Evidence map›Paper›PMID 17015669›Full record

ArticleJournal of bacteriology2006

Comparative phylogenomics of Clostridium difficile reveals clade specificity and microevolution of hypervirulent strains.

R A Stabler, D N Gerding, J G Songer, D Drudy, J S Brazier, H T Trinh, A A Witney, J Hinds, B W Wren

Abstract readComparative Study
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 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing 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

117 citing papers in PubMed.

  1. Contact dependent suppression ofbioRxiv : the preprint server for biology · 2026
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  2. The critical role ofApplied and environmental microbiology · 2026
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  3. Development of a high-throughput screening platform forAntimicrobial agents and chemotherapy · 2026
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  4. Comparative Genomics of Clostridioides difficile.Advances in experimental medicine and biology · 2024
    Article
  5. Ribotypes and New Virulent Strains Across Europe.Advances in experimental medicine and biology · 2024
    Review
  6. Article
  7. Detection and Genomic Characterisation ofPathogens (Basel, Switzerland) · 2022
    Article
  8. Capturing the environment of the Clostridioides difficile infection cycle.Nature reviews. Gastroenterology & hepatology · 2022
    Review
  9. Review
  10. Article
  11. Transition From PCR-Ribotyping to Whole Genome Sequencing Based Typing ofFrontiers in cellular and infection microbiology · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2020
    Review
  17. Article
  18. Enterotoxic Clostridia:Microbiology spectrum · 2019
    Review
  19. Article
  20. Article

57 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

9 authors.

R A StablerDepartment of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, United Kingdom.
D N Gerding
J G Songer
D Drudy
J S Brazier
H T Trinh
A A Witney
J Hinds
B W Wren

Funding

Wellcome Trust 062511
6 · The paper itself

Abstract

Clostridium difficile is the most frequent cause of nosocomial diarrhea worldwide, and recent reports suggested the emergence of a hypervirulent strain in North America and Europe. In this study, we applied comparative phylogenomics (whole-genome comparisons using DNA microarrays combined with Bayesian phylogenies) to model the phylogeny of C. difficile, including 75 diverse isolates comprising hypervirulent, toxin-variable, and animal strains. The analysis identified four distinct statistically supported clusters comprising a hypervirulent clade, a toxin A(-) B(+) clade, and two clades with human and animal isolates. Genetic differences among clades revealed several genetic islands relating to virulence and niche adaptation, including antibiotic resistance, motility, adhesion, and enteric metabolism. Only 19.7% of genes were shared by all strains, confirming that this enteric species readily undergoes genetic exchange. This study has provided insight into the possible origins of C. difficile and its evolution that may have implications in disease control strategies.

Indexed as

Genome, BacterialPhylogenyAnimalsBacterial AdhesionBacterial ToxinsClostridioides difficileCluster AnalysisDNA, BacterialDrug Resistance, BacterialGene Transfer, HorizontalGenomic IslandsHumansMovementNucleic Acid HybridizationOligonucleotide Array Sequence AnalysisVirulenceBacterial ToxinsDNA, Bacterial

Identifiers

PMID17015669
PMCPMC1636221

What OpenQuestion holds

Textmetadata
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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.