Abstract
Abstract
Metabolic cross-feeding is central to microbial life. Theory predicts that spatial structure favors cross- feeding by affording cells preferential access to the exchanged metabolites. Yet recent evidence shows that spatial structure can, in some contexts, disfavor cross-feeding. Here, we resolve this contradiction by structuring cross-feeding interactions into three dimensions: (i) directionality, (ii) investment, and (iii) metabolic dependency. We then investigated their combined effects using a spatially explicit individual- based model. We find that the effect of spatial structure on cross-feeding is determined not by physical proximity alone, but by how microbial growth depends on exchanged metabolites. Metabolic dependence shapes the spatial organization of cells and metabolite fluxes, and this emergent organization, in turn, reshapes the ecological outcome of cross-feeding. Our results reconcile previously conflicting observations and provide a general framework for predicting and engineering metabolically interdependent microbial communities.
Significance Statement
Cross-feeding, the sharing of metabolites among microbes, is one of the most common interactions in nature, and it helps build the communities that drive processes ranging from gut digestion and crop production to global nutrient cycling. A long-standing view says that physical association among microbes should promote this sharing. Here, we show this view is incomplete. Whether spatial structure strengthens or weakens cross-feeding depends on the type of metabolic dependence between the partners, not on the physical association alone. This finding reconciles conflicting experimental and theoretical observations reported over the past decade and provides a predictive framework for understanding metabolite exchange in natural microbial communities.
Graphical Abstract