Decoding the intensity of sensory input by two glutamate receptors in one C. elegans interneuron

How neurons are capable of decoding stimulus intensity and translate this information into complex behavioral outputs is poorly defined. Here, we demonstrate that the C. elegans interneuron AIB regulates two types of behaviors: reversal initiation and feeding suppression in response to different concentrations of quinine. Low concentrations of quinine are decoded in AIB by a low-threshold, fast-inactivation glutamate receptor GLR-1 and translated into reversal initiation. In contrast, high concentrations of quinine are decoded by a high-threshold, slow-inactivation glutamate receptor GLR-5 in AIB. After activation, GLR-5 evokes sustained Ca 2+ release from the inositol 1,4,5-trisphosphate (IP 3 )-sensitive Ca 2+ stores and triggers neuropeptide secretion, which in turn activates the downstream neuron RIM and inhibits feeding. Our results reveal that distinct signal patterns in a single interneuron AIB can encode differential behavioral outputs depending on the stimulus intensity, thus highlighting the importance of functional mapping of information propagation at the single-neuron level during connectome construction. Little is known about how stimuli of different intensities result in different behavioral outcomes in C. elegans . In this study, the authors demonstrate how distinct signal patterns, involving different glutamate receptors, in a single interneuron AIB can encode differential behavioral outputs depending on the stimulus intensity