Evidence map›Paper›PMID 12228295›Full record

ArticleInfection and immunity2002

Legionella pneumophila feoAB promotes ferrous iron uptake and intracellular infection.

Marianne Robey, Nicholas P Cianciotto

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

76 citing papers in PubMed, 172 citations in OpenAlex.

  1. Article
  2. Article
  3. Molecular evolution and adaptations ofFrontiers in cellular and infection microbiology · 2026
    Review
  4. Article
  5. Journal of bacteriology · 2024
    Review
  6. Iron Homeostasis inBiology · 2023
    Review
  7. Article
  8. Complete Genome Sequence of Legionella cardiaca Strain H63Microbiology resource announcements · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. International journal of molecular sciences · 2021
    Article
  13. Metallomics : integrated biometal science · 2020
    Article
  14. Article
  15. Article
  16. A NovelmBio · 2020
    Article
  17. IroT/MavN Is aBiochemistry · 2019
    Article
  18. The iron-regulated vacuolarProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Toward a mechanistic understanding of Feo-mediated ferrous iron uptake.Metallomics : integrated biometal science · 2018
    Review
  20. Article

16 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

2 authors at 1 institution in 1 country.

Marianne RobeyDepartment of Microbiology-Immunology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Nicholas P Cianciotto
Northwestern University · US

Funding

GENETICS OF IRON ACQUISITION BY LEGIONELLA PNEUMOPHILAR01AI034937 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CIANCIOTTO, NICHOLAS P · 1995 to 2014
$4.5M
NIAID NIH HHS AI34937NIAID NIH HHS R01 AI034937
6 · The paper itself

Abstract

In order to determine the role of ferrous iron transport in Legionella pathogenesis, we identified and mutated the feoB gene in virulent Legionella pneumophila strain 130b. As it is in Escherichia coli, the L. pneumophila feoB gene was contained within a putative feoAB operon. L. pneumophila feoB insertion mutants exhibited decreased ferrous but not ferric iron uptake compared to the wild type. Growth on standard buffered charcoal yeast extract agar or buffered yeast extract broth was unaffected by the loss of L. pneumophila FeoB. However, the L. pneumophila feoB mutant had a reduced ability to grow on buffered charcoal yeast extract agar with a reduced amount of its usual iron supplementation, a phenotype that could be complemented by the addition of feoB in trans. In unsupplemented buffered yeast extract broth, the feoB mutant also had a growth defect, which was further exacerbated by the addition of the ferrous iron chelator, 2,2'-dipyridyl. The feoB mutant was also 2.5 logs more resistant to streptonigrin than wild-type 130b, confirming its decreased ability to acquire iron during extracellular growth. Decreased replication of the feoB mutant was noted within iron-depleted Hartmannella vermiformis amoebae and human U937 cell macrophages. The reduced intracellular infectivity of the feoB mutant was complemented by the introduction of a plasmid containing feoAB. The L. pneumophila feoB gene conferred a modest growth advantage for the wild type over the mutant in a competition assay within the lungs of A/J mice. Taken together, these results indicate that L. pneumophila FeoB is a ferrous iron transporter that is important for extracellular and intracellular growth, especially in iron-limited environments. These data represent the first evidence for the importance of ferrous iron transport for intracellular replication by a human pathogen.

Indexed as

AnimalsBacterial ProteinsBase SequenceCation Transport ProteinsDNA, BacterialDrug Resistance, BacterialGenes, BacterialGenetic Complementation TestHartmannellaHumansIronLegionella pneumophilaLegionnaires' DiseaseMacrophagesMiceMice, Inbred ABacterial ProteinsCation Transport ProteinsDNA, BacterialFeoB protein, Helicobacter pyloriIronStreptonigrin

Identifiers

PMID12228295
PMCPMC128349
OpenAlexW2116089904

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.