Evidence map›Paper›PMID 30206380›Full record

ArticleScientific reports2018

Population level mitogenomics of long-lived bats reveals dynamic heteroplasmy and challenges the Free Radical Theory of Ageing.

David Jebb, Nicole M Foley, Conor V Whelan, Frédéric Touzalin, Sebastien J Puechmaille, Emma C Teeling

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Molecular evolution of animal aging.The EMBO journal · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Unparalleled mitochondrial heteroplasmy andCurrent research in insect science · 2022
    Article
  11. Article
  12. Ageing European lobsters (Evolutionary applications · 2021
    Article
  13. Article
  14. Alternative Animal Models of Aging Research.Frontiers in molecular biosciences · 2021
    Review
  15. Review
  16. Article
  17. Review
  18. Faraway, so close. The comparative method and the potential of non-model animals in mitochondrial research.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  19. Novel Insights Into Immune Systems of Bats.Frontiers in immunology · 2020
    Review
  20. 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

6 authors.

David JebbSchool of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland.
Nicole M FoleySchool of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland.ORCID 0000-0002-8169-9436
Conor V WhelanSchool of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland.
Frédéric TouzalinLaboratoire Evolution et Diversité Biologique, Université Toulouse 3, Paul Sabatier, 31062, Toulouse Cedex 09, France.
Sebastien J PuechmailleSchool of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland.
Emma C TeelingSchool of Biology and Environmental Science, University College Dublin, Belfield, Dublin 4, Ireland. emma.teeling@ucd.ie.

Funding

EC | European Research Council (ERC) ERC-2012-StG311000
6 · The paper itself

Abstract

Bats are the only mammals capable of true, powered flight, which drives an extremely high metabolic rate. The "Free Radical Theory of Ageing" (FTRA) posits that a high metabolic rate causes mitochondrial heteroplasmy and the progressive ageing phenotype. Contrary to this, bats are the longest-lived order of mammals given their small size and high metabolic rate. To investigate if bats exhibit increased mitochondrial heteroplasmy with age, we performed targeted, deep sequencing of mitogenomes and measured point heteroplasmy in wild, long lived Myotis myotis. Blood was sampled from 195 individuals, aged between <1 and at 6+ years old, and whole mitochondria deep-sequenced, with a subset sampled over multiple years. The majority of heteroplasmies were at a low frequency and were transitions. Oxidative mutations were present in only a small number of individuals, suggesting local oxidative stress events. Cohort data showed no significant increase in heteroplasmy with age, while longitudinal data from recaptured individuals showed heteroplasmy is dynamic, and does not increase uniformly over time. We show that bats do not suffer from the predicted, inevitable increase in heteroplasmy as posited by the FRTA, instead heteroplasmy was found to be dynamic, questioning its presumed role as a primary driver of ageing.

Indexed as

MutationAgingAnimalsChiropteraDNA, MitochondrialFree RadicalsHigh-Throughput Nucleotide SequencingDNA, MitochondrialFree Radicals

Identifiers

PMID30206380
PMCPMC6134106

What OpenQuestion holds

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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.