Evidence map›Paper›PMID 33290416›Full record

ArticlePloS one2020

Interferon-gamma promotes iron export in human macrophages to limit intracellular bacterial replication.

Rodrigo Abreu, Lauren Essler, Pramod Giri, Frederick Quinn

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. TargetingRSC medicinal chemistry · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Observational
  14. Article
  15. Article
  16. The Iron Response ofFrontiers in cellular and infection microbiology · 2022
    Review
  17. Drug Repositioning in Friedreich Ataxia.Frontiers in neuroscience · 2022
    Review
  18. Article
  19. The Roles of Inflammasomes in Host Defense againstPathogens (Basel, Switzerland) · 2021
    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

4 authors at 1 institution in 1 country.

Rodrigo AbreuDepartment of Infectious Diseases, University of Georgia, Athens, Georgia, United States of America.
Lauren EsslerDepartment of Infectious Diseases, University of Georgia, Athens, Georgia, United States of America.
Pramod GiriDepartment of Infectious Diseases, University of Georgia, Athens, Georgia, United States of America.
Frederick QuinnDepartment of Infectious Diseases, University of Georgia, Athens, Georgia, United States of America.ORCID 0000-0002-6413-0184
University of Georgia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Salmonellosis and listeriosis together accounted for more than one third of foodborne illnesses in the United States and almost half the hospitalizations for gastrointestinal diseases in 2018 while tuberculosis afflicted over 10 million people worldwide causing almost 2 million deaths. Regardless of the intrinsic virulence differences among Listeria monocytogenes, Salmonella enterica and Mycobacterium tuberculosis, these intracellular pathogens share the ability to survive and persist inside the macrophage and other cells and thrive in iron rich environments. Interferon-gamma (IFN-γ) is a central cytokine in host defense against intracellular pathogens and has been shown to promote iron export in macrophages. We hypothesize that IFN-γ decreases iron availability to intracellular pathogens consequently limiting replication in these cells. In this study, we show that IFN-γ regulates the expression of iron-related proteins hepcidin, ferroportin, and ferritin to induce iron export from macrophages. Listeria monocytogenes, S. enterica, and M. tuberculosis infections significantly induce iron sequestration in human macrophages. In contrast, IFN-γ significantly reduces hepcidin secretion in S. enterica and M. tuberculosis infected macrophages. Similarly, IFN-γ-activated macrophages express higher ferroportin levels than untreated controls even after infection with L. monocytogenes bacilli; bacterial infection greatly down-regulates ferroportin expression. Collectively, IFN-γ significantly inhibits pathogen-associated intracellular iron sequestration in macrophages and consequently retards the growth of intracellular bacterial pathogens by decreasing iron availability.

Indexed as

Biological Transport, ActiveCation Transport ProteinsFerritinsFerroportinHepcidinsHost Microbial InteractionsHumansImmunity, InnateInterferon-gammaIronListeria monocytogenesMacrophagesMycobacterium tuberculosisRecombinant ProteinsSalmonella entericaTHP-1 CellsCation Transport ProteinsFerritinsFerroportinHAMP protein, humanHepcidinsInterferon-gammaIronRecombinant Proteins

Identifiers

PMID33290416
PMCPMC7723272
OpenAlexW3112899019

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.