Hierarchical communities in the larval Drosophila connectome: Links to cellular annotations and network topology

Abstract

One of the longstanding aims of network neuroscience is to link a connectomes topological properties-i.e. features defined from connectivity alone-with an organisms neurobiology. One approach for doing so is to compare connectome properties with maps of metabolic, functional, and neurochemical annotations. This type of analysis is popular at the meso-/macro-scale, but is less common at the nano-scale, owing to a paucity of neuron-level connectome data. However, recent methodological advances have made possible the reconstruction of whole-brain connectomes at single-neuron resolution for a select set of organisms. These include the fruit fly, Drosophila melanogaster, and its developing larvae. In addition to fine-scale descriptions of neuron-to-neuron connectivity, these datasets are accompanied by rich annotations, documenting cell type and function. Here, we use a hierarchical and weighted variant of the stochastic blockmodel to detect multi-level communities in a recently published larval Drosophila connectome. We find that these communities partition neurons based on function and cell type. We find that communities mostly interact assortatively, reflecting the principle of functional segregation. However, a small number of communities interact non-assortatively. The neurons that make up these communities also form a "rich-club", composed mostly of interneurons that receive sensory/ascending inputs and deliver outputs along descending pathways. Next, we investigate the role of community structure in shaping neuron-to-neuron communication patterns. We find that polysynaptic signaling follows specific trajectories across modular hierarchies, with interneurons playing a key role in mediating communication routes between modules and hierarchical scales. Our work suggests a relationship between the system-level architecture of an organisms complete neuronal wiring network and the precise biological function and classification of its individual neurons. We envision our study as an important step towards bridging the gap between complex systems and neurobiological lines of investigation in brain sciences.