Evidence map›Paper›PMID 23984967›Full record

ArticleBMC genomics2013

Comparative genomics of Campylobacter concisus isolates reveals genetic diversity and provides insights into disease association.

Nandan P Deshpande, Nadeem O Kaakoush, Marc R Wilkins, Hazel M Mitchell

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
8.4field-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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Genetic Diversity ofMicroorganisms · 2025
    Article
  2. Genomic diversity and taxonomic marker forFrontiers in microbiology · 2023
    Article
  3. Review
  4. Review
  5. Analysis of completeMicrobial genomics · 2020
    Article
  6. Review
  7. Pathogenomics of EmergingClinical microbiology reviews · 2019
    Review
  8. NovelJournal of lipid research · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Complete Genome Sequence ofGenome announcements · 2017
    Article
  14. Frontiers in physiology · 2017
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Global Epidemiology of Campylobacter Infection.Clinical microbiology reviews · 2015
    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 at 1 institution in 1 country.

Nandan P DeshpandeSchool of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney 2052, NSW, Australia. H.Mitchell@unsw.edu.au.
Nadeem O Kaakoush
Marc R Wilkins
Hazel M Mitchell
UNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn spite of its association with gastroenteritis and inflammatory bowel diseases, the isolation of Campylobacter concisus from both diseased and healthy individuals has led to controversy regarding its role as an intestinal pathogen. One proposed reason for this is the presence of high genetic diversity among the genomes of C. concisus strains.

resultsIn this study the genomes of six C. concisus strains were sequenced, assembled and annotated including two strains isolated from Crohn's disease patients (UNSW2 and UNSW3), three from gastroenteritis patients (UNSW1, UNSWCS and ATCC 51562) and one from a healthy individual (ATCC 51561). The genomes of C. concisus BAA-1457 and UNSWCD, available from NCBI, were included in subsequent comparative genomic analyses. The Pan and Core genomes for the sequenced C. concisus strains consisted of 3254 and 1556 protein coding genes, respectively.

conclusionGenes were identified with specific conservation in C. concisus strains grouped by phenotypes such as invasiveness, adherence, motility and diseased states. Phylogenetic trees based on ribosomal RNA sequences and concatenated host-related pathways for the eight C. concisus strains were generated using the neighbor-joining method, of which the 16S rRNA gene and peptidoglycan biosynthesis grouped the C. concisus strains according to their pathogenic phenotypes. Furthermore, 25 non-synonymous amino acid changes with 14 affecting functional domains, were identified within proteins of conserved host-related pathways, which had possible associations with the pathogenic potential of C. concisus strains. Finally, the genomes of the eight C. concisus strains were compared to the nine available genomes of the well-established pathogen Campylobacter jejuni, which identified several important differences in the respiration pathways of these two species. Our findings indicate that C. concisus strains are genetically diverse, and suggest the genomes of this bacterium contain respiration pathways and modifications in the peptidoglycan layer that may play an important role in its virulence.

Indexed as

Polymorphism, Single NucleotideBacterial AdhesionCampylobacterCampylobacter InfectionsCrohn DiseaseGastroenteritisGene OntologyGenome, BacterialGenomicsHost-Pathogen InteractionsHumansPhenotypePhylogenyPlasmidsRNA, BacterialRNA, RibosomalRNA, BacterialRNA, Ribosomal

Identifiers

PMID23984967
PMCPMC3765806
OpenAlexW1983204233

What OpenQuestion holds

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LicenceCC BY
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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.