Mucus-penetrating microbiota drive chronic low-grade intestinal inflammation and metabolic dysregulation

被引:1
|
作者
Kordahi, Melissa C. [1 ,2 ,5 ]
Daniel, Noemie [1 ,2 ,6 ]
Gewirtz, Andrew T. [3 ]
Chassaing, Benoit [1 ,2 ,4 ]
机构
[1] Univ Paris Cite, Inst Pasteur, Microbiome Host Interact, INSERM,U1306,CNRS,UMR6047, 25 Rue Docteur Roux, F-75015 Paris, France
[2] Univ Paris Cite, Mucosal microbiota chron inflammatory Dis, INSERM, CNRS,UMR8104,U1016, Paris, France
[3] Georgia State Univ, Inst Biomed Sci, Ctr Inflammat Immun & Infect, Digest Dis Res Grp, Atlanta, GA USA
[4] CHRU Nancy, IHU Infiny, Nancy, France
[5] Univ Paris Saclay, Inflammat Microbiome & Immunosurveillance, INSERM, U996, Orsay, France
[6] Symrise AG, 15 Rue Mozart 92 110, Clichy, France
基金
欧洲研究理事会;
关键词
Microbiota; mucus; encroachment; inflammation; metabolic deregulations; GUT MICROBIOTA; EMULSIFIERS; BACTERIA; COLITIS; MUCINS;
D O I
10.1080/19490976.2025.2455790
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Metabolic syndrome is, in humans, associated with alterations in the composition and localization of the intestinal microbiota, including encroachment of bacteria within the colon's inner mucus layer. Possible promoters of these events include dietary emulsifiers, such as carboxymethylcellulose (CMC) and polysorbate-80 (P80), which, in mice, result in altered microbiota composition, encroachment, low-grade inflammation and metabolic syndrome. While assessments of gut microbiota composition have largely focused on fecal/luminal samples, we hypothesize an outsized role for changes in mucus microbiota in driving low-grade inflammation and its consequences. In support of this notion, we herein report that both CMC and P80 led to stark changes in the mucus microbiome, markedly distinct from those observed in feces. Moreover, transfer of mucus microbiota from CMC- and P80-fed mice to germfree mice resulted in microbiota encroachment, low-grade inflammation, and various features of metabolic syndrome. Thus, we conclude that mucus-associated bacteria are pivotal determinants of intestinal inflammatory tone and host metabolism.
引用
收藏
页数:18
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