Cargando…

Sequestration of host metabolism by an intracellular pathogen

For intracellular pathogens, residence in a vacuole provides a shelter against cytosolic host defense to the cost of limited access to nutrients. The human pathogen Chlamydia trachomatis grows in a glycogen-rich vacuole. How this large polymer accumulates there is unknown. We reveal that host glycog...

Descripción completa

Detalles Bibliográficos
Autores principales: Gehre, Lena, Gorgette, Olivier, Perrinet, Stéphanie, Prevost, Marie-Christine, Ducatez, Mathieu, Giebel, Amanda M, Nelson, David E, Ball, Steven G, Subtil, Agathe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829429/
https://www.ncbi.nlm.nih.gov/pubmed/26981769
http://dx.doi.org/10.7554/eLife.12552
_version_ 1782426744522801152
author Gehre, Lena
Gorgette, Olivier
Perrinet, Stéphanie
Prevost, Marie-Christine
Ducatez, Mathieu
Giebel, Amanda M
Nelson, David E
Ball, Steven G
Subtil, Agathe
author_facet Gehre, Lena
Gorgette, Olivier
Perrinet, Stéphanie
Prevost, Marie-Christine
Ducatez, Mathieu
Giebel, Amanda M
Nelson, David E
Ball, Steven G
Subtil, Agathe
author_sort Gehre, Lena
collection PubMed
description For intracellular pathogens, residence in a vacuole provides a shelter against cytosolic host defense to the cost of limited access to nutrients. The human pathogen Chlamydia trachomatis grows in a glycogen-rich vacuole. How this large polymer accumulates there is unknown. We reveal that host glycogen stores shift to the vacuole through two pathways: bulk uptake from the cytoplasmic pool, and de novo synthesis. We provide evidence that bacterial glycogen metabolism enzymes are secreted into the vacuole lumen through type 3 secretion. Our data bring strong support to the following scenario: bacteria co-opt the host transporter SLC35D2 to import UDP-glucose into the vacuole, where it serves as substrate for de novo glycogen synthesis, through a remarkable adaptation of the bacterial glycogen synthase. Based on these findings we propose that parasitophorous vacuoles not only offer protection but also provide a microorganism-controlled metabolically active compartment essential for redirecting host resources to the pathogens. DOI: http://dx.doi.org/10.7554/eLife.12552.001
format Online
Article
Text
id pubmed-4829429
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-48294292016-04-15 Sequestration of host metabolism by an intracellular pathogen Gehre, Lena Gorgette, Olivier Perrinet, Stéphanie Prevost, Marie-Christine Ducatez, Mathieu Giebel, Amanda M Nelson, David E Ball, Steven G Subtil, Agathe eLife Cell Biology For intracellular pathogens, residence in a vacuole provides a shelter against cytosolic host defense to the cost of limited access to nutrients. The human pathogen Chlamydia trachomatis grows in a glycogen-rich vacuole. How this large polymer accumulates there is unknown. We reveal that host glycogen stores shift to the vacuole through two pathways: bulk uptake from the cytoplasmic pool, and de novo synthesis. We provide evidence that bacterial glycogen metabolism enzymes are secreted into the vacuole lumen through type 3 secretion. Our data bring strong support to the following scenario: bacteria co-opt the host transporter SLC35D2 to import UDP-glucose into the vacuole, where it serves as substrate for de novo glycogen synthesis, through a remarkable adaptation of the bacterial glycogen synthase. Based on these findings we propose that parasitophorous vacuoles not only offer protection but also provide a microorganism-controlled metabolically active compartment essential for redirecting host resources to the pathogens. DOI: http://dx.doi.org/10.7554/eLife.12552.001 eLife Sciences Publications, Ltd 2016-03-16 /pmc/articles/PMC4829429/ /pubmed/26981769 http://dx.doi.org/10.7554/eLife.12552 Text en © 2016, Gehre et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Gehre, Lena
Gorgette, Olivier
Perrinet, Stéphanie
Prevost, Marie-Christine
Ducatez, Mathieu
Giebel, Amanda M
Nelson, David E
Ball, Steven G
Subtil, Agathe
Sequestration of host metabolism by an intracellular pathogen
title Sequestration of host metabolism by an intracellular pathogen
title_full Sequestration of host metabolism by an intracellular pathogen
title_fullStr Sequestration of host metabolism by an intracellular pathogen
title_full_unstemmed Sequestration of host metabolism by an intracellular pathogen
title_short Sequestration of host metabolism by an intracellular pathogen
title_sort sequestration of host metabolism by an intracellular pathogen
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829429/
https://www.ncbi.nlm.nih.gov/pubmed/26981769
http://dx.doi.org/10.7554/eLife.12552
work_keys_str_mv AT gehrelena sequestrationofhostmetabolismbyanintracellularpathogen
AT gorgetteolivier sequestrationofhostmetabolismbyanintracellularpathogen
AT perrinetstephanie sequestrationofhostmetabolismbyanintracellularpathogen
AT prevostmariechristine sequestrationofhostmetabolismbyanintracellularpathogen
AT ducatezmathieu sequestrationofhostmetabolismbyanintracellularpathogen
AT giebelamandam sequestrationofhostmetabolismbyanintracellularpathogen
AT nelsondavide sequestrationofhostmetabolismbyanintracellularpathogen
AT ballsteveng sequestrationofhostmetabolismbyanintracellularpathogen
AT subtilagathe sequestrationofhostmetabolismbyanintracellularpathogen