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Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee
Flowers attract pollinating insects like honeybees by sophisticated compositions of olfactory and visual cues. Using honeybees as a model to study olfactory–visual integration at the neuronal level, we focused on mushroom body (MB) output neurons (MBON). From a neuronal circuit perspective, MBONs re...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830775/ https://www.ncbi.nlm.nih.gov/pubmed/29515886 http://dx.doi.org/10.1098/rsos.171785 |
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author | Strube-Bloss, Martin F. Rössler, Wolfgang |
author_facet | Strube-Bloss, Martin F. Rössler, Wolfgang |
author_sort | Strube-Bloss, Martin F. |
collection | PubMed |
description | Flowers attract pollinating insects like honeybees by sophisticated compositions of olfactory and visual cues. Using honeybees as a model to study olfactory–visual integration at the neuronal level, we focused on mushroom body (MB) output neurons (MBON). From a neuronal circuit perspective, MBONs represent a prominent level of sensory-modality convergence in the insect brain. We established an experimental design allowing electrophysiological characterization of olfactory, visual, as well as olfactory–visual induced activation of individual MBONs. Despite the obvious convergence of olfactory and visual pathways in the MB, we found numerous unimodal MBONs. However, a substantial proportion of MBONs (32%) responded to both modalities and thus integrated olfactory–visual information across MB input layers. In these neurons, representation of the olfactory–visual compound was significantly increased compared with that of single components, suggesting an additive, but nonlinear integration. Population analyses of olfactory–visual MBONs revealed three categories: (i) olfactory, (ii) visual and (iii) olfactory–visual compound stimuli. Interestingly, no significant differentiation was apparent regarding different stimulus qualities within these categories. We conclude that encoding of stimulus quality within a modality is largely completed at the level of MB input, and information at the MB output is integrated across modalities to efficiently categorize sensory information for downstream behavioural decision processing. |
format | Online Article Text |
id | pubmed-5830775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58307752018-03-07 Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee Strube-Bloss, Martin F. Rössler, Wolfgang R Soc Open Sci Cellular and Molecular Biology Flowers attract pollinating insects like honeybees by sophisticated compositions of olfactory and visual cues. Using honeybees as a model to study olfactory–visual integration at the neuronal level, we focused on mushroom body (MB) output neurons (MBON). From a neuronal circuit perspective, MBONs represent a prominent level of sensory-modality convergence in the insect brain. We established an experimental design allowing electrophysiological characterization of olfactory, visual, as well as olfactory–visual induced activation of individual MBONs. Despite the obvious convergence of olfactory and visual pathways in the MB, we found numerous unimodal MBONs. However, a substantial proportion of MBONs (32%) responded to both modalities and thus integrated olfactory–visual information across MB input layers. In these neurons, representation of the olfactory–visual compound was significantly increased compared with that of single components, suggesting an additive, but nonlinear integration. Population analyses of olfactory–visual MBONs revealed three categories: (i) olfactory, (ii) visual and (iii) olfactory–visual compound stimuli. Interestingly, no significant differentiation was apparent regarding different stimulus qualities within these categories. We conclude that encoding of stimulus quality within a modality is largely completed at the level of MB input, and information at the MB output is integrated across modalities to efficiently categorize sensory information for downstream behavioural decision processing. The Royal Society Publishing 2018-02-21 /pmc/articles/PMC5830775/ /pubmed/29515886 http://dx.doi.org/10.1098/rsos.171785 Text en © 2018 The Authors. 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 | Cellular and Molecular Biology Strube-Bloss, Martin F. Rössler, Wolfgang Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee |
title | Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee |
title_full | Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee |
title_fullStr | Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee |
title_full_unstemmed | Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee |
title_short | Multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee |
title_sort | multimodal integration and stimulus categorization in putative mushroom body output neurons of the honeybee |
topic | Cellular and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830775/ https://www.ncbi.nlm.nih.gov/pubmed/29515886 http://dx.doi.org/10.1098/rsos.171785 |
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