Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology

Polyamines are essential for Trypanosoma cruzi, the causative agent of Chagas disease. As T. cruzi behaves as a natural auxotrophic organism, it relies on host polyamines biosynthesis. In this paper we obtained a double-transfected T. cruzi parasite that expresses the green fluorescent protein (GFP)...

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Publicado: 2011
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_20900406_v2011_n1_p_Barclay
http://hdl.handle.net/20.500.12110/paper_20900406_v2011_n1_p_Barclay
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spelling paper:paper_20900406_v2011_n1_p_Barclay2023-06-08T16:34:17Z Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology green fluorescent protein ornithine ornithine decarboxylase polyamine animal cell article auxotrophy Chagas disease controlled study enzyme activity enzyme kinetics fluorescence analysis genetic transfection nonhuman parasite survival parasite transmission pathogenesis priority journal protein expression Trypanosoma cruzi Vero cell Trypanosoma cruzi Polyamines are essential for Trypanosoma cruzi, the causative agent of Chagas disease. As T. cruzi behaves as a natural auxotrophic organism, it relies on host polyamines biosynthesis. In this paper we obtained a double-transfected T. cruzi parasite that expresses the green fluorescent protein (GFP) and a heterologous ornithine decarboxylase (ODC), used itself as a novel selectable marker. These autotrophic and fluorescent parasites were characterized; the ODC presented an apparent Km for ornithine of 0.51 0.16 mM and an estimated Vvalue of 476.2 nmoles/h/mg of protein. These expressing ODC parasites showed higher metacyclogenesis capacity than the auxotrophic counterpart, supporting the idea that polyamines are engaged in this process. This double-transfected T. cruzi parasite results in a powerful tool - easy to follow by its fluorescence - to study the role of polyamines in Chagas disease pathology and in related processes such as parasite survival, invasion, proliferation, metacyclogenesis, and tissue spreading. © 2011 Jeremías José Barclay et al. 2011 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_20900406_v2011_n1_p_Barclay http://hdl.handle.net/20.500.12110/paper_20900406_v2011_n1_p_Barclay
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic green fluorescent protein
ornithine
ornithine decarboxylase
polyamine
animal cell
article
auxotrophy
Chagas disease
controlled study
enzyme activity
enzyme kinetics
fluorescence analysis
genetic transfection
nonhuman
parasite survival
parasite transmission
pathogenesis
priority journal
protein expression
Trypanosoma cruzi
Vero cell
Trypanosoma cruzi
spellingShingle green fluorescent protein
ornithine
ornithine decarboxylase
polyamine
animal cell
article
auxotrophy
Chagas disease
controlled study
enzyme activity
enzyme kinetics
fluorescence analysis
genetic transfection
nonhuman
parasite survival
parasite transmission
pathogenesis
priority journal
protein expression
Trypanosoma cruzi
Vero cell
Trypanosoma cruzi
Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology
topic_facet green fluorescent protein
ornithine
ornithine decarboxylase
polyamine
animal cell
article
auxotrophy
Chagas disease
controlled study
enzyme activity
enzyme kinetics
fluorescence analysis
genetic transfection
nonhuman
parasite survival
parasite transmission
pathogenesis
priority journal
protein expression
Trypanosoma cruzi
Vero cell
Trypanosoma cruzi
description Polyamines are essential for Trypanosoma cruzi, the causative agent of Chagas disease. As T. cruzi behaves as a natural auxotrophic organism, it relies on host polyamines biosynthesis. In this paper we obtained a double-transfected T. cruzi parasite that expresses the green fluorescent protein (GFP) and a heterologous ornithine decarboxylase (ODC), used itself as a novel selectable marker. These autotrophic and fluorescent parasites were characterized; the ODC presented an apparent Km for ornithine of 0.51 0.16 mM and an estimated Vvalue of 476.2 nmoles/h/mg of protein. These expressing ODC parasites showed higher metacyclogenesis capacity than the auxotrophic counterpart, supporting the idea that polyamines are engaged in this process. This double-transfected T. cruzi parasite results in a powerful tool - easy to follow by its fluorescence - to study the role of polyamines in Chagas disease pathology and in related processes such as parasite survival, invasion, proliferation, metacyclogenesis, and tissue spreading. © 2011 Jeremías José Barclay et al.
title Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology
title_short Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology
title_full Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology
title_fullStr Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology
title_full_unstemmed Trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology
title_sort trypanosoma cruzi coexpressing ornithine decarboxylase and green fluorescence proteins as a tool to study the role of polyamines in chagas disease pathology
publishDate 2011
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_20900406_v2011_n1_p_Barclay
http://hdl.handle.net/20.500.12110/paper_20900406_v2011_n1_p_Barclay
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