Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/25993
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dc.contributor.authorWilck, Nicola-
dc.contributor.authorMatus, Mariana G.-
dc.contributor.authorKearney, Sean M.-
dc.contributor.authorOlesen, Scott W.-
dc.contributor.authorForslund, Kristoffer-
dc.contributor.authorBartolomaeus, Hendrik-
dc.contributor.authorJörg, Stefanie-
dc.contributor.authorMähler, Anja-
dc.contributor.authorBalogh, András-
dc.contributor.authorMarkó, Lajos-
dc.contributor.authorVvedenskaya, Olga-
dc.contributor.authorKleiner, Friedrich H.-
dc.contributor.authorTsvetkov, Dmitry-
dc.contributor.authorKlug, Lars-
dc.contributor.authorCostea, Paul I.-
dc.contributor.authorSunagawa, Shinichi-
dc.contributor.authorMaier, Lisa-
dc.contributor.authorRakova, Natalia-
dc.contributor.authorSchatz, Valentin-
dc.contributor.authorNeubert, Patrick-
dc.contributor.authorFrätzer, Christian-
dc.contributor.authorKrannich, Alexander-
dc.contributor.authorGollasch, Maik-
dc.contributor.authorGrohme, Diana A.-
dc.contributor.authorCôrte-Real, Beatriz F.-
dc.contributor.authorGerlach, Roman G.-
dc.contributor.authorBasic, Marijana-
dc.contributor.authorTypas, Athanasios-
dc.contributor.authorWu, Chuan-
dc.contributor.authorTitze, Jens M.-
dc.contributor.authorJantsch, Jonathan-
dc.contributor.authorBoschmann, Michael-
dc.contributor.authorDechend, Ralf-
dc.contributor.authorKLEINEWIETFELD, Markus-
dc.contributor.authorKempa, Stefan-
dc.contributor.authorBork, Peer-
dc.contributor.authorLinker, Ralf A.-
dc.contributor.authorAlm, Eric J.-
dc.contributor.authorMüller, Dominik N.-
dc.date.accessioned2018-05-17T08:07:43Z-
dc.date.available2018-05-17T08:07:43Z-
dc.date.issued2017-
dc.identifier.citationNATURE, 551(7682), p. 585-589-
dc.identifier.issn0028-0836-
dc.identifier.urihttp://hdl.handle.net/1942/25993-
dc.description.abstractA Western lifestyle with high salt consumption can lead to hypertension and cardiovascular disease. High salt may additionally drive autoimmunity by inducing T helper 17 (TH17) cells, which can also contribute to hypertension. Induction of TH17 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 TH17 cells. In line with these findings, a moderate high-salt challenge in a pilot study in humans reduced intestinal survival of Lactobacillus spp., increased TH17 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.-
dc.description.sponsorshipThis study was funded by grants from the German Centre for Cardiovascular Research (DZHK; BER 1.1 VD), the Center for Microbiome Informatics and Therapeutics, and the MetaCardis consortium. D.N.M., J.J. and M.G. were supported by the German Research Foundation (DFG). R.A.L. holds an endowed professorship supported by Novartis Pharma. M.K. was supported by the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (640116), by a SALK-grant from the government of Flanders, Belgium and by an Odysseus-grant of the Research Foundation Flanders (FWO), Belgium. L. reuteri was provided by L. Romani.-
dc.language.isoen-
dc.rights© 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.-
dc.titleSalt-responsive gut commensal modulates TH17 axis and disease-
dc.typeJournal Contribution-
dc.identifier.epage589-
dc.identifier.issue7682-
dc.identifier.spage585-
dc.identifier.volume551-
local.bibliographicCitation.jcatA1-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.type.programmeH2020-
local.relation.h2020640116-
dc.identifier.doi10.1038/nature24628-
dc.identifier.isi000416520400034-
item.validationecoom 2019-
item.fulltextWith Fulltext-
item.fullcitationWilck, Nicola; Matus, Mariana G.; Kearney, Sean M.; Olesen, Scott W.; Forslund, Kristoffer; Bartolomaeus, Hendrik; Jörg, Stefanie; Mähler, Anja; Balogh, András; Markó, Lajos; Vvedenskaya, Olga; Kleiner, Friedrich H.; Tsvetkov, Dmitry; Klug, Lars; Costea, Paul I.; Sunagawa, Shinichi; Maier, Lisa; Rakova, Natalia; Schatz, Valentin; Neubert, Patrick; Frätzer, Christian; Krannich, Alexander; Gollasch, Maik; Grohme, Diana A.; Côrte-Real, Beatriz F.; Gerlach, Roman G.; Basic, Marijana; Typas, Athanasios; Wu, Chuan; Titze, Jens M.; Jantsch, Jonathan; Boschmann, Michael; Dechend, Ralf; KLEINEWIETFELD, Markus; Kempa, Stefan; Bork, Peer; Linker, Ralf A.; Alm, Eric J. & Müller, Dominik N. (2017) Salt-responsive gut commensal modulates TH17 axis and disease. In: NATURE, 551(7682), p. 585-589.-
item.accessRightsOpen Access-
item.contributorWilck, Nicola-
item.contributorMatus, Mariana G.-
item.contributorKearney, Sean M.-
item.contributorOlesen, Scott W.-
item.contributorForslund, Kristoffer-
item.contributorBartolomaeus, Hendrik-
item.contributorJörg, Stefanie-
item.contributorMähler, Anja-
item.contributorBalogh, András-
item.contributorMarkó, Lajos-
item.contributorVvedenskaya, Olga-
item.contributorKleiner, Friedrich H.-
item.contributorTsvetkov, Dmitry-
item.contributorKlug, Lars-
item.contributorCostea, Paul I.-
item.contributorSunagawa, Shinichi-
item.contributorMaier, Lisa-
item.contributorRakova, Natalia-
item.contributorSchatz, Valentin-
item.contributorNeubert, Patrick-
item.contributorFrätzer, Christian-
item.contributorKrannich, Alexander-
item.contributorGollasch, Maik-
item.contributorGrohme, Diana A.-
item.contributorCôrte-Real, Beatriz F.-
item.contributorGerlach, Roman G.-
item.contributorBasic, Marijana-
item.contributorTypas, Athanasios-
item.contributorWu, Chuan-
item.contributorTitze, Jens M.-
item.contributorJantsch, Jonathan-
item.contributorBoschmann, Michael-
item.contributorDechend, Ralf-
item.contributorKLEINEWIETFELD, Markus-
item.contributorKempa, Stefan-
item.contributorBork, Peer-
item.contributorLinker, Ralf A.-
item.contributorAlm, Eric J.-
item.contributorMüller, Dominik N.-
crisitem.journal.issn0028-0836-
crisitem.journal.eissn1476-4687-
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