Evidence map›Paper›PMID 31233488›Full record

ArticlePLoS biology2019

An endocytic-secretory cycle participates in Toxoplasma gondii in motility.

Simon Gras, Elena Jimenez-Ruiz, Christen M Klinger, Katja Schneider, Andreas Klingl, Leandro Lemgruber, Markus Meissner

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.5field-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

32 citing papers in PubMed, 64 citations in OpenAlex.

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  15. Review
  16. Regulation of phosphoinositide metabolism in Apicomplexan parasites.Frontiers in cell and developmental biology · 2023
    Review
  17. Article
  18. Article
  19. Review
  20. Frontiers in cellular and infection microbiology · 2022
    Article
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

7 authors at 3 institutions in 3 countries.

Simon GrasLehrstuhl für experimentelle Parasitologie, Ludwig-Maximilians-Universität, LMU, Tierärztliche Fakultät, München, Germany.
Elena Jimenez-RuizLehrstuhl für experimentelle Parasitologie, Ludwig-Maximilians-Universität, LMU, Tierärztliche Fakultät, München, Germany.ORCID 0000-0003-2695-0947
Christen M KlingerWellcome Centre for Integrative Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, Glasgow, United Kingdom.
Katja SchneiderPflanzliche Entwicklungsbiologie, Biozentrum der Ludwig-Maximilians-Universität, Planegg-Martinsried, Germany.
Andreas KlinglPflanzliche Entwicklungsbiologie, Biozentrum der Ludwig-Maximilians-Universität, Planegg-Martinsried, Germany.
Leandro LemgruberWellcome Centre for Integrative Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0003-2832-6806
Markus MeissnerLehrstuhl für experimentelle Parasitologie, Ludwig-Maximilians-Universität, LMU, Tierärztliche Fakultät, München, Germany.ORCID 0000-0002-4816-5221
Wellcome Centre for Molecular Parasitology · GBLudwig-Maximilians-Universität München · DEUniversity of Alberta · CA

Funding

Wellcome TrustWellcome Trust 085349Wellcome Trust 087582/Z/08/Z
6 · The paper itself

Abstract

Apicomplexan parasites invade host cells in an active process involving their ability to move by gliding motility. While the acto-myosin system of the parasite plays a crucial role in the formation and release of attachment sites during this process, there are still open questions regarding the involvement of other mechanisms in parasite motility. In many eukaryotes, a secretory-endocytic cycle leads to the recycling of receptors (integrins), necessary to form attachment sites, regulation of surface area during motility, and generation of retrograde membrane flow. Here, we demonstrate that endocytosis operates during gliding motility in Toxoplasma gondii and appears to be crucial for the establishment of retrograde membrane flow, because inhibition of endocytosis blocks retrograde flow and motility. We demonstrate that extracellular parasites can efficiently incorporate exogenous material, such as labelled phospholipids, nanogold particles (NGPs), antibodies, and Concanavalin A (ConA). Using labelled phospholipids, we observed that the endocytic and secretory pathways of the parasite converge, and endocytosed lipids are subsequently secreted, demonstrating the operation of an endocytic-secretory cycle. Together our data consolidate previous findings, and we propose an additional model, working in parallel to the acto-myosin motor, that reconciles parasite motility with observations in other eukaryotes: an apicomplexan fountain-flow-model for parasite motility.

Indexed as

ActinsAnimalsCell AdhesionCell MovementCell Surface ExtensionsEndocytosisMembrane ProteinsMyosinsParasitesProtozoan ProteinsSecretory PathwayToxoplasmaActinsMembrane ProteinsMyosinsProtozoan Proteins

Identifiers

PMID31233488
PMCPMC6611640
OpenAlexW2949584587

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.