Statistical signature of subtle behavioral changes in large-scale assays
The central nervous system can generate various behaviors, including motor responses, which we can observe through video recordings. Recent advances in gene manipulation, automated behavioral acquisition at scale, and machine learning enable us to causally link behaviors to their underlying neural mechanisms. Moreover, in some animals, such as the Drosophila melanogaster larva, this mapping is possible at the unprecedented scale of single neurons, allowing us to identify the neural microcircuits generating particular behaviors. These high-throughput screening efforts, linking the activation or suppression of specific neurons to behavioral patterns in millions of animals, provide a rich dataset to explore the diversity of nervous system responses to the same stimuli. However, important challenges remain in identifying subtle behaviors, including immediate and delayed responses to neural activation or suppression, and understanding these behaviors on a large scale. We here introduce several statistically robust methods for analyzing behavioral data in response to these challenges: 1) A generative physical model that regularizes the inference of larval shapes across the entire dataset. 2) An unsupervised kernel-based method for statistical testing in learned behavioral spaces aimed at detecting subtle deviations in behavior. 3) A generative model for larval behavioral sequences, providing a benchmark for identifying higher-order behavioral changes. 4) A comprehensive analysis technique using suffix trees to categorize genetic lines into clusters based on common action sequences. We showcase these methodologies through a behavioral screen focused on responses to an air puff, analyzing data from 280 716 larvae across 569 genetic lines.
Authors
- Benjamin M.W. Jones
- Peter Hague (ORCID: https://orcid.org/0000-0003-3603-4272)
- Alex Barbier–Chebbah (ORCID: https://orcid.org/0000-0002-9523-8411)
- Alexandre Blanc (ORCID: https://orcid.org/0000-0001-9148-5223)
- Chloé Barré (ORCID: https://orcid.org/0000-0002-4551-8984)
- Hugues Van Assel
- François Laurent (ORCID: https://orcid.org/0000-0002-1615-6400)
- Tihana Jovanic (ORCID: https://orcid.org/0000-0002-0525-8620)
- Rayan Chikhi (ORCID: https://orcid.org/0000-0003-1099-8735)
- Marta Zlatic (ORCID: https://orcid.org/0000-0002-3149-2250)
- Christian L. Vestergaard (ORCID: https://orcid.org/0000-0001-5329-475X)
- Jean‐Baptiste Masson (ORCID: https://orcid.org/0000-0002-5484-9056)
- Ben Cocanougher (ORCID: https://orcid.org/0000-0003-0648-554X)
Institutions
- École Normale Supérieure de Lyon (FR)
- Centre National de la Recherche Scientifique (FR)
- Institut national de recherche en sciences et technologies du numérique (FR)
- Howard Hughes Medical Institute (US)
- Institut Pasteur (FR)
- MRC Laboratory of Molecular Biology (GB)
- Janelia Research Campus (US)
- Université Paris Cité (FR)
- University of Cambridge (GB)
- Université Paris-Saclay (FR)
- Institut des Neurosciences Paris-Saclay (FR)
Publication Details
- Journal
- PLoS Computational Biology
- Published
- 2025-04-21
- DOI
- https://doi.org/10.1371/journal.pcbi.1012990
- Citations
- 2
- Primary Topic
- Neurobiology and Insect Physiology Research
- Type
- article
- Field-Weighted Citation Impact
- 1.82
Funders
- Agence Nationale de la Recherche
- H2020 European Research Council