Evidence map›Paper›PMID 31257182›Full record

ArticleCell chemical biology2019

Discovery of Druggable Host Factors Critical to Plasmodium Liver-Stage Infection.

Rene Raphemot, Maria Toro-Moreno, Kuan-Yi Lu, Dora Posfai, Emily Rose Derbyshire

Open access · bronzeAbstract read
In one paragraph

Article in Cell chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. mSphere · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Forward Genetics in Apicomplexa Biology: The Host Side of the Story.Frontiers in cellular and infection microbiology · 2022
    Review
  14. Recent Advances in Host-Directed Therapies for Tuberculosis and Malaria.Frontiers in cellular and infection microbiology · 2022
    Review
  15. Host-parasite interactions duringFrontiers in immunology · 2022
    Review
  16. COPB2: a transport protein with multifaceted roles in cancer development and progression.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Review
  17. Review
  18. Review
  19. Chemoproteomics for Plasmodium Parasite Drug Target Discovery.Chembiochem : a European journal of chemical biology · 2021
    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

5 authors at 1 institution in 1 country.

Rene RaphemotDepartment of Chemistry, Duke University, 124 Science Drive, Durham, NC 27708, USA.
Maria Toro-MorenoDepartment of Chemistry, Duke University, 124 Science Drive, Durham, NC 27708, USA.
Kuan-Yi LuDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, 213 Research Drive, Durham, NC 27710, USA.
Dora PosfaiDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, 213 Research Drive, Durham, NC 27710, USA.
Emily Rose DerbyshireDepartment of Chemistry, Duke University, 124 Science Drive, Durham, NC 27708, USA; Department of Molecular Genetics and Microbiology, Duke University Medical Center, 213 Research Drive, Durham, NC 27710, USA. Electronic address: emily.derbyshire@duke.edu.
Duke University · US

Funding

Enabling Host Processes for Defense Against Liver Stage Malaria InfectionDP2AI138239 · NIAID · DUKE UNIVERSITY · PI DERBYSHIRE, EMILY R · 2017 to 2017
$2.3M
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
Discovery of novel liver host targets for malaria treatmentF32AI118294 · NIAID · DUKE UNIVERSITY · PI RAPHEMOT, RENE · 2016 to 2017
$75k
NIAID NIH HHS DP2 AI138239NIAID NIH HHS F32 AI118294NIH HHS S10 OD018164
6 · The paper itself

Abstract

Plasmodium parasites undergo an obligatory and asymptomatic developmental stage within the liver before infecting red blood cells to cause malaria. The hijacked host pathways critical to parasite infection during this hepatic phase remain poorly understood. Here, we implemented a forward genetic screen to identify over 100 host factors within the human druggable genome that are critical to P. berghei infection in hepatoma cells. Notably, we found knockdown of genes involved in protein trafficking pathways to be detrimental to parasite infection. The disruption of protein trafficking modulators, including COPB2 and GGA1, decreases P. berghei parasite size, and an immunofluorescence study suggests that these proteins are recruited to the Plasmodium parasitophorous vacuole in infected hepatocytes. These findings reveal that various host intracellular protein trafficking pathways are subverted by Plasmodium parasites during the liver stage and provide new insights into their manipulation for growth and development.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsCarcinoma, HepatocellularCell LineCoatomer ProteinCommunicable DiseasesHepatocytesHep G2 CellsHumansLiverMalariaMiceParasitesPlasmodiumPlasmodium bergheiProtein TransportAdaptor Proteins, Vesicular TransportCoatomer ProteinCOPB2 protein, humanGGA adaptor proteinsCOPB2GGA1Host factorshost-parasite interactionsLiver stagemalariaPlasmodiumRNAi screen

Identifiers

PMID31257182
PMCPMC6754275
OpenAlexW2953466448

What OpenQuestion holds

Textmetadata
LicenceTDM
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.