Evidence map›Paper›PMID 19265156›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Virulent Toxoplasma gondii evade immunity-related GTPase-mediated parasite vacuole disruption within primed macrophages.

Yanlin Zhao, David J P Ferguson, Douglas C Wilson, Jonathan C Howard, L David Sibley, George S Yap

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
98citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

98 citing papers in PubMed, 1 synthesis or guideline pooled it, 145 citations in OpenAlex.

  1. Pooled it
  2. Review
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  10. Nitric oxide in parasitic infections: a friend or foe?Journal of parasitic diseases : official organ of the Indian Society for Parasitology · 2022
    Review
  11. Modulation of autophagy as a therapeutic strategy forFrontiers in cellular and infection microbiology · 2022
    Review
  12. Article
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  14. Cell-autonomousLife science alliance · 2021
    Article
  15. Review
  16. Article
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  20. Article

38 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 5 countries.

Yanlin ZhaoDepartment of Medicine and Center for Immunity and Inflammation, University of Medicine and Dentistry of New Jersey-New Jersey Medical School, Newark, NJ 07101, USA.
David J P Ferguson
Douglas C Wilson
Jonathan C Howard
L David Sibley
George S Yap
University Hospital, Newark · USNuffield Orthopaedic Centre · GBUniversity of Cologne · DEWashington University in St. Louis · US

Funding

MOLECULAR BASIS OF TOXOPLASMOSIS IN AIDS PATIENTSR01AI036629 · NIAID · WASHINGTON UNIVERSITY · PI SIBLEY, L. DAVID · 1994 to 2013
$5.3M
TARGETING ESSENTIAL ROP KINASES IN TOXOPLASMAR01AI082423 · NIAID · WASHINGTON UNIVERSITY · PI SIBLEY, L. DAVID · 2009 to 2015
$2.9M
Pathogenic and Protective T cells in ToxoplasmosisR01AI083405 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI YAP, GEORGE S. · 2010 to 2014
$1.9M
Autophagic Defense Against Intracellular ParasitesR21AI074919 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI YAP, GEORGE S. · 2008 to 2009
$423k
NIAID NIH HHS AI036629NIAID NIH HHS AI074914NIAID NIH HHS R01 AI036629NIAID NIH HHS R01 AI082423NIAID NIH HHS R01 AI083405NIAID NIH HHS R21 AI074919
6 · The paper itself

Abstract

Cytokine-activated macrophages restrain the replication of intracellular parasites and disrupt the integrity of vacuolar pathogens. In this study, we show that inducible nitric oxide synthase and the immunity-related GTPase (IRG) family member Irgm3, respectively, are required for the ability of in vivo primed macrophages to restrain the growth of Toxoplasma gondii and to destroy the parasite's intracellular niche. Remarkably, virulent Type I strains of T. gondii evade IRG-dependent vacuolar disruption, while remaining susceptible to iNOS-dependent restriction. The ability of virulent T. gondii to escape killing by macrophages is controlled at the level of the individual vacuole and is associated with differential permissiveness for association of the IRG proteins Irga6 (IIGP1) and Irgb6 (TGTP) to the vacuolar membrane. Surprisingly, expression of the Type I ROP-18 virulence determinant in an avirulent strain did not confer the evasive phenotype. These results pinpoint evasion of vacuolar disruption by IRG proteins as a new determinant of pathogen virulence.

Indexed as

AnimalsGTP-Binding ProteinsGTP PhosphohydrolasesMacrophage ActivationMacrophages, PeritonealMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNitric Oxide Synthase Type IIToxoplasmaVacuolesVirulenceGTP-Binding ProteinsGTP PhosphohydrolasesIfi1 protein, mouseIgtp protein, mouseNitric Oxide Synthase Type IINos2 protein, mouse

Identifiers

PMID19265156
PMCPMC2848815
OpenAlexW2129052947

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.