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Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline

Trypanosoma brucei, a protist responsible for human African trypanosomiasis (sleeping sickness), is transmitted by the tsetse fly where the procyclic forms of the parasite develop in the proline-rich (1–2 mM) and glucose-depleted digestive tract. Proline is essential for the midgut colonization of t...

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Autores principales: Villafraz, Oriana, Biran, Marc, Pineda, Erika, Plazolles, Nicolas, Cahoreau, Edern, Ornitz Oliveira Souza, Rodolpho, Thonnus, Magali, Allmann, Stefan, Tetaud, Emmanuel, Rivière, Loïc, Silber, Ariel M., Barrett, Michael P., Zíková, Alena, Boshart, Michael, Portais, Jean-Charles, Bringaud, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951978/
https://www.ncbi.nlm.nih.gov/pubmed/33647053
http://dx.doi.org/10.1371/journal.ppat.1009204
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author Villafraz, Oriana
Biran, Marc
Pineda, Erika
Plazolles, Nicolas
Cahoreau, Edern
Ornitz Oliveira Souza, Rodolpho
Thonnus, Magali
Allmann, Stefan
Tetaud, Emmanuel
Rivière, Loïc
Silber, Ariel M.
Barrett, Michael P.
Zíková, Alena
Boshart, Michael
Portais, Jean-Charles
Bringaud, Frédéric
author_facet Villafraz, Oriana
Biran, Marc
Pineda, Erika
Plazolles, Nicolas
Cahoreau, Edern
Ornitz Oliveira Souza, Rodolpho
Thonnus, Magali
Allmann, Stefan
Tetaud, Emmanuel
Rivière, Loïc
Silber, Ariel M.
Barrett, Michael P.
Zíková, Alena
Boshart, Michael
Portais, Jean-Charles
Bringaud, Frédéric
author_sort Villafraz, Oriana
collection PubMed
description Trypanosoma brucei, a protist responsible for human African trypanosomiasis (sleeping sickness), is transmitted by the tsetse fly where the procyclic forms of the parasite develop in the proline-rich (1–2 mM) and glucose-depleted digestive tract. Proline is essential for the midgut colonization of the parasite in the insect vector, however other carbon sources could be available and used to feed its central metabolism. Here we show that procyclic trypanosomes can consume and metabolize metabolic intermediates, including those excreted from glucose catabolism (succinate, alanine and pyruvate), with the exception of acetate, which is the ultimate end-product excreted by the parasite. Among the tested metabolites, tricarboxylic acid (TCA) cycle intermediates (succinate, malate and α-ketoglutarate) stimulated growth of the parasite in the presence of 2 mM proline. The pathways used for their metabolism were mapped by proton-NMR metabolic profiling and phenotypic analyses of thirteen RNAi and/or null mutants affecting central carbon metabolism. We showed that (i) malate is converted to succinate by both the reducing and oxidative branches of the TCA cycle, which demonstrates that procyclic trypanosomes can use the full TCA cycle, (ii) the enormous rate of α-ketoglutarate consumption (15-times higher than glucose) is possible thanks to the balanced production and consumption of NADH at the substrate level and (iii) α-ketoglutarate is toxic for trypanosomes if not appropriately metabolized as observed for an α-ketoglutarate dehydrogenase null mutant. In addition, epimastigotes produced from procyclics upon overexpression of RBP6 showed a growth defect in the presence of 2 mM proline, which is rescued by α-ketoglutarate, suggesting that physiological amounts of proline are not sufficient per se for the development of trypanosomes in the fly. In conclusion, these data show that trypanosomes can metabolize multiple metabolites, in addition to proline, which allows them to confront challenging environments in the fly.
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spelling pubmed-79519782021-03-22 Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline Villafraz, Oriana Biran, Marc Pineda, Erika Plazolles, Nicolas Cahoreau, Edern Ornitz Oliveira Souza, Rodolpho Thonnus, Magali Allmann, Stefan Tetaud, Emmanuel Rivière, Loïc Silber, Ariel M. Barrett, Michael P. Zíková, Alena Boshart, Michael Portais, Jean-Charles Bringaud, Frédéric PLoS Pathog Research Article Trypanosoma brucei, a protist responsible for human African trypanosomiasis (sleeping sickness), is transmitted by the tsetse fly where the procyclic forms of the parasite develop in the proline-rich (1–2 mM) and glucose-depleted digestive tract. Proline is essential for the midgut colonization of the parasite in the insect vector, however other carbon sources could be available and used to feed its central metabolism. Here we show that procyclic trypanosomes can consume and metabolize metabolic intermediates, including those excreted from glucose catabolism (succinate, alanine and pyruvate), with the exception of acetate, which is the ultimate end-product excreted by the parasite. Among the tested metabolites, tricarboxylic acid (TCA) cycle intermediates (succinate, malate and α-ketoglutarate) stimulated growth of the parasite in the presence of 2 mM proline. The pathways used for their metabolism were mapped by proton-NMR metabolic profiling and phenotypic analyses of thirteen RNAi and/or null mutants affecting central carbon metabolism. We showed that (i) malate is converted to succinate by both the reducing and oxidative branches of the TCA cycle, which demonstrates that procyclic trypanosomes can use the full TCA cycle, (ii) the enormous rate of α-ketoglutarate consumption (15-times higher than glucose) is possible thanks to the balanced production and consumption of NADH at the substrate level and (iii) α-ketoglutarate is toxic for trypanosomes if not appropriately metabolized as observed for an α-ketoglutarate dehydrogenase null mutant. In addition, epimastigotes produced from procyclics upon overexpression of RBP6 showed a growth defect in the presence of 2 mM proline, which is rescued by α-ketoglutarate, suggesting that physiological amounts of proline are not sufficient per se for the development of trypanosomes in the fly. In conclusion, these data show that trypanosomes can metabolize multiple metabolites, in addition to proline, which allows them to confront challenging environments in the fly. Public Library of Science 2021-03-01 /pmc/articles/PMC7951978/ /pubmed/33647053 http://dx.doi.org/10.1371/journal.ppat.1009204 Text en © 2021 Villafraz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Villafraz, Oriana
Biran, Marc
Pineda, Erika
Plazolles, Nicolas
Cahoreau, Edern
Ornitz Oliveira Souza, Rodolpho
Thonnus, Magali
Allmann, Stefan
Tetaud, Emmanuel
Rivière, Loïc
Silber, Ariel M.
Barrett, Michael P.
Zíková, Alena
Boshart, Michael
Portais, Jean-Charles
Bringaud, Frédéric
Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline
title Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline
title_full Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline
title_fullStr Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline
title_full_unstemmed Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline
title_short Procyclic trypanosomes recycle glucose catabolites and TCA cycle intermediates to stimulate growth in the presence of physiological amounts of proline
title_sort procyclic trypanosomes recycle glucose catabolites and tca cycle intermediates to stimulate growth in the presence of physiological amounts of proline
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951978/
https://www.ncbi.nlm.nih.gov/pubmed/33647053
http://dx.doi.org/10.1371/journal.ppat.1009204
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