Evidence map›Paper›PMID 28100223›Full record

ArticleBMC biology2017

Surface attachment, promoted by the actomyosin system of Toxoplasma gondii is important for efficient gliding motility and invasion.

Jamie A Whitelaw, Fernanda Latorre-Barragan, Simon Gras, Gurman S Pall, Jacqueline M Leung, Aoife Heaslip, Saskia Egarter, Nicole Andenmatten, Shane R Nelson, David M Warshaw and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
12.5field-weighted citation impact, top 1% 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

41 citing papers in PubMed, 182 citations in OpenAlex.

  1. HarnessingAnnals of medicine · 2026
    Review
  2. Review
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  5. Motility-dependent processes inbioRxiv : the preprint server for biology · 2024
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  7. Propulsive cell entry diverts pathogens from immune degradation by remodeling the phagocytic synapse.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. bioRxiv : the preprint server for biology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Refractile bodies ofFrontiers in cellular and infection microbiology · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Phosphoproteomic Comparison of FourInternational journal of molecular sciences · 2021
    Article
  18. Review
  19. Article
  20. 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

12 authors at 2 institutions in 2 countries.

Jamie A WhitelawWellcome Trust Centre For Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK.
Fernanda Latorre-BarraganWellcome Trust Centre For Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK.
Simon GrasWellcome Trust Centre For Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK.
Gurman S PallWellcome Trust Centre For Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK.
Jacqueline M LeungDepartment of Biology, Indiana University, Bloomington, Myers Hall 240, 915 E 3rd St Bloomington, Bloomington, IN, 47405, USA.
Aoife HeaslipUniversity of Vermont, Department of Molecular Physiology and Biophysics Burlington, Vermont, 05405, USA.
Saskia EgarterWellcome Trust Centre For Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK.
Nicole AndenmattenWellcome Trust Centre For Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK.
Shane R NelsonUniversity of Vermont, Department of Molecular Physiology and Biophysics Burlington, Vermont, 05405, USA.
David M WarshawUniversity of Vermont, Department of Molecular Physiology and Biophysics Burlington, Vermont, 05405, USA.
Gary E WardUniversity of Vermont, Department of Microbiology and Molecular Genetics, College of Medicine, Burlington, VT, 05405, USA.
Markus MeissnerWellcome Trust Centre For Molecular Parasitology, Institute of Infection, Immunity & Inflammation, Glasgow Biomedical Research Centre, University of Glasgow, 120 University Place, Glasgow, G12 8TA, UK. markus.meissner@glasgow.ac.uk.ORCID 0000-0002-4816-5221
Wellcome Centre for Molecular Parasitology · GBUniversity of Vermont · US

Funding

Vermont Immunology/Infectious Diseases CenterP30GM118228 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BUDD, RALPH C · 2016 to 2021
$6.8M
Small Molecule Approaches to Studying T. gondii InvasionR01AI054961 · NIAID · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI WARD, GARY E · 2003 to 2014
$4.5M
Myosin Va Cargo Transport: In Vitro Model SystemsR01GM094229 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WARSHAW, DAVID M · 2011 to 2020
$2.7M
Small Molecule Approaches to Studying T. gondi InvasionR56AI054961 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI WARD, GARY E · 2008 to 2008
$312k
NIAID NIH HHS R01 AI054961NIAID NIH HHS R56 AI054961NIGMS NIH HHS P30 GM118228NIGMS NIH HHS R01 GM094229Wellcome Trust 085349Wellcome Trust 087582/Z/08/Z
6 · The paper itself

Abstract

backgroundApicomplexan parasites employ a unique form of movement, termed gliding motility, in order to invade the host cell. This movement depends on the parasite's actomyosin system, which is thought to generate the force during gliding. However, recent evidence questions the exact molecular role of this system, since mutants for core components of the gliding machinery, such as parasite actin or subunits of the MyoA-motor complex (the glideosome), remain motile and invasive, albeit at significantly reduced efficiencies. While compensatory mechanisms and unusual polymerisation kinetics of parasite actin have been evoked to explain these findings, the actomyosin system could also play a role distinct from force production during parasite movement.

resultsIn this study, we compared the phenotypes of different mutants for core components of the actomyosin system in Toxoplasma gondii to decipher their exact role during gliding motility and invasion. We found that, while some phenotypes (apicoplast segregation, host cell egress, dense granule motility) appeared early after induction of the act1 knockout and went to completion, a small percentage of the parasites remained capable of motility and invasion well past the point at which actin levels were undetectable. Those act1 conditional knockout (cKO) and mlc1 cKO that continue to move in 3D do so at speeds similar to wildtype parasites. However, these mutants are virtually unable to attach to a collagen-coated substrate under flow conditions, indicating an important role for the actomyosin system of T. gondii in the formation of attachment sites.

conclusionWe demonstrate that parasite actin is essential during the lytic cycle and cannot be compensated by other molecules. Our data suggest a conventional polymerisation mechanism in vivo that depends on a critical concentration of G-actin. Importantly, we demonstrate that the actomyosin system of the parasite functions in attachment to the surface substrate, and not necessarily as force generator.

Indexed as

Cell MovementActinsActomyosinAnimalsApicoplastsCell AdhesionCell MembraneCells, CulturedCytoplasmic GranulesGene Knockout TechniquesKineticsMutationParasitesPhenotypeProtozoan ProteinsRheologyActinsActomyosinProtozoan ProteinsSirolimusActinApicomplexaAttachmentHost cell invasionMembrane flowMotilityMyosinToxoplasma

Identifiers

PMID28100223
PMCPMC5242020
OpenAlexW2572179555

What OpenQuestion holds

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LicenceCC BY
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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.