Evidence map›Paper›PMID 17172337›Full record

ArticleJournal of bacteriology2007

Evolution of Mycobacterium ulcerans and other mycolactone-producing mycobacteria from a common Mycobacterium marinum progenitor.

Marcus J Yip, Jessica L Porter, Janet A M Fyfe, Caroline J Lavender, Françoise Portaels, Martha Rhodes, Howard Kator, Angelo Colorni, Grant A Jenkin, Tim Stinear

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
10.1field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 166 citations in OpenAlex.

  1. Review
  2. Systematic review: Global host range, case fatality and detection rates ofJournal of clinical tuberculosis and other mycobacterial diseases · 2024
    Review
  3. Cracking the antigenic code of mycobacteria: CFP-10/ESAT-6 tuberculosis skin test and misleading results.Journal of clinical tuberculosis and other mycobacterial diseases · 2024
    Article
  4. Unlocking Opportunities forACS infectious diseases · 2024
    Review
  5. Article
  6. Review
  7. Linking theOne health (Amsterdam, Netherlands) · 2021
    Review
  8. Review
  9. Article
  10. Article
  11. Human genetics of Buruli ulcer.Human genetics · 2020
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Discovery and Characterization ofFrontiers in microbiology · 2018
    Article
  18. Buruli Ulcer: a Review of the Current Knowledge.Current tropical medicine reports · 2018
    Review
  19. Article
  20. Mycobacterium marinum.Microbiology spectrum · 2017
    Review

20 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

10 authors at 5 institutions in 4 countries.

Marcus J YipDepartment of Microbiology, Monash University, Wellington Road, Clayton 3800, Australia.
Jessica L Porter
Janet A M Fyfe
Caroline J Lavender
Françoise Portaels
Martha Rhodes
Howard Kator
Angelo Colorni
Grant A Jenkin
Tim Stinear
Monash University · AUVictorian Infectious Diseases Reference Laboratory · AUWilliam & Mary · USInstituut voor Tropische Geneeskunde · BEIsrael Oceanographic and Limnological Research · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It had been assumed that production of the cytotoxic polyketide mycolactone was strictly associated with Mycobacterium ulcerans, the causative agent of Buruli ulcer. However, a recent study has uncovered a broader distribution of mycolactone-producing mycobacteria (MPM) that includes mycobacteria cultured from diseased fish and frogs in the United States and from diseased fish in the Red and Mediterranean Seas. All of these mycobacteria contain versions of the M. ulcerans pMUM plasmid, produce mycolactones, and show a high degree of genetic relatedness to both M. ulcerans and Mycobacterium marinum. Here, we show by multiple genetic methods, including multilocus sequence analysis and DNA-DNA hybridization, that all MPM have evolved from a common M. marinum progenitor to form a genetically cohesive group among a more diverse assemblage of M. marinum strains. Like M. ulcerans, the fish and frog MPM show multiple copies of the insertion sequence IS2404. Comparisons of pMUM and chromosomal gene sequences demonstrate that plasmid acquisition and the subsequent ability to produce mycolactone were probably the key drivers of speciation. Ongoing evolution among MPM has since produced at least two genetically distinct ecotypes that can be broadly divided into those typically causing disease in ectotherms (but also having a high zoonotic potential) and those causing disease in endotherms, such as humans.

Indexed as

Bacterial ToxinsBase SequenceDNA Transposable ElementsEvolution, MolecularMacrolidesMinisatellite RepeatsMolecular Sequence DataMycobacterium marinumMycobacterium ulceransNucleic Acid HybridizationPlasmidsSequence Analysis, DNABacterial ToxinsDNA Transposable ElementsMacrolidesmycolactone

Identifiers

PMID17172337
PMCPMC1855710
OpenAlexW1975649026

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.