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Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen

Food limitation is a universal stressor for wildlife populations and is increasingly exacerbated by human activities. Anthropogenic environmental change can significantly alter the availability and quality of food resources for reservoir hosts and impact host–pathogen interactions in the wild. The s...

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Autores principales: Owen, J. C., Landwerlen, H. R., Dupuis, A. P., Belsare, A. V., Sharma, D. B., Wang, S., Ciota, A. T., Kramer, L. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354750/
https://www.ncbi.nlm.nih.gov/pubmed/34375559
http://dx.doi.org/10.1098/rspb.2021.0881
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author Owen, J. C.
Landwerlen, H. R.
Dupuis, A. P.
Belsare, A. V.
Sharma, D. B.
Wang, S.
Ciota, A. T.
Kramer, L. D.
author_facet Owen, J. C.
Landwerlen, H. R.
Dupuis, A. P.
Belsare, A. V.
Sharma, D. B.
Wang, S.
Ciota, A. T.
Kramer, L. D.
author_sort Owen, J. C.
collection PubMed
description Food limitation is a universal stressor for wildlife populations and is increasingly exacerbated by human activities. Anthropogenic environmental change can significantly alter the availability and quality of food resources for reservoir hosts and impact host–pathogen interactions in the wild. The state of the host's nutritional reserves at the time of infection is a key factor influencing infection outcomes by altering host resistance. Combining experimental and model-based approaches, we investigate how an environmental stressor affects host resistance to West Nile virus (WNV). Using American robins (Turdus migratorius), a species considered a superspreader of WNV, we tested the effect of acute food deprivation immediately prior to infection on host viraemia. Here, we show that robins food deprived for 48 h prior to infection, developed higher virus titres and were infectious longer than robins fed normally. To gain an understanding about the epidemiological significance of food-stressed hosts, we developed an agent-based model that simulates transmission dynamics of WNV between an avian host and the mosquito vector. When simulating a nutritionally stressed host population, the mosquito infection rate rose significantly, reaching levels that represent an epidemiological risk. An understanding of the infection disease dynamics in wild populations is critical to predict and mitigate zoonotic disease outbreaks.
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spelling pubmed-83547502021-08-17 Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen Owen, J. C. Landwerlen, H. R. Dupuis, A. P. Belsare, A. V. Sharma, D. B. Wang, S. Ciota, A. T. Kramer, L. D. Proc Biol Sci Ecology Food limitation is a universal stressor for wildlife populations and is increasingly exacerbated by human activities. Anthropogenic environmental change can significantly alter the availability and quality of food resources for reservoir hosts and impact host–pathogen interactions in the wild. The state of the host's nutritional reserves at the time of infection is a key factor influencing infection outcomes by altering host resistance. Combining experimental and model-based approaches, we investigate how an environmental stressor affects host resistance to West Nile virus (WNV). Using American robins (Turdus migratorius), a species considered a superspreader of WNV, we tested the effect of acute food deprivation immediately prior to infection on host viraemia. Here, we show that robins food deprived for 48 h prior to infection, developed higher virus titres and were infectious longer than robins fed normally. To gain an understanding about the epidemiological significance of food-stressed hosts, we developed an agent-based model that simulates transmission dynamics of WNV between an avian host and the mosquito vector. When simulating a nutritionally stressed host population, the mosquito infection rate rose significantly, reaching levels that represent an epidemiological risk. An understanding of the infection disease dynamics in wild populations is critical to predict and mitigate zoonotic disease outbreaks. The Royal Society 2021-08-11 2021-08-11 /pmc/articles/PMC8354750/ /pubmed/34375559 http://dx.doi.org/10.1098/rspb.2021.0881 Text en © 2021 The Authors. https://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/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Ecology
Owen, J. C.
Landwerlen, H. R.
Dupuis, A. P.
Belsare, A. V.
Sharma, D. B.
Wang, S.
Ciota, A. T.
Kramer, L. D.
Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen
title Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen
title_full Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen
title_fullStr Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen
title_full_unstemmed Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen
title_short Reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen
title_sort reservoir hosts experiencing food stress alter transmission dynamics for a zoonotic pathogen
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354750/
https://www.ncbi.nlm.nih.gov/pubmed/34375559
http://dx.doi.org/10.1098/rspb.2021.0881
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