# Muribaculum intestinale in brain-gut axis regulation: promises and limitations for therapeutic applications

**Authors:** Ruijun Wang, Zhanbiao He, Zhiqi Li, Yuanming Pan, Shuang Bai

PMC · DOI: 10.3389/fmicb.2026.1723051 · Frontiers in Microbiology · 2026-02-20

## TL;DR

This paper explores how the gut bacterium Muribaculum intestinale influences the gut-brain axis and its potential for treating brain and metabolic disorders.

## Contribution

The paper systematically reviews the novel regulatory mechanisms and therapeutic potential of Muribaculum intestinale in the gut-brain axis.

## Key findings

- M. intestinale modulates neurotransmitters, immune responses, and intestinal barrier function through metabolites like short-chain fatty acids.
- Its abundance is influenced by diet, exercise, and antibiotics, with high-fiber diets and exercise increasing its presence.
- Clinical translation faces challenges like technical limitations and individual variability, requiring future strategies like humanized models.

## Abstract

In recent years, the role of gut microbiota in the regulation of the gut-brain axis has garnered increasing attention, with Muribaculum intestinale (M. intestinale) emerging as a novel member of the gut microbiota, exhibiting unique biological characteristics and potential therapeutic value. This article systematically reviews the regulatory mechanisms of M. intestinale in the gut-brain axis and its associations with various diseases. M. intestinale modulates host neurotransmitter synthesis, immune responses, and intestinal barrier function through metabolites such as short-chain fatty acids, succinate, and 3-hydroxybutyrate, thereby influencing the progression of neurodegenerative disorders, psychiatric diseases, and metabolic diseases. Additionally, this article explores the distribution differences of M. intestinale in the intestines of mice and humans, as well as its susceptibility to external factors like diet, antibiotics, and exercise. Although current research has unveiled the potential roles of M. intestinale, its clinical translation still faces challenges such as technical bottlenecks and individual variability. Future studies should focus on humanized model construction, synthetic biology modifications, and multi-target intervention strategies to achieve precise microbiota-targeted therapies.

Infographic divided into four panels illustrating the relationship between gut microbiota, diet, health, and research challenges. Panel A shows dietary fiber leading to immune modulation and barrier protection in the gut. Panel B depicts a human silhouette linking gut factors to brain disorders, metabolism, and neurodegeneration. Panel C compares increased M. intestinale abundance from a high-fiber diet plus exercise versus reduced abundance from a high-fat diet plus antibiotics. Panel D outlines research challenges and future perspectives, including technical bottlenecks and strategies such as humanized models and synthetic biology.

## Linked entities

- **Chemicals:** succinate (PubChem CID 160419), 3-hydroxybutyrate (PubChem CID 92135)
- **Species:** Muribaculum intestinale (taxon 1796646), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cldn5 (claudin 5) [NCBI Gene 12741] {aka MBEC1, Tmvcf}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 13385] {aka Dlgh4, PSD-95, PSD95, SAP90, SAP90A}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}, Tph1 (tryptophan hydroxylase 1) [NCBI Gene 21990] {aka Tph}, Mucin [NCBI Gene 100508689], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Fdxr (ferredoxin reductase) [NCBI Gene 14149] {aka AR}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, Ffar2 (free fatty acid receptor 2) [NCBI Gene 233079] {aka GPCR43, Gpr43}, Ahr (aryl-hydrocarbon receptor) [NCBI Gene 11622] {aka Ah, Ahh, Ahre, In, bHLHe76}, Ido1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 15930] {aka Ido, Indo}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il23a (interleukin 23, alpha subunit p19) [NCBI Gene 83430] {aka IL-23, p19}, Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 21803] {aka TGF-beta1, TGFbeta1, Tgfb, Tgfb-1}, Tdo2 (tryptophan 2,3-dioxygenase) [NCBI Gene 56720] {aka TDO, TO, chky}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Gdnf (glial cell line derived neurotrophic factor) [NCBI Gene 14573] {aka ATF}, Il22 (interleukin 22) [NCBI Gene 50929] {aka IL-22, IL-22a, ILTIFa, If2b1, Iltif}, Tlr1 (toll-like receptor 1) [NCBI Gene 21897], Muc2 (mucin 2) [NCBI Gene 17831] {aka 2010015E03Rik, MCM, wnn}, Tlr2 (toll-like receptor 2) [NCBI Gene 24088] {aka Ly105}
- **Diseases:** cachexia (MESH:D002100), HPA (MESH:D007029), obese (MESH:D009765), Metabolic diseases (MESH:D008659), mitochondrial dysfunction (MESH:D028361), Neuro-degenerative diseases (MESH:D019636), chronic inflammation (MESH:D007249), muscle wasting (MESH:D009133), metabolic disturbances (MESH:D024821), Acute pancreatitis (MESH:D010195), Neuroinflammation (MESH:D000090862), anxiety (MESH:D001007), AD (MESH:D000544), mental disorders (MESH:D001523), inflammatory damage (MESH:D018746), dysbiosis (MESH:D064806), cancer cachexia (MESH:D009369), muscle loss (MESH:D009135), Colitis-associated cancer (MESH:D000083023), beta-amyloid (MESH:C000718787), systemic (MESH:D015619), pulmonary fibrosis (MESH:D011658), Sleep deprivation (MESH:D012892), Diabetic neuropathic pain (MESH:D009437), Depression (MESH:D003866), neuronal damage and dysfunction (MESH:D007674), cognitive impairment (MESH:D003072), gastric hemorrhage (MESH:D006471), impaired spatial memory (MESH:D008569), brain (MESH:D001927), anemia (MESH:D000740), neuro-diseases (MESH:C536203), Vitamin K deficiency (MESH:D014813), insulin resistance (MESH:D007333), gut-brain inflammation (MESH:D004660), infection (MESH:D007239)
- **Chemicals:** vancomycin (MESH:D014640), disaccharide (MESH:D004187), propionic acid (MESH:C029658), Arbutin (MESH:D001104), lipid A (MESH:D008050), dicarboxylic acids (MESH:D003998), blood sugar (MESH:D001786), quinolinic acid (MESH:D017378), GABA (MESH:D005680), AG (MESH:D012834), kynurenine (MESH:D007737), BLM (MESH:D001761), sugar (MESH:D000073893), chitosan (MESH:D048271), oxygen (MESH:D010100), alginate (MESH:D000464), Azoxymethane (MESH:D001397), 3-HB (MESH:D020155), Succinate (MESH:D019802), saline (MESH:D012965), SFN (MESH:C016766), carbon (MESH:D002244), metronidazole (MESH:D008795), polysaccharide (MESH:D011134), cortisol (MESH:D006854), nitrogen (MESH:D009584), LPS (MESH:D008070), lipid (MESH:D008055), resistant starch (MESH:D000084922), hyperforin (MESH:C001654), ampicillin (MESH:D000667), polyphenol (MESH:D059808), Ginsenoside Rd (MESH:C049863), 5-HT (MESH:D012701), Flavonoids (MESH:D005419), Indole (MESH:C030374), SCFA (MESH:D005232), neomycin (MESH:D009355), Heterophyllin B (MESH:C000608358), Tryptophan (MESH:D014364), hydrogen (MESH:D006859), AAD (-), bile acid (MESH:D001647), Propionate (MESH:D011422), hypericin (MESH:C004965), Carbohydrate (MESH:D002241), vitamin K (MESH:D014812), butyrate (MESH:D002087), amino acid (MESH:D000596), Dimethyl itaconate (MESH:C518953)
- **Species:** Chrysanthemum indicum (species) [taxon 146995], Desulfovibrio (genus) [taxon 872], Muribaculum intestinale (species) [taxon 1796646], Parasutterella excrementihominis (species) [taxon 487175], Zingiber officinale (ginger, species) [taxon 94328], Salmonella enterica subsp. enterica serovar Typhimurium (no rank) [taxon 90371], Bacteroides uniformis (species) [taxon 820], Mucispirillum schaedleri (species) [taxon 248039], Nannospalax leucodon (lesser mole rat, species) [taxon 30638], Escherichia coli (E. coli, species) [taxon 562], Ligilactobacillus murinus (species) [taxon 1622], Lachnospiraceae (family) [taxon 186803], Deferribacterota (phylum) [taxon 200930], Prevotella sp. (species) [taxon 59823], Mus musculus (house mouse, species) [taxon 10090], Citrus unshiu (satsuma mandarin, species) [taxon 55188], Oryza sativa (Asian cultivated rice, species) [taxon 4530], Curcuma longa (turmeric, species) [taxon 136217], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Bacteroidia (class) [taxon 200643], Bacteroides caecimuris (species) [taxon 1796613], Bacteroidales (order) [taxon 171549], Prevotella sp. MGM2 (species) [taxon 2033406], Faecalibaculum rodentium (species) [taxon 1702221], Akkermansia muciniphila (species) [taxon 239935], Sargassum fusiforme (species) [taxon 590727], Bifidobacterium (genus) [taxon 1678], Spirochaetia (class) [taxon 203692], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Muribaculum (genus) [taxon 1918540], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW), Caco-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12963064/full.md

## References

102 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963064/full.md

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Source: https://tomesphere.com/paper/PMC12963064