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Yeast volatiles double starvation survival in Drosophila

Organisms make decisions based on the information they gather from their environment, the effects of which affect their fitness. Understanding how these interactions affect physiology may generate interventions that improve the length and quality of life. Here, we provide evidence that exposure to l...

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Autores principales: Luo, Yuan, Johnson, Jacob C., Chakraborty, Tuhin S., Piontkowski, Austin, Gendron, Christi M., Pletcher, Scott D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115925/
https://www.ncbi.nlm.nih.gov/pubmed/33980491
http://dx.doi.org/10.1126/sciadv.abf8896
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author Luo, Yuan
Johnson, Jacob C.
Chakraborty, Tuhin S.
Piontkowski, Austin
Gendron, Christi M.
Pletcher, Scott D.
author_facet Luo, Yuan
Johnson, Jacob C.
Chakraborty, Tuhin S.
Piontkowski, Austin
Gendron, Christi M.
Pletcher, Scott D.
author_sort Luo, Yuan
collection PubMed
description Organisms make decisions based on the information they gather from their environment, the effects of which affect their fitness. Understanding how these interactions affect physiology may generate interventions that improve the length and quality of life. Here, we provide evidence that exposure to live yeast volatiles during starvation significantly extends survival, increases activity, and slows the rate of triacylglyceride (TAG) decline independent of canonical sensory perception. We demonstrate that ethanol (EtOH) is one of the active components in yeast volatiles that influences these phenotypes and that EtOH metabolites mediate dynamic mechanisms to promote Drosophila survival. Silencing R4d neurons reverses the ability of high EtOH concentrations to promote starvation survival, and their activation promotes EtOH metabolism. The transcription factor foxo promotes EtOH resistance, likely by protection from EtOH toxicity. Our results suggest that food-related cues recruit neural circuits and modulate stress signaling pathways to promote survival during starvation.
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spelling pubmed-81159252021-05-19 Yeast volatiles double starvation survival in Drosophila Luo, Yuan Johnson, Jacob C. Chakraborty, Tuhin S. Piontkowski, Austin Gendron, Christi M. Pletcher, Scott D. Sci Adv Research Articles Organisms make decisions based on the information they gather from their environment, the effects of which affect their fitness. Understanding how these interactions affect physiology may generate interventions that improve the length and quality of life. Here, we provide evidence that exposure to live yeast volatiles during starvation significantly extends survival, increases activity, and slows the rate of triacylglyceride (TAG) decline independent of canonical sensory perception. We demonstrate that ethanol (EtOH) is one of the active components in yeast volatiles that influences these phenotypes and that EtOH metabolites mediate dynamic mechanisms to promote Drosophila survival. Silencing R4d neurons reverses the ability of high EtOH concentrations to promote starvation survival, and their activation promotes EtOH metabolism. The transcription factor foxo promotes EtOH resistance, likely by protection from EtOH toxicity. Our results suggest that food-related cues recruit neural circuits and modulate stress signaling pathways to promote survival during starvation. American Association for the Advancement of Science 2021-05-12 /pmc/articles/PMC8115925/ /pubmed/33980491 http://dx.doi.org/10.1126/sciadv.abf8896 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Luo, Yuan
Johnson, Jacob C.
Chakraborty, Tuhin S.
Piontkowski, Austin
Gendron, Christi M.
Pletcher, Scott D.
Yeast volatiles double starvation survival in Drosophila
title Yeast volatiles double starvation survival in Drosophila
title_full Yeast volatiles double starvation survival in Drosophila
title_fullStr Yeast volatiles double starvation survival in Drosophila
title_full_unstemmed Yeast volatiles double starvation survival in Drosophila
title_short Yeast volatiles double starvation survival in Drosophila
title_sort yeast volatiles double starvation survival in drosophila
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115925/
https://www.ncbi.nlm.nih.gov/pubmed/33980491
http://dx.doi.org/10.1126/sciadv.abf8896
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