Evidence map›Paper›PMID 41316404›Full record

ArticleAnimal microbiome2025

Bsal susceptibility depends on host origin but not on skin microbiota in captive Pleurodeles waltl.

Léa Fieschi-Méric, Frank Pasmans, Eduardo Fernández Meléndez, Sofie De Bruyckere, Ellen Blomme, Elin Verbrugghe, An Martel

Abstract read
In one paragraph

Article in Animal microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Co-Exposure with the Herbicide 2,4-D Does Not ExacerbateAnimals : an open access journal from MDPI · 2025
    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

7 authors.

Léa Fieschi-MéricWildlife Health Ghent, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, B9820, Belgium. lea.fieschimeric@ugent.be.
Frank PasmansWildlife Health Ghent, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, B9820, Belgium.
Eduardo Fernández MeléndezWildlife Health Ghent, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, B9820, Belgium.
Sofie De BruyckereWildlife Health Ghent, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, B9820, Belgium.
Ellen BlommeWildlife Health Ghent, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, B9820, Belgium.
Elin VerbruggheWildlife Health Ghent, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, B9820, Belgium.
An MartelWildlife Health Ghent, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, Merelbeke, B9820, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmidst the current biodiversity crisis, amphibians are particularly endangered by the emergence of infectious diseases. The skin disease chytridiomycosis is caused by the fungi Batrachochytrium dendrobatidis (Bd) and B. salamandrivorans (Bsal), which may interact with bacterial symbionts present on the amphibian epidermis. Extensive research has explored the interactions between the amphibian microbiota and Bd; yet, little is known about its interactions with Bsal. In this paper, we used the ribbed newt (Pleurodeles waltl), a model species displaying pronounced among-individual variation in response to Bsal, to (1) determine whether susceptibility to Bsal and individual microbiota vary between source groups; (2) test whether susceptibility to Bsal can be predicted from skin microbiota before exposure and (3) quantify microbiota volatility over time to determine whether Bsal infection intensity and chytridiomycosis severity correlate with the magnitude of shifts in bacterial communities caused by Bsal exposure.

resultsOur results demonstrate that newts of different origin harbor distinct microbiota even under uniform rearing conditions. We show that Bsal infection intensity and disease severity cannot be predicted from the diversity, structure, or composition of the skin microbiota of P. waltl. Instead, a strong relation between newts' source group and their response to Bsal suggests that other factors might underpin among-individual variation in Bsal susceptibility in this species. Moreover, our results indicate that the intensity of early Bsal infection and longer-term severity of chytridiomycosis do not correlate with the magnitude of microbiota change following Bsal exposure.

conclusionThese results demonstrate a limited involvement of the microbiota in Bsal dynamics in P. waltl, suggesting that other mechanisms contribute to individual Bsal susceptibility. Further research on the relation between chytrid pathogens and their amphibian hosts will be instrumental to improve the conservation of the most endangered vertebrate class on earth.

Indexed as

AmphibiaBatrachochytrium salamandrivoransChytridiomycosisDisease severityEmerging infectious diseasesMicrobiomeMicrobiome volatilityUrodela

Identifiers

PMID41316404
PMCPMC12661705

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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.