4.8 Article

In vitro interaction network of a synthetic gut bacterial community

期刊

ISME JOURNAL
卷 16, 期 4, 页码 1095-1109

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SPRINGERNATURE
DOI: 10.1038/s41396-021-01153-z

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资金

  1. German Research Foundation (DFG, German Research Foundation) [395357507-SFB 1371, 279971426, 315980449]
  2. European Research Council (ERC) under the European Union [865615]
  3. German Center for Infection Research (DZIF)
  4. Center for Gastrointestinal Microbiome Research (CEGIMIR)
  5. Collaborative Research Centre 1182-'Origin and Function of Metaorganisms'-Deutsche Forschungsgemeinschaft
  6. Cluster of Excellence 2167-'Precision medicine in chronic inflammation'-Deutsche Forschungsgemeinschaft
  7. German Ministry for Education and Research within the context of iTREAT [01ZX1902A]
  8. Care-for-Rare Foundation
  9. European Research Council (ERC) [865615] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

This study focuses on the growth and metabolic interactions of the Oligo-Mouse-Microbiota (OMM12) synthetic bacterial community in gut microbiome research. By conducting experiments, it was found that the OMM12 interaction network is influenced by exploitative and interference competition, with Enterococcus faecalis KB1 identified as an important driver of community composition.
A key challenge in microbiome research is to predict the functionality of microbial communities based on community membership and (meta)-genomic data. As central microbiota functions are determined by bacterial community networks, it is important to gain insight into the principles that govern bacteria-bacteria interactions. Here, we focused on the growth and metabolic interactions of the Oligo-Mouse-Microbiota (OMM12) synthetic bacterial community, which is increasingly used as a model system in gut microbiome research. Using a bottom-up approach, we uncovered the directionality of strain-strain interactions in mono- and pairwise co-culture experiments as well as in community batch culture. Metabolic network reconstruction in combination with metabolomics analysis of bacterial culture supernatants provided insights into the metabolic potential and activity of the individual community members. Thereby, we could show that the OMM12 interaction network is shaped by both exploitative and interference competition in vitro in nutrient-rich culture media and demonstrate how community structure can be shifted by changing the nutritional environment. In particular, Enterococcus faecalis KB1 was identified as an important driver of community composition by affecting the abundance of several other consortium members in vitro. As a result, this study gives fundamental insight into key drivers and mechanistic basis of the OMM12 interaction network in vitro, which serves as a knowledge base for future mechanistic in vivo studies.

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