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Serotonin promotes exploitation in complex environments by accelerating decision-making
BACKGROUND: Fast responses can provide a competitive advantage when resources are inhomogeneously distributed. The nematode Caenorhabditis elegans was shown to modulate locomotion on a lawn of bacterial food in serotonin (5-HT)-dependent manners. However, potential roles for serotonergic signaling i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743430/ https://www.ncbi.nlm.nih.gov/pubmed/26847342 http://dx.doi.org/10.1186/s12915-016-0232-y |
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author | Iwanir, Shachar Brown, Adam S. Nagy, Stanislav Najjar, Dana Kazakov, Alexander Lee, Kyung Suk Zaslaver, Alon Levine, Erel Biron, David |
author_facet | Iwanir, Shachar Brown, Adam S. Nagy, Stanislav Najjar, Dana Kazakov, Alexander Lee, Kyung Suk Zaslaver, Alon Levine, Erel Biron, David |
author_sort | Iwanir, Shachar |
collection | PubMed |
description | BACKGROUND: Fast responses can provide a competitive advantage when resources are inhomogeneously distributed. The nematode Caenorhabditis elegans was shown to modulate locomotion on a lawn of bacterial food in serotonin (5-HT)-dependent manners. However, potential roles for serotonergic signaling in responding to food discovery are poorly understood. RESULTS: We found that 5-HT signaling in C. elegans facilitates efficient exploitation in complex environments by mediating a rapid response upon encountering food. Genetic or cellular manipulations leading to deficient serotonergic signaling resulted in gradual responses and defective exploitation of a patchy foraging landscape. Physiological imaging revealed that the NSM serotonergic neurons responded acutely upon encounter with newly discovered food and were key to rapid responses. In contrast, the onset of responses of ADF serotonergic neurons preceded the physical encounter with the food. The serotonin-gated chloride channel MOD-1 and the ortholog of mammalian 5-HT1 metabotropic serotonin receptors SER-4 acted in synergy to accelerate decision-making. The relevance of responding rapidly was demonstrated in patchy environments, where the absence of 5-HT signaling was detrimental to exploitation. CONCLUSIONS: Our results implicate 5-HT in a novel form of decision-making, demonstrate its fitness consequences, suggest that NSM and ADF act in concert to modulate locomotion in complex environments, and identify the synergistic action of a channel and a metabotropic receptor in accelerating C. elegans decision-making. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0232-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4743430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47434302016-02-06 Serotonin promotes exploitation in complex environments by accelerating decision-making Iwanir, Shachar Brown, Adam S. Nagy, Stanislav Najjar, Dana Kazakov, Alexander Lee, Kyung Suk Zaslaver, Alon Levine, Erel Biron, David BMC Biol Research Article BACKGROUND: Fast responses can provide a competitive advantage when resources are inhomogeneously distributed. The nematode Caenorhabditis elegans was shown to modulate locomotion on a lawn of bacterial food in serotonin (5-HT)-dependent manners. However, potential roles for serotonergic signaling in responding to food discovery are poorly understood. RESULTS: We found that 5-HT signaling in C. elegans facilitates efficient exploitation in complex environments by mediating a rapid response upon encountering food. Genetic or cellular manipulations leading to deficient serotonergic signaling resulted in gradual responses and defective exploitation of a patchy foraging landscape. Physiological imaging revealed that the NSM serotonergic neurons responded acutely upon encounter with newly discovered food and were key to rapid responses. In contrast, the onset of responses of ADF serotonergic neurons preceded the physical encounter with the food. The serotonin-gated chloride channel MOD-1 and the ortholog of mammalian 5-HT1 metabotropic serotonin receptors SER-4 acted in synergy to accelerate decision-making. The relevance of responding rapidly was demonstrated in patchy environments, where the absence of 5-HT signaling was detrimental to exploitation. CONCLUSIONS: Our results implicate 5-HT in a novel form of decision-making, demonstrate its fitness consequences, suggest that NSM and ADF act in concert to modulate locomotion in complex environments, and identify the synergistic action of a channel and a metabotropic receptor in accelerating C. elegans decision-making. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0232-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-04 /pmc/articles/PMC4743430/ /pubmed/26847342 http://dx.doi.org/10.1186/s12915-016-0232-y Text en © Iwanir et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Iwanir, Shachar Brown, Adam S. Nagy, Stanislav Najjar, Dana Kazakov, Alexander Lee, Kyung Suk Zaslaver, Alon Levine, Erel Biron, David Serotonin promotes exploitation in complex environments by accelerating decision-making |
title | Serotonin promotes exploitation in complex environments by accelerating decision-making |
title_full | Serotonin promotes exploitation in complex environments by accelerating decision-making |
title_fullStr | Serotonin promotes exploitation in complex environments by accelerating decision-making |
title_full_unstemmed | Serotonin promotes exploitation in complex environments by accelerating decision-making |
title_short | Serotonin promotes exploitation in complex environments by accelerating decision-making |
title_sort | serotonin promotes exploitation in complex environments by accelerating decision-making |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743430/ https://www.ncbi.nlm.nih.gov/pubmed/26847342 http://dx.doi.org/10.1186/s12915-016-0232-y |
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