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Climate forcing of an emerging pathogenic fungus across a montane multi-host community

Changes in the timings of seasonality as a result of anthropogenic climate change are predicted to occur over the coming decades. While this is expected to have widespread impacts on the dynamics of infectious disease through environmental forcing, empirical data are lacking. Here, we investigated w...

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Autores principales: Clare, Frances C., Halder, Julia B., Daniel, Olivia, Bielby, Jon, Semenov, Mikhail A., Jombart, Thibaut, Loyau, Adeline, Schmeller, Dirk S., Cunningham, Andrew A., Rowcliffe, Marcus, Garner, Trenton W. J., Bosch, Jaime, Fisher, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095533/
https://www.ncbi.nlm.nih.gov/pubmed/28080980
http://dx.doi.org/10.1098/rstb.2015.0454
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author Clare, Frances C.
Halder, Julia B.
Daniel, Olivia
Bielby, Jon
Semenov, Mikhail A.
Jombart, Thibaut
Loyau, Adeline
Schmeller, Dirk S.
Cunningham, Andrew A.
Rowcliffe, Marcus
Garner, Trenton W. J.
Bosch, Jaime
Fisher, Matthew C.
author_facet Clare, Frances C.
Halder, Julia B.
Daniel, Olivia
Bielby, Jon
Semenov, Mikhail A.
Jombart, Thibaut
Loyau, Adeline
Schmeller, Dirk S.
Cunningham, Andrew A.
Rowcliffe, Marcus
Garner, Trenton W. J.
Bosch, Jaime
Fisher, Matthew C.
author_sort Clare, Frances C.
collection PubMed
description Changes in the timings of seasonality as a result of anthropogenic climate change are predicted to occur over the coming decades. While this is expected to have widespread impacts on the dynamics of infectious disease through environmental forcing, empirical data are lacking. Here, we investigated whether seasonality, specifically the timing of spring ice-thaw, affected susceptibility to infection by the emerging pathogenic fungus Batrachochytrium dendrobatidis (Bd) across a montane community of amphibians that are suffering declines and extirpations as a consequence of this infection. We found a robust temporal association between the timing of the spring thaw and Bd infection in two host species, where we show that an early onset of spring forced high prevalences of infection. A third highly susceptible species (the midwife toad, Alytes obstetricans) maintained a high prevalence of infection independent of time of spring thaw. Our data show that perennially overwintering midwife toad larvae may act as a year-round reservoir of infection with variation in time of spring thaw determining the extent to which infection spills over into sympatric species. We used future temperature projections based on global climate models to demonstrate that the timing of spring thaw in this region will advance markedly by the 2050s, indicating that climate change will further force the severity of infection. Our findings on the effect of annual variability on multi-host infection dynamics show that the community-level impact of fungal infectious disease on biodiversity will need to be re-evaluated in the face of climate change. This article is part of the themed issue ‘Tackling emerging fungal threats to animal health, food security and ecosystem resilience’.
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spelling pubmed-50955332016-12-05 Climate forcing of an emerging pathogenic fungus across a montane multi-host community Clare, Frances C. Halder, Julia B. Daniel, Olivia Bielby, Jon Semenov, Mikhail A. Jombart, Thibaut Loyau, Adeline Schmeller, Dirk S. Cunningham, Andrew A. Rowcliffe, Marcus Garner, Trenton W. J. Bosch, Jaime Fisher, Matthew C. Philos Trans R Soc Lond B Biol Sci Articles Changes in the timings of seasonality as a result of anthropogenic climate change are predicted to occur over the coming decades. While this is expected to have widespread impacts on the dynamics of infectious disease through environmental forcing, empirical data are lacking. Here, we investigated whether seasonality, specifically the timing of spring ice-thaw, affected susceptibility to infection by the emerging pathogenic fungus Batrachochytrium dendrobatidis (Bd) across a montane community of amphibians that are suffering declines and extirpations as a consequence of this infection. We found a robust temporal association between the timing of the spring thaw and Bd infection in two host species, where we show that an early onset of spring forced high prevalences of infection. A third highly susceptible species (the midwife toad, Alytes obstetricans) maintained a high prevalence of infection independent of time of spring thaw. Our data show that perennially overwintering midwife toad larvae may act as a year-round reservoir of infection with variation in time of spring thaw determining the extent to which infection spills over into sympatric species. We used future temperature projections based on global climate models to demonstrate that the timing of spring thaw in this region will advance markedly by the 2050s, indicating that climate change will further force the severity of infection. Our findings on the effect of annual variability on multi-host infection dynamics show that the community-level impact of fungal infectious disease on biodiversity will need to be re-evaluated in the face of climate change. This article is part of the themed issue ‘Tackling emerging fungal threats to animal health, food security and ecosystem resilience’. The Royal Society 2016-12-05 /pmc/articles/PMC5095533/ /pubmed/28080980 http://dx.doi.org/10.1098/rstb.2015.0454 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Clare, Frances C.
Halder, Julia B.
Daniel, Olivia
Bielby, Jon
Semenov, Mikhail A.
Jombart, Thibaut
Loyau, Adeline
Schmeller, Dirk S.
Cunningham, Andrew A.
Rowcliffe, Marcus
Garner, Trenton W. J.
Bosch, Jaime
Fisher, Matthew C.
Climate forcing of an emerging pathogenic fungus across a montane multi-host community
title Climate forcing of an emerging pathogenic fungus across a montane multi-host community
title_full Climate forcing of an emerging pathogenic fungus across a montane multi-host community
title_fullStr Climate forcing of an emerging pathogenic fungus across a montane multi-host community
title_full_unstemmed Climate forcing of an emerging pathogenic fungus across a montane multi-host community
title_short Climate forcing of an emerging pathogenic fungus across a montane multi-host community
title_sort climate forcing of an emerging pathogenic fungus across a montane multi-host community
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095533/
https://www.ncbi.nlm.nih.gov/pubmed/28080980
http://dx.doi.org/10.1098/rstb.2015.0454
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