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Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation
Resources are a core currency of species interactions and ecology in general (e.g., think of food webs or competition). Within parasite-infected hosts, resources are divided among the competing demands of host immunity and growth as well as parasite reproduction and growth. Effects of resources on i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766659/ https://www.ncbi.nlm.nih.gov/pubmed/29358937 http://dx.doi.org/10.3389/fimmu.2017.01914 |
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author | Budischak, Sarah A. Hansen, Christina B. Caudron, Quentin Garnier, Romain Kartzinel, Tyler R. Pelczer, István Cressler, Clayton E. van Leeuwen, Anieke Graham, Andrea L. |
author_facet | Budischak, Sarah A. Hansen, Christina B. Caudron, Quentin Garnier, Romain Kartzinel, Tyler R. Pelczer, István Cressler, Clayton E. van Leeuwen, Anieke Graham, Andrea L. |
author_sort | Budischak, Sarah A. |
collection | PubMed |
description | Resources are a core currency of species interactions and ecology in general (e.g., think of food webs or competition). Within parasite-infected hosts, resources are divided among the competing demands of host immunity and growth as well as parasite reproduction and growth. Effects of resources on immune responses are increasingly understood at the cellular level (e.g., metabolic predictors of effector function), but there has been limited consideration of how these effects scale up to affect individual energetic regimes (e.g., allocation trade-offs), susceptibility to infection, and feeding behavior (e.g., responses to local resource quality and quantity). We experimentally rewilded laboratory mice (strain C57BL/6) in semi-natural enclosures to investigate the effects of dietary protein and gastrointestinal nematode (Trichuris muris) infection on individual-level immunity, activity, and behavior. The scale and realism of this field experiment, as well as the multiple physiological assays developed for laboratory mice, enabled us to detect costs, trade-offs, and potential compensatory mechanisms that mice employ to battle infection under different resource conditions. We found that mice on a low-protein diet spent more time feeding, which led to higher body fat stores (i.e., concentration of a satiety hormone, leptin) and altered metabolite profiles, but which did not fully compensate for the effects of poor nutrition on albumin or immune defenses. Specifically, immune defenses measured as interleukin 13 (IL13) (a primary cytokine coordinating defense against T. muris) and as T. muris-specific IgG1 titers were lower in mice on the low-protein diet. However, these reduced defenses did not result in higher worm counts in mice with poorer diets. The lab mice, living outside for the first time in thousands of generations, also consumed at least 26 wild plant species occurring in the enclosures, and DNA metabarcoding revealed that the consumption of different wild foods may be associated with differences in leptin concentrations. When individual foraging behavior was accounted for, worm infection significantly reduced rates of host weight gain. Housing laboratory mice in outdoor enclosures provided new insights into the resource costs of immune defense to helminth infection and how hosts modify their behavior to compensate for those costs. |
format | Online Article Text |
id | pubmed-5766659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57666592018-01-22 Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation Budischak, Sarah A. Hansen, Christina B. Caudron, Quentin Garnier, Romain Kartzinel, Tyler R. Pelczer, István Cressler, Clayton E. van Leeuwen, Anieke Graham, Andrea L. Front Immunol Immunology Resources are a core currency of species interactions and ecology in general (e.g., think of food webs or competition). Within parasite-infected hosts, resources are divided among the competing demands of host immunity and growth as well as parasite reproduction and growth. Effects of resources on immune responses are increasingly understood at the cellular level (e.g., metabolic predictors of effector function), but there has been limited consideration of how these effects scale up to affect individual energetic regimes (e.g., allocation trade-offs), susceptibility to infection, and feeding behavior (e.g., responses to local resource quality and quantity). We experimentally rewilded laboratory mice (strain C57BL/6) in semi-natural enclosures to investigate the effects of dietary protein and gastrointestinal nematode (Trichuris muris) infection on individual-level immunity, activity, and behavior. The scale and realism of this field experiment, as well as the multiple physiological assays developed for laboratory mice, enabled us to detect costs, trade-offs, and potential compensatory mechanisms that mice employ to battle infection under different resource conditions. We found that mice on a low-protein diet spent more time feeding, which led to higher body fat stores (i.e., concentration of a satiety hormone, leptin) and altered metabolite profiles, but which did not fully compensate for the effects of poor nutrition on albumin or immune defenses. Specifically, immune defenses measured as interleukin 13 (IL13) (a primary cytokine coordinating defense against T. muris) and as T. muris-specific IgG1 titers were lower in mice on the low-protein diet. However, these reduced defenses did not result in higher worm counts in mice with poorer diets. The lab mice, living outside for the first time in thousands of generations, also consumed at least 26 wild plant species occurring in the enclosures, and DNA metabarcoding revealed that the consumption of different wild foods may be associated with differences in leptin concentrations. When individual foraging behavior was accounted for, worm infection significantly reduced rates of host weight gain. Housing laboratory mice in outdoor enclosures provided new insights into the resource costs of immune defense to helminth infection and how hosts modify their behavior to compensate for those costs. Frontiers Media S.A. 2018-01-08 /pmc/articles/PMC5766659/ /pubmed/29358937 http://dx.doi.org/10.3389/fimmu.2017.01914 Text en Copyright © 2018 Budischak, Hansen, Caudron, Garnier, Kartzinel, Pelczer, Cressler, van Leeuwen and Graham. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Budischak, Sarah A. Hansen, Christina B. Caudron, Quentin Garnier, Romain Kartzinel, Tyler R. Pelczer, István Cressler, Clayton E. van Leeuwen, Anieke Graham, Andrea L. Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation |
title | Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation |
title_full | Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation |
title_fullStr | Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation |
title_full_unstemmed | Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation |
title_short | Feeding Immunity: Physiological and Behavioral Responses to Infection and Resource Limitation |
title_sort | feeding immunity: physiological and behavioral responses to infection and resource limitation |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766659/ https://www.ncbi.nlm.nih.gov/pubmed/29358937 http://dx.doi.org/10.3389/fimmu.2017.01914 |
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