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Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem
1. Predators may create healthier prey populations by selectively removing diseased individuals. Predators typically prefer some ages of prey over others, which may, or may not, align with those prey ages that are most likely to be diseased. 2. The interaction of age‐specific infection and predation...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9912199/ https://www.ncbi.nlm.nih.gov/pubmed/34994978 http://dx.doi.org/10.1111/1365-2656.13661 |
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author | Brandell, Ellen E. Cross, Paul C. Smith, Douglas W. Rogers, Will Galloway, Nathan L. MacNulty, Daniel R. Stahler, Daniel R. Treanor, John Hudson, Peter J. |
author_facet | Brandell, Ellen E. Cross, Paul C. Smith, Douglas W. Rogers, Will Galloway, Nathan L. MacNulty, Daniel R. Stahler, Daniel R. Treanor, John Hudson, Peter J. |
author_sort | Brandell, Ellen E. |
collection | PubMed |
description | 1. Predators may create healthier prey populations by selectively removing diseased individuals. Predators typically prefer some ages of prey over others, which may, or may not, align with those prey ages that are most likely to be diseased. 2. The interaction of age‐specific infection and predation has not been previously explored and likely has sizable effects on disease dynamics. We hypothesize that predator cleansing effects will be greater when the disease and predation occur in the same prey age groups. 3. We examine the predator cleansing effect using a model where both vulnerability to predators and pathogen prevalence vary with age. We tailor this model to chronic wasting disease (CWD) in mule deer and elk populations in the Greater Yellowstone Ecosystem, with empirical data from Yellowstone grey wolves and cougars. 4. Model results suggest that under moderate, yet realistic, predation pressure from cougars and wolves independently, predators may decrease CWD outbreak size substantially and delay the accumulation of symptomatic deer and elk. The magnitude of this effect is driven by the ability of predators to selectively remove late‐stage CWD infections that are likely the most responsible for transmission, but this may not be the age class they typically select. Thus, predators that select for infected young adults over uninfected juveniles have a stronger cleansing effect, and these effects are strengthened when transmission rates increase with increasing prey morbidity. There are also trade‐offs from a management perspective—that is, increasing predator kill rates can result in opposing forces on prey abundance and CWD prevalence. 5. Our modelling exploration shows that predators have the potential to reduce prevalence in prey populations when prey age and disease severity are considered, yet the strength of this effect is influenced by predators' selection for demography or body condition. Current CWD management focuses on increasing cervid hunting as the primary management tool, and our results suggest predators may also be a useful tool under certain conditions, but not necessarily without additional impacts on host abundance and demography. Protected areas with predator populations will play a large role in informing the debate over predator impacts on disease. |
format | Online Article Text |
id | pubmed-9912199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99121992023-02-11 Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem Brandell, Ellen E. Cross, Paul C. Smith, Douglas W. Rogers, Will Galloway, Nathan L. MacNulty, Daniel R. Stahler, Daniel R. Treanor, John Hudson, Peter J. J Anim Ecol Research Articles 1. Predators may create healthier prey populations by selectively removing diseased individuals. Predators typically prefer some ages of prey over others, which may, or may not, align with those prey ages that are most likely to be diseased. 2. The interaction of age‐specific infection and predation has not been previously explored and likely has sizable effects on disease dynamics. We hypothesize that predator cleansing effects will be greater when the disease and predation occur in the same prey age groups. 3. We examine the predator cleansing effect using a model where both vulnerability to predators and pathogen prevalence vary with age. We tailor this model to chronic wasting disease (CWD) in mule deer and elk populations in the Greater Yellowstone Ecosystem, with empirical data from Yellowstone grey wolves and cougars. 4. Model results suggest that under moderate, yet realistic, predation pressure from cougars and wolves independently, predators may decrease CWD outbreak size substantially and delay the accumulation of symptomatic deer and elk. The magnitude of this effect is driven by the ability of predators to selectively remove late‐stage CWD infections that are likely the most responsible for transmission, but this may not be the age class they typically select. Thus, predators that select for infected young adults over uninfected juveniles have a stronger cleansing effect, and these effects are strengthened when transmission rates increase with increasing prey morbidity. There are also trade‐offs from a management perspective—that is, increasing predator kill rates can result in opposing forces on prey abundance and CWD prevalence. 5. Our modelling exploration shows that predators have the potential to reduce prevalence in prey populations when prey age and disease severity are considered, yet the strength of this effect is influenced by predators' selection for demography or body condition. Current CWD management focuses on increasing cervid hunting as the primary management tool, and our results suggest predators may also be a useful tool under certain conditions, but not necessarily without additional impacts on host abundance and demography. Protected areas with predator populations will play a large role in informing the debate over predator impacts on disease. John Wiley and Sons Inc. 2022-01-27 2022-07 /pmc/articles/PMC9912199/ /pubmed/34994978 http://dx.doi.org/10.1111/1365-2656.13661 Text en © 2022 The Authors. Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Brandell, Ellen E. Cross, Paul C. Smith, Douglas W. Rogers, Will Galloway, Nathan L. MacNulty, Daniel R. Stahler, Daniel R. Treanor, John Hudson, Peter J. Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem |
title | Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem |
title_full | Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem |
title_fullStr | Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem |
title_full_unstemmed | Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem |
title_short | Examination of the interaction between age‐specific predation and chronic disease in the Greater Yellowstone Ecosystem |
title_sort | examination of the interaction between age‐specific predation and chronic disease in the greater yellowstone ecosystem |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9912199/ https://www.ncbi.nlm.nih.gov/pubmed/34994978 http://dx.doi.org/10.1111/1365-2656.13661 |
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