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Migration distance does not predict blood parasitism in a migratory songbird

Migration can influence host–parasite dynamics in animals by increasing exposure to parasites, by reducing the energy available for immune defense, or by culling of infected individuals. These mechanisms have been demonstrated in several comparative analyses; however, few studies have investigated w...

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Autores principales: Sorensen, Marjorie C., Dixit, Tanmay, Kardynal, Kevin J., Newton, Jason, Hobson, Keith A., Bensch, Staffan, Jenni‐Eiermann, Susanne, Spottiswoode, Claire N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662322/
https://www.ncbi.nlm.nih.gov/pubmed/31380090
http://dx.doi.org/10.1002/ece3.5404
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author Sorensen, Marjorie C.
Dixit, Tanmay
Kardynal, Kevin J.
Newton, Jason
Hobson, Keith A.
Bensch, Staffan
Jenni‐Eiermann, Susanne
Spottiswoode, Claire N.
author_facet Sorensen, Marjorie C.
Dixit, Tanmay
Kardynal, Kevin J.
Newton, Jason
Hobson, Keith A.
Bensch, Staffan
Jenni‐Eiermann, Susanne
Spottiswoode, Claire N.
author_sort Sorensen, Marjorie C.
collection PubMed
description Migration can influence host–parasite dynamics in animals by increasing exposure to parasites, by reducing the energy available for immune defense, or by culling of infected individuals. These mechanisms have been demonstrated in several comparative analyses; however, few studies have investigated whether conspecific variation in migration distance may also be related to infection risk. Here, we ask whether autumn migration distance, inferred from stable hydrogen isotope analysis of summer‐grown feathers (δ (2)H(f)) in Europe, correlates with blood parasite prevalence and intensity of infection for willow warblers (Phylloscopus trochilus) wintering in Zambia. We also investigated whether infection was correlated with individual condition (assessed via corticosterone, scaled mass index, and feather quality). We found that 43% of birds were infected with Haemoproteus palloris (lineage WW1). Using generalized linear models, we found no relationship between migration distance and either Haemoproteus infection prevalence or intensity. There was spatial variation in breeding ground origins of infected versus noninfected birds, with infected birds originating from more northern sites than noninfected birds, but this difference translated into only slightly longer estimated migration distances (~214 km) for infected birds. We found no relationship between body condition indices and Haemoproteus infection prevalence or intensity. Our results do not support any of the proposed mechanisms for migration effects on host–parasite dynamics and cautiously suggest that other factors may be more important for determining individual susceptibility to disease in migratory bird species.
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spelling pubmed-66623222019-08-02 Migration distance does not predict blood parasitism in a migratory songbird Sorensen, Marjorie C. Dixit, Tanmay Kardynal, Kevin J. Newton, Jason Hobson, Keith A. Bensch, Staffan Jenni‐Eiermann, Susanne Spottiswoode, Claire N. Ecol Evol Original Research Migration can influence host–parasite dynamics in animals by increasing exposure to parasites, by reducing the energy available for immune defense, or by culling of infected individuals. These mechanisms have been demonstrated in several comparative analyses; however, few studies have investigated whether conspecific variation in migration distance may also be related to infection risk. Here, we ask whether autumn migration distance, inferred from stable hydrogen isotope analysis of summer‐grown feathers (δ (2)H(f)) in Europe, correlates with blood parasite prevalence and intensity of infection for willow warblers (Phylloscopus trochilus) wintering in Zambia. We also investigated whether infection was correlated with individual condition (assessed via corticosterone, scaled mass index, and feather quality). We found that 43% of birds were infected with Haemoproteus palloris (lineage WW1). Using generalized linear models, we found no relationship between migration distance and either Haemoproteus infection prevalence or intensity. There was spatial variation in breeding ground origins of infected versus noninfected birds, with infected birds originating from more northern sites than noninfected birds, but this difference translated into only slightly longer estimated migration distances (~214 km) for infected birds. We found no relationship between body condition indices and Haemoproteus infection prevalence or intensity. Our results do not support any of the proposed mechanisms for migration effects on host–parasite dynamics and cautiously suggest that other factors may be more important for determining individual susceptibility to disease in migratory bird species. John Wiley and Sons Inc. 2019-07-01 /pmc/articles/PMC6662322/ /pubmed/31380090 http://dx.doi.org/10.1002/ece3.5404 Text en © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Sorensen, Marjorie C.
Dixit, Tanmay
Kardynal, Kevin J.
Newton, Jason
Hobson, Keith A.
Bensch, Staffan
Jenni‐Eiermann, Susanne
Spottiswoode, Claire N.
Migration distance does not predict blood parasitism in a migratory songbird
title Migration distance does not predict blood parasitism in a migratory songbird
title_full Migration distance does not predict blood parasitism in a migratory songbird
title_fullStr Migration distance does not predict blood parasitism in a migratory songbird
title_full_unstemmed Migration distance does not predict blood parasitism in a migratory songbird
title_short Migration distance does not predict blood parasitism in a migratory songbird
title_sort migration distance does not predict blood parasitism in a migratory songbird
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662322/
https://www.ncbi.nlm.nih.gov/pubmed/31380090
http://dx.doi.org/10.1002/ece3.5404
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