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Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee
Understanding of the neural bases for complex behaviors in Hymenoptera insect species has been limited by a lack of tools that allow measuring neuronal activity simultaneously in different brain regions. Here, we developed the first pan-neuronal genetic driver in a Hymenopteran model organism, the h...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917304/ https://www.ncbi.nlm.nih.gov/pubmed/36719927 http://dx.doi.org/10.1371/journal.pbio.3001984 |
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author | Carcaud, Julie Otte, Marianne Grünewald, Bernd Haase, Albrecht Sandoz, Jean-Christophe Beye, Martin |
author_facet | Carcaud, Julie Otte, Marianne Grünewald, Bernd Haase, Albrecht Sandoz, Jean-Christophe Beye, Martin |
author_sort | Carcaud, Julie |
collection | PubMed |
description | Understanding of the neural bases for complex behaviors in Hymenoptera insect species has been limited by a lack of tools that allow measuring neuronal activity simultaneously in different brain regions. Here, we developed the first pan-neuronal genetic driver in a Hymenopteran model organism, the honey bee, and expressed the calcium indicator GCaMP6f under the control of the honey bee synapsin promoter. We show that GCaMP6f is widely expressed in the honey bee brain, allowing to record neural activity from multiple brain regions. To assess the power of this tool, we focused on the olfactory system, recording simultaneous responses from the antennal lobe, and from the more poorly investigated lateral horn (LH) and mushroom body (MB) calyces. Neural responses to 16 distinct odorants demonstrate that odorant quality (chemical structure) and quantity are faithfully encoded in the honey bee antennal lobe. In contrast, odor coding in the LH departs from this simple physico-chemical coding, supporting the role of this structure in coding the biological value of odorants. We further demonstrate robust neural responses to several bee pheromone odorants, key drivers of social behavior, in the LH. Combined, these brain recordings represent the first use of a neurogenetic tool for recording large-scale neural activity in a eusocial insect and will be of utility in assessing the neural underpinnings of olfactory and other sensory modalities and of social behaviors and cognitive abilities. |
format | Online Article Text |
id | pubmed-9917304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99173042023-02-11 Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee Carcaud, Julie Otte, Marianne Grünewald, Bernd Haase, Albrecht Sandoz, Jean-Christophe Beye, Martin PLoS Biol Methods and Resources Understanding of the neural bases for complex behaviors in Hymenoptera insect species has been limited by a lack of tools that allow measuring neuronal activity simultaneously in different brain regions. Here, we developed the first pan-neuronal genetic driver in a Hymenopteran model organism, the honey bee, and expressed the calcium indicator GCaMP6f under the control of the honey bee synapsin promoter. We show that GCaMP6f is widely expressed in the honey bee brain, allowing to record neural activity from multiple brain regions. To assess the power of this tool, we focused on the olfactory system, recording simultaneous responses from the antennal lobe, and from the more poorly investigated lateral horn (LH) and mushroom body (MB) calyces. Neural responses to 16 distinct odorants demonstrate that odorant quality (chemical structure) and quantity are faithfully encoded in the honey bee antennal lobe. In contrast, odor coding in the LH departs from this simple physico-chemical coding, supporting the role of this structure in coding the biological value of odorants. We further demonstrate robust neural responses to several bee pheromone odorants, key drivers of social behavior, in the LH. Combined, these brain recordings represent the first use of a neurogenetic tool for recording large-scale neural activity in a eusocial insect and will be of utility in assessing the neural underpinnings of olfactory and other sensory modalities and of social behaviors and cognitive abilities. Public Library of Science 2023-01-31 /pmc/articles/PMC9917304/ /pubmed/36719927 http://dx.doi.org/10.1371/journal.pbio.3001984 Text en © 2023 Carcaud 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 | Methods and Resources Carcaud, Julie Otte, Marianne Grünewald, Bernd Haase, Albrecht Sandoz, Jean-Christophe Beye, Martin Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee |
title | Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee |
title_full | Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee |
title_fullStr | Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee |
title_full_unstemmed | Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee |
title_short | Multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee |
title_sort | multisite imaging of neural activity using a genetically encoded calcium sensor in the honey bee |
topic | Methods and Resources |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9917304/ https://www.ncbi.nlm.nih.gov/pubmed/36719927 http://dx.doi.org/10.1371/journal.pbio.3001984 |
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