Feedback inhibition by a descending GABAergic neuron regulates timing of escape behavior in Drosophila larvae

Author:

Zhu Jiayi12,Boivin Jean-Christophe12,Garner Alastair12,Ning Jing1,Zhao Yi Q1,Ohyama Tomoko13ORCID

Affiliation:

1. Department of Biology, McGill University

2. Integrated Program of Neuroscience, McGill University

3. Alan Edwards Center for Research on Pain, McGill University

Abstract

Escape behaviors help animals avoid harm from predators and other threats in the environment. Successful escape relies on integrating information from multiple stimulus modalities (of external or internal origin) to compute trajectories toward safe locations, choose between actions that satisfy competing motivations, and execute other strategies that ensure survival. To this end, escape behaviors must be adaptive. When a Drosophila melanogaster larva encounters a noxious stimulus, such as the focal pressure a parasitic wasp applies to the larval cuticle via its ovipositor, it initiates a characteristic escape response. The escape sequence consists of an initial abrupt bending, lateral rolling, and finally rapid crawling. Previous work has shown that the detection of noxious stimuli primarily relies on class IV multi-dendritic arborization neurons (Class IV neurons) located beneath the body wall, and more recent studies have identified several important components in the nociceptive neural circuitry involved in rolling. However, the neural mechanisms that underlie the rolling-escape sequence remain unclear. Here, we present both functional and anatomical evidence suggesting that bilateral descending neurons within the subesophageal zone of D. melanogaster larva play a crucial role in regulating the termination of rolling and subsequent transition to escape crawling. We demonstrate that these descending neurons (designated SeIN128) are inhibitory and receive inputs from a second-order interneuron upstream (Basin-2) and an ascending neuron downstream of Basin-2 (A00c). Together with optogenetic experiments showing that co-activation of SeIN128 neurons and Basin-2 influence the temporal dynamics of rolling, our findings collectively suggest that the ensemble of SeIN128, Basin-2, and A00c neurons forms a GABAergic feedback loop onto Basin-2, which inhibits rolling and thereby facilitates the shift to escape crawling.

Funder

Natural Sciences and Engineering Research Council of Canada

Canadian Institutes of Health Research

Fonds de recherche du Québec – Nature et technologies

Fonds de Recherche du Québec - Santé

Canada Foundation for Innovation

Publisher

eLife Sciences Publications, Ltd

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