Evidence map›Paper›PMID 31065106›Full record

ArticleCell death and differentiation2020

Liver stage malaria infection is controlled by host regulators of lipid peroxidation.

Heather S Kain, Elizabeth K K Glennon, Kamalakannan Vijayan, Nadia Arang, Alyse N Douglass, Chelsea L Fortin, Meghan Zuck, Adam J Lewis, Samantha L Whiteside, Denali R Dudgeon and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.2field-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

48 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Article
  5. Recent progress in understanding ferroptosis mechanisms in infectious diseases.Frontiers in cellular and infection microbiology · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Tick HRF-dependent ferroptosis pathway to promote tick acquisition ofFrontiers in cellular and infection microbiology · 2025
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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

14 authors at 2 institutions in 1 country.

Heather S KainCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Elizabeth K K GlennonCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Kamalakannan VijayanCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Nadia ArangCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-8167-2188
Alyse N DouglassCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Chelsea L FortinDepartments of Bioengineering & Pathology, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-6931-0862
Meghan ZuckCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Adam J LewisCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Samantha L WhitesideCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Denali R DudgeonCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Jarrod S JohnsonCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Alan AderemCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA.
Kelly R StevensDepartments of Bioengineering & Pathology, Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, USA.
Alexis KaushanskyCenter for Infectious Disease Research, Seattle Biomedical Research Institute, Seattle, WA, USA. alexis.kaushansky@seattlechildrens.org.
Center for Infectious Disease Research · USUniversity of Washington · US

Funding

Systems Biology CoreU19AI100627 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI ULEVITCH, RICHARD J · 2012 to 2021
$49.1M
LPS Signaling in Macrophages: The Roll of TollR01AI032972 · NIAID · UNIVERSITY OF WASHINGTON · PI ADEREM, ALAN A · 1992 to 2020
$14.6M
LPS REGULATION OF MACROPHAGE FUNCTIONR01AI025032 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI ADEREM, ALAN A · 1987 to 2016
$6.7M
Diseases of Public Health Importance Training GrantT32AI007509 · NIAID · UNIVERSITY OF WASHINGTON · PI LUND, JENNIFER M · 1997 to 2024
$6.3M
Perturbations of host cell signaling by a complex hepatotropic pathogenR01GM101183 · NIGMS · SEATTLE CHILDREN'S HOSPITAL · PI KAUSHANSKY, ALEXIS · 2013 to 2021
$3.6M
Investigating hepatocyte signaling driven by host-pathogen interactionsR00AI111785 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI KAUSHANSKY, ALEXIS · 2016 to 2017
$498k
NIAID NIH HHS R00 AI111785NIAID NIH HHS R01 AI025032NIAID NIH HHS R01 AI032972NIAID NIH HHS T32 AI007509NIAID NIH HHS U19 AI100627NIGMS NIH HHS R01 GM101183
6 · The paper itself

Abstract

The facets of host control during Plasmodium liver infection remain largely unknown. We find that the SLC7a11-GPX4 pathway, which has been associated with the production of reactive oxygen species, lipid peroxidation, and a form of cell death called ferroptosis, plays a critical role in control of Plasmodium liver stage infection. Specifically, blocking GPX4 or SLC7a11 dramatically reduces Plasmodium liver stage parasite infection. In contrast, blocking negative regulators of this pathway, NOX1 and TFR1, leads to an increase in liver stage infection. We have shown previously that increased levels of P53 reduces Plasmodium LS burden in an apoptosis-independent manner. Here, we demonstrate that increased P53 is unable to control parasite burden during NOX1 or TFR1 knockdown, or in the presence of ROS scavenging or when lipid peroxidation is blocked. Additionally, SLC7a11 inhibitors Erastin and Sorafenib reduce infection. Thus, blocking the host SLC7a11-GPX4 pathway serves to selectively elevate lipid peroxides in infected cells, which localize within the parasite and lead to the elimination of liver stage parasites.

Indexed as

Lipid PeroxidationAmino Acid Transport System y+AnimalsCell LineCells, CulturedFerroptosisLiver DiseasesMalariaMice, Inbred C57BLMice, KnockoutNADPH Oxidase 1Phospholipid Hydroperoxide Glutathione PeroxidaseReactive Oxygen SpeciesReceptors, TransferrinSignal TransductionTumor Suppressor Protein p53Amino Acid Transport System y+glutathione peroxidase 4, mouseNADPH Oxidase 1NOX1 protein, mousePhospholipid Hydroperoxide Glutathione PeroxidaseReactive Oxygen SpeciesReceptors, TransferrinSlc7a11 protein, mouseTfrc protein, mouseTrp53 protein, mouseTumor Suppressor Protein p53

Identifiers

PMID31065106
PMCPMC7206113
OpenAlexW2944572531

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.