Resource limitation and population fluctuation drive spatiotemporal order in microbial communities

Abstract

Microbial communities display complex spatiotemporal behaviors leading to spatially-structured and ordered organization driven by species interactions and environmental factors. Resource availability plays a pivotal role in shaping the dynamics of bacterial colonies. In this study, we delve into the intricate interplay between resource limitation and the emergent properties of a growing colony of two visually distinct bacterial strains having similar growth and mechanical properties. Employing an agent-based modeling and computer simulations, we analyze the resource-driven effect on segregation and sectoring, cell length regulation and nematic ordering within a growing colony. We introduce a dimensionless parameter referred to as the active layer thickness, derived from nutrient diffusion equations, indicating effective population participation due to local resource availability. Our results reveal that lower values of active layer thickness arising from decreased resource abundance lead to rougher colony fronts, fostering heightened population fluctuations within the colony and faster spatial genetic diversity loss. Our temporal analyses unveil the dynamics of mean cell length and fluctuations, showcasing how initial disturbances evolve as colonies are exposed to nutrients and subsequently settle. Furthermore, examining microscopic details, we find that lower resource levels yield diverse cell lengths and enhanced nematic ordering, driven by the increased prevalence of longer rod-shaped cells. Our investigation sheds light on the multifaceted relationship between resource constraints and bacterial colony dynamics, revealing insights into their spatiotemporal organization.