Structured Interactions Drive Abrupt Transitions in the Spatial Organization of Microbial Communities

Abstract

Bacteria possess diverse mechanisms to regulate their motility in response to environmental and physiological signals, enabling them to navigate complex habitats and adapt their behavior. Among these mechanisms, interspecies recognition enables cells to modulate their movement based on the ecological identity of neighboring species. Here, we introduce a model in which we assume bacterial species recognizes each other and interact via local signals that either enhance or suppress the motility of neighboring cells. Through large-scale simulations and a coarse-grained stochastic model, we demonstrate the emergence of a sharp transition driven by nucleation processes: increasing the density of motility-suppressing interactions drives the system from a fully mixed, motile phase to a state characterized by large, stationary bacterial clusters. Remarkably, in systems with a large number of interacting species, this transition can be triggered solely by altering the structure of the motility-regulation interaction matrix while maintaining species and interaction densities constant. In particular, we find that heterogeneous and modular interactions promote the transition more readily than homogeneous random ones. These results contribute to the ongoing effort to understand microbial interactions, suggesting that structured, non-random ones may be key to reproducing commonly observed spatial patterns in microbial communities.

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