bioRxivNeurosciencePreprint
A novel epifluorescence microscope design and soft-ware package to record naturalistic behaviour and cell activity in freely moving Caenorhabditis elegans.
Sebastian N. WittekindtiD, Hannah OwensiD, Lennard Wittekindt, Aurélie GuisnetiD, Michael HendricksiD
Abstract
Understanding how neural circuits drive behavior requires imaging methods that capture cellular dynamics in freely moving animals. Here, we introduce Wormspy, a compact, flexible, and cost-effective microscope system paired with an open-source software package, specifically designed for high-magnification epifluorescence imaging in Caenorhabditis elegans. By integrating dual-channel fluorescence optics, off-the-shelf components, and a motorized stage, Wormspy enables simultaneous recording of neuronal activity and behavioral dynamics without restraining the animal. Our system incorporates both manual and automated tracking--including DeepLabCut-based feature extraction--to maintain precise centering of the subject, even during complex locomotor behaviors. We demonstrate the utility of Wormspy across multiple paradigms: quantifying body wall muscle calcium transients during locomotion, capturing rapid sensory-evoked responses in the polymodal ASH neuron during aversive stimuli, and resolving food-related activity in the AWCON neuron. Notably, Wormspy further distinguishes subcellular calcium events in the RIA axonal compartments that correlate with head bending kinematics. This versatile platform not only reproduces known phenotypes, such as altered gait in gar-3 mutants, but also uncovers nuanced sensorimotor correlations previously inaccessible with conventional methods. Wormspys modular design and open-source framework lower the technical and financial barriers to high-resolution, behaviorally relevant neural imaging. Our findings establish Wormspy as a robust tool for dissecting the neural underpinnings of behavior in freely moving organisms, with potential applications extending to other small model systems.
- organism: C. elegans
- assay: imaging
- research focus: cell type annotation
- research focus: cell-cell communication
- approach: experimental assay
- Citations
- 2
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Microfluidics-Enabled Simultaneous Imaging of Neural Activity and Behavior in Chemically Stimulated, Head-Fixed C. elegans
Hyun Jee Lee, Julia E. Vallier, Hang Lu·bioRxiv·Nov 3, 2025
- Simultaneous optogenetic manipulation and calcium imaging in freely moving C. elegans
Frederick B. Shipley, Christopher M. Clark, … Andrew M. Leifer·Frontiers in Neural CircuitsPeer-reviewed·Mar 24, 2014
- A Real-Time Automated Deep Learning Workflow for Non-invasive High-Magnification Imaging of C. elegans
Parsa Safaeian, Tasnuva Binte Mahbub, … Salman Sohrabi·BioengineeringPeer-reviewed·Oct 25, 2026
- A MULTI-PURPOSE WORM TRACKER BASED ON FIM
Matthias Kiel, Dimitri Berh, … Benjamin Risse·bioRxiv·Jun 21, 2018
- Track-A-Worm 2.0: A Software Suite for Quantifying Properties of C. elegans Locomotion, Bending, Sleep, and Action Potentials
Kiranmayi Vedantham, Longgang Niu, … Zhao‐Wen Wang·eNeuroPeer-reviewed·Aug 1, 2025
- Large vision model framework for automated C. elegans analysis: From static morphometry to dynamic neural activity
Aurélie Guisnet, Michael Hendricks·PLoS Computational BiologyPeer-reviewed·Jul 22, 2026