Serotonergic Signaling Governs <i>Caenorhabditis elegans</i> Sensory Response to Conflicting Chemosensory Stimuli

Neural circuits that consolidate sensory cues are essential for neurological functioning. Neural circuits that perform sensory integration can vary greatly because the sensory processing regions of the brain employ various neural motifs. Here, we investigate a neural circuit that mediates the response to conflicting stimuli in <i>Caenorhabditis elegans</i> We concurrently expose animals to an aversive dispersal pheromone, osas#9, and an attractive bacterial extract. While worms usually avoid osas#9 alone, they suppress this avoidance behavior in the presence of a bacterial extract. Loss-of-function mutants and cell-specific rescues reveal that signaling from the ADF and NSM neurons is essential for bacterial extract-induced osas#9 avoidance attenuation. The inhibitory serotonin receptor, MOD-1, which is widely expressed on interneurons and motor neurons, is required for this sensory integration, suggesting that serotonin acts in an inhibitory manner. By performing calcium imaging on the ADF neurons in synaptic signaling (<i>unc-13</i>) and peptidergic (<i>unc-31</i>) signaling mutant backgrounds, we show that the ADF neurons require input from other neurons to respond to food extracts. We reveal a cue integration neural circuit in which serotonergic signaling and sensory neurons silence an aversive neural signal.