Evidence map›Paper›PMID 23209419›Full record

ArticlePLoS pathogens2012

A forward genetic screen reveals that calcium-dependent protein kinase 3 regulates egress in Toxoplasma.

Erin Garrison, Moritz Treeck, Emma Ehret, Heidi Butz, Tamila Garbuz, Benji P Oswald, Matt Settles, John Boothroyd, Gustavo Arrizabalaga

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
6.8field-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

85 citing papers in PubMed, 137 citations in OpenAlex.

  1. Article
  2. Article
  3. Molecular biology of the cell · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Identification ofmSphere · 2023
    Article
  13. Article
  14. mSphere · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Frontiers in immunology · 2022
    Article
  19. Review
  20. Protein kinases in Toxoplasma gondii.International journal for parasitology · 2021
    Review

25 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

9 authors at 3 institutions in 1 country.

Erin GarrisonUniversity of Idaho, Department of Biological Sciences, Moscow, Idaho, United States of America.
Moritz Treeck
Emma Ehret
Heidi Butz
Tamila Garbuz
Benji P Oswald
Matt Settles
John Boothroyd
Gustavo Arrizabalaga
University of Idaho · USIndiana University School of MedicineStanford University · US

Funding

The Evolution of Protein FlexibilityP20RR016448 · NCRR · UNIVERSITY OF IDAHO · PI ROBISON, BARRIE D · 2002 to 2011
$19.3M
Toxoplasma Rhoptry FunctionR01AI021423 · NIAID · STANFORD UNIVERSITY · PI BOOTHROYD, JOHN C · 1985 to 2018
$7.8M
ANTIGENS OF TOXOPLASMA GONDII AND THEIR GENESR37AI021423 · NIAID · STANFORD UNIVERSITY · PI BOOTHROYD, JOHN C · 1994 to 2003
$1.6M
Dissecting a novel mechanism of drug-induced death in Toxoplasma gondiiR01AI089808 · NIAID · UNIVERSITY OF IDAHO · PI ARRIZABALAGA, GUSTAVO A · 2010 to 2013
$882k
NCRR NIH HHS P20 RR016448NCRR NIH HHS P20RR16448NIAID NIH HHS AI21423NIAID NIH HHS R01 AI021423NIAID NIH HHS R01 AI089808NIAID NIH HHS R01 AI 89808-01NIAID NIH HHS R37 AI021423
6 · The paper itself

Abstract

Egress from the host cell is a crucial and highly regulated step in the biology of the obligate intracellular parasite, Toxoplasma gondii. Active egress depends on calcium fluxes and appears to be a crucial step in escaping the attack from the immune system and, potentially, in enabling the parasites to shuttle into appropriate cells for entry into the brain of the host. Previous genetic screens have yielded mutants defective in both ionophore-induced egress and ionophore-induced death. Using whole genome sequencing of one mutant and subsequent analysis of all mutants from these screens, we find that, remarkably, four independent mutants harbor a mis-sense mutation in the same gene, TgCDPK3, encoding a calcium-dependent protein kinase. All four mutations are predicted to alter key regions of TgCDPK3 and this is confirmed by biochemical studies of recombinant forms of each. By complementation we confirm a crucial role for TgCDPK3 in the rapid induction of parasite egress and we establish that TgCDPK3 is critical for formation of latent stages in the brains of mice. Genetic knockout of TgCDPK3 confirms a crucial role for this kinase in parasite egress and a non-essential role for it in the lytic cycle.

Indexed as

AnimalsBrainCalcium-Binding ProteinsGene Knockdown TechniquesMiceProtein KinasesProtozoan ProteinsToxoplasmaToxoplasmosisCalcium-Binding ProteinsProtein KinasesProtozoan Proteins

Identifiers

PMID23209419
PMCPMC3510250
OpenAlexW2083614398

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.