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Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet

The geometric framework of nutrition predicts that populations restricted to a single imbalanced diet should evolve post-ingestive nutritional compensation mechanisms bringing the blend of assimilated nutrients closer to physiological optimum. The evolution of such nutritional compensation is though...

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Autores principales: Cavigliasso, Fanny, Dupuis, Cindy, Savary, Loriane, Spangenberg, Jorge E., Kawecki, Tadeusz J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739944/
https://www.ncbi.nlm.nih.gov/pubmed/33259760
http://dx.doi.org/10.1098/rspb.2020.2684
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author Cavigliasso, Fanny
Dupuis, Cindy
Savary, Loriane
Spangenberg, Jorge E.
Kawecki, Tadeusz J.
author_facet Cavigliasso, Fanny
Dupuis, Cindy
Savary, Loriane
Spangenberg, Jorge E.
Kawecki, Tadeusz J.
author_sort Cavigliasso, Fanny
collection PubMed
description The geometric framework of nutrition predicts that populations restricted to a single imbalanced diet should evolve post-ingestive nutritional compensation mechanisms bringing the blend of assimilated nutrients closer to physiological optimum. The evolution of such nutritional compensation is thought to be mainly driven by the ratios of major nutrients rather than overall nutritional content of the diet. We report experimental evolution of divergence in post-ingestive nutritional compensation in populations of Drosophila melanogaster adapted to diets that contained identical imbalanced nutrient ratios but differed in total nutrient concentration. Larvae from ‘Selected’ populations maintained for over 200 generations on a nutrient-poor diet with a 1 : 13.5 protein : carbohydrate ratio showed enhanced assimilation of nitrogen from yeasts and reduced assimilation of carbon from sucrose than ‘Control’ populations evolved on a diet with the same nutrient ratio but fourfold greater nutrient concentration. Compared to the Controls, the Selected larvae also accumulated less triglycerides relative to protein. This implies that the Selected populations evolved a higher assimilation rate of amino acids from the poor imbalanced diet and a lower assimilation of carbohydrates than Controls. Thus, the evolution of nutritional compensation may be driven by changes in total nutrient abundance, even if the ratios of different nutrients remain unchanged.
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spelling pubmed-77399442020-12-31 Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet Cavigliasso, Fanny Dupuis, Cindy Savary, Loriane Spangenberg, Jorge E. Kawecki, Tadeusz J. Proc Biol Sci Evolution The geometric framework of nutrition predicts that populations restricted to a single imbalanced diet should evolve post-ingestive nutritional compensation mechanisms bringing the blend of assimilated nutrients closer to physiological optimum. The evolution of such nutritional compensation is thought to be mainly driven by the ratios of major nutrients rather than overall nutritional content of the diet. We report experimental evolution of divergence in post-ingestive nutritional compensation in populations of Drosophila melanogaster adapted to diets that contained identical imbalanced nutrient ratios but differed in total nutrient concentration. Larvae from ‘Selected’ populations maintained for over 200 generations on a nutrient-poor diet with a 1 : 13.5 protein : carbohydrate ratio showed enhanced assimilation of nitrogen from yeasts and reduced assimilation of carbon from sucrose than ‘Control’ populations evolved on a diet with the same nutrient ratio but fourfold greater nutrient concentration. Compared to the Controls, the Selected larvae also accumulated less triglycerides relative to protein. This implies that the Selected populations evolved a higher assimilation rate of amino acids from the poor imbalanced diet and a lower assimilation of carbohydrates than Controls. Thus, the evolution of nutritional compensation may be driven by changes in total nutrient abundance, even if the ratios of different nutrients remain unchanged. The Royal Society 2020-12-09 2020-12-02 /pmc/articles/PMC7739944/ /pubmed/33259760 http://dx.doi.org/10.1098/rspb.2020.2684 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Cavigliasso, Fanny
Dupuis, Cindy
Savary, Loriane
Spangenberg, Jorge E.
Kawecki, Tadeusz J.
Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet
title Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet
title_full Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet
title_fullStr Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet
title_full_unstemmed Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet
title_short Experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet
title_sort experimental evolution of post-ingestive nutritional compensation in response to a nutrient-poor diet
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739944/
https://www.ncbi.nlm.nih.gov/pubmed/33259760
http://dx.doi.org/10.1098/rspb.2020.2684
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