Evidence map›Paper›PMID 25257508›Full record

ArticleEMBO molecular medicine2014

ZIPCO, a putative metal ion transporter, is crucial for Plasmodium liver-stage development.

Tejram Sahu, Bertrand Boisson, Céline Lacroix, Emmanuel Bischoff, Quentin Richier, Pauline Formaglio, Sabine Thiberge, Irina Dobrescu, Robert Ménard, Patricia Baldacci

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Identification of a divalent metal transporter required for cellular iron metabolism in malaria parasites.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Iron transport pathways in the human malaria parasiteFrontiers in cellular and infection microbiology · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Oxidative Stress in Malaria: Potential Benefits of Antioxidant Therapy.International journal of molecular sciences · 2022
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Malaria Parasite Liver Infection and Exoerythrocytic Biology.Cold Spring Harbor perspectives in medicine · 2017
    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

10 authors at 4 institutions in 2 countries.

Tejram SahuInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, Rockville, MD, USA.
Bertrand BoissonInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France St. Giles Laboratory of Human Genetics of Infectious Diseases, The Rockefeller University, New York, NY, USA.
Céline LacroixInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France Institut de Biologie et Chimie des Protéines, Lyon Cedex 07, France.
Emmanuel BischoffInstitut Pasteur Plateforme Puces à ADN Génopole, Paris Cedex 15, France.
Quentin RichierInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France.
Pauline FormaglioInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France.
Sabine ThibergeInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France.
Irina DobrescuInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France.
Robert MénardInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France.
Patricia BaldacciInstitut Pasteur Unité de Biologie et Génétique du Paludisme, Paris Cedex 15, France patricia.baldacci@pasteur.fr.
Institut Pasteur · FRGenopole (France) · FRNational Institute of Allergy and Infectious Diseases · USRockefeller University · US

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

The malaria parasite, Plasmodium, requires iron for growth, but how it imports iron remains unknown. We characterize here a protein that belongs to the ZIP (Zrt-, Irt-like Protein) family of metal ion transport proteins and have named ZIP domain-containing protein (ZIPCO). Inactivation of the ZIPCO-encoding gene in Plasmodium berghei, while not affecting the parasite's ability to multiply in mouse blood and to infect mosquitoes, greatly impairs its capacity to develop inside hepatocytes. Iron/zinc supplementation and depletion experiments suggest that ZIPCO is required for parasite utilization of iron and possibly zinc, consistent with its predicted function as a metal transporter. This is the first report of a ZIP protein having a crucial role in Plasmodium liver-stage development, as well as the first metal ion transporter identified in Plasmodium pre-erythrocytic stages. Because of the drastic dependence on iron of Plasmodium growth, ZIPCO and related proteins might constitute attractive drug targets to fight against malaria.

Indexed as

Amino Acid SequenceAnimalsAnophelesFemaleGene Knockout TechniquesHepatocytesHep G2 CellsHumansIonsIronLiverMalariaMembrane Transport ProteinsMiceMice, Inbred C57BLMolecular Sequence DataIonsIronMembrane Transport ProteinsZincironliver stagePlasmodiumtransporterZIP

Identifiers

PMID25257508
PMCPMC4237467
OpenAlexW2107062947

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.