Abstract

SummaryThe eco-evolutionary dynamics of microbial communities are predicted to affect both the tempo and trajectory of evolution in constituent species [1]. While community composition determines available niche space, species sorting dynamically alters composition, changing over time the distribution of vacant niches to which species adapt [2], altering evolutionary trajectories [3, 4]. Competition for the same niche can limit evolutionary potential if population size and mutation supply are reduced [5, 6] but, alternatively, could stimulate evolutionary divergence to exploit vacant niches if character displacement results from the coevolution of competitors [7, 8]. Under more complex ecological scenarios, species can create new niches through their exploitation of complex resources, enabling others to adapt to occupy these newly formed niches [9, 10]. Disentangling the drivers of natural selection within such communities is extremely challenging, and it is thus unclear how eco-evolutionary dynamics drive the evolution of constituent taxa. We tracked the metabolic evolution of a focal species during adaptation to wheat straw as a resource both in monoculture and in polycultures wherein on-going eco-evolutionary community dynamics were either permitted or prevented. Species interactions accelerated metabolic evolution. Eco-evolutionary dynamics drove increased use of recalcitrant substrates by the focal species, whereas greater exploitation of readily digested substrate niches created by other species evolved if on-going eco-evolutionary dynamics were prevented. Increased use of recalcitrant substrates was associated with parallel evolution of tctE, encoding a carbon metabolism regulator. Species interactions and species sorting set, respectively, the tempo and trajectory of evolutionary divergence among communities, selecting distinct ecological functions in otherwise equivalent ecosystems.

Highlights

  • In competition against the ancestral polyculture community, the RP-evolved Stenotrophomonas sp. reached a higher final relative abundance than its ancestor or the evolved Stenotrophomonas sp. from the DP or MC treatments. This suggests that the on-going eco-evolutionary dynamics of communities limited the evolution of exploitative metabolic strategies by the focal species

  • We previously showed that this Bacillus sp. strain is a labile substrate specialist [28], suggesting it would have competed strongly for labile substrates, potentially driving the observed niche differentiation by Stenotrophomonas sp. toward recalcitrant substrate use

  • The higher frequency of tctE mutations in DP-evolved compared to RP-evolved clones suggests that these mutations could be linked to the observed increase in the use of recalcitrant substrates by DPevolved Stenotrophomonas populations (Figure 1, Figure S1)

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Summary

Introduction

Significantly diverged between treatments over time (Figure S1; linear mixed model, treatment 3 substrate 3 time interaction, F12,777 = 7.8661, p < 2.2 3 10À16). Evolutionary paths varied significantly between treatments (Figure 1; permutational manova, treatment 3 time interaction, F = 8.97, p < 0.001). The RP treatment took an evolutionary trajectory whose direction was distinct from either the MC or DP treatments (pairwise differences in path angle, RP:DP Z = 2.028, p = 0.039; RP:MC Z = 1.88, p = 0.034).

Results
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