Evidence map›Paper›PMID 29942072›Full record

ArticleThe ISME journal2018

Genetic variability and ontogeny predict microbiome structure in a disease-challenged montane amphibian.

Sarah M Griffiths, Xavier A Harrison, Ché Weldon, Michael D Wood, Abigail Pretorius, Kevin Hopkins, Graeme Fox, Richard F Preziosi, Rachael E Antwis

Abstract read
In one paragraph

Article in The ISME journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
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  5. Archival mitogenomes identify invasion by theProceedings. Biological sciences · 2024
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  7. Environment predictsEcology and evolution · 2024
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  20. Chytrid fungi and global amphibian declines.Nature reviews. Microbiology · 2020
    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

9 authors.

Sarah M GriffithsSchool of Science and the Environment, Manchester Metropolitan University, Manchester, UK. griffiths.sarahm@gmail.com.ORCID http://orcid.org/0000-0003-4743-049X
Xavier A HarrisonInstitute of Zoology, Zoological Society of London, London, UK. xav.harrison@gmail.com.ORCID http://orcid.org/0000-0002-2004-3601
Ché WeldonUnit for Environmental Research and Management, Faculty of Natural Science, North-West University, Potchefstroom, South Africa.
Michael D WoodSchool of Environment and Life Sciences, University of Salford, Salford, UK.ORCID http://orcid.org/0000-0002-0635-2387
Abigail PretoriusUnit for Environmental Research and Management, Faculty of Natural Science, North-West University, Potchefstroom, South Africa.
Kevin HopkinsInstitute of Zoology, Zoological Society of London, London, UK.
Graeme FoxSchool of Science and the Environment, Manchester Metropolitan University, Manchester, UK.ORCID http://orcid.org/0000-0001-7980-6944
Richard F PreziosiSchool of Science and the Environment, Manchester Metropolitan University, Manchester, UK.ORCID http://orcid.org/0000-0003-0468-6655
Rachael E AntwisUnit for Environmental Research and Management, Faculty of Natural Science, North-West University, Potchefstroom, South Africa. r.e.antwis@salford.ac.uk.ORCID http://orcid.org/0000-0002-8849-8194

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amphibian populations worldwide are at risk of extinction from infectious diseases, including chytridiomycosis caused by the fungal pathogen Batrachochytrium dendrobatidis (Bd). Amphibian cutaneous microbiomes interact with Bd and can confer protective benefits to the host. The composition of the microbiome itself is influenced by many environment- and host-related factors. However, little is known about the interacting effects of host population structure, genetic variation and developmental stage on microbiome composition and Bd prevalence across multiple sites. Here we explore these questions in Amietia hymenopus, a disease-affected frog in southern Africa. We use microsatellite genotyping and 16S amplicon sequencing to show that the microbiome associated with tadpole mouthparts is structured spatially, and is influenced by host genotype and developmental stage. We observed strong genetic structure in host populations based on rivers and geographic distances, but this did not correspond to spatial patterns in microbiome composition. These results indicate that demographic and host genetic factors affect microbiome composition within sites, but different factors are responsible for host population structure and microbiome structure at the between-site level. Our results help to elucidate complex within- and among- population drivers of microbiome structure in amphibian populations. That there is a genetic basis to microbiome composition in amphibians could help to inform amphibian conservation efforts against infectious diseases.

Indexed as

ChytridiomycotaMicrobiotaAmphibiansAnimalsAnuraGenetic Predisposition to DiseaseMycosesSkinSouth Africa

Identifiers

PMID29942072
PMCPMC6155040

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.