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Natural Selection, The Microbiome, and Public Health

The microbiome is composed of hundreds of interacting species that have co-evolved with the host and alterations in microbiome composition have been associated with health and disease. Insights from evolutionary ecology may aid efforts to ameliorate microbiome-associated diseases. One step toward th...

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Autores principales: Swain Ewald, Holly A., Ewald, Paul W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: YJBM 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302615/
https://www.ncbi.nlm.nih.gov/pubmed/30588210
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author Swain Ewald, Holly A.
Ewald, Paul W.
author_facet Swain Ewald, Holly A.
Ewald, Paul W.
author_sort Swain Ewald, Holly A.
collection PubMed
description The microbiome is composed of hundreds of interacting species that have co-evolved with the host and alterations in microbiome composition have been associated with health and disease. Insights from evolutionary ecology may aid efforts to ameliorate microbiome-associated diseases. One step toward this goal involves recognition that the idea of commensalism has been applied too broadly to human/microbe symbioses. Commensalism is most accurately viewed on a symbiosis continuum as a dividing line that separates a spectrum of mutualisms of decreasing positive interdependence from parasitisms of increasing severity. Insights into the evolution of the gut microbial symbiosis continuum will help distinguish between human actions that will advance or hinder health. Theory and research indicate that a major benefit of mutualistic microbes will be protection against pathogens. Mismatches between current and ancestral diets may disfavor mutualists, resulting in microbiome effects on health problems, including obesity, diabetes, autism, and childhood allergy. Evolutionary theory indicates that mutualisms will be favored when symbionts depend on resources that are not used by the host. These resources, which are referred to as human-inaccessible microbiota-accessible carbohydrates (HIMACs), can be supplied naturally through diet. Public health interventions need to consider the position of gut microbes on the mutualist-parasite continuum and the specific associations between prebiotics, such as HIMACs, and the mutualists they support. Otherwise interventions may fail to restore the match between human adaptations, diet, and microbiome function and may thereby fail to improve health and even inadvertently promote illness.
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spelling pubmed-63026152018-12-26 Natural Selection, The Microbiome, and Public Health Swain Ewald, Holly A. Ewald, Paul W. Yale J Biol Med Review The microbiome is composed of hundreds of interacting species that have co-evolved with the host and alterations in microbiome composition have been associated with health and disease. Insights from evolutionary ecology may aid efforts to ameliorate microbiome-associated diseases. One step toward this goal involves recognition that the idea of commensalism has been applied too broadly to human/microbe symbioses. Commensalism is most accurately viewed on a symbiosis continuum as a dividing line that separates a spectrum of mutualisms of decreasing positive interdependence from parasitisms of increasing severity. Insights into the evolution of the gut microbial symbiosis continuum will help distinguish between human actions that will advance or hinder health. Theory and research indicate that a major benefit of mutualistic microbes will be protection against pathogens. Mismatches between current and ancestral diets may disfavor mutualists, resulting in microbiome effects on health problems, including obesity, diabetes, autism, and childhood allergy. Evolutionary theory indicates that mutualisms will be favored when symbionts depend on resources that are not used by the host. These resources, which are referred to as human-inaccessible microbiota-accessible carbohydrates (HIMACs), can be supplied naturally through diet. Public health interventions need to consider the position of gut microbes on the mutualist-parasite continuum and the specific associations between prebiotics, such as HIMACs, and the mutualists they support. Otherwise interventions may fail to restore the match between human adaptations, diet, and microbiome function and may thereby fail to improve health and even inadvertently promote illness. YJBM 2018-12-21 /pmc/articles/PMC6302615/ /pubmed/30588210 Text en Copyright ©2018, Yale Journal of Biology and Medicine https://creativecommons.org/licenses/by-nc/3.0/ This is an open access article distributed under the terms of the Creative Commons CC BY-NC license, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use the material for commercial purposes.
spellingShingle Review
Swain Ewald, Holly A.
Ewald, Paul W.
Natural Selection, The Microbiome, and Public Health
title Natural Selection, The Microbiome, and Public Health
title_full Natural Selection, The Microbiome, and Public Health
title_fullStr Natural Selection, The Microbiome, and Public Health
title_full_unstemmed Natural Selection, The Microbiome, and Public Health
title_short Natural Selection, The Microbiome, and Public Health
title_sort natural selection, the microbiome, and public health
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302615/
https://www.ncbi.nlm.nih.gov/pubmed/30588210
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