Evidence map›Paper›PMID 28642498›Full record

ArticleScientific reports2017

Uptake and metabolism of arginine impact Plasmodium development in the liver.

Patrícia Meireles, António M Mendes, Rita I Aroeira, Bryan C Mounce, Marco Vignuzzi, Henry M Staines, Miguel Prudêncio

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. The intersection of hostMicrobiology and molecular biology reviews : MMBR · 2024
    Review
  4. Article
  5. Article
  6. Insights into Antimalarial Activity ofMolecules (Basel, Switzerland) · 2022
    Article
  7. iScience · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Characterization ofFrontiers in microbiology · 2018
    Article
  15. Review
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 4 countries.

Patrícia MeirelesInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
António M MendesInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
Rita I AroeiraInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.
Bryan C MounceInstitut Pasteur, Viral Populations and Pathogenesis Unit, CNRS UMR 3569, 25-28 rue du Dr. Roux, Paris, France.
Marco VignuzziInstitut Pasteur, Viral Populations and Pathogenesis Unit, CNRS UMR 3569, 25-28 rue du Dr. Roux, Paris, France.
Henry M StainesInstitute for Infection & Immunity, St. George's, University of London, Cranmer Terrace, London, UK.
Miguel PrudêncioInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal. mprudencio@medicina.ulisboa.pt.ORCID 0000-0003-1746-6029
University of Lisbon · PTCentre National de la Recherche Scientifique · FRSt George's, University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prior to infecting erythrocytes and causing malaria symptoms, Plasmodium parasites undergo an obligatory phase of invasion and extensive replication inside their mammalian host's liver cells that depends on the parasite's ability to obtain the nutrients it requires for its intra-hepatic growth and multiplication. Here, we show that L-arginine (Arg) uptake through the host cell's SLC7A2-encoded transporters is essential for the parasite's development and maturation in the liver. Our data suggest that the Arg that is taken up is primarily metabolized by the arginase pathway to produce the polyamines required for Plasmodium growth. Although the parasite may hijack the host's biosynthesis pathway, it relies mainly upon its own arginase-AdoMetDC/ODC pathway to acquire the polyamines it needs to develop. These results identify for the first time a pivotal role for Arg-dependent polyamine production during Plasmodium's hepatic development and pave the way to the exploitation of strategies to impact liver infection by the malaria parasite through the modulation of Arg uptake and polyamine synthesis.

Indexed as

PlasmodiumAnimalsArginineCationic Amino Acid Transporter 2Cell LineDisease Models, AnimalGene Expression RegulationHepatocytesHost-Pathogen InteractionsHumansLiverMalariaMiceMice, KnockoutPlasmodium bergheiArginineCationic Amino Acid Transporter 2

Identifiers

PMID28642498
PMCPMC5481400
OpenAlexW2626594896

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.