Evidence map›Paper›PMID 16980451›Full record

ArticleJournal of bacteriology2006

Heme utilization in Campylobacter jejuni.

Kristian A Ridley, Jonathan D Rock, Ying Li, Julian M Ketley

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

48 citing papers in PubMed, 86 citations in OpenAlex.

  1. TheProceedings of the National Academy of Sciences of the United States of America · 2026
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  4. Comparison of Media for the Detection ofPathogens (Basel, Switzerland) · 2025
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  8. InFrontiers in genetics · 2023
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  9. Current perspectives on irritable bowel syndrome: a narrative review.The Journal of international medical research · 2022
    Review
  10. Article
  11. Article
  12. Hydrogen Sulfide and Carbon Monoxide Tolerance in Bacteria.Antioxidants (Basel, Switzerland) · 2021
    Review
  13. Review
  14. Experimental Evolution ofFrontiers in microbiology · 2020
    Article
  15. Heme Uptake and Utilization by Gram-Negative Bacterial Pathogens.Frontiers in cellular and infection microbiology · 2019
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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.

Kristian A RidleyDepartment of Genetics, University of Leicester, Adrian Building, University Road, Leicester LE1 7RH, United Kingdom.
Jonathan D Rock
Ying Li
Julian M Ketley
University of Leicester · GB

Funding

Biotechnology and Biological Sciences Research Council D19661
6 · The paper itself

Abstract

A putative iron- and Fur-regulated hemin uptake gene cluster, composed of the transport genes chuABCD and a putative heme oxygenase gene (Cj1613c), has been identified in Campylobacter jejuni NCTC 11168. Mutation of chuA or Cj1613c leads to an inability to grow in the presence of hemin or hemoglobin as a sole source of iron. Mutation of chuB, -C, or -D only partially attenuates growth where hemin is the sole iron source, suggesting that an additional inner membrane (IM) ABC (ATP-binding cassette) transport system(s) for heme is present in C. jejuni. Genotyping experiments revealed that Cj1613c is highly conserved in 32 clinical isolates. One strain did not possess chuC, though it was still capable of using hemin/hemoglobin as a sole iron source, supporting the hypothesis that additional IM transport genes are present. In two other strains, sequence variations within the gene cluster were apparent and may account for an observed negative heme utilization phenotype. Analysis of promoter activity within the Cj1613c-chuA intergenic spacer region revealed chuABCD and Cj1613c are expressed from separate iron-repressed promoters and that this region also specifically binds purified recombinant Fur(Cj) in gel retardation studies. Absorbance spectroscopy of purified recombinant His(6)-Cj1613c revealed a 1:1 heme:His(6)-Cj1613c binding ratio. The complex was oxidatively degraded in the presence of ascorbic acid as the electron donor, indicating that the Cj1613c gene product functions as a heme oxygenase. In conclusion, we confirm the involvement of Cj1613c and ChuABCD in heme/hemoglobin utilization in C. jejuni.

Indexed as

Bacterial ProteinsBiological TransportCampylobacter InfectionsCampylobacter jejuniCulture MediaHemeHeme Oxygenase (Decyclizing)HeminHemoglobinsHumansMultigene FamilyOxidation-ReductionPhylogenyPromoter Regions, GeneticReceptors, Cell SurfaceBacterial ProteinsCulture MediaHemeHeme Oxygenase (Decyclizing)HeminHemoglobinsReceptors, Cell Surface

Identifiers

PMID16980451
PMCPMC1636299
OpenAlexW2125195630

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.