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Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs

Endothermy and homeothermy are mammalian characteristics whose evolutionary origins are poorly understood. Given that fungal species rapidly lose their capacity for growth above ambient temperatures, we have proposed that mammalian endothermy enhances fitness by creating exclusionary thermal zones t...

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Detalles Bibliográficos
Autores principales: Bergman, Aviv, Casadevall, Arturo
Formato: Texto
Lenguaje:English
Publicado: American Society of Microbiology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975364/
https://www.ncbi.nlm.nih.gov/pubmed/21060737
http://dx.doi.org/10.1128/mBio.00212-10
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author Bergman, Aviv
Casadevall, Arturo
author_facet Bergman, Aviv
Casadevall, Arturo
author_sort Bergman, Aviv
collection PubMed
description Endothermy and homeothermy are mammalian characteristics whose evolutionary origins are poorly understood. Given that fungal species rapidly lose their capacity for growth above ambient temperatures, we have proposed that mammalian endothermy enhances fitness by creating exclusionary thermal zones that protect against fungal disease. According to this view, the relative paucity of invasive fungal diseases in immunologically intact mammals relative to other infectious diseases would reflect an inability of most fungal species to establish themselves in a mammalian host. In this study, that hypothesis was tested by modeling the fitness increase with temperature versus its metabolic costs. We analyzed the tradeoff involved between the costs of the excess metabolic rates required to maintain a body temperature and the benefit gained by creating a thermal exclusion zone that protects against environmental microbes such as fungi. The result yields an optimum at 36.7°C, which closely approximates mammalian body temperatures. This calculation is consistent with and supportive of the notion that an intrinsic thermally based resistance against fungal diseases could have contributed to the success of mammals in the Tertiary relative to that of other vertebrates.
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spelling pubmed-29753642010-11-09 Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs Bergman, Aviv Casadevall, Arturo mBio Observation Endothermy and homeothermy are mammalian characteristics whose evolutionary origins are poorly understood. Given that fungal species rapidly lose their capacity for growth above ambient temperatures, we have proposed that mammalian endothermy enhances fitness by creating exclusionary thermal zones that protect against fungal disease. According to this view, the relative paucity of invasive fungal diseases in immunologically intact mammals relative to other infectious diseases would reflect an inability of most fungal species to establish themselves in a mammalian host. In this study, that hypothesis was tested by modeling the fitness increase with temperature versus its metabolic costs. We analyzed the tradeoff involved between the costs of the excess metabolic rates required to maintain a body temperature and the benefit gained by creating a thermal exclusion zone that protects against environmental microbes such as fungi. The result yields an optimum at 36.7°C, which closely approximates mammalian body temperatures. This calculation is consistent with and supportive of the notion that an intrinsic thermally based resistance against fungal diseases could have contributed to the success of mammals in the Tertiary relative to that of other vertebrates. American Society of Microbiology 2010-11-09 /pmc/articles/PMC2975364/ /pubmed/21060737 http://dx.doi.org/10.1128/mBio.00212-10 Text en Copyright © 2010 Bergman and Casadevall. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Observation
Bergman, Aviv
Casadevall, Arturo
Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs
title Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs
title_full Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs
title_fullStr Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs
title_full_unstemmed Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs
title_short Mammalian Endothermy Optimally Restricts Fungi and Metabolic Costs
title_sort mammalian endothermy optimally restricts fungi and metabolic costs
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975364/
https://www.ncbi.nlm.nih.gov/pubmed/21060737
http://dx.doi.org/10.1128/mBio.00212-10
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