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Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition

When facing microbes, animals engage in behaviors that lower the impact of the infection. We previously demonstrated that internal sensing of bacterial peptidoglycan reduces Drosophila female oviposition via NF-κB pathway activation in some neurons (Kurz et al., 2017). Although we showed that the ne...

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Autores principales: Masuzzo, Ambra, Manière, Gérard, Viallat-Lieutaud, Annelise, Avazeri, Émilie, Zugasti, Olivier, Grosjean, Yaël, Kurz, C Léopold, Royet, Julien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819134/
https://www.ncbi.nlm.nih.gov/pubmed/31661076
http://dx.doi.org/10.7554/eLife.50559
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author Masuzzo, Ambra
Manière, Gérard
Viallat-Lieutaud, Annelise
Avazeri, Émilie
Zugasti, Olivier
Grosjean, Yaël
Kurz, C Léopold
Royet, Julien
author_facet Masuzzo, Ambra
Manière, Gérard
Viallat-Lieutaud, Annelise
Avazeri, Émilie
Zugasti, Olivier
Grosjean, Yaël
Kurz, C Léopold
Royet, Julien
author_sort Masuzzo, Ambra
collection PubMed
description When facing microbes, animals engage in behaviors that lower the impact of the infection. We previously demonstrated that internal sensing of bacterial peptidoglycan reduces Drosophila female oviposition via NF-κB pathway activation in some neurons (Kurz et al., 2017). Although we showed that the neuromodulator octopamine is implicated, the identity of the involved neurons, as well as the physiological mechanism blocking egg-laying, remained unknown. In this study, we identified few ventral nerve cord and brain octopaminergic neurons expressing an NF-κB pathway component. We functionally demonstrated that NF-κB pathway activation in the brain, but not in the ventral nerve cord octopaminergic neurons, triggers an egg-laying drop in response to infection. Furthermore, we demonstrated via calcium imaging that the activity of these neurons can be directly modulated by peptidoglycan and that these cells do not control other octopamine-dependent behaviors such as female receptivity. This study shows that by sensing peptidoglycan and hence activating NF-κB cascade, a couple of brain neurons modulate a specific octopamine-dependent behavior to adapt female physiology status to their infectious state.
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spelling pubmed-68191342019-10-31 Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition Masuzzo, Ambra Manière, Gérard Viallat-Lieutaud, Annelise Avazeri, Émilie Zugasti, Olivier Grosjean, Yaël Kurz, C Léopold Royet, Julien eLife Neuroscience When facing microbes, animals engage in behaviors that lower the impact of the infection. We previously demonstrated that internal sensing of bacterial peptidoglycan reduces Drosophila female oviposition via NF-κB pathway activation in some neurons (Kurz et al., 2017). Although we showed that the neuromodulator octopamine is implicated, the identity of the involved neurons, as well as the physiological mechanism blocking egg-laying, remained unknown. In this study, we identified few ventral nerve cord and brain octopaminergic neurons expressing an NF-κB pathway component. We functionally demonstrated that NF-κB pathway activation in the brain, but not in the ventral nerve cord octopaminergic neurons, triggers an egg-laying drop in response to infection. Furthermore, we demonstrated via calcium imaging that the activity of these neurons can be directly modulated by peptidoglycan and that these cells do not control other octopamine-dependent behaviors such as female receptivity. This study shows that by sensing peptidoglycan and hence activating NF-κB cascade, a couple of brain neurons modulate a specific octopamine-dependent behavior to adapt female physiology status to their infectious state. eLife Sciences Publications, Ltd 2019-10-29 /pmc/articles/PMC6819134/ /pubmed/31661076 http://dx.doi.org/10.7554/eLife.50559 Text en © 2019, Masuzzo et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Masuzzo, Ambra
Manière, Gérard
Viallat-Lieutaud, Annelise
Avazeri, Émilie
Zugasti, Olivier
Grosjean, Yaël
Kurz, C Léopold
Royet, Julien
Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition
title Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition
title_full Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition
title_fullStr Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition
title_full_unstemmed Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition
title_short Peptidoglycan-dependent NF-κB activation in a small subset of brain octopaminergic neurons controls female oviposition
title_sort peptidoglycan-dependent nf-κb activation in a small subset of brain octopaminergic neurons controls female oviposition
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819134/
https://www.ncbi.nlm.nih.gov/pubmed/31661076
http://dx.doi.org/10.7554/eLife.50559
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