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Microbiota-Modulated Metabolites Shape the Intestinal Microenvironment by Regulating NLRP6 Inflammasome Signaling
Open accessAbstract
Host-microbiome co-evolution drives homeostasis and disease susceptibility, yet regulatory principles governing the integrated intestinal host-commensal microenvironment remain obscure. While inflammasome signaling participates in these interactions, its activators and microbiome-modulating mechanisms are unknown. Here, we demonstrate that the microbiota-associated metabolites taurine, histamine, and spermine shape the host-microbiome interface by co-modulating NLRP6 inflammasome signaling, epithelial IL-18 secretion, and downstream anti-microbial peptide (AMP) profiles. Distortion of this balanced AMP landscape by inflammasome deficiency drives dysbiosis development. Upon fecal transfer, colitis-inducing microbiota hijacks this microenvironment-orchestrating machinery through metabolite-mediated inflammasome suppression, leading to distorted AMP balance favoring its preferential colonization. Restoration of the metabolite-inflammasome-AMP axis reinstates a normal microbiota and ameliorates colitis. Together, we identify microbial modulators of the NLRP6 inflammasome and highlight mechanisms by which microbiome-host interactions cooperatively drive microbial community stability through metabolite-mediated innate immune modulation. Therefore, targeted "postbiotic" metabolomic intervention may restore a normal microenvironment as treatment or prevention of dysbiosis-driven diseases.
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In the citing paper
“free taurine generated by deconjugation can enhance the activation of the NLRP6 inflammasome and thereby increase production of IL-18 by the intestinal epithelium, which supports epithelial barrier function and maintenance (Levy et al., 2015).”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Levy et al., 2015
In the citing paper
“Spermine and the monoamine histamine both inhibit activation of the NLRP6 inflammasome, a protein complex expressed by epithelial cells that regulates IL-18 secretion.”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Levy et al., 2015
In the citing paper
“Levy et al. recently reported that exogenous polyamines can reduce the release of IL-18, a cytokine that promotes epithelial repair and barrier function.”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Levy et al., 2015
In the citing paper
“taurine, another microbial metabolite that derives from host-produced bile acids (see below), counteracts the effects of spermine and histamine, indicating a finely tuned balance of opposing bacterial stimuli (Levy et al., 2015).”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Levy et al., 2015
In the citing paper
“NLRP6 inflammasome signaling is co-modulated by microbiota-derived metabolites, which regulates epithelial IL-18 secretion and AMP expression profiles.71”
From Interaction between microbiota and immunity in health and disease (2020) · cites this paper as [71]
In the citing paper
“NLRP6 KO mice show dysbiosis and increased incidence of inflammation-associated CRC [135,136,137].”
From Gut Microbiota and Cancer: From Pathogenesis to Therapy (2019) · cites this paper as [136]
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QIIME allows analysis of high-throughput community sequencing data
Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887
KEGG: Kyoto Encyclopedia of Genes and Genomes
Ogata, H., Goto, S., Sato, K., Fujibuchi, W., Bono, H., & Kanehisa, M. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.1.29 · Cited by 31,232
An obesity-associated gut microbiome with increased capacity for energy harvest
Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444
A human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624
Diet rapidly and reproducibly alters the human gut microbiome
David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100
Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria
Ivanov, I. I., Atarashi, K., Manel, N., Brodie, E. L., Shima, T., Karaoz, U., Wei, D., Goldfarb, K. C., Santee, C. A., Lynch, S. V., et al. (2009) · Cell · doi:10.1016/j.cell.2009.09.033 · Cited by 4,554
Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis
Rakoff-Nahoum, S., Paglino, J., Eslami-Varzaneh, F., Edberg, S., & Medzhitov, R. (2004) · Cell · doi:10.1016/j.cell.2004.07.002 · Cited by 4,251
Interactions Between the Microbiota and the Immune System
Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173
Human Genetics Shape the Gut Microbiome
Goodrich, J. K., Waters, J. L., Poole, A. C., Sutter, J. L., Koren, O., Blekhman, R., Beaumont, M., Van Treuren, W., Knight, R., Bell, J. T., et al. (2014) · Cell · doi:10.1016/j.cell.2014.09.053 · Cited by 3,164
Data, information, knowledge and principle: back to metabolism in KEGG
Kanehisa, M. I., Goto, S., Sato, Y., Kawashima, M., Furumichi, M., & Tanabe, M. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1076 · Cited by 3,103
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Additional file 1 of The important role of NLRP6 inflammasome in Pasteurella multocida infection
Wu, X., Zeng, Z., Tian, H., Peng, L., Xu, D., Wang, Y., Ye, C., Peng, Y., & Fang, R. (2022) · Figshare · doi:10.6084/m9.figshare.21321631
Cui, W., Hull, L., Zizzo, A., Wang, L., Lin, B., Zhai, M., & Xiao, M. (2023) · Figshare · doi:10.6084/m9.figshare.24104405
Cui, W., Hull, L., Zizzo, A., Wang, L., Lin, B., Zhai, M., & Xiao, M. (2023) · Figshare · doi:10.6084/m9.figshare.24104411
Zhang, F.-L., Chen, X.-W., Wang, Y.-F., Hu, Z., Zhang, W.-J., Zhou, B.-W., Ci, P.-F., & Liu, K. (2023) · Figshare · doi:10.6084/m9.figshare.22655282
Cui, W., Hull, L., Zizzo, A., Wang, L., Lin, B., Zhai, M., & Xiao, M. (2023) · Figshare · doi:10.6084/m9.figshare.24104414
Zhang, F.-L., Chen, X.-W., Wang, Y.-F., Hu, Z., Zhang, W.-J., Zhou, B.-W., Ci, P.-F., & Liu, K. (2023) · Figshare · doi:10.6084/m9.figshare.22655285
Cui, W., Hull, L., Zizzo, A., Wang, L., Lin, B., Zhai, M., & Xiao, M. (2023) · Figshare · doi:10.6084/m9.figshare.24104408
Cui, W., Hull, L., Zizzo, A., Wang, L., Lin, B., Zhai, M., & Xiao, M. (2023) · Figshare · doi:10.6084/m9.figshare.24104402
Cui, W., Hull, L., Zizzo, A., Wang, L., Lin, B., Zhai, M., & Xiao, M. (2023) · Figshare · doi:10.6084/m9.figshare.24104399
Tan, J., Wang, M., Huang, K., Xie, M., Zheng, Y., Luo, J., Tang, J., Zhai, X., He, Q., & Zhao, J. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02683-9
Zeng, M., Xing, W., Liang, G., Yuan, F., Wang, W., Liu, J., & He, Z. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.116305
Mahato, M., Mondal, P., & Bhattacharyya, S. (2026) · Bratislavské lekárske listy/Bratislava medical journal · doi:10.1007/s44411-026-00528-y
Inflammasome activation and signalling in the ischemic-reperfused myocardium
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Martin‐Gallausiaux, C. (2018) · theses.fr (ABES) · doi:10.70675/c6162413z61d4z4a51z889bze8ca8724b717
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Cornut, M. (2020) · theses.fr (ABES) · doi:10.70675/fa5bf18bz82a6z4879za183z27963c062531
Lustig, R., Watkins, W. J., Natella, S., Velasquez‐Mieyer, P., & Jones, L. (2026) · Research Square · doi:10.21203/rs.3.rs-9252335/v1
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Guerville, F. (2023) · theses.fr (ABES) · doi:10.70675/eac3286czda71z4606z9c90z3d3efeaf1afe
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Zheng, X. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-31402-5.00001-3
Zhang, J., Bao, L., Li, X., Li, J., 崔珈衔, Qiao, L., He, X., Zhang, M., Lu, J., Zhang, X., et al. (2026) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2026.5834
Sun, L., Huang, K., Yang, X., Huang, X., & Zhai, Q. (2026) · Burns · doi:10.1016/j.burns.2026.108032
Andrusiów, S., Brzoza, A., Łacina, P., Dratwa-Kuźmin, M., Raczkowska, J., Kujawa, D., Romańczuk, K., Gancarek, M., Bochen, P., Dziadkowiak, E., et al. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1802462
Hu, Y., Chen, J.-S., Zhou, M., Huang, H., Zhou, Y.-F., Zhou, H.-Y., & Lv, Z. (2026) · Infectious Diseases of Poverty · doi:10.1186/s40249-026-01436-7
Inflammasomes in digestive diseases: mechanisms and therapeutic potential
Zhang, Y., Zhao, X., Tian, Z., Li, M., Luo, N., Chu, X., Chen, S., Jiang, T., Wang, S., & Liu, Z. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12245-4
Nakase, H., Shimomori, Y., & Kurumi, H. (2026) · Internal Medicine · doi:10.2169/internalmedicine.7768-26
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Wu, J. J., Wang, Q., & Mao, X. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1869733
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Zhang, Z.-Y., Li, Z.-D., Peng, C.-W., Peng, H., Zou, X., Yuan-xia, Z., Liao, W.-L., Tian-ke, L., & Li, R. H. (2026) · Therapeutic Advances in Gastroenterology · doi:10.1177/17562848261467814
Chan, Y.-T., Lu, P., Zou, J., Jiang, Z., Xu, L., & Wang, N. (2026) · Cancer Biome and Targeted Therapy · doi:10.66505/cbtt.v1i3.42
Puri, M., Kumar, M., Haleagrahara, N., Sahkumara, H., Rowarth, S., Robertson, K., Subbian, S., Warner, J., Rush, C. M., Ruscher, R., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.16.743391
Babu, P., Prakash, V., Subhash, S., Vanuopadath, M., Haripriyan, J., Rajan, K., Anu, A. G., Padmakumar, S., Kumar, G. B., Nair, B. G., et al. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1905445 · Cited by 1
Gut instincts: Multi-level control and neural pathways involved in gastrointestinal interoception
Chai, X.-Y., Wongkrasant, P., Morales‐Soto, W., Meerschaert, K. A., Wang, X. J., & Smith, K. (2026) · Autonomic Neuroscience · doi:10.1016/j.autneu.2026.103476
The NLRP3 inflammasome at the crossroads of innate immune signaling and cell death
Xiao, N., Lu, Z., Cooper, D. K., & Chen, J. (2026) · Cellular and Molecular Immunology · doi:10.1038/s41423-026-01463-2 · Cited by 2
Microbiota-derived metabolite-GPCR signalling in neurodegeneration
Sharma, A., & Jatana, N. (2026) · Neuroscience · doi:10.1016/j.neuroscience.2026.09.001
Martínez-García, J. J., Rodríguez, S., Guijarro, A., Quevedo-Romero, I., Mateo, S. V., Molina‐López, C., Hurtado‐Navarro, L., Baroja‐Mazo, A., & Pelegrín, P. (2026) · Metabolism · doi:10.1016/j.metabol.2026.156766
Structural mechanisms for ATP-mediated inhibition of human NLRP6 inflammasome
Cui, Z., Sheng, Q., Son, M., Goo, Y. A., & Shen, C. (2026) · Nature Structural & Molecular Biology · doi:10.1038/s41594-026-01878-5
Emfietzoglou, M., Bantounou, M. A., Osmani, S., Narimatsu, T., Baroutis, K. G., Varsamidaki, A., Skondra, D., Papaconstantinou, D., Theodossiadis, P., Chatziralli, I., et al. (2026) · PLoS ONE · doi:10.1371/journal.pone.0357009
Meng, X.-W., Tian, C., Zhu, Y.-J., & Zheng, D.-P. (2026) · Microorganisms · doi:10.3390/microorganisms14092108
Du, Y., Fu, J., Lai, X., Zhu, H., & Wang, K. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1898429
Düll, M. M., Rauh, M., Dietrich, P., Vetter, M., Schmid, J., Mettang, T., & Kremer, A. E. (2026) · JEADV Clinical Practice · doi:10.1002/jvc2.70447
Context-dependent roles of resistin-like molecule β in mucosal defense and inflammatory diseases
Ai, Q., Chen, W., Chen, W., & Tuo, Q. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1882146
Ali, S., Ali, B., Shaukat, A., Alghamdi, S. A., Kabrah, A. M., Ahmed, M., & Zhang, L. (2026) · Veterinary Research Communications · doi:10.1007/s11259-026-11535-3
The gasdermin family: from pyroptosis mechanisms to therapeutic targets
Xu, W., Liu, S., Yu, Z., Shi, J., Yang, Y., & Shi, F. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02867-2
Xu, H., Xianyu, D.-W., Jin, W.-W., Chen, K.-Z., Deng, Y.-H., Li, J.-X., Zhu, Y.-M., Fu, C.-H., Chen, G.-X., & Yu, L.-J. (2026) · Foods · doi:10.3390/foods15193528
Dong, J., & Zhou, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1948343
Xu, C., Wu, X., He, Q., Yang, L., Talib, S., & Li, K. (2026) · Microbiology Spectrum · doi:10.1128/spectrum.03662-25
Wang, S., Zhu, H., Li, Y., Zou, J., Mu, P., Yu, X., Liu, Y., Zhang, J., Jiang, L., Yu, J., et al. (2026) · Biology · doi:10.3390/biology15201870
Molecular mechanisms of NLR proteins in inflammasome activation
Liu, Y., Ji, K., & Zhang, L. (2026) · Communications Biology · doi:10.1038/s42003-026-11169-w
Gheblawi, M., Khoramjoo, M., Elaish, M., Wang, K., Puttagunta, L., Wang, F., Zhabyeyev, P., Ogando, N. S., Basu, R., Zhang, A., et al. (2026) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2026.101691
BindingDB (2019) · UC San Diego · doi:10.7270/q2jd507r
Gut epithelial barriers as regulators of metabolite-driven immune responses
Tyagi, A., Tayal, R., Bhatt, D. N., Srivastava, S., Kumar, A., Kumar, A., & Kumar, V. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1959305
Metadata
- Authors
- Levy, M., Thaiss, C. A., Zeevi, D., Dohnalová, L., Zilberman-Schapira, G., Mahdi, J. A., David, E., Savidor, A., Korem, T., Herzig, Y., Pevsner-Fischer, M., Shapiro, H., Christ, A., Harmelin, A., Halpern, Z., Latz, E., Flavell, R. A., Amit, I., Segal, E., & Elinav, E.
- Affiliations
- Weizmann Institute of Science (IL)
- Ben-Gurion University of the Negev (IL)
- University of Bonn (DE)
- Tel Aviv University (IL)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Segal, Eran
- Elinav, Eran
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2015-12
- Volume
- 163
- Issue
- 6
- Pages
- 1428-1443
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC5665753
- OpenAlex
- W2188593832
- Cited by
- 960
- References
- 51
- Citations by year
- 2026: 63 · 2025: 67 · 2024: 95 · 2023: 106 · 2022: 109 · 2021: 112 · 2020: 96 · 2019: 108 · 2018: 69 · 2017: 78 · 2016: 51 · 2015: 3
- FWCI
- 29.08
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 368 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Cancer Institute (P30CA016359)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK034989)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- gut microbiota, NLRP6 inflammasome, host-microbiome interactions, taurine, histamine, spermine, IL-18, antimicrobial peptides, dysbiosis, colitis, fecal microbiota transplantation, postbiotics, innate immune modulation, intestinal epithelium
- MeSH terms
- Animals, Colitis, Colon, Germ-Free Life, Mice, Inbred C57BL, Receptors, Cell Surface, Taurine, Inflammatory Bowel Diseases, Signal Transduction, Interleukin-18, Antimicrobial Cationic Peptides, Mice, Inflammasomes, Microbiota, Dysbiosis
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