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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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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 |
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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 |
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