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Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans

Nervous systems extract and process information from the environment to alter animal behavior and physiology. Despite progress in understanding how different stimuli are represented by changes in neuronal activity, less is known about how they affect broader neural network properties. We developed a...

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Detalles Bibliográficos
Autores principales: How, Javier J., Navlakha, Saket, Chalasani, Sreekanth H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604368/
https://www.ncbi.nlm.nih.gov/pubmed/34752447
http://dx.doi.org/10.1371/journal.pcbi.1009591
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author How, Javier J.
Navlakha, Saket
Chalasani, Sreekanth H.
author_facet How, Javier J.
Navlakha, Saket
Chalasani, Sreekanth H.
author_sort How, Javier J.
collection PubMed
description Nervous systems extract and process information from the environment to alter animal behavior and physiology. Despite progress in understanding how different stimuli are represented by changes in neuronal activity, less is known about how they affect broader neural network properties. We developed a framework for using graph-theoretic features of neural network activity to predict ecologically relevant stimulus properties, in particular stimulus identity. We used the transparent nematode, Caenorhabditis elegans, with its small nervous system to define neural network features associated with various chemosensory stimuli. We first immobilized animals using a microfluidic device and exposed their noses to chemical stimuli while monitoring changes in neural activity of more than 50 neurons in the head region. We found that graph-theoretic features, which capture patterns of interactions between neurons, are modulated by stimulus identity. Further, we show that a simple machine learning classifier trained using graph-theoretic features alone, or in combination with neural activity features, can accurately predict salt stimulus. Moreover, by focusing on putative causal interactions between neurons, the graph-theoretic features were almost twice as predictive as the neural activity features. These results reveal that stimulus identity modulates the broad, network-level organization of the nervous system, and that graph theory can be used to characterize these changes.
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spelling pubmed-86043682021-11-20 Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans How, Javier J. Navlakha, Saket Chalasani, Sreekanth H. PLoS Comput Biol Research Article Nervous systems extract and process information from the environment to alter animal behavior and physiology. Despite progress in understanding how different stimuli are represented by changes in neuronal activity, less is known about how they affect broader neural network properties. We developed a framework for using graph-theoretic features of neural network activity to predict ecologically relevant stimulus properties, in particular stimulus identity. We used the transparent nematode, Caenorhabditis elegans, with its small nervous system to define neural network features associated with various chemosensory stimuli. We first immobilized animals using a microfluidic device and exposed their noses to chemical stimuli while monitoring changes in neural activity of more than 50 neurons in the head region. We found that graph-theoretic features, which capture patterns of interactions between neurons, are modulated by stimulus identity. Further, we show that a simple machine learning classifier trained using graph-theoretic features alone, or in combination with neural activity features, can accurately predict salt stimulus. Moreover, by focusing on putative causal interactions between neurons, the graph-theoretic features were almost twice as predictive as the neural activity features. These results reveal that stimulus identity modulates the broad, network-level organization of the nervous system, and that graph theory can be used to characterize these changes. Public Library of Science 2021-11-09 /pmc/articles/PMC8604368/ /pubmed/34752447 http://dx.doi.org/10.1371/journal.pcbi.1009591 Text en © 2021 How 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
How, Javier J.
Navlakha, Saket
Chalasani, Sreekanth H.
Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans
title Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans
title_full Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans
title_fullStr Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans
title_full_unstemmed Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans
title_short Neural network features distinguish chemosensory stimuli in Caenorhabditis elegans
title_sort neural network features distinguish chemosensory stimuli in caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604368/
https://www.ncbi.nlm.nih.gov/pubmed/34752447
http://dx.doi.org/10.1371/journal.pcbi.1009591
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