Evidence map›Paper›PMID 26565995›Full record

ArticlePLoS biology2015

Phosphatidylthreonine and Lipid-Mediated Control of Parasite Virulence.

Ruben D Arroyo-Olarte, Jos F Brouwers, Arunakar Kuchipudi, J Bernd Helms, Aindrila Biswas, Ildiko R Dunay, Richard Lucius, Nishith Gupta

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 57 citations in OpenAlex.

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  8. Host cell-specific metabolism of linoleic acid controlsbioRxiv : the preprint server for biology · 2024
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  9. Review
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  11. Apigeninidin chloride disruptsFrontiers in cellular and infection microbiology · 2024
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  15. Article
  16. Plasticity and therapeutic potential of cAMP and cGMP-specific phosphodiesterases inComputational and structural biotechnology journal · 2022
    Article
  17. Computational and structural biotechnology journal · 2021
    Article
  18. Article
  19. Key Limitations and New Insights Into theFrontiers in cellular and infection microbiology · 2020
    Review
  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

8 authors at 4 institutions in 2 countries.

Ruben D Arroyo-OlarteDepartment of Molecular Parasitology, Humboldt University, Berlin, Germany.
Jos F BrouwersDepartment of Biochemistry and Cell Biology, Institute of Biomembranes, Utrecht University, The Netherlands.
Arunakar KuchipudiDepartment of Molecular Parasitology, Humboldt University, Berlin, Germany.
J Bernd HelmsDepartment of Biochemistry and Cell Biology, Institute of Biomembranes, Utrecht University, The Netherlands.
Aindrila BiswasInstitute of Medical Microbiology, Otto von Guericke University, Magdeburg, Germany.
Ildiko R DunayInstitute of Medical Microbiology, Otto von Guericke University, Magdeburg, Germany.
Richard LuciusDepartment of Molecular Parasitology, Humboldt University, Berlin, Germany.
Nishith GuptaDepartment of Molecular Parasitology, Humboldt University, Berlin, Germany.
Humboldt-Universität zu Berlin · DEOtto-von-Guericke University Magdeburg · DEUtrecht University · NLMax Planck Institute for Infection Biology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The major membrane phospholipid classes, described thus far, include phosphatidylcholine (PtdCho), phosphatidylethanolamine (PtdEtn), phosphatidylserine (PtdSer), and phosphatidylinositol (PtdIns). Here, we demonstrate the natural occurrence and genetic origin of an exclusive and rather abundant lipid, phosphatidylthreonine (PtdThr), in a common eukaryotic model parasite, Toxoplasma gondii. The parasite expresses a novel enzyme PtdThr synthase (TgPTS) to produce this lipid in its endoplasmic reticulum. Genetic disruption of TgPTS abrogates de novo synthesis of PtdThr and impairs the lytic cycle and virulence of T. gondii. The observed phenotype is caused by a reduced gliding motility, which blights the parasite egress and ensuing host cell invasion. Notably, the PTS mutant can prevent acute as well as yet-incurable chronic toxoplasmosis in a mouse model, which endorses its potential clinical utility as a metabolically attenuated vaccine. Together, the work also illustrates the functional speciation of two evolutionarily related membrane phospholipids, i.e., PtdThr and PtdSer.

Indexed as

AnimalsBrainCells, CulturedEndoplasmic ReticulumGlycerophospholipidsHumansMiceMolecular Sequence DataMutationOrganisms, Genetically ModifiedParasite EncystmentPeptide FragmentsProtein Interaction Domains and MotifsProtozoan ProteinsProtozoan VaccinesRecombinant Fusion ProteinsGlycerophospholipidsPeptide FragmentsphosphatidylthreonineProtozoan ProteinsProtozoan VaccinesRecombinant Fusion ProteinsThreonineTransferases (Other Substituted Phosphate Groups)Vaccines, Attenuated

Identifiers

PMID26565995
PMCPMC4643901
OpenAlexW2175688467

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.