Origin of biogeographically distinct ecotypes during laboratory evolution

Abstract

Resource partitioning within microbial communities is central to their incredible productivity, including over 1 gigaton of annual methane emissions through syntrophic interactions. Here, we show how isogenic strains of a sulfate reducing bacterium (Desulfovibrio vulgaris, Dv) and a methanogen (Methanococcus maripaludis, Mm) underwent evolutionary diversification over 300-1,000 generations in a purely planktonic environmental context giving rise to coexisting ecotypes that could partition resources and improve overall stability, cooperativity, and productivity in a simulated subsurface environment. We discovered that mutations in just 15 Dv and 7 Mm genes gave rise to ecotypes within each species that were spatially enriched between sediment and planktonic phases over the course of only a few generations after transferring the evolved populations to a fluidized bed reactor (FBR). While lactate utilization by Dv in the attached community was significantly greater, the resulting H2 was partially consumed by low affinity hydrogenases in Mm within the same attached phase. The unutilized H2 was scavenged by high affinity hydrogenases in the planktonic phase Mm, generating copious amounts of methane and higher ratio of Mm to Dv. Our findings show how a handful of mutations that arise in one environmental context can drive resource partitioning by ecologically differentiated variants in another environmental context, whose interplay synergistically improves productivity of the entire mutualistic community.