4.8 Article

Salt-responsive gut commensal modulates TH17 axis and disease

Journal

NATURE
Volume 551, Issue 7682, Pages 585-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/nature24628

Keywords

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Funding

  1. German Centre for Cardiovascular Research (DZHK) [BER 1.1 VD]
  2. Center for Microbiome Informatics and Therapeutics
  3. MetaCardis consortium
  4. German Research Foundation (DFG)
  5. Novartis Pharma
  6. European Research Council (ERC) under the European Union [640116]
  7. government of Flanders, Belgium
  8. Research Foundation Flanders (FWO), Belgium

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A Western lifestyle with high salt consumption can lead to hypertension and cardiovascular disease. High salt may additionally drive autoimmunity by inducing T helper 17 (T(H)17) cells, which can also contribute to hypertension. Induction of T(H)17 cells depends on gut microbiota; however, the effect of salt on the gut microbiome is unknown. Here we show that high salt intake affects the gut microbiome in mice, particularly by depleting Lactobacillus murinus. Consequently, treatment of mice with L. murinus prevented salt-induced aggravation of actively induced experimental autoimmune encephalomyelitis and salt-sensitive hypertension by modulating T(H)17 cells. In line with these findings, a moderate high-salt challenge in a pilot study in humans reduced intestinal survival of Lactobacillus spp., increased T(H)17 cells and increased blood pressure. Our results connect high salt intake to the gut-immune axis and highlight the gut microbiome as a potential therapeutic target to counteract salt-sensitive conditions.

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