Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins

<jats:p><jats:italic>Toxoplasma gondii</jats:italic> is a master manipulator capable of effectively siphoning the resources from the host cell for its intracellular subsistence. However, the molecular underpinnings of how the parasite gains resources from its host remain largely un...

Full description

Bibliographic Details
Main Authors: Rivera-Cuevas, Yolanda, Mayoral, Joshua, Di Cristina, Manlio, Lawrence, Anna-Lisa E, Olafsson, Einar B, Patel, Romir K, Thornhill, Dishari, Waldman, Benjamin S, Ono, Akira, Sexton, Jonathan Z, Lourido, Sebastian, Weiss, Louis M, Carruthers, Vern B
Other Authors: Massachusetts Institute of Technology. Department of Biology
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022
Online Access:https://hdl.handle.net/1721.1/146900
_version_ 1811077286461440000
author Rivera-Cuevas, Yolanda
Mayoral, Joshua
Di Cristina, Manlio
Lawrence, Anna-Lisa E
Olafsson, Einar B
Patel, Romir K
Thornhill, Dishari
Waldman, Benjamin S
Ono, Akira
Sexton, Jonathan Z
Lourido, Sebastian
Weiss, Louis M
Carruthers, Vern B
author2 Massachusetts Institute of Technology. Department of Biology
author_facet Massachusetts Institute of Technology. Department of Biology
Rivera-Cuevas, Yolanda
Mayoral, Joshua
Di Cristina, Manlio
Lawrence, Anna-Lisa E
Olafsson, Einar B
Patel, Romir K
Thornhill, Dishari
Waldman, Benjamin S
Ono, Akira
Sexton, Jonathan Z
Lourido, Sebastian
Weiss, Louis M
Carruthers, Vern B
author_sort Rivera-Cuevas, Yolanda
collection MIT
description <jats:p><jats:italic>Toxoplasma gondii</jats:italic> is a master manipulator capable of effectively siphoning the resources from the host cell for its intracellular subsistence. However, the molecular underpinnings of how the parasite gains resources from its host remain largely unknown. Residing within a non-fusogenic parasitophorous vacuole (PV), the parasite must acquire resources across the limiting membrane of its replicative niche, which is decorated with parasite proteins including those secreted from dense granules. We discovered a role for the host Endosomal Sorting Complex Required for Transport (ESCRT) machinery in host cytosolic protein uptake by <jats:italic>T</jats:italic>. <jats:italic>gondii</jats:italic> by disrupting host ESCRT function. We identified the transmembrane dense granule protein TgGRA14, which contains motifs homologous to the late domain motifs of HIV-1 Gag, as a candidate for the recruitment of the host ESCRT machinery to the PV membrane. Using an HIV-1 virus-like particle (VLP) release assay, we found that the motif-containing portion of TgGRA14 is sufficient to substitute for HIV-1 Gag late domain to mediate ESCRT-dependent VLP budding. We also show that TgGRA14 is proximal to and interacts with host ESCRT components and other dense granule proteins during infection. Furthermore, analysis of TgGRA14-deficient parasites revealed a marked reduction in ingestion of a host cytosolic protein compared to WT parasites. Thus, we propose a model in which <jats:italic>T</jats:italic>. <jats:italic>gondii</jats:italic> recruits the host ESCRT machinery to the PV where it can interact with TgGRA14 for the internalization of host cytosolic proteins across the PV membrane (PVM). These findings provide new insight into how <jats:italic>T</jats:italic>. <jats:italic>gondii</jats:italic> accesses contents of the host cytosol by exploiting a key pathway for vesicular budding and membrane scission.</jats:p>
first_indexed 2024-09-23T10:40:32Z
format Article
id mit-1721.1/146900
institution Massachusetts Institute of Technology
language English
last_indexed 2024-09-23T10:40:32Z
publishDate 2022
publisher Public Library of Science (PLoS)
record_format dspace
spelling mit-1721.1/1469002022-12-17T03:34:28Z Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins Rivera-Cuevas, Yolanda Mayoral, Joshua Di Cristina, Manlio Lawrence, Anna-Lisa E Olafsson, Einar B Patel, Romir K Thornhill, Dishari Waldman, Benjamin S Ono, Akira Sexton, Jonathan Z Lourido, Sebastian Weiss, Louis M Carruthers, Vern B Massachusetts Institute of Technology. Department of Biology <jats:p><jats:italic>Toxoplasma gondii</jats:italic> is a master manipulator capable of effectively siphoning the resources from the host cell for its intracellular subsistence. However, the molecular underpinnings of how the parasite gains resources from its host remain largely unknown. Residing within a non-fusogenic parasitophorous vacuole (PV), the parasite must acquire resources across the limiting membrane of its replicative niche, which is decorated with parasite proteins including those secreted from dense granules. We discovered a role for the host Endosomal Sorting Complex Required for Transport (ESCRT) machinery in host cytosolic protein uptake by <jats:italic>T</jats:italic>. <jats:italic>gondii</jats:italic> by disrupting host ESCRT function. We identified the transmembrane dense granule protein TgGRA14, which contains motifs homologous to the late domain motifs of HIV-1 Gag, as a candidate for the recruitment of the host ESCRT machinery to the PV membrane. Using an HIV-1 virus-like particle (VLP) release assay, we found that the motif-containing portion of TgGRA14 is sufficient to substitute for HIV-1 Gag late domain to mediate ESCRT-dependent VLP budding. We also show that TgGRA14 is proximal to and interacts with host ESCRT components and other dense granule proteins during infection. Furthermore, analysis of TgGRA14-deficient parasites revealed a marked reduction in ingestion of a host cytosolic protein compared to WT parasites. Thus, we propose a model in which <jats:italic>T</jats:italic>. <jats:italic>gondii</jats:italic> recruits the host ESCRT machinery to the PV where it can interact with TgGRA14 for the internalization of host cytosolic proteins across the PV membrane (PVM). These findings provide new insight into how <jats:italic>T</jats:italic>. <jats:italic>gondii</jats:italic> accesses contents of the host cytosol by exploiting a key pathway for vesicular budding and membrane scission.</jats:p> 2022-12-16T17:40:02Z 2022-12-16T17:40:02Z 2021 2022-12-16T17:36:15Z Article http://purl.org/eprint/type/JournalArticle https://hdl.handle.net/1721.1/146900 Rivera-Cuevas, Yolanda, Mayoral, Joshua, Di Cristina, Manlio, Lawrence, Anna-Lisa E, Olafsson, Einar B et al. 2021. "Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins." PLoS Pathogens, 17 (12). en 10.1371/JOURNAL.PPAT.1010138 PLoS Pathogens Creative Commons Attribution 4.0 International license https://creativecommons.org/licenses/by/4.0/ application/pdf Public Library of Science (PLoS) PLoS
spellingShingle Rivera-Cuevas, Yolanda
Mayoral, Joshua
Di Cristina, Manlio
Lawrence, Anna-Lisa E
Olafsson, Einar B
Patel, Romir K
Thornhill, Dishari
Waldman, Benjamin S
Ono, Akira
Sexton, Jonathan Z
Lourido, Sebastian
Weiss, Louis M
Carruthers, Vern B
Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins
title Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins
title_full Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins
title_fullStr Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins
title_full_unstemmed Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins
title_short Toxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteins
title_sort toxoplasma gondii exploits the host escrt machinery for parasite uptake of host cytosolic proteins
url https://hdl.handle.net/1721.1/146900
work_keys_str_mv AT riveracuevasyolanda toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT mayoraljoshua toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT dicristinamanlio toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT lawrenceannalisae toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT olafssoneinarb toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT patelromirk toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT thornhilldishari toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT waldmanbenjamins toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT onoakira toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT sextonjonathanz toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT louridosebastian toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT weisslouism toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins
AT carruthersvernb toxoplasmagondiiexploitsthehostescrtmachineryforparasiteuptakeofhostcytosolicproteins