Evidence map›Paper›PMID 24551260›Full record

ArticlePLoS neglected tropical diseases2014

Laboratory colonisation and genetic bottlenecks in the tsetse fly Glossina pallidipes.

Marc Ciosi, Daniel K Masiga, Charles M R Turner

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Dual suppression ofFrontiers in microbiology · 2024
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  15. Differential virulence and tsetse fly transmissibility ofThe Onderstepoort journal of veterinary research · 2017
    Article
  16. Article
  17. 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

3 authors.

Marc CiosiMolecular Biology and Bioinformatics Unit, ICIPE, Nairobi, Kenya ; Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, United Kingdom.
Daniel K MasigaMolecular Biology and Bioinformatics Unit, ICIPE, Nairobi, Kenya ; Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, United Kingdom.
Charles M R TurnerInstitute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, United Kingdom.

Funding

Wellcome TrustWellcome Trust 093692
6 · The paper itself

Abstract

backgroundThe IAEA colony is the only one available for mass rearing of Glossina pallidipes, a vector of human and animal African trypanosomiasis in eastern Africa. This colony is the source for Sterile Insect Technique (SIT) programs in East Africa. The source population of this colony is unclear and its genetic diversity has not previously been evaluated and compared to field populations. METHODOLOGY/PRINCIPAL

findingsWe examined the genetic variation within and between the IAEA colony and its potential source populations in north Zimbabwe and the Kenya/Uganda border at 9 microsatellites loci to retrace the demographic history of the IAEA colony. We performed classical population genetics analyses and also combined historical and genetic data in a quantitative analysis using Approximate Bayesian Computation (ABC). There is no evidence of introgression from the north Zimbabwean population into the IAEA colony. Moreover, the ABC analyses revealed that the foundation and establishment of the colony was associated with a genetic bottleneck that has resulted in a loss of 35.7% of alleles and 54% of expected heterozygosity compared to its source population. Also, we show that tsetse control carried out in the 1990's is likely reduced the effective population size of the Kenya/Uganda border population. CONCLUSIONS/SIGNIFICANCE: All the analyses indicate that the area of origin of the IAEA colony is the Kenya/Uganda border and that a genetic bottleneck was associated with the foundation and establishment of the colony. Genetic diversity associated with traits that are important for SIT may potentially have been lost during this genetic bottleneck which could lead to a suboptimal competitiveness of the colony males in the field. The genetic diversity of the colony is lower than that of field populations and so, studies using colony flies should be interpreted with caution when drawing general conclusions about G. pallidipes biology.

Indexed as

Genetic DriftAnimalsAnimals, LaboratoryAnimals, WildBayes TheoremBiomedical ResearchGenetic VariationKenyaTsetse FliesUgandaZimbabwe

Identifiers

PMID24551260
PMCPMC3923722

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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.