Evidence map›Paper›PMID 16933993›Full record

ArticlePLoS pathogens2006

Staphylococcus aureus redirects central metabolism to increase iron availability.

David B Friedman, Devin L Stauff, Gleb Pishchany, Corbin W Whitwell, Victor J Torres, Eric P Skaar

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

122 citing papers in PubMed, 217 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Pathogenicity Mechanisms ofInternational journal of molecular sciences · 2025
    Review
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  7. Article
  8. Article
  9. Review
  10. Review
  11. ThebioRxiv : the preprint server for biology · 2024
    Article
  12. SilversolPharmaceutics · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

62 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

6 authors at 1 institution in 1 country.

David B FriedmanMass Spectrometry Research Center, Department of Biochemistry, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Devin L Stauff
Gleb Pishchany
Corbin W Whitwell
Victor J Torres
Eric P Skaar
Vanderbilt University Medical Center · US

Funding

Immunobiology of Blood and Vascular Systems Training ProgramT32HL069765 · NHLBI · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2002 to 2016
$6.5M
Mechanism and function of heme-iron utilization in staphylococcal pathogenesisR01AI069233 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SKAAR, ERIC P · 2006 to 2020
$5.6M
Mechanisms of heme utilization by Staphylococcus aureusF32AI071487 · NIAID · VANDERBILT UNIVERSITY · PI TORRES, VICTOR J. · 2006 to 2008
$118k
NHLBI NIH HHS T32 HL069765NHLBI NIH HHS T32 HL069765-05NIAID NIH HHS AI071487NIAID NIH HHS AI69233NIAID NIH HHS F32 AI071487NIAID NIH HHS R01 AI069233
6 · The paper itself

Abstract

Staphylococcus aureus pathogenesis is significantly influenced by the iron status of the host. However, the regulatory impact of host iron sources on S. aureus gene expression remains unknown. In this study, we combine multivariable difference gel electrophoresis and mass spectrometry with multivariate statistical analyses to systematically cluster cellular protein response across distinct iron-exposure conditions. Quadruplicate samples were simultaneously analyzed for alterations in protein abundance and/or post-translational modification state in response to environmental (iron chelation, hemin treatment) or genetic (Deltafur) alterations in bacterial iron exposure. We identified 120 proteins representing several coordinated biochemical pathways that are affected by changes in iron-exposure status. Highlighted in these experiments is the identification of the heme-regulated transport system (HrtAB), a novel transport system which plays a critical role in staphylococcal heme metabolism. Further, we show that regulated overproduction of acidic end-products brought on by iron starvation decreases local pH resulting in the release of iron from the host iron-sequestering protein transferrin. These findings reveal novel strategies used by S. aureus to acquire scarce nutrients in the hostile host environment and begin to define the iron and heme-dependent regulons of S. aureus.

Indexed as

Gene Expression Regulation, BacterialBacterial ProteinsBiological AvailabilityElectrophoresis, Gel, Two-DimensionalHemeHydrogen-Ion ConcentrationIronIron-Binding ProteinsIron DeficienciesMass SpectrometryProteomicsRepressor ProteinsStaphylococcus aureusTransferrinBacterial Proteinsferric uptake regulating proteins, bacterialHemeIronIron-Binding ProteinsRepressor ProteinsTransferrin

Identifiers

PMID16933993
PMCPMC1557832
OpenAlexW2113638991

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.