Evidence map›Paper›PMID 26809473›Full record

ArticleeLife2016

Population genomics reveals the origin and asexual evolution of human infective trypanosomes.

William Weir, Paul Capewell, Bernardo Foth, Caroline Clucas, Andrew Pountain, Pieter Steketee, Nicola Veitch, Mathurin Koffi, Thierry De Meeûs, Jacques Kaboré and 7 more

Abstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
  2. Extensive heterozygosity and genetic exchange among natural populations ofProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Genome diversity ofFrontiers in cellular and infection microbiology · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Haplotype divergence supports long-term asexuality in the oribatid miteProceedings of the National Academy of Sciences of the United States of America · 2021
    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

17 authors.

William WeirWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Paul CapewellWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Bernardo FothSanger Institute, Wellcome Trust Genome Campus, Cambridge, United Kingdom.
Caroline ClucasWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Andrew PountainWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Pieter SteketeeWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Nicola VeitchWest Medical Building, Office 350, University of Glasgow, Glasgow, Scotland.
Mathurin KoffiUFR Environnement, Laboratoire des Interactions Hôte-Microorganismes-Environnement et Evolution (LIHME), Université Jean Lorougnon GUEDE, Daloa, Côte d'Ivoire.
Thierry De MeeûsInstitut de Recherche pour le Développement, Campus International de Baillarguet, Montpellier, France.ORCID http://orcid.org/0000-0001-8807-241X
Jacques KaboréCentre International de Recherche-Développement de l'Elevage en zone Subhumide, Bobo-Dioulasso, Burkina Faso.
Mamadou CamaraProgramme National de Lutte contre la Trypanosomiase Humaine Africaine, Conakry, Guinea.
Anneli CooperWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Andy TaitWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Vincent JamonneauInstitut de Recherche pour le Développement, Campus International de Baillarguet, Montpellier, France.
Bruno BuchetonInstitut de Recherche pour le Développement, Campus International de Baillarguet, Montpellier, France.
Matt BerrimanSanger Institute, Wellcome Trust Genome Campus, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0002-9581-0377
Annette MacLeodWellcome Centre for Molecular Parasitology, College of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.

Funding

Wellcome Trust 085349Wellcome Trust 098051
6 · The paper itself

Abstract

Evolutionary theory predicts that the lack of recombination and chromosomal re-assortment in strictly asexual organisms results in homologous chromosomes irreversibly accumulating mutations and thus evolving independently of each other, a phenomenon termed the Meselson effect. We apply a population genomics approach to examine this effect in an important human pathogen, Trypanosoma brucei gambiense. We determine that T.b. gambiense is evolving strictly asexually and is derived from a single progenitor, which emerged within the last 10,000 years. We demonstrate the Meselson effect for the first time at the genome-wide level in any organism and show large regions of loss of heterozygosity, which we hypothesise to be a short-term compensatory mechanism for counteracting deleterious mutations. Our study sheds new light on the genomic and evolutionary consequences of strict asexuality, which this pathogen uses as it exploits a new biological niche, the human population.

Indexed as

Evolution, MolecularReproduction, AsexualHumansMetagenomicsMutationTrypanosoma brucei gambienseTrypanosomiasisevolutionary biologygenomicsinfectious diseaseMeselson effectmicrobiologypopulation genomicsTrypanosoma brucei gambiensetrypanosomiasis

Identifiers

PMID26809473
PMCPMC4739771

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.