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High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies

All organisms react to noxious and mechanical stimuli but we still lack a complete understanding of cellular and molecular mechanisms by which somatosensory information is transformed into appropriate motor outputs. The small number of neurons and excellent genetic tools make Drosophila larva an esp...

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Autores principales: Ohyama, Tomoko, Jovanic, Tihana, Denisov, Gennady, Dang, Tam C., Hoffmann, Dominik, Kerr, Rex A., Zlatic, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748116/
https://www.ncbi.nlm.nih.gov/pubmed/23977118
http://dx.doi.org/10.1371/journal.pone.0071706
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author Ohyama, Tomoko
Jovanic, Tihana
Denisov, Gennady
Dang, Tam C.
Hoffmann, Dominik
Kerr, Rex A.
Zlatic, Marta
author_facet Ohyama, Tomoko
Jovanic, Tihana
Denisov, Gennady
Dang, Tam C.
Hoffmann, Dominik
Kerr, Rex A.
Zlatic, Marta
author_sort Ohyama, Tomoko
collection PubMed
description All organisms react to noxious and mechanical stimuli but we still lack a complete understanding of cellular and molecular mechanisms by which somatosensory information is transformed into appropriate motor outputs. The small number of neurons and excellent genetic tools make Drosophila larva an especially tractable model system in which to address this problem. We developed high throughput assays with which we can simultaneously expose more than 1,000 larvae per man-hour to precisely timed noxious heat, vibration, air current, or optogenetic stimuli. Using this hardware in combination with custom software we characterized larval reactions to somatosensory stimuli in far greater detail than possible previously. Each stimulus evoked a distinctive escape strategy that consisted of multiple actions. The escape strategy was context-dependent. Using our system we confirmed that the nociceptive class IV multidendritic neurons were involved in the reactions to noxious heat. Chordotonal (ch) neurons were necessary for normal modulation of head casting, crawling and hunching, in response to mechanical stimuli. Consistent with this we observed increases in calcium transients in response to vibration in ch neurons. Optogenetic activation of ch neurons was sufficient to evoke head casting and crawling. These studies significantly increase our understanding of the functional roles of larval ch neurons. More generally, our system and the detailed description of wild type reactions to somatosensory stimuli provide a basis for systematic identification of neurons and genes underlying these behaviors.
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spelling pubmed-37481162013-08-23 High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies Ohyama, Tomoko Jovanic, Tihana Denisov, Gennady Dang, Tam C. Hoffmann, Dominik Kerr, Rex A. Zlatic, Marta PLoS One Research Article All organisms react to noxious and mechanical stimuli but we still lack a complete understanding of cellular and molecular mechanisms by which somatosensory information is transformed into appropriate motor outputs. The small number of neurons and excellent genetic tools make Drosophila larva an especially tractable model system in which to address this problem. We developed high throughput assays with which we can simultaneously expose more than 1,000 larvae per man-hour to precisely timed noxious heat, vibration, air current, or optogenetic stimuli. Using this hardware in combination with custom software we characterized larval reactions to somatosensory stimuli in far greater detail than possible previously. Each stimulus evoked a distinctive escape strategy that consisted of multiple actions. The escape strategy was context-dependent. Using our system we confirmed that the nociceptive class IV multidendritic neurons were involved in the reactions to noxious heat. Chordotonal (ch) neurons were necessary for normal modulation of head casting, crawling and hunching, in response to mechanical stimuli. Consistent with this we observed increases in calcium transients in response to vibration in ch neurons. Optogenetic activation of ch neurons was sufficient to evoke head casting and crawling. These studies significantly increase our understanding of the functional roles of larval ch neurons. More generally, our system and the detailed description of wild type reactions to somatosensory stimuli provide a basis for systematic identification of neurons and genes underlying these behaviors. Public Library of Science 2013-08-20 /pmc/articles/PMC3748116/ /pubmed/23977118 http://dx.doi.org/10.1371/journal.pone.0071706 Text en © 2013 Ohyama et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ohyama, Tomoko
Jovanic, Tihana
Denisov, Gennady
Dang, Tam C.
Hoffmann, Dominik
Kerr, Rex A.
Zlatic, Marta
High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies
title High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies
title_full High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies
title_fullStr High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies
title_full_unstemmed High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies
title_short High-Throughput Analysis of Stimulus-Evoked Behaviors in Drosophila Larva Reveals Multiple Modality-Specific Escape Strategies
title_sort high-throughput analysis of stimulus-evoked behaviors in drosophila larva reveals multiple modality-specific escape strategies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748116/
https://www.ncbi.nlm.nih.gov/pubmed/23977118
http://dx.doi.org/10.1371/journal.pone.0071706
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