Evidence map›Paper›PMID 10992462›Full record

ArticleInfection and immunity2000

Gallium disrupts iron metabolism of mycobacteria residing within human macrophages.

O Olakanmi, B E Britigan, L S Schlesinger

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

82 citing papers in PubMed, 216 citations in OpenAlex.

  1. iScience · 2026
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  8. Drug resistantbioRxiv : the preprint server for biology · 2024
    Article
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  18. Evolution of gallium applications in medicine and microbiology: a timeline.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2022
    Review
  19. Article
  20. Review

22 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 2 countries.

O OlakanmiDivision of Infectious Diseases, Department of Medicine, The University of Iowa College of Medicine, Iowa City, Iowa 52242, USA.
B E Britigan
L S Schlesinger
Office of Infectious Diseases · US

Funding

MACROPHAGE COMPLEMENT RECEPTORS IN TUBERCULOSISR01AI033004 · NIAID · UNIVERSITY OF IOWA · PI SCHLESINGER, LARRY S. · 1998 to 2002
$693k
SURFACTANT PROTEINS IN THE PATHOGENESIS OF TUBERCULOSISR01HL051990 · NHLBI · UNIVERSITY OF IOWA · PI SCHLESINGER, LARRY S. · 1993 to 1997
–
MACROPHAGE COMPLEMENT RECEPTORS IN TUBERCULOSISR29AI033004 · NIAID · UNIVERSITY OF IOWA · PI SCHLESINGER, LARRY S. · 1992 to 1996
–
NHLBI NIH HHS HL51990NIAID NIH HHS AI24954NIAID NIH HHS AI33004
6 · The paper itself

Abstract

Mycobacterium tuberculosis and M. avium complex (MAC) enter and multiply within monocytes and macrophages in phagosomes. In vitro growth studies using standard culture media indicate that siderophore-mediated iron (Fe) acquisition plays a critical role in the growth and metabolism of both M. tuberculosis and MAC. However, the applicability of such studies to conditions within the macrophage phagosome is unclear, due in part to the absence of experimental means to inhibit such a process. Based on the ability of gallium (Ga(3+)) to concentrate within mononuclear phagocytes and on evidence that Ga disrupts cellular Fe-dependent metabolic pathways by substituting for Fe(3+) and failing to undergo redox cycling, we hypothesized that Ga could disrupt Fe acquisition and Fe-dependent metabolic pathways of mycobacteria. We find that Ga(NO(3))(3) and Ga-transferrin produce an Fe-reversible concentration-dependent growth inhibition of M. tuberculosis strains and MAC grown extracellularly and within human macrophages. Ga is bactericidal for M. tuberculosis growing extracellularly and within macrophages. Finally, we provide evidence that exogenously added Fe is acquired by intraphagosomal M. tuberculosis and that Ga inhibits this Fe acquisition. Thus, Ga(NO(3))(3) disruption of mycobacterial Fe metabolism may serve as an experimental means to study the mechanism of Fe acquisition by intracellular mycobacteria and the role of Fe in intracellular survival. Furthermore, given the inability of biological systems to discriminate between Ga and Fe, this approach could have broad applicability to the study of Fe metabolism of other intracellular pathogens.

Indexed as

Cells, CulturedCulture MediaGalliumHumansIronMacrophagesMacrophages, AlveolarMicroscopy, Electron, ScanningMonocytesMycobacterium avium ComplexMycobacterium tuberculosisTransferrinCulture MediaGalliumgallium nitrateIronTransferrin

Identifiers

PMID10992462
PMCPMC101514
OpenAlexW2161032017

What OpenQuestion holds

Textmetadata
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.