Specific Eco-evolutionary Contexts in the Mouse Gut Reveal Escherichia coli Metabolic Versatility

Members of the gut microbiota are thought to experience strong competition for nutrients. However, how such competition shapes their evolutionary dynamics and depends on intra- and interspecies interactions is poorly understood. Here, we test the hypothesis that Escherichia coli evolution in the mou...

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Veröffentlicht in:Current biology 2020-03, Vol.30 (6), p.1049-1062.e7
Hauptverfasser: Barroso-Batista, João, Pedro, Miguel F., Sales-Dias, Joana, Pinto, Catarina J.G., Thompson, Jessica A., Pereira, Helena, Demengeot, Jocelyne, Gordo, Isabel, Xavier, Karina B.
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container_end_page 1062.e7
container_issue 6
container_start_page 1049
container_title Current biology
container_volume 30
creator Barroso-Batista, João
Pedro, Miguel F.
Sales-Dias, Joana
Pinto, Catarina J.G.
Thompson, Jessica A.
Pereira, Helena
Demengeot, Jocelyne
Gordo, Isabel
Xavier, Karina B.
description Members of the gut microbiota are thought to experience strong competition for nutrients. However, how such competition shapes their evolutionary dynamics and depends on intra- and interspecies interactions is poorly understood. Here, we test the hypothesis that Escherichia coli evolution in the mouse gut is more predictable across hosts in the absence of interspecies competition than in the presence of other microbial species. In support, we observed that lrp, a gene encoding a global regulator of amino acid metabolism, was repeatedly selected in germ-free mice 2 weeks after mono-colonization by this bacterium. We established that this specific genetic adaptation increased E. coli’s ability to compete for amino acids, and analysis of gut metabolites identified serine and threonine as the metabolites preferentially consumed by E. coli in the mono-colonized mouse gut. Preference for serine consumption was further supported by testing a set of mutants that showed loss of advantage of an lrp mutant impaired in serine metabolism in vitro and in vivo. Remarkably, the presence of a single additional member of the microbiota, Blautia coccoides, was sufficient to alter the gut metabolome and, consequently, the evolutionary path of E. coli. In this environment, the fitness advantage of the lrp mutant bacteria is lost, and mutations in genes involved in anaerobic respiration were selected instead, recapitulating the eco-evolutionary context from mice with a complex microbiota. Together, these results highlight the metabolic plasticity and evolutionary versatility of E. coli, tailored to the specific ecology it experiences in the gut. [Display omitted] •Evolution of E. coli in the mono-colonized mouse gut is highly predictable•Preference for serine consumption is a major driver for adaptation•Co-colonization with B. coccoides alters the gut metabolome and E. coli evolution•Evolution in co-colonized mice recapitulates the process seen with complex microbiota Competition is thought to shape the dynamics of gut microbiota evolution. Barroso-Batista et al. show that evolution of Escherichia coli in mono-colonized mice is highly predictable and selects for mutants in amino acid metabolism. The presence of a competitor species alters the metabolic environment and E. coli’s metabolism and evolutionary path.
doi_str_mv 10.1016/j.cub.2020.01.050
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However, how such competition shapes their evolutionary dynamics and depends on intra- and interspecies interactions is poorly understood. Here, we test the hypothesis that Escherichia coli evolution in the mouse gut is more predictable across hosts in the absence of interspecies competition than in the presence of other microbial species. In support, we observed that lrp, a gene encoding a global regulator of amino acid metabolism, was repeatedly selected in germ-free mice 2 weeks after mono-colonization by this bacterium. We established that this specific genetic adaptation increased E. coli’s ability to compete for amino acids, and analysis of gut metabolites identified serine and threonine as the metabolites preferentially consumed by E. coli in the mono-colonized mouse gut. Preference for serine consumption was further supported by testing a set of mutants that showed loss of advantage of an lrp mutant impaired in serine metabolism in vitro and in vivo. Remarkably, the presence of a single additional member of the microbiota, Blautia coccoides, was sufficient to alter the gut metabolome and, consequently, the evolutionary path of E. coli. In this environment, the fitness advantage of the lrp mutant bacteria is lost, and mutations in genes involved in anaerobic respiration were selected instead, recapitulating the eco-evolutionary context from mice with a complex microbiota. Together, these results highlight the metabolic plasticity and evolutionary versatility of E. coli, tailored to the specific ecology it experiences in the gut. [Display omitted] •Evolution of E. coli in the mono-colonized mouse gut is highly predictable•Preference for serine consumption is a major driver for adaptation•Co-colonization with B. coccoides alters the gut metabolome and E. coli evolution•Evolution in co-colonized mice recapitulates the process seen with complex microbiota Competition is thought to shape the dynamics of gut microbiota evolution. 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Remarkably, the presence of a single additional member of the microbiota, Blautia coccoides, was sufficient to alter the gut metabolome and, consequently, the evolutionary path of E. coli. In this environment, the fitness advantage of the lrp mutant bacteria is lost, and mutations in genes involved in anaerobic respiration were selected instead, recapitulating the eco-evolutionary context from mice with a complex microbiota. Together, these results highlight the metabolic plasticity and evolutionary versatility of E. coli, tailored to the specific ecology it experiences in the gut. [Display omitted] •Evolution of E. coli in the mono-colonized mouse gut is highly predictable•Preference for serine consumption is a major driver for adaptation•Co-colonization with B. coccoides alters the gut metabolome and E. coli evolution•Evolution in co-colonized mice recapitulates the process seen with complex microbiota Competition is thought to shape the dynamics of gut microbiota evolution. Barroso-Batista et al. show that evolution of Escherichia coli in mono-colonized mice is highly predictable and selects for mutants in amino acid metabolism. 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source Cell Press Free Archives; Access via ScienceDirect (Elsevier); EZB-FREE-00999 freely available EZB journals
subjects amino acid metabolism
Blautia coccoides
Escherichia coli
evolution
germ-free
gnotobiology
gut, metabolomics
lrp
serine metabolism
title Specific Eco-evolutionary Contexts in the Mouse Gut Reveal Escherichia coli Metabolic Versatility
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