Summary
A bacterial colony rarely exists in isolation - in natural habitats, colonies interact to form spatially structured communities across length and time scales. Eco-evolutionary feedbacks link these scales, such that structure at one level can influence another, yet the interplay between single- and multi-colony organization remains poorly understood. As a step toward addressing this, we develop a high-throughput platform to track population dynamics across spatially extended networks of colonies. A common structural feature observed at the multi-colony scale is the formation of a stable gap region between colonies, even when they are isogenic. Numerous studies observe similar patterns of behavior across species, with few resolving the underlying mechanism. Here, we ask: what are the minimal ingredients shaping this multi-colony structure? We focus on colonies of the opportunistic pathogen Enterococcus faecalis, a model organism for which this behavior has yet to be reported. By combining modeling and experiments, we show that both nutrient competition and direct growth inhibition control colony morphology and expansion of interacting colonies. We identify distinct regimes of gap formation, relating intra- and inter-colony spatial patterns to ecological interactions mediated at the cellular scale. Together, our results suggest that antagonism, even between isogenic populations through self-inhibition, is likely a common behavior of bacterial species in general.
Outcomes reported
A bacterial colony rarely exists in isolation - in natural habitats, colonies interact to form spatially structured communities across length and time scales. Eco-evolutionary feedbacks link these scales, such that structure at one level can influence another, yet the interplay between single- and multi-colony organization remains poorly understood. As a step toward addressing this, we develop a high-throughput platform to track population dynamics across spatially extended networks of colonies. A common structural feature observed at the multi-colony scale is the formation of a stable gap region between colonies, even when they are isogenic. Numerous studies observe similar patterns of behavior across species, with few resolving the underlying mechanism. Here, we ask: what are the minimal ingredients shaping this multi-colony structure? We focus on colonies of the opportunistic pathogen Enterococcus faecalis, a model organism for which this behavior has yet to be reported. By combining modeling and experiments, we show that both nutrient competition and direct growth inhibition control colony morphology and expansion of interacting colonies. We identify distinct regimes of gap formation, relating intra- and inter-colony spatial patterns to ecological interactions mediated at the cellular scale. Together, our results suggest that antagonism, even between isogenic populations through self-inhibition, is likely a common behavior of bacterial species in general.
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