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HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY
Many have argued that we may be able to extend life and improve human health through hormesis, the beneficial effects of low-level toxins and other stressors. But, studies of hormesis in model systems have not yet established whether stress-induced benefits are cost free, artifacts of inbreeding, or...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282086/ https://www.ncbi.nlm.nih.gov/pubmed/24862588 http://dx.doi.org/10.1111/evo.12453 |
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author | McClure, Colin D Zhong, Weihao Hunt, Vicky L Chapman, Fiona M Hill, Fiona V Priest, Nicholas K |
author_facet | McClure, Colin D Zhong, Weihao Hunt, Vicky L Chapman, Fiona M Hill, Fiona V Priest, Nicholas K |
author_sort | McClure, Colin D |
collection | PubMed |
description | Many have argued that we may be able to extend life and improve human health through hormesis, the beneficial effects of low-level toxins and other stressors. But, studies of hormesis in model systems have not yet established whether stress-induced benefits are cost free, artifacts of inbreeding, or come with deleterious side effects. Here, we provide evidence that hormesis results in trade-offs with immunity. We find that a single topical dose of dead spores of the entomopathogenic fungus, Metarhizium robertsii, increases the longevity of the fruit fly, Drosophila melanogaster, without significant decreases in fecundity. We find that hormetic benefits of pathogen challenge are greater in lines that lack key components of antifungal immunity (Dif and Turandot M). And, in outbred fly lines, we find that topical pathogen challenge enhances both survival and fecundity, but reduces ability to fight off live infections. The results provide evidence that hormesis is manifested by stress-induced trade-offs with immunity, not cost-free benefits or artifacts of inbreeding. Our findings illuminate mechanisms underlying pathogen-induced life-history trade-offs, and indicate that reduced immune function may be an ironic side effect of the “elixirs of life.” |
format | Online Article Text |
id | pubmed-4282086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42820862015-01-15 HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY McClure, Colin D Zhong, Weihao Hunt, Vicky L Chapman, Fiona M Hill, Fiona V Priest, Nicholas K Evolution Original Articles Many have argued that we may be able to extend life and improve human health through hormesis, the beneficial effects of low-level toxins and other stressors. But, studies of hormesis in model systems have not yet established whether stress-induced benefits are cost free, artifacts of inbreeding, or come with deleterious side effects. Here, we provide evidence that hormesis results in trade-offs with immunity. We find that a single topical dose of dead spores of the entomopathogenic fungus, Metarhizium robertsii, increases the longevity of the fruit fly, Drosophila melanogaster, without significant decreases in fecundity. We find that hormetic benefits of pathogen challenge are greater in lines that lack key components of antifungal immunity (Dif and Turandot M). And, in outbred fly lines, we find that topical pathogen challenge enhances both survival and fecundity, but reduces ability to fight off live infections. The results provide evidence that hormesis is manifested by stress-induced trade-offs with immunity, not cost-free benefits or artifacts of inbreeding. Our findings illuminate mechanisms underlying pathogen-induced life-history trade-offs, and indicate that reduced immune function may be an ironic side effect of the “elixirs of life.” BlackWell Publishing Ltd 2014-08 2014-06-20 /pmc/articles/PMC4282086/ /pubmed/24862588 http://dx.doi.org/10.1111/evo.12453 Text en © 2014 The Author(s). http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles McClure, Colin D Zhong, Weihao Hunt, Vicky L Chapman, Fiona M Hill, Fiona V Priest, Nicholas K HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY |
title | HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY |
title_full | HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY |
title_fullStr | HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY |
title_full_unstemmed | HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY |
title_short | HORMESIS RESULTS IN TRADE-OFFS WITH IMMUNITY |
title_sort | hormesis results in trade-offs with immunity |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282086/ https://www.ncbi.nlm.nih.gov/pubmed/24862588 http://dx.doi.org/10.1111/evo.12453 |
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