Audiovisual integration in the Mauthner cell enhances escape probability and reduces response latency

• Published in: Scientific reports 2022-01, Vol.12 (1), p.1097-1097, Article 1097
• Main Authors: Martorell, Nicolás, Medan, Violeta
• Format: Article
• Language: English
• Subjects: 631/114/116; 631/114/116/1925; 631/1647/2198; 631/378/2613; 631/378/2613/1483; 631/378/2629; 631/378/2632; 631/378/2649/1409; 631/378/3917; 631/378/3920; Acoustic Stimulation; Animals; Auditory Perception - physiology; Auditory stimuli; Behavior; Computational neuroscience; Cues; Decision making; Escape behavior; Escape Reaction - physiology; Female; Goldfish - physiology; Hearing; Humanities and Social Sciences; Latency; Male; multidisciplinary; Neurons - physiology; Reaction Time - physiology; Rhombencephalon - physiology; Risk assessment; Science; Science (multidisciplinary); Sensory integration; Velocity; Visual Perception - physiology; Visual stimuli
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-04998-2

Fast and accurate threat detection is critical for animal survival. Reducing perceptual ambiguity by integrating multiple sources of sensory information can enhance perception and reduce response latency. However, studies addressing the link between behavioral correlates of multisensory integration and its underlying neural basis are rare. Fish that detect an urgent threat escape with an explosive behavior known as C-start. The C-start is driven by an identified neural circuit centered on the Mauthner cell, an identified neuron capable of triggering escapes in response to visual and auditory stimuli. Here we demonstrate that goldfish can integrate visual looms and brief auditory stimuli to increase C-start probability. This multisensory enhancement is inversely correlated to the salience of the stimuli, with weaker auditory cues producing a proportionally stronger multisensory effect. We also show that multisensory stimuli reduced C-start response latency, with most escapes locked to the presentation of the auditory cue. We make a direct link between behavioral data and its underlying neural mechanism by reproducing the behavioral data with an integrate-and-fire computational model of the Mauthner cell. This model of the Mauthner cell circuit suggests that excitatory inputs integrated at the soma are key elements in multisensory decision making during fast C-start escapes. This provides a simple but powerful mechanism to enhance threat detection and survival.