Cargando…

Glycerol suppresses glucose consumption in trypanosomes through metabolic contest

Microorganisms must make the right choice for nutrient consumption to adapt to their changing environment. As a consequence, bacteria and yeasts have developed regulatory mechanisms involving nutrient sensing and signaling, known as “catabolite repression,” allowing redirection of cell metabolism to...

Descripción completa

Detalles Bibliográficos
Autores principales: Allmann, Stefan, Wargnies, Marion, Plazolles, Nicolas, Cahoreau, Edern, Biran, Marc, Morand, Pauline, Pineda, Erika, Kulyk, Hanna, Asencio, Corinne, Villafraz, Oriana, Rivière, Loïc, Tetaud, Emmanuel, Rotureau, Brice, Mourier, Arnaud, 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/PMC8386887/
https://www.ncbi.nlm.nih.gov/pubmed/34388147
http://dx.doi.org/10.1371/journal.pbio.3001359
_version_ 1783742340800708608
author Allmann, Stefan
Wargnies, Marion
Plazolles, Nicolas
Cahoreau, Edern
Biran, Marc
Morand, Pauline
Pineda, Erika
Kulyk, Hanna
Asencio, Corinne
Villafraz, Oriana
Rivière, Loïc
Tetaud, Emmanuel
Rotureau, Brice
Mourier, Arnaud
Portais, Jean-Charles
Bringaud, Frédéric
author_facet Allmann, Stefan
Wargnies, Marion
Plazolles, Nicolas
Cahoreau, Edern
Biran, Marc
Morand, Pauline
Pineda, Erika
Kulyk, Hanna
Asencio, Corinne
Villafraz, Oriana
Rivière, Loïc
Tetaud, Emmanuel
Rotureau, Brice
Mourier, Arnaud
Portais, Jean-Charles
Bringaud, Frédéric
author_sort Allmann, Stefan
collection PubMed
description Microorganisms must make the right choice for nutrient consumption to adapt to their changing environment. As a consequence, bacteria and yeasts have developed regulatory mechanisms involving nutrient sensing and signaling, known as “catabolite repression,” allowing redirection of cell metabolism to maximize the consumption of an energy-efficient carbon source. Here, we report a new mechanism named “metabolic contest” for regulating the use of carbon sources without nutrient sensing and signaling. Trypanosoma brucei is a unicellular eukaryote transmitted by tsetse flies and causing human African trypanosomiasis, or sleeping sickness. We showed that, in contrast to most microorganisms, the insect stages of this parasite developed a preference for glycerol over glucose, with glucose consumption beginning after the depletion of glycerol present in the medium. This “metabolic contest” depends on the combination of 3 conditions: (i) the sequestration of both metabolic pathways in the same subcellular compartment, here in the peroxisomal-related organelles named glycosomes; (ii) the competition for the same substrate, here ATP, with the first enzymatic step of the glycerol and glucose metabolic pathways both being ATP-dependent (glycerol kinase and hexokinase, respectively); and (iii) an unbalanced activity between the competing enzymes, here the glycerol kinase activity being approximately 80-fold higher than the hexokinase activity. As predicted by our model, an approximately 50-fold down-regulation of the GK expression abolished the preference for glycerol over glucose, with glucose and glycerol being metabolized concomitantly. In theory, a metabolic contest could be found in any organism provided that the 3 conditions listed above are met.
format Online
Article
Text
id pubmed-8386887
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-83868872021-08-26 Glycerol suppresses glucose consumption in trypanosomes through metabolic contest Allmann, Stefan Wargnies, Marion Plazolles, Nicolas Cahoreau, Edern Biran, Marc Morand, Pauline Pineda, Erika Kulyk, Hanna Asencio, Corinne Villafraz, Oriana Rivière, Loïc Tetaud, Emmanuel Rotureau, Brice Mourier, Arnaud Portais, Jean-Charles Bringaud, Frédéric PLoS Biol Research Article Microorganisms must make the right choice for nutrient consumption to adapt to their changing environment. As a consequence, bacteria and yeasts have developed regulatory mechanisms involving nutrient sensing and signaling, known as “catabolite repression,” allowing redirection of cell metabolism to maximize the consumption of an energy-efficient carbon source. Here, we report a new mechanism named “metabolic contest” for regulating the use of carbon sources without nutrient sensing and signaling. Trypanosoma brucei is a unicellular eukaryote transmitted by tsetse flies and causing human African trypanosomiasis, or sleeping sickness. We showed that, in contrast to most microorganisms, the insect stages of this parasite developed a preference for glycerol over glucose, with glucose consumption beginning after the depletion of glycerol present in the medium. This “metabolic contest” depends on the combination of 3 conditions: (i) the sequestration of both metabolic pathways in the same subcellular compartment, here in the peroxisomal-related organelles named glycosomes; (ii) the competition for the same substrate, here ATP, with the first enzymatic step of the glycerol and glucose metabolic pathways both being ATP-dependent (glycerol kinase and hexokinase, respectively); and (iii) an unbalanced activity between the competing enzymes, here the glycerol kinase activity being approximately 80-fold higher than the hexokinase activity. As predicted by our model, an approximately 50-fold down-regulation of the GK expression abolished the preference for glycerol over glucose, with glucose and glycerol being metabolized concomitantly. In theory, a metabolic contest could be found in any organism provided that the 3 conditions listed above are met. Public Library of Science 2021-08-13 /pmc/articles/PMC8386887/ /pubmed/34388147 http://dx.doi.org/10.1371/journal.pbio.3001359 Text en © 2021 Allmann et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Allmann, Stefan
Wargnies, Marion
Plazolles, Nicolas
Cahoreau, Edern
Biran, Marc
Morand, Pauline
Pineda, Erika
Kulyk, Hanna
Asencio, Corinne
Villafraz, Oriana
Rivière, Loïc
Tetaud, Emmanuel
Rotureau, Brice
Mourier, Arnaud
Portais, Jean-Charles
Bringaud, Frédéric
Glycerol suppresses glucose consumption in trypanosomes through metabolic contest
title Glycerol suppresses glucose consumption in trypanosomes through metabolic contest
title_full Glycerol suppresses glucose consumption in trypanosomes through metabolic contest
title_fullStr Glycerol suppresses glucose consumption in trypanosomes through metabolic contest
title_full_unstemmed Glycerol suppresses glucose consumption in trypanosomes through metabolic contest
title_short Glycerol suppresses glucose consumption in trypanosomes through metabolic contest
title_sort glycerol suppresses glucose consumption in trypanosomes through metabolic contest
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386887/
https://www.ncbi.nlm.nih.gov/pubmed/34388147
http://dx.doi.org/10.1371/journal.pbio.3001359
work_keys_str_mv AT allmannstefan glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT wargniesmarion glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT plazollesnicolas glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT cahoreauedern glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT biranmarc glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT morandpauline glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT pinedaerika glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT kulykhanna glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT asenciocorinne glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT villafrazoriana glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT riviereloic glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT tetaudemmanuel glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT rotureaubrice glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT mourierarnaud glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT portaisjeancharles glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest
AT bringaudfrederic glycerolsuppressesglucoseconsumptionintrypanosomesthroughmetaboliccontest