A single pair of interneurons commands the Drosophila feeding motor program

Many feeding behaviors represent stereotyped, organized sequences of motor patterns that have been the subject of neuroethological studies(1,2) such as electrophysiological characterization of neurons governing prey capture in toads(1,3). Technical limitations, however, have prevented detailed study of the functional role of these neurons as in other studies on vertebrate organisms. Complexities involved in studies of whole animal behavior can be resolved in Drosophila, where remote activation of brain cells by genetic means(4) allows one to interrogate the nervous system in freely moving animals to identify neurons that govern a specific behavior, and then to repeatedly target and manipulate these neurons to characterize their function. Here we show finding of neurons that generate the feeding motor program in Drosophila. We performed an unbiased screen using remote neuronal activation and identified a critical pair of brain cells that induces the entire feeding sequence when activated. These Fdg (feeding)-neurons are also essential for normal feeding as their suppression or ablation eliminates the sugar-induced feeding behavior. Activation of a single Fdg-neuron induced asymmetric feeding behavior and ablation of a single Fdg-neuron distorted the sugar-induced feeding behavior to be asymmetric, indicating the direct role of these neurons in shaping motor program execution. Simultaneously recording neuronal activity with calcium imaging during feeding behavior(5) further revealed that the Fdg-neurons respond to food presentation, but only in starved flies. Our results demonstrate that Fdg-neurons operate firmly within the sensori-motor watershed, downstream of sensory and metabolic cues and at the top of the feeding motor hierarchy to execute the decision to feed.