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The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation
Emerging fungal pathogens have substantial consequences for infected hosts, as revealed by the global decline of amphibian species from the chytrid fungus. According to the “curse of the Pharaoh” hypothesis, free-living infectious stages typical of fungal pathogens lengthen the timespan of transmiss...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438611/ https://www.ncbi.nlm.nih.gov/pubmed/25992836 http://dx.doi.org/10.1038/srep10368 |
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author | Al-Shorbaji, Farah N. Gozlan, Rodolphe E. Roche, Benjamin Robert Britton, J. Andreou, Demetra |
author_facet | Al-Shorbaji, Farah N. Gozlan, Rodolphe E. Roche, Benjamin Robert Britton, J. Andreou, Demetra |
author_sort | Al-Shorbaji, Farah N. |
collection | PubMed |
description | Emerging fungal pathogens have substantial consequences for infected hosts, as revealed by the global decline of amphibian species from the chytrid fungus. According to the “curse of the Pharaoh” hypothesis, free-living infectious stages typical of fungal pathogens lengthen the timespan of transmission. Free-living infectious stages whose lifespan exceeds the infection time of their hosts are not constrained by virulence, enabling them to persist at high levels and continue transmitting to further sensitive hosts. Using the only Mesomycetozoea fungal species that can be cultured, Sphaerothecum destruens, we obtained tractable data on infectivity and pathogen life cycle for the first time. Here, based on the outcomes of a set of infectious trials and combined with an epidemiological model, we show a high level of dependence on direct transmission in crowded, confined environments and establish that incubation rate and length of infection dictate the epidemic dynamics of fungal disease. The spread of Mesomycetozoea in the wild raise ecological concerns for a range of susceptible species including birds, amphibians and mammals. Our results shed light on the risks associated with farming conditions and highlight the additional risk posed by invasive species that are highly abundant and can act as infectious reservoir hosts. |
format | Online Article Text |
id | pubmed-4438611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44386112015-06-01 The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation Al-Shorbaji, Farah N. Gozlan, Rodolphe E. Roche, Benjamin Robert Britton, J. Andreou, Demetra Sci Rep Article Emerging fungal pathogens have substantial consequences for infected hosts, as revealed by the global decline of amphibian species from the chytrid fungus. According to the “curse of the Pharaoh” hypothesis, free-living infectious stages typical of fungal pathogens lengthen the timespan of transmission. Free-living infectious stages whose lifespan exceeds the infection time of their hosts are not constrained by virulence, enabling them to persist at high levels and continue transmitting to further sensitive hosts. Using the only Mesomycetozoea fungal species that can be cultured, Sphaerothecum destruens, we obtained tractable data on infectivity and pathogen life cycle for the first time. Here, based on the outcomes of a set of infectious trials and combined with an epidemiological model, we show a high level of dependence on direct transmission in crowded, confined environments and establish that incubation rate and length of infection dictate the epidemic dynamics of fungal disease. The spread of Mesomycetozoea in the wild raise ecological concerns for a range of susceptible species including birds, amphibians and mammals. Our results shed light on the risks associated with farming conditions and highlight the additional risk posed by invasive species that are highly abundant and can act as infectious reservoir hosts. Nature Publishing Group 2015-05-20 /pmc/articles/PMC4438611/ /pubmed/25992836 http://dx.doi.org/10.1038/srep10368 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Al-Shorbaji, Farah N. Gozlan, Rodolphe E. Roche, Benjamin Robert Britton, J. Andreou, Demetra The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation |
title | The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation |
title_full | The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation |
title_fullStr | The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation |
title_full_unstemmed | The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation |
title_short | The alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation |
title_sort | alternate role of direct and environmental transmission in fungal infectious disease in wildlife: threats for biodiversity conservation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438611/ https://www.ncbi.nlm.nih.gov/pubmed/25992836 http://dx.doi.org/10.1038/srep10368 |
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