Show simple item record

dc.contributor.authorRivera-Cuevas, Yolanda
dc.contributor.authorMayoral, Joshua
dc.contributor.authorDi Cristina, Manlio
dc.contributor.authorLawrence, Anna-Lisa E
dc.contributor.authorOlafsson, Einar B
dc.contributor.authorPatel, Romir K
dc.contributor.authorThornhill, Dishari
dc.contributor.authorWaldman, Benjamin S
dc.contributor.authorOno, Akira
dc.contributor.authorSexton, Jonathan Z
dc.contributor.authorLourido, Sebastian
dc.contributor.authorWeiss, Louis M
dc.contributor.authorCarruthers, Vern B
dc.date.accessioned2022-12-16T17:40:02Z
dc.date.available2022-12-16T17:40:02Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/146900
dc.description.abstract<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>en_US
dc.language.isoen
dc.publisherPublic Library of Science (PLoS)en_US
dc.relation.isversionof10.1371/JOURNAL.PPAT.1010138en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourcePLoSen_US
dc.titleToxoplasma gondii exploits the host ESCRT machinery for parasite uptake of host cytosolic proteinsen_US
dc.typeArticleen_US
dc.identifier.citationRivera-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).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journalPLoS Pathogensen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-12-16T17:36:15Z
dspace.orderedauthorsRivera-Cuevas, Y; Mayoral, J; Di Cristina, M; Lawrence, A-LE; Olafsson, EB; Patel, RK; Thornhill, D; Waldman, BS; Ono, A; Sexton, JZ; Lourido, S; Weiss, LM; Carruthers, VBen_US
dspace.date.submission2022-12-16T17:36:18Z
mit.journal.volume17en_US
mit.journal.issue12en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record