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The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network

Many intracellular pathogens subvert host membrane trafficking pathways to promote their replication. Toxoplasma multiplies in a membrane-bound parasitophorous vacuole (PV) that interacts with mammalian host organelles and intercepts Golgi Rab vesicles to acquire sphingolipids. The mechanisms of hos...

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Autores principales: Romano, Julia D., Nolan, Sabrina J., Porter, Corey, Ehrenman, Karen, Hartman, Eric J., Hsia, Ru-ching, Coppens, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716271/
https://www.ncbi.nlm.nih.gov/pubmed/29070609
http://dx.doi.org/10.1083/jcb.201701108
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author Romano, Julia D.
Nolan, Sabrina J.
Porter, Corey
Ehrenman, Karen
Hartman, Eric J.
Hsia, Ru-ching
Coppens, Isabelle
author_facet Romano, Julia D.
Nolan, Sabrina J.
Porter, Corey
Ehrenman, Karen
Hartman, Eric J.
Hsia, Ru-ching
Coppens, Isabelle
author_sort Romano, Julia D.
collection PubMed
description Many intracellular pathogens subvert host membrane trafficking pathways to promote their replication. Toxoplasma multiplies in a membrane-bound parasitophorous vacuole (PV) that interacts with mammalian host organelles and intercepts Golgi Rab vesicles to acquire sphingolipids. The mechanisms of host vesicle internalization and processing within the PV remain undefined. We demonstrate that Toxoplasma sequesters a broad range of Rab vesicles into the PV. Correlative light and electron microscopy analysis of infected cells illustrates that intravacuolar Rab1A vesicles are surrounded by the PV membrane, suggesting a phagocytic-like process for vesicle engulfment. Rab11A vesicles concentrate to an intravacuolar network (IVN), but this is reduced in Δgra2 and Δgra2Δgra6 parasites, suggesting that tubules stabilized by the TgGRA2 and TgGRA6 proteins secreted by the parasite within the PV contribute to host vesicle sequestration. Overexpression of a phospholipase TgLCAT, which is localized to the IVN, results in a decrease in the number of intravacuolar GFP-Rab11A vesicles, suggesting that TgLCAT controls lipolytic degradation of Rab vesicles for cargo release.
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spelling pubmed-57162712018-06-04 The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network Romano, Julia D. Nolan, Sabrina J. Porter, Corey Ehrenman, Karen Hartman, Eric J. Hsia, Ru-ching Coppens, Isabelle J Cell Biol Research Articles Many intracellular pathogens subvert host membrane trafficking pathways to promote their replication. Toxoplasma multiplies in a membrane-bound parasitophorous vacuole (PV) that interacts with mammalian host organelles and intercepts Golgi Rab vesicles to acquire sphingolipids. The mechanisms of host vesicle internalization and processing within the PV remain undefined. We demonstrate that Toxoplasma sequesters a broad range of Rab vesicles into the PV. Correlative light and electron microscopy analysis of infected cells illustrates that intravacuolar Rab1A vesicles are surrounded by the PV membrane, suggesting a phagocytic-like process for vesicle engulfment. Rab11A vesicles concentrate to an intravacuolar network (IVN), but this is reduced in Δgra2 and Δgra2Δgra6 parasites, suggesting that tubules stabilized by the TgGRA2 and TgGRA6 proteins secreted by the parasite within the PV contribute to host vesicle sequestration. Overexpression of a phospholipase TgLCAT, which is localized to the IVN, results in a decrease in the number of intravacuolar GFP-Rab11A vesicles, suggesting that TgLCAT controls lipolytic degradation of Rab vesicles for cargo release. The Rockefeller University Press 2017-12-04 /pmc/articles/PMC5716271/ /pubmed/29070609 http://dx.doi.org/10.1083/jcb.201701108 Text en © 2017 Romano et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Romano, Julia D.
Nolan, Sabrina J.
Porter, Corey
Ehrenman, Karen
Hartman, Eric J.
Hsia, Ru-ching
Coppens, Isabelle
The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network
title The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network
title_full The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network
title_fullStr The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network
title_full_unstemmed The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network
title_short The parasite Toxoplasma sequesters diverse Rab host vesicles within an intravacuolar network
title_sort parasite toxoplasma sequesters diverse rab host vesicles within an intravacuolar network
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716271/
https://www.ncbi.nlm.nih.gov/pubmed/29070609
http://dx.doi.org/10.1083/jcb.201701108
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