Microbial communities often exhibit complex spatial structures that are important for their functioning, ecology, and evolution. While the role of biochemical interactions is extensively studied, how physical interactions contribute to structuring typically multispecies and phenotypically diverse bacterial communities is unclear. Here, we examined how motility, a major bacterial trait, affects the organization of model binary mixtures of motile and nonmotile bacteria, revealing a novel type of active self-organization. Motile bacteria induce large-scale, fluctuating density patterns in nonmotile bacteria across a wide range of physiologically relevant cell densities. Combining experiments and quantitative modeling, we demonstrate that this pattern formation solely results from physical interactions and relies on two key ingredients: By swimming in circles at surfaces, the motile bacteria generate recirculating hydrodynamic flows that advect nonmotile cells, and the breaking of vertical symmetry by gravity permits local density accumulation. The density patterns fluctuate as the advection landscape slowly rearrange with motile cells configurations on the surfaces. This new nonequilibrium mechanism for pattern formation in bacteria belongs to a different class compared to previous models for self-organization in self-propelled systems, which rely on localized traffic jamming in two dimensions. It is instead similar to fluctuation-dominated phase ordering in active nematics. The behavior also drives the formation of large scale and highly structured aggregates of nonmotile cells that express adhesins in the mixture, and it showcases how motile species activity can shape the spatial organization of complex microbial communities. Published by the American Physical Society 2024
Read full abstract