TY - JOUR
T1 - Linking brain and behavior states in Zebrafish Larvae locomotion using hidden Markov models
AU - Dommanget-Kott, Mattéo
AU - Fernandez-de-Cossio-Diaz, Jorge
AU - Coraggioso, Monica
AU - Bormuth, Volker
AU - Monasson, Rémi
AU - Debrégeas, Georges
AU - Cocco, Simona
N1 - Publisher Copyright:
Copyright: © 2026 Dommanget-Kott et al. 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 credited.
PY - 2026/1/1
Y1 - 2026/1/1
N2 - Understanding how collective neuronal activity in the brain orchestrates behavior is a central question in integrative neuroscience. Addressing this question requires models that can offer a unified interpretation of multimodal data. In this study, we jointly examine video-recordings of zebrafish larvae freely exploring their environment and calcium imaging of the Anterior Rhombencephalic Turning Region (ARTR) circuit, which is known to control swimming orientation, recorded in vivo under tethered conditions. We show that both behavioral and neural data can be accurately modeled using a Hidden Markov Model (HMM) with three hidden states. In the context of behavior, the hidden states correspond to leftward, rightward, and forward swimming. The HMM robustly captures the key statistical features of the swimming motion, including bout-type persistence and its dependence on bath temperature, while also revealing inter-individual phenotypic variability. For neural data, the three states are found to correspond to left- and right-lateral activation of the ARTR circuit, known to govern the selection of left vs. right reorientation, and a balanced state, which likely corresponds to the behavioral forward state. To further unify the two analyses, we exploit the generative nature of the HMM, using neural sequences to generate synthetic swimming trajectories, whose statistical properties are similar to the behavioral data. Overall, this work demonstrates how state-space models can be used to link neuronal and behavioral data, providing insights into the mechanisms of self-generated action.
AB - Understanding how collective neuronal activity in the brain orchestrates behavior is a central question in integrative neuroscience. Addressing this question requires models that can offer a unified interpretation of multimodal data. In this study, we jointly examine video-recordings of zebrafish larvae freely exploring their environment and calcium imaging of the Anterior Rhombencephalic Turning Region (ARTR) circuit, which is known to control swimming orientation, recorded in vivo under tethered conditions. We show that both behavioral and neural data can be accurately modeled using a Hidden Markov Model (HMM) with three hidden states. In the context of behavior, the hidden states correspond to leftward, rightward, and forward swimming. The HMM robustly captures the key statistical features of the swimming motion, including bout-type persistence and its dependence on bath temperature, while also revealing inter-individual phenotypic variability. For neural data, the three states are found to correspond to left- and right-lateral activation of the ARTR circuit, known to govern the selection of left vs. right reorientation, and a balanced state, which likely corresponds to the behavioral forward state. To further unify the two analyses, we exploit the generative nature of the HMM, using neural sequences to generate synthetic swimming trajectories, whose statistical properties are similar to the behavioral data. Overall, this work demonstrates how state-space models can be used to link neuronal and behavioral data, providing insights into the mechanisms of self-generated action.
UR - https://www.scopus.com/pages/publications/105027418648
U2 - 10.1371/journal.pcbi.1013762
DO - 10.1371/journal.pcbi.1013762
M3 - Article
C2 - 41490239
AN - SCOPUS:105027418648
SN - 1553-734X
VL - 22
SP - e1013762
JO - PLoS Computational Biology
JF - PLoS Computational Biology
IS - 1
ER -