Computer-guided design of optimal microbial consortia for immune system modulation.
basic_science · Level V
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- Record sourced from PubMed, PMID 29664397.
- Also identified by DOI 10.7554/eLife.30916 and PMC identifier 5959721.
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Abstract
Manipulation of the gut microbiota holds great promise for the treatment of diseases. However, a major challenge is the identification of therapeutically potent microbial consortia that colonize the host effectively while maximizing immunologic outcome. Here, we propose a novel workflow to select optimal immune-inducing consortia from microbiome compositicon and immune effectors measurements. Using published and newly generated microbial and regulatory T-cell (T<sub>reg</sub>) data from germ-free mice, we estimate the contributions of twelve Clostridia strains with known immune-modulating effect to T<sub>reg</sub> induction. Combining this with a longitudinal data-constrained ecological model, we predict the ability of every attainable and ecologically stable subconsortium in promoting T<sub>reg</sub> activation and rank them by the T<sub>reg</sub> Induction Score (TrIS). Experimental validation of selected consortia indicates a strong and statistically significant correlation between predicted TrIS and measured T<sub>reg</sub>. We argue that computational indexes, such as the TrIS, are valuable tools for the systematic selection of immune-modulating bacteriotherapeutics.
Medical subject headings
- Bacillota
- Host Microbial Interactions
- Immunity, Cellular
- Microbial Consortia
- T-Lymphocytes, Regulatory