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Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish

BACKGROUND: Animals use sensory cues to efficiently locate resources, but when sensory information is insufficient, they may rely on internally coded search strategies. Despite the importance of search behavior, there is limited understanding of the underlying neural mechanisms in vertebrates. RESUL...

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Detalles Bibliográficos
Autores principales: Horstick, Eric J., Bayleyen, Yared, Sinclair, Jennifer L., Burgess, Harold A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5267475/
https://www.ncbi.nlm.nih.gov/pubmed/28122559
http://dx.doi.org/10.1186/s12915-016-0346-2
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author Horstick, Eric J.
Bayleyen, Yared
Sinclair, Jennifer L.
Burgess, Harold A.
author_facet Horstick, Eric J.
Bayleyen, Yared
Sinclair, Jennifer L.
Burgess, Harold A.
author_sort Horstick, Eric J.
collection PubMed
description BACKGROUND: Animals use sensory cues to efficiently locate resources, but when sensory information is insufficient, they may rely on internally coded search strategies. Despite the importance of search behavior, there is limited understanding of the underlying neural mechanisms in vertebrates. RESULTS: Here, we report that loss of illumination initiates sophisticated light-search behavior in larval zebrafish. Using three-dimensional tracking, we show that at the onset of darkness larvae swim in a helical trajectory that is spatially restricted in the horizontal plane, before gradually transitioning to an outward movement profile. Local and outward swim patterns display characteristic features of area-restricted and roaming search strategies, differentially enhancing phototaxis to nearby and remote sources of light. Retinal signaling is only required to initiate area-restricted search, implying that photoreceptors within the brain drive the transition to the roaming search state. Supporting this, orthopediaA mutant larvae manifest impaired transition to roaming search, a phenotype which is recapitulated by loss of the non-visual opsin opn4a and somatostatin signaling. CONCLUSION: These findings define distinct neuronal pathways for area-restricted and roaming search behaviors and clarify how internal drives promote goal-directed activity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0346-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-52674752017-02-01 Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish Horstick, Eric J. Bayleyen, Yared Sinclair, Jennifer L. Burgess, Harold A. BMC Biol Research Article BACKGROUND: Animals use sensory cues to efficiently locate resources, but when sensory information is insufficient, they may rely on internally coded search strategies. Despite the importance of search behavior, there is limited understanding of the underlying neural mechanisms in vertebrates. RESULTS: Here, we report that loss of illumination initiates sophisticated light-search behavior in larval zebrafish. Using three-dimensional tracking, we show that at the onset of darkness larvae swim in a helical trajectory that is spatially restricted in the horizontal plane, before gradually transitioning to an outward movement profile. Local and outward swim patterns display characteristic features of area-restricted and roaming search strategies, differentially enhancing phototaxis to nearby and remote sources of light. Retinal signaling is only required to initiate area-restricted search, implying that photoreceptors within the brain drive the transition to the roaming search state. Supporting this, orthopediaA mutant larvae manifest impaired transition to roaming search, a phenotype which is recapitulated by loss of the non-visual opsin opn4a and somatostatin signaling. CONCLUSION: These findings define distinct neuronal pathways for area-restricted and roaming search behaviors and clarify how internal drives promote goal-directed activity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0346-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-26 /pmc/articles/PMC5267475/ /pubmed/28122559 http://dx.doi.org/10.1186/s12915-016-0346-2 Text en © Burgess et al. 2017 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
Horstick, Eric J.
Bayleyen, Yared
Sinclair, Jennifer L.
Burgess, Harold A.
Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish
title Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish
title_full Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish
title_fullStr Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish
title_full_unstemmed Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish
title_short Search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish
title_sort search strategy is regulated by somatostatin signaling and deep brain photoreceptors in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5267475/
https://www.ncbi.nlm.nih.gov/pubmed/28122559
http://dx.doi.org/10.1186/s12915-016-0346-2
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