Changes to Skin Microbiome Community Dynamics Support Resistance to Enzootic and Epizootic Strains of Batrachochytrium dendrobatidis (Bd) in the Spotted Salamander (Ambystoma maculatum).

Bibliographic Details
Title: Changes to Skin Microbiome Community Dynamics Support Resistance to Enzootic and Epizootic Strains of Batrachochytrium dendrobatidis (Bd) in the Spotted Salamander (Ambystoma maculatum).
Authors: Cambridge TW; Department of Biology, Trent University, Peterborough, Ontario, Canada., Kyle CJ; Forensic Science Department, Trent University, Peterborough, Ontario, Canada., Lesbarrères D; Environment and Climate Change Canada, Université de Sudbury, Sudbury, Ontario, Canada., Murray DL; Department of Biology, Trent University, Peterborough, Ontario, Canada.
Source: Molecular ecology [Mol Ecol] 2026 Aug; Vol. 35 (16), pp. e70514.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Language: English
Journal Info: Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 9214478 Publication Model: Print Cited Medium: Internet ISSN: 1365-294X (Electronic) Linking ISSN: 09621083 NLM ISO Abbreviation: Mol Ecol Subsets: MEDLINE
Imprint Name(s): Original Publication: Oxford, UK : Blackwell Scientific Publications, c1992-
MeSH Terms: Batrachochytrium*/pathogenicity , Ambystoma*/microbiology , Disease Resistance*/genetics , Skin*/microbiology , Mycoses*/veterinary , Mycoses*/microbiology , Skin Microbiome* , Microbiota*, RNA, Ribosomal, 16S/genetics ; Animals ; Host-Pathogen Interactions ; Chytridiomycota
Abstract: Global spread of animal pathogens has contributed to species declines and extinctions. In regions where a particular disease is enzootic, pathogen inhibition may arise through protection provided by host-associated microbiomes. Amphibians skin microbiomes can inhibit growth of the fungal pathogen Batrachochytrium dendrobatidis (Bd), preventing emergence of disease through a range of microbe-mediated antifungal mechanisms, allowing hosts to resist Bd infection. However, it remains unclear how skin microbiomes may shift in community composition or structure following infection by different Bd strain types. We assessed infection dynamics of Bd-resistant amphibians (Ambystoma maculatum) following experimental exposure to enzootic and epizootic strains of Bd-GPL and tracking pathogen load and bacterial skin microbiome community responses from exposure through to recovery, using 16S rRNA metabarcoding. We found that microbiome communities shifted post-exposure, with increasing diversity, dominance, abundance and total proportion of known Bd-inhibitory microbes, indicating microbial rescue effects during infection. We also observed lower intra-host variation in diversity during recovery, indicating a shared functional response across the host population and broadly indicative of microbial community resilience. Salamanders exposed to enzootic Bd had greater pathogen loads over time and demonstrated more prolonged community changes and more putatively protective microbiomes, whereas epizootic Bd infection was more rapidly cleared following temporary increase in inhibitory microbes. Collectively, these results indicate that skin microbiomes may offer a crucial barrier to fungal disease in Bd-resistant amphibians, with exposure to pathogens inducing changes in microbial community structure that benefit hosts, possibly driven by localized coevolutionary changes in infection dynamics. Our work illustrates how complex host-pathogen interactions are mediated by skin microbiomes through changes in microbial community dynamics that favour pathogen resistant microbes.
(© 2026 The Author(s). Molecular Ecology published by John Wiley & Sons Ltd.)
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Grant Information: Natural Sciences and Engineering Research Council of Canada
Contributed Indexing: Keywords: Batrachochytrium dendrobatidis; community resilience; disease resistance; host‐associated microbiome; local adaptation; microbial rescue
Molecular Sequence: BioProject PRJNA1354488
Substance Nomenclature: 0 (RNA, Ribosomal, 16S)
Entry Date(s): Date Created: 20260819 Date Completed: 20260819 Latest Revision: 20260902
Update Code: 20260903
PubMed Central ID: PMC13487513
DOI: 10.1111/mec.70514
PMID: 42615103
Database: MEDLINE
Description
ISSN:1365-294X
DOI:10.1111/mec.70514