Cargando…

A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function

The optomotor response (OMR) is central to the locomotory behavior in diverse animal species including insects, fish and mammals. Furthermore, the study of the OMR in larval zebrafish has become a key model system for investigating the neural basis of sensorimotor control. However, a comprehensive u...

Descripción completa

Detalles Bibliográficos
Autores principales: Holman, John G., Lai, Winnie W. K., Pichler, Paul, Saska, Daniel, Lagnado, Leon, Buckley, Christopher L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998047/
https://www.ncbi.nlm.nih.gov/pubmed/36821587
http://dx.doi.org/10.1371/journal.pcbi.1010924
_version_ 1784903390741921792
author Holman, John G.
Lai, Winnie W. K.
Pichler, Paul
Saska, Daniel
Lagnado, Leon
Buckley, Christopher L.
author_facet Holman, John G.
Lai, Winnie W. K.
Pichler, Paul
Saska, Daniel
Lagnado, Leon
Buckley, Christopher L.
author_sort Holman, John G.
collection PubMed
description The optomotor response (OMR) is central to the locomotory behavior in diverse animal species including insects, fish and mammals. Furthermore, the study of the OMR in larval zebrafish has become a key model system for investigating the neural basis of sensorimotor control. However, a comprehensive understanding of the underlying control algorithms is still outstanding. In fish it is often assumed that the OMR, by reducing average optic flow across the retina, serves to stabilize position with respect to the ground. Yet the degree to which this is achieved, and how it could emerge from the intermittent burst dynamics of larval zebrafish swimming, are unclear. Here, we combine detailed computational modeling with a new approach to free-swimming experiments in which we control the amount of visual feedback produced by a given motor effort by varying the height of the larva above a moving grid stimulus. We develop an account of underlying feedback control mechanisms that describes both the bout initiation process and the control of swim speed during bouts. We observe that the degree to which fish stabilize their position is only partial and height-dependent, raising questions about its function. We find the relative speed profile during bouts follows a fixed temporal pattern independent of absolute bout speed, suggesting that bout speed and bout termination are not separately controlled. We also find that the reverse optic flow, experienced when the fish is swimming faster than the stimulus, plays a minimal role in control of the OMR despite carrying most of the sensory information about self-movement. These results shed new light on the underlying dynamics of the OMR in larval zebrafish and will be crucial for future work aimed at identifying the neural basis of this behavior.
format Online
Article
Text
id pubmed-9998047
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-99980472023-03-10 A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function Holman, John G. Lai, Winnie W. K. Pichler, Paul Saska, Daniel Lagnado, Leon Buckley, Christopher L. PLoS Comput Biol Research Article The optomotor response (OMR) is central to the locomotory behavior in diverse animal species including insects, fish and mammals. Furthermore, the study of the OMR in larval zebrafish has become a key model system for investigating the neural basis of sensorimotor control. However, a comprehensive understanding of the underlying control algorithms is still outstanding. In fish it is often assumed that the OMR, by reducing average optic flow across the retina, serves to stabilize position with respect to the ground. Yet the degree to which this is achieved, and how it could emerge from the intermittent burst dynamics of larval zebrafish swimming, are unclear. Here, we combine detailed computational modeling with a new approach to free-swimming experiments in which we control the amount of visual feedback produced by a given motor effort by varying the height of the larva above a moving grid stimulus. We develop an account of underlying feedback control mechanisms that describes both the bout initiation process and the control of swim speed during bouts. We observe that the degree to which fish stabilize their position is only partial and height-dependent, raising questions about its function. We find the relative speed profile during bouts follows a fixed temporal pattern independent of absolute bout speed, suggesting that bout speed and bout termination are not separately controlled. We also find that the reverse optic flow, experienced when the fish is swimming faster than the stimulus, plays a minimal role in control of the OMR despite carrying most of the sensory information about self-movement. These results shed new light on the underlying dynamics of the OMR in larval zebrafish and will be crucial for future work aimed at identifying the neural basis of this behavior. Public Library of Science 2023-02-23 /pmc/articles/PMC9998047/ /pubmed/36821587 http://dx.doi.org/10.1371/journal.pcbi.1010924 Text en © 2023 Holman et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Holman, John G.
Lai, Winnie W. K.
Pichler, Paul
Saska, Daniel
Lagnado, Leon
Buckley, Christopher L.
A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function
title A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function
title_full A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function
title_fullStr A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function
title_full_unstemmed A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function
title_short A behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function
title_sort behavioral and modeling study of control algorithms underlying the translational optomotor response in larval zebrafish with implications for neural circuit function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998047/
https://www.ncbi.nlm.nih.gov/pubmed/36821587
http://dx.doi.org/10.1371/journal.pcbi.1010924
work_keys_str_mv AT holmanjohng abehavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT laiwinniewk abehavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT pichlerpaul abehavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT saskadaniel abehavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT lagnadoleon abehavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT buckleychristopherl abehavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT holmanjohng behavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT laiwinniewk behavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT pichlerpaul behavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT saskadaniel behavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT lagnadoleon behavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction
AT buckleychristopherl behavioralandmodelingstudyofcontrolalgorithmsunderlyingthetranslationaloptomotorresponseinlarvalzebrafishwithimplicationsforneuralcircuitfunction