requiring metabolic adaptation to environmental fluctuations.
- Understanding signal transduction in trypanosomatids is limited, hindering the development of targeted interventions.
Purpose of the Study:
- To investigate the role and components of the TOR pathway in Trypanosoma cruzi.
- To integrate existing data and perform in silico analysis of the parasite's genome for TOR pathway components.
- To propose potential effectors and processes regulated by the TOR pathway in this parasite.
Main Methods:
- Bibliographic data integration.
- In silico analysis of the Trypanosoma cruzi genome.
- Bioinformatic approaches for pathway modeling.
Main Results:
- Identification and characterization of potential TOR pathway components in Trypanosoma cruzi.
- In silico model of the TOR pathway, predicting its involvement in parasite adaptation.
- Hypothesized effectors and regulated processes offer a framework for future research.
Conclusions:
- The TOR pathway is a likely mediator of environmental sensing and metabolic adaptation in Trypanosoma cruzi.
- The presented in silico model serves as a foundation for experimental validation.
- This research provides a reference for future studies on signal transduction in trypanosomatids and potential Chagas disease therapeutics.
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