Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.

The p47 GTPases are essential for interferon-gamma-induced cell-autonomous immunity against the protozoan parasite, Toxoplasma gondii, in mice, but the mechanism of resistance is poorly understood. We show that the p47 GTPases, including IIGP1, accumulate at vacuoles containing T. gondii. The accumu...

Full description

Bibliographic Details
Main Authors: Sascha Martens, Iana Parvanova, Jens Zerrahn, Gareth Griffiths, Gudrun Schell, Gaby Reichmann, Jonathan C Howard
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2005-11-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.0010024
id doaj-9ccf5167388344ea98140a79c43b99b0
record_format Article
spelling doaj-9ccf5167388344ea98140a79c43b99b02021-04-21T17:18:59ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742005-11-0113e2410.1371/journal.ppat.0010024Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.Sascha MartensIana ParvanovaJens ZerrahnGareth GriffithsGudrun SchellGaby ReichmannJonathan C HowardThe p47 GTPases are essential for interferon-gamma-induced cell-autonomous immunity against the protozoan parasite, Toxoplasma gondii, in mice, but the mechanism of resistance is poorly understood. We show that the p47 GTPases, including IIGP1, accumulate at vacuoles containing T. gondii. The accumulation is GTP-dependent and requires live parasites. Vacuolar IIGP1 accumulations undergo a maturation-like process accompanied by vesiculation of the parasitophorous vacuole membrane. This culminates in disruption of the parasitophorous vacuole and finally of the parasite itself. Over-expression of IIGP1 leads to accelerated vacuolar disruption whereas a dominant negative form of IIGP1 interferes with interferon-gamma-mediated killing of intracellular parasites. Targeted deletion of the IIGP1 gene results in partial loss of the IFN-gamma-mediated T. gondii growth restriction in mouse astrocytes.https://doi.org/10.1371/journal.ppat.0010024
collection DOAJ
language English
format Article
sources DOAJ
author Sascha Martens
Iana Parvanova
Jens Zerrahn
Gareth Griffiths
Gudrun Schell
Gaby Reichmann
Jonathan C Howard
spellingShingle Sascha Martens
Iana Parvanova
Jens Zerrahn
Gareth Griffiths
Gudrun Schell
Gaby Reichmann
Jonathan C Howard
Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.
PLoS Pathogens
author_facet Sascha Martens
Iana Parvanova
Jens Zerrahn
Gareth Griffiths
Gudrun Schell
Gaby Reichmann
Jonathan C Howard
author_sort Sascha Martens
title Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.
title_short Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.
title_full Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.
title_fullStr Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.
title_full_unstemmed Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.
title_sort disruption of toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance gtpases.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2005-11-01
description The p47 GTPases are essential for interferon-gamma-induced cell-autonomous immunity against the protozoan parasite, Toxoplasma gondii, in mice, but the mechanism of resistance is poorly understood. We show that the p47 GTPases, including IIGP1, accumulate at vacuoles containing T. gondii. The accumulation is GTP-dependent and requires live parasites. Vacuolar IIGP1 accumulations undergo a maturation-like process accompanied by vesiculation of the parasitophorous vacuole membrane. This culminates in disruption of the parasitophorous vacuole and finally of the parasite itself. Over-expression of IIGP1 leads to accelerated vacuolar disruption whereas a dominant negative form of IIGP1 interferes with interferon-gamma-mediated killing of intracellular parasites. Targeted deletion of the IIGP1 gene results in partial loss of the IFN-gamma-mediated T. gondii growth restriction in mouse astrocytes.
url https://doi.org/10.1371/journal.ppat.0010024
work_keys_str_mv AT saschamartens disruptionoftoxoplasmagondiiparasitophorousvacuolesbythemousep47resistancegtpases
AT ianaparvanova disruptionoftoxoplasmagondiiparasitophorousvacuolesbythemousep47resistancegtpases
AT jenszerrahn disruptionoftoxoplasmagondiiparasitophorousvacuolesbythemousep47resistancegtpases
AT garethgriffiths disruptionoftoxoplasmagondiiparasitophorousvacuolesbythemousep47resistancegtpases
AT gudrunschell disruptionoftoxoplasmagondiiparasitophorousvacuolesbythemousep47resistancegtpases
AT gabyreichmann disruptionoftoxoplasmagondiiparasitophorousvacuolesbythemousep47resistancegtpases
AT jonathanchoward disruptionoftoxoplasmagondiiparasitophorousvacuolesbythemousep47resistancegtpases
_version_ 1714666294963339264