Evidence map›Paper›PMID 23813677›Full record

ArticleMicrobiology (Reading, England)2013

Distribution and diversity of the haemoglobin-haptoglobin iron-acquisition systems in pathogenic and non-pathogenic Neisseria.

Odile B Harrison, Julia S Bennett, Jeremy P Derrick, Martin C J Maiden, Christopher D Bayliss

Abstract readComparative Study
In one paragraph

Article in Microbiology (Reading, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Pirates of the haemoglobin.Microbial cell (Graz, Austria) · 2022
    Review
  6. Article
  7. Review
  8. Review
  9. Acquisition of virulence genes by a carrier strain gave rise to the ongoing epidemics of meningococcal disease in West Africa.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. Review
  11. Article
  12. Article
  13. Heme Synthesis and Acquisition in Bacterial Pathogens.Journal of molecular biology · 2016
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

5 authors.

Odile B HarrisonDepartment of Zoology, University of Oxford, South Parks Road, Oxford OX1 3SY, UK.
Julia S BennettDepartment of Zoology, University of Oxford, South Parks Road, Oxford OX1 3SY, UK.
Jeremy P DerrickFaculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK.
Martin C J MaidenDepartment of Zoology, University of Oxford, South Parks Road, Oxford OX1 3SY, UK.
Christopher D BaylissDepartment of Genetics, University of Leicester, Leicester LE1 7RH, UK.

Funding

Wellcome Trust 087622
6 · The paper itself

Abstract

A new generation of vaccines containing multiple protein components that aim to provide broad protection against serogroup B meningococci has been developed. One candidate, 4CMenB (4 Component MenB), has been approved by the European Medicines Agency, but is predicted to provide at most 70-80 % strain coverage; hence there is a need for second-generation vaccines that achieve higher levels of coverage. Prior knowledge of the diversity of potential protein vaccine components is a key step in vaccine design. A number of iron import systems have been targeted in meningococcal vaccine development, including the HmbR and HpuAB outer-membrane proteins, which mediate the utilization of haemoglobin or haemoglobin-haptoglobin complexes as iron sources. While the genetic diversity of HmbR has been described, little is known of the diversity of HpuAB. Using whole genome sequences deposited in a Bacterial Isolate Genome Sequence Database (BIGSDB), the prevalence and diversity of HpuAB among Neisseria were investigated. HpuAB was widely present in a range of Neisseria species whereas HmbR was mainly limited to the pathogenic species Neisseria meningitidis and Neisseria gonorrhoeae. Patterns of sequence variation in sequences from HpuAB proteins were suggestive of recombination and diversifying selection consistent with strong immune selection. HpuAB was subject to repeat-mediated phase variation in pathogenic Neisseria and the closely related non-pathogenic Neisseria species Neisseria lactamica and Neisseria polysaccharea but not in the majority of other commensal Neisseria species. These findings are consistent with HpuAB being subject to frequent genetic transfer potentially limiting the efficacy of this receptor as a vaccine candidate.

Indexed as

Bacterial Outer Membrane ProteinsBacterial ProteinsGenetic VariationHaptoglobinsHemoglobinsHumansIronMolecular Sequence DataNeisseriaNeisseriaceae InfectionsPhylogenyProtein ConformationReceptors, Cell SurfaceBacterial Outer Membrane ProteinsBacterial ProteinsHaptoglobinsHemoglobinsHmbR protein, Neisseria meningitidisHpuA protein, NeisseriaHpuB protein, NeisseriaIronReceptors, Cell Surface

Identifiers

PMID23813677
PMCPMC3783016

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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.