4.8 Article

Gut microbiome-mediated metabolism effects on immunity in rural and urban African populations

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NATURE COMMUNICATIONS
卷 12, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41467-021-25213-2

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资金

  1. Center for the Study of Inflammatory Bowel Disease (CSIBD) [P30DK043351]
  2. Center for Microbiome Informatics and Therapeutics
  3. CCIB development funds
  4. European Union [727565]
  5. The Joint Programming Initiative-A Healthy Diet for a Healthy Life (JPI-HDHL) [529051018]
  6. ZonMw (the Netherlands Organisation for Health Research and Development)
  7. Radboud Revolving Research Funds (3R-Fund)
  8. Spinoza Prize [NWO SPI94-212]
  9. ERC [833247]
  10. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [EXC2151 - 390873048]

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The study reveals a gradient of gut microbial profiles from rural through urban Tanzania towards Western populations, with associations found between immune responses, circulating metabolites, and specific immunomodulatory microbes. Rural populations show higher intestinal microbial diversity, with Bacteroidetes and fungi playing key roles in influencing immune responses.
The human gut microbiota is increasingly recognized as an important factor in modulating innate and adaptive immunity through release of ligands and metabolites that translocate into circulation. Urbanizing African populations harbor large intestinal diversity due to a range of lifestyles, providing the necessary variation to gauge immunomodulatory factors. Here, we uncover a gradient of intestinal microbial compositions from rural through urban Tanzanian, towards European samples, manifested both in relative abundance and genomic variation observed in stool metagenomics. The rural population shows increased Bacteroidetes, led by Prevotella copri, but also presence of fungi. Measured ex vivo cytokine responses were significantly associated with 34 immunomodulatory microbes, which have a larger impact on circulating metabolites than non-significant microbes. Pathway effects on cytokines, notably TNF-alpha and IFN-gamma, differential metabolome analysis and enzyme copy number enrichment converge on histidine and arginine metabolism as potential immunomodulatory pathways mediated by Bifidobacterium longum and Akkermansia muciniphila. The authors profile stool metagenomics and plasma metabolomics in Tanzanian individuals and uncover a gradient of gut microbial profiles, from rural through urban Tanzania towards Western populations. Integration with ex vivo blood microbial stimulations reveals immune responses associated with histidine and arginine pathways, mediated by Bifidobacterium longum and Akkermansia muciniphila.

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