Capillary interactions drive the self-organization of bacterial colonies.

Many bacteria inhabit thin water layers on solid surfaces. These thin films occur both naturally - in soils, on hosts, on textiles - and in the lab on agar hydrogels. In these environments, cells the water menisci formed around bacteria lead to capillary attraction between cells while still allowing them to slide past one another. We develop an experimental apparatus that allows us to control bacterial collective experience capillary forces but it is unclear how these forces shape bacterial collective behavior. Here, we show that behavior by varying the strength and range of capillary forces. Combining three-dimensional imaging and cell tracking with agent-based modelling, we demonstrate that capillary attraction organizes rod-shaped bacteria into densely packed, nematic groups, and influences their collective dynamics and morphologies. Our results suggest that capillary forces may be a ubiquitous physical ingredient in shaping microbial communities in partially hydrated environments.