Evidence map›Paper›PMID 29931811›Full record

ArticleMicrobiologyOpen2019

Bacteroides fragilis requires the ferrous-iron transporter FeoAB and the CobN-like proteins BtuS1 and BtuS2 for assimilation of iron released from heme.

Edson R Rocha, Hector A Bergonia, Svetlana Gerdes, Charles Jeffrey Smith

Abstract read
In one paragraph

Article in MicrobiologyOpen, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Biochemical and functional characterization ofFrontiers in microbiology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. HmuY proteins of theFrontiers in cellular and infection microbiology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Frontiers in cellular and infection microbiology · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Analysis of SixInfection and immunity · 2022
    Article
  15. Article
  16. Article
  17. International journal of molecular sciences · 2021
    Article
  18. Article
  19. TheInfection and immunity · 2020
    Article
  20. Transition metals and host-microbe interactions in the inflamed intestine.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2019
    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.

Edson R RochaDepartment of Microbiology and Immunology, Brody School of Medicine, Greenville, North Carolina.ORCID 0000-0002-3472-8951
Hector A BergoniaIron and Heme Core, Division of Hematology, University of Utah School of Medicine, Salt Lake City, Utah.
Svetlana GerdesFellowship for Interpretation of Genomes, Burr Ridge, Illinois.
Charles Jeffrey SmithDepartment of Microbiology and Immunology, Brody School of Medicine, Greenville, North Carolina.

Funding

Proteomics CoreU54DK110858 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Anna E Beaudin, JAMES Eric COX · 2016 to 2026
$8.6M
Strategies of Bacteroides fragilis to acquire iron in the intestinal tract.R21AI125921 · NIAID · EAST CAROLINA UNIVERSITY · PI ROCHA, EDSON R · 2017 to 2018
$406k
NIAID NIH HHS R21 AI125921NIDDK NIH HHS U54 DK110858
6 · The paper itself

Abstract

The intestinal commensal and opportunistic anaerobic pathogen Bacteroides fragilis has an essential requirement for both heme and free iron to support growth in extraintestinal infections. In the absence of free iron, B. fragilis can utilize heme as the sole source of iron. However, the mechanisms to remove iron from heme are not completely understood. In this study, we show that the inner membrane ferrous iron transporter ∆feoAB mutant strain is no longer able to grow with heme as the sole source of iron. Genetic complementation with the feoAB gene operon completely restored growth. Our data indicate that iron is removed from heme in the periplasmic space, and the released iron is transported by the FeoAB system. Interestingly, when B. fragilis utilizes iron from heme, it releases heme-derived porphyrins by a dechelatase activity which is upregulated under low iron conditions. This is supported by the findings showing that formation of heme-derived porphyrins in the ∆feoAB mutant and the parent strain increased 30-fold and fivefold (respectively) under low iron conditions compared to iron replete conditions. Moreover, the btuS1 btuS2 double-mutant strain (lacking the predicted periplasmic, membrane anchored CobN-like proteins) also showed growth defect with heme as the sole source of iron, suggesting that BtuS1 and BtuS2 are involved in heme-iron assimilation. Though the dechelatase mechanism remains uncharacterized, assays performed in bacterial crude extracts show that BtuS1 and BtuS2 affect the regulation of the dechelatase-specific activities in an iron-dependent manner. These findings suggest that the mechanism to extract iron from heme in Bacteroides requires a group of proteins, which spans the periplasmic space to make iron available for cellular functions.

Indexed as

Bacterial ProteinsBacteroides fragilisBiological TransportCation Transport ProteinsHemeIronBacterial ProteinsCation Transport ProteinsHemeIronanaerobesanaerobic bacteriaBacteroideschelatasedechelatasedemetallasehemeiron

Identifiers

PMID29931811
PMCPMC6460266

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Registered trials

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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.