Akkermansia muciniphila-derived hypoacylated rough-type lipopolysaccharides alleviate diet-induced obesity via activation of TLR4−IL-23−IL-22 immune axis

Li Sun , Yuting Zhang , Wang Dong , Jingzu Sun , Tao Wang , Fei Shao , Huanqin Dai , Junjie Han , Wenzhao Wang , Shuo Wang , Tong Zhao , Liangliang Wang , Chang Liu , Shuangjiang Liu , Hongwei Liu

iMeta ›› 2025, Vol. 4 ›› Issue (5) : e70066

PDF
iMeta ›› 2025, Vol. 4 ›› Issue (5) :e70066 DOI: 10.1002/imt2.70066
RESEARCH ARTICLE
Akkermansia muciniphila-derived hypoacylated rough-type lipopolysaccharides alleviate diet-induced obesity via activation of TLR4−IL-23−IL-22 immune axis
Author information +
History +
PDF

Abstract

Lipopolysaccharides (LPS) derived from intestinal symbionts plays a critical role in modulating and maintaining mucosal immunity. In this study, we investigated the chemical characteristics and antiobesity properties of Akkermansia muciniphila HW07 LPS (ALPS). ALPS was identified as hypo-acylated, mono/bis-phosphorylated, rough-type LPS. Compared to Escherichia coli LPS (ELPS), ALPS functions as a weak agonist of TLR4/TLR2. Intraperitoneal administration of ALPS in diet-induced obese (DIO) mice suppressed weight gain, improved metabolic parameters, restored gut barrier integrity, and modulated the gut microbiota. Notably, ALPS treatment significantly increased plasma interleukin (IL)-22 levels. Furthermore, neutralizing IL-22 with an antibody eliminated the antiobesity effects of ALPS in DIO mice. Mechanistically, ALPS upregulated the expression of both IL-22 and its upstream cytokine IL-23 in a TLR4-dependent manner. These findings confirm that activation of the TLR4−IL-23−IL-22 immune axis is a key mechanism underlying the antiobesity effect of ALPS. In acute toxicity assessment, no fatalities were observed in ALPS-treated mice, whereas ELPS treatment led to a 40% mortality rate. Collectively, our results demonstrate that hypo-acylated LPS from A. muciniphila functions as a metabolically beneficial immune modulator that exerts immunomodulatory effects through the TLR4−IL-22 axis and suggests ALPS as a promising novel therapeutic strategy for metabolic disorders.

Keywords

Akkermansia muciniphila / antiobesity / hypoacylated rough-type LPS / TLR4−IL-23−IL-22 immune axis

Cite this article

Download citation ▾
Li Sun, Yuting Zhang, Wang Dong, Jingzu Sun, Tao Wang, Fei Shao, Huanqin Dai, Junjie Han, Wenzhao Wang, Shuo Wang, Tong Zhao, Liangliang Wang, Chang Liu, Shuangjiang Liu, Hongwei Liu. Akkermansia muciniphila-derived hypoacylated rough-type lipopolysaccharides alleviate diet-induced obesity via activation of TLR4−IL-23−IL-22 immune axis. iMeta, 2025, 4(5): e70066 DOI:10.1002/imt2.70066

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Wu, Guojun, Ting Xu, Naisi Zhao, Yan Y. Lam, Xiaoying Ding, Dongqin Wei, Jian Fan, et al. 2024. “A Core Microbiome Signature as an Indicator of Health.” Cell 187: 6550-6565. https://doi.org/10.1016/j.cell.2024.09.019

[2]

Zhao, Liping, Feng Zhang, Xiaoying Ding, Guojun Wu, Yan Y. Lam, Xuejiao Wang, Huaqing Fu, et al. 2018. “Gut Bacteria Selectively Promoted by Dietary Fibers Alleviate Type 2 Diabetes.” Science 359: 1151-1156. https://doi.org/10.1126/science.aao5774

[3]

Chen, Jiali, Yuhang Xiao, Dongmei Li, Shiqing Zhang, Yingzi Wu, Qing Zhang, and Weibin Bai. 2023. “New Insights into the Mechanisms of High-Fat Diet Mediated Gut Microbiota in Chronic Diseases.” iMeta 2: e69. https://doi.org/10.1002/imt2.69

[4]

Warmbrunn, Moritz V., Hilde Herrema, Judith Aron-Wisnewsky, Maarten R. Soeters, Daniel H. Van Raalte, and Max Nieuwdorp. 2020. “Gut Microbiota: A Promising Target against Cardiometabolic Diseases.” Expert Review of Endocrinology & Metabolism 15: 13-27. https://doi.org/10.1080/17446651.2020.1720511

[5]

Depommier, Clara, Matthias Van Hul, Amandine Everard, Nathalie M. Delzenne, Willem M. De Vos, and Patrice D. Cani. 2020. “Pasteurized Akkermansia muciniphila Increases Whole-Body Energy Expenditure and Fecal Energy Excretion in Diet-Induced Obese Mice.” Gut Microbes 11: 1231-1245. https://doi.org/10.1080/19490976.2020.1737307

[6]

Chang, Chih-Jung, Tzu-Lung Lin, Yu-Ling Tsai, Tsung-Ru Wu, Wei-Fan Lai, Chia-Chen Lu, and Hsin-Chih Lai. 2019. “Next Generation Probiotics in Disease Amelioration.” Journal of Food and Drug Analysis 27: 615-622. https://doi.org/10.1016/j.jfda.2018.12.011

[7]

Earley, Helen, Grainne Lennon, Áine Balfe, J. Calvin Coffey, Desmond C. Winter, and P. Ronan O'Connell. 2019. “The Abundance of Akkermansia muciniphila and Its Relationship with Sulphated Colonic Mucins in Health and Ulcerative Colitis.” Scientific Reports 9: 15683. https://doi.org/10.1038/s41598-019-51878-3

[8]

Hasani, Alka, Saba Ebrahimzadeh, Fatemeh Hemmati, Aytak Khabbaz, Akbar Hasani, and Pourya Gholizadeh. 2021. “The Role of Akkermansia muciniphila in Obesity, Diabetes and Atherosclerosis.” Journal of Medical Microbiology 70: 001435. https://doi.org/10.1099/jmm.0.001435

[9]

Plovier, Hubert, Amandine Everard, Céline Druart, Clara Depommier, Matthias Van Hul, Lucie Geurts, Julien Chilloux, et al. 2017. “A Purified Membrane Protein from Akkermansia muciniphila or the Pasteurized Bacterium Improves Metabolism in Obese and Diabetic Mice.” Nature Medicine 23: 107-113. https://doi.org/10.1038/nm.4236

[10]

Liu, Yaojiang, Min Yang, Li Tang, Fengchao Wang, Shengjie Huang, Shuang Liu, Yuanyuan Lei, et al. 2022. “TLR4 Regulates RORγt+ Regulatory T-Cell Responses and Susceptibility to Colon Inflammation Through Interaction With Akkermansia muciniphila.” Microbiome 10: 98. https://doi.org/10.1186/s40168-022-01296-x

[11]

Yoon, Hyo Shin, Chung Hwan Cho, Myeong Sik Yun, Sung Jae Jang, Hyun Ju You, Jun-hyeong Kim, Dohyun Han, et al. 2021. “Akkermansia muciniphila Secretes a Glucagon-Like Peptide-1-Inducing Protein That Improves Glucose Homeostasis and Ameliorates Metabolic Disease in Mice.” Nature Microbiology 6: 563-573. https://doi.org/10.1038/s41564-021-00880-5

[12]

Routy, Bertrand, Emmanuelle Le Chatelier, Lisa Derosa, Connie P. M. Duong, Maryam Tidjani Alou, Romain Daillère, Aurélie Fluckiger, et al. 2018. “Gut Microbiome Influences Efficacy of PD-1-Based Immunotherapy Against Epithelial Tumors.” Science 359: 91-97. https://doi.org/10.1126/science.aan3706

[13]

Li, Jin, Shaoqiang Lin, Paul M. Vanhoutte, Connie W. Woo, and Aimin Xu. 2016. “Akkermansia muciniphila Protects Against Atherosclerosis by Preventing Metabolic Endotoxemia-Induced Inflammation in ApoE−/− Mice.” Circulation 133: 2434-2446. https://doi.org/10.1161/CIRCULATIONAHA.115.019645

[14]

Everard, Amandine, Clara Belzer, Lucie Geurts, Janneke P. Ouwerkerk, Céline Druart, Laure B. Bindels, Yves Guiot, et al. 2013. “Cross-Talk between Akkermansia muciniphila and Intestinal Epithelium Controls Diet-Induced Obesity.” Proceedings of the National Academy of Sciences 110: 9066-9071. https://doi.org/10.1073/pnas.1219451110

[15]

Depommier, Clara, Amandine Everard, Céline Druart, Hubert Plovier, Matthias Van Hul, Sara Vieira-Silva, Gwen Falony, et al. 2019. “Supplementation With Akkermansia muciniphila in Overweight and Obese Human Volunteers: A Proof-of-Concept Exploratory Study.” Nature Medicine 25: 1096-1103. https://doi.org/10.1038/s41591-019-0495-2

[16]

Xie, Shihao, Jiaxin Li, Fengyuan Lyu, Qingming Xiong, Peng Gu, Yuqi Chen, Meiling Chen, et al. 2024. “Novel Tripeptide RKH Derived From Akkermansia muciniphila Protects against Lethal Sepsis.” Gut 73: 78-91. https://doi.org/10.1136/gutjnl-2023-329996

[17]

Bae, Munhyung, Chelsi D. Cassilly, Xiaoxi Liu, Sung-Moo Park, Betsabeh Khoramian Tusi, Xiangjun Chen, Jaeyoung Kwon, et al. 2022. “Akkermansia muciniphila Phospholipid Induces Homeostatic Immune Responses.” Nature 608: 168-173. https://doi.org/10.1038/s41586-022-04985-7

[18]

Kim, Su-Man, Shinhye Park, Seung-Ho Hwang, Eun-Young Lee, Jong-Hwan Kim, Ga Seul Lee, Giljae Lee, et al. 2023. “Secreted Akkermansia muciniphila threonyl-tRNA Synthetase Functions to Monitor and Modulate Immune Homeostasis.” Cell Host & Microbe 31: 1021-1037. https://doi.org/10.1016/j.chom.2023.05.007

[19]

Kang, Eun-Jung, Jae-Hoon Kim, Young Eun Kim, Hana Lee, Kwang Bo Jung, Dong-Ho Chang, Youngjin Lee, et al. 2024. “The Secreted Protein Amuc_1409 From Akkermansia muciniphila Improves Gut Health Through Intestinal Stem Cell Regulation.” Nature Communications 15: 2983. https://doi.org/10.1038/s41467-024-47275-8

[20]

Vatanen, Tommi, Aleksandar D. Kostic, Eva d'Hennezel, Heli Siljander, Eric A. Franzosa, Moran Yassour, Raivo Kolde, et al. 2016. “Variation in Microbiome LPS Immunogenicity Contributes to Autoimmunity in Humans.” Cell 165: 842-853. https://doi.org/10.1016/j.cell.2016.04.007

[21]

Steimle, Alex, Lena Michaelis, Flaviana Di Lorenzo, Thorsten Kliem, Tobias Münzner, Jan Kevin Maerz, Andrea Schäfer, et al. 2019. “Weak Agonistic LPS Restores Intestinal Immune Homeostasis.” Molecular Therapy 27: 1974-1991. https://doi.org/10.1016/j.ymthe.2019.07.007

[22]

Di Lorenzo, Flaviana, Molly D. Pither, Michela Martufi, Ilaria Scarinci, Joan Guzmán-Caldentey, Ewelina Łakomiec, Wojciech Jachymek, et al. 2020. “Pairing Bacteroides vulgatus LPS Structure With Its Immunomodulatory Effects on Human Cellular Models.” ACS Central Science 6: 1602-1616. https://doi.org/10.1021/acscentsci.0c00791

[23]

Anhê, Fernando F., Nicole G. Barra, Joseph F. Cavallari, Brandyn D. Henriksbo, and Jonathan D. Schertzer. 2021. “Metabolic Endotoxemia Is Dictated by the Type of Lipopolysaccharide.” Cell Reports 36: 109691. https://doi.org/10.1016/j.celrep.2021.109691

[24]

Lai, Hsin-Chih, Tzu-Lung Lin, Ting-Wen Chen, Yu-Lun Kuo, Chih-Jung Chang, Tsung-Ru Wu, Ching-Chung Shu, Ying-Huang Tsai, Simon Swift, Chia-Chen Lu, et al. 2022. “Gut Microbiota Modulates COPD Pathogenesis: Role of Anti-Inflammatory Parabacteroides goldsteinii Lipopolysaccharide.” Gut 71: 309-321. https://doi.org/10.1136/gutjnl-2020-322599

[25]

Yang, Wenjing, Tianming Yu, Xiangsheng Huang, Anthony J. Bilotta, Leiqi Xu, Yao Lu, Jiaren Sun, et al. 2020. “Intestinal Microbiota-Derived Short-Chain Fatty Acids Regulation of Immune Cell IL-22 Production and Gut Immunity.” Nature Communications 11: 4457. https://doi.org/10.1038/s41467-020-18262-6

[26]

Mar, Jordan S., Naruhisa Ota, Nick D. Pokorzynski, Yutian Peng, Allan Jaochico, Dewakar Sangaraju, Elizabeth Skippington, et al. 2023. “IL-22 Alters Gut Microbiota Composition and Function to Increase Aryl Hydrocarbon Receptor Activity in Mice and Humans.” Microbiome 11: 47. https://doi.org/10.1186/s40168-023-01486-1

[27]

Montaldo, Elisa, Kerstin Juelke, and Chiara Romagnani. 2015. “Group 3 Innate Lymphoid Cells (ILC3s): Origin, Differentiation, and Plasticity in Humans and Mice.” European Journal of Immunology 45: 2171-2182. https://doi.org/10.1002/eji.201545598

[28]

Xiong, Le, Shanti Diwakarla, Roxanne Chatzis, Olivia Artaiz, Matthew Macowan, Shengbo Zhang, Alexandra Garnham, et al. 2025. “Acute Exposure to High-Fat Diet Impairs ILC3 Functions and Gut Homeostasis.” Immunity 58: 1185-1200. https://doi.org/10.1016/j.immuni.2025.03.017

[29]

Wang, Xiaoting, Naruhisa Ota, Paolo Manzanillo, Lance Kates, Jose Zavala-Solorio, Celine Eidenschenk, Juan Zhang, et al. 2014. “Interleukin-22 Alleviates Metabolic Disorders and Restores Mucosal Immunity in Diabetes.” Nature 514: 237-241. https://doi.org/10.1038/nature13564

[30]

Apicella, Michael A. 2008. Isolation and characterization of lipopolysaccharides. Bacterial Pathogenesis: Methods and Protocols Humana Press, 3−13. https://doi.org/10.1007/978-1-60327-032-8_1

[31]

Garcia-Vello, Pilar, Hanne L. P. Tytgat, Janneke Elzinga, Matthias Van Hul, Hubert Plovier, Marta Tiemblo-Martin, Patrice D. Cani, et al. 2024. “The Lipooligosaccharide of the Gut Symbiont Akkermansia muciniphila Exhibits a Remarkable Structure and TLR Signaling Capacity.” Nature Communications 15: 8411. https://doi.org/10.1038/s41467-024-52683-x

[32]

Tillander, Veronika, Stefan E. H. Alexson, and David E. Cohen. 2017. “Deactivating Fatty Acids: Acyl-CoA Thioesterase-Mediated Control of Lipid Metabolism.” Trends in Endocrinology & Metabolism 28: 473-484. https://doi.org/10.1016/j.tem.2017.03.001

[33]

Li, Tingting, Yun Shi, Jieyun Yin, Qin Qin, Sheng Wei, Shaofa Nie, Li Liu, and Li Liu. 2015. “The Association between Lipid Metabolism Gene Polymorphisms and Nephropathy in Type 2 Diabetes: A Meta-Analysis.” International Urology and Nephrology 47: 117-130. https://doi.org/10.1007/s11255-014-0843-6

[34]

Yang, Zhihong, Tyler Cappello, and Li Wang. 2015. “Emerging Role of microRNAs in Lipid Metabolism.” Acta Pharmaceutica Sinica B 5: 145-150. https://doi.org/10.1016/j.apsb.2015.01.002

[35]

Colaço-Gaspar, Mariana, Peter Hofer, Monika Oberer, and Rudolf Zechner. 2024. “PNPLA-mediated Lipid Hydrolysis and Transacylation at the Intersection of Catabolism and Anabolism.” Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1869: 159410. https://doi.org/10.1016/j.bbalip.2023.159410

[36]

Ouyang, Wenjun, Sascha Rutz, Natasha K. Crellin, Patricia A. Valdez, and Sarah G. Hymowitz. 2011. “Regulation and Functions of the IL-10 Family of Cytokines in Inflammation and Disease.” Annual Review of Immunology 29: 71-109. https://doi.org/10.1146/annurev-immunol-031210-101312

[37]

Colonna, Marco. 2009. “Interleukin-22-Producing Natural Killer Cells and Lymphoid Tissue Inducer-Like Cells in Mucosal Immunity.” Immunity 31: 15-23. https://doi.org/10.1016/j.immuni.2009.06.008

[38]

Sajiir, Haressh, Grant A. Ramm, Graeme A. Macdonald, Michael A. McGuckin, Johannes B. Prins, and Sumaira Z. Hasnain. 2025. “Harnessing IL-22 for Metabolic Health: Promise and Pitfalls.” Trends in Molecular Medicine 31: 574-584. https://doi.org/10.1016/j.molmed.2024.10.016

[39]

Gaudino, Stephen J., Ankita Singh, Huakang Huang, Jyothi Padiadpu, Makheni Jean-Pierre, Cody Kempen, Tej Bahadur, et al. 2024. “Intestinal IL-22RA1 Signaling Regulates Intrinsic and Systemic Lipid and Glucose Metabolism to Alleviate Obesity-Associated Disorders.” Nature Communications 15: 1597. https://doi.org/10.1038/s41467-024-45568-6

[40]

Yin, Ruopeng, Tao Wang, Jingzu Sun, Huanqin Dai, Yuting Zhang, Ningning Liu, and Hongwei Liu. 2024. “Postbiotics from Lactobacillus johnsonii Activates Gut Innate Immunity to Mitigate Alcohol-Associated Liver Disease.” Advanced Science 12: e2405781. https://doi.org/10.1002/advs.202405781

[41]

Yin, Ruopeng, Tao Wang, Huanqin Dai, Junjie Han, Jingzu Sun, Ningning Liu, Wang Dong, Jin Zhong, and Hongwei Liu. 2023. “Immunogenic Molecules Associated With Gut Bacterial Cell Walls: Chemical Structures, Immune-Modulating Functions, and Mechanisms.” Protein & Cell 14: 776-785. https://doi.org/10.1093/procel/pwad016

[42]

Lee, Heetae, and GwangPyo Ko. 2014. “Effect of Metformin on Metabolic Improvement and Gut Microbiota.” Applied and Environmental Microbiology 80: 5935-5943. https://doi.org/10.1128/aem.01357-14

[43]

Gu, Jun-Fei, Shu-Lan Su, Jian-Ming Guo, Yue Zhu, Ming Zhao, and Jin-Ao Duan. 2017. “The Aerial Parts of Salvia miltiorrhiza Bge. Strengthen Intestinal Barrier and Modulate Gut Microbiota Imbalance in Streptozocin-Induced Diabetic Mice.” Journal of Functional Foods 36: 362-374. https://doi.org/10.1016/j.jff.2017.06.010

[44]

Wang, Kai, Mingfang Liao, Nan Zhou, Li Bao, Ke Ma, Zhongyong Zheng, Yujing Wang, et al. 2019. “Parabacteroides distasonis Alleviates Obesity and Metabolic Dysfunctions via Production of Succinate and Secondary Bile Acids.” Cell Reports 26: 222-235. https://doi.org/10.1016/j.celrep.2018.12.028

[45]

Sun, Li, Tao Wang, Baosong Chen, Cui Guo, Shanshan Qiao, Jinghan Lin, Huan Liao, et al. 2024. “Sugarcane Leaves-Derived Polyphenols Alleviate Metabolic Syndrome and Modulate Gut Microbiota of ob/ob Mice.” Food Science and Human Wellness 13: 633-648. https://doi.org/10.26599/fshw.2022.9250048

[46]

Ivanov, Ivaylo I., Koji Atarashi, Nicolas Manel, Eoin L. Brodie, Tatsuichiro Shima, Ulas Karaoz, Dongguang Wei, et al. 2009. “Induction of Intestinal Th17 Cells by Segmented Filamentous Bacteria.” Cell 139: 485-498. https://doi.org/10.1016/j.cell.2009.09.033

[47]

Pither, Molly Dorothy, Anna Illiano, Chiara Pagliuca, Amy Jacobson, Giuseppe Mantova, Alessia Stornaiuolo, Roberta Colicchio, et al. 2022. “Bacteroides thetaiotaomicron Rough-Type Lipopolysaccharide: The Chemical Structure and the Immunological Activity.” Carbohydrate Polymers 297: 120040. https://doi.org/10.1016/j.carbpol.2022.120040

[48]

Wang, Yunru, Koji Hosomi, Atsushi Shimoyama, Ken Yoshii, Takahiro Nagatake, Yukari Fujimoto, Hiroshi Kiyono, Koichi Fukase, and Jun Kunisawa. 2021. “Lipopolysaccharide Derived from the Lymphoid-Resident Commensal Bacteria Alcaligenes faecalis Functions as an Effective Nasal Adjuvant to Augment IgA Antibody and Th17 Cell Responses.” Frontiers in Immunology 12: 699349. https://doi.org/10.3389/fimmu.2021.699349

[49]

Pither, Molly Dorothy, Emanuela Andretta, Giuseppe Rocca, Fabio Balzarini, Alejandra Matamoros-Recio, Roberta Colicchio, Paola Salvatore, et al. 2024. “Deciphering the Chemical Language of the Immunomodulatory Properties of Veillonella parvula Lipopolysaccharide.” Angewandte Chemie International Edition 63: e202401541. https://doi.org/10.1002/anie.202401541

[50]

Cani, Patrice D., Clara Depommier, Muriel Derrien, Amandine Everard, and Willem M. de Vos. 2022. “Akkermansia muciniphila: Paradigm for Next-Generation Beneficial Microorganisms.” Nature Reviews Gastroenterology & Hepatology 19: 625-637. https://doi.org/10.1038/s41575-022-00631-9

[51]

Rodrigues, Vanessa Fernandes, Jefferson Elias-Oliveira, Ítalo Sousa Pereira, Jéssica Assis Pereira, Sara Cândida Barbosa, Melissa Santana Gonsalez Machado, and Daniela Carlos. 2022. “Akkermansia muciniphila and Gut Immune System: A Good Friendship That Attenuates Inflammatory Bowel Disease, Obesity, and Diabetes.” Frontiers in Immunology 13: 934695. https://doi.org/10.3389/fimmu.2022.934695

[52]

Wang, Haifeng, Juan Guo, Xing Chen, and Hongxuan He. 2023. “The Metabolomics Changes in Luria-Bertani Broth Medium under Different Sterilization Methods and Their Effects on Bacillus Growth.” Metabolites 13: 958. https://doi.org/10.3390/metabo13080958

[53]

Garcia-Vello, Pilar, Flaviana Di Lorenzo, Daniele Zucchetta, Alla Zamyatina, Cristina De Castro, and Antonio Molinaro. 2022. “Lipopolysaccharide Lipid A: A Promising Molecule for New Immunity-Based Therapies and Antibiotics.” Pharmacology & Therapeutics 230: 107970. https://doi.org/10.1016/j.pharmthera.2021.107970

[54]

Pinedo-Rivilla, Cristina, Josefina Aleu, and Rosa Durán-Patrón. 2022. “Cryptic Metabolites From Marine-Derived Microorganisms Using OSMAC and Epigenetic Approaches.” Marine Drugs 20: 84. https://doi.org/10.3390/md20020084

[55]

Park, Beom Seok, Dong Hyun Song, Ho Min Kim, Byong-Seok Choi, Hayyoung Lee, and Jie-Oh Lee. 2009. “The Structural Basis of Lipopolysaccharide Recognition by the TLR4-Md-2 Complex.” Nature 458: 1191-1195. https://doi.org/10.1038/nature07830

[56]

Vatanen, Tommi, Aleksandar D. Kostic, Eva d'Hennezel, Heli Siljander, Eric A. Franzosa, Moran Yassour, Raivo Kolde, et al. 2016. “Variation in Microbiome LPS Immunogenicity Contributes to Autoimmunity in Humans.” Cell 165: 1551. https://doi.org/10.1016/j.cell.2016.05.056

[57]

Maeshima, Nina, and Rachel C. Fernandez. 2013. “Recognition of Lipid A Variants by the TLR4-Md-2 Receptor Complex.” Frontiers in Cellular and Infection Microbiology 3: 3. https://doi.org/10.3389/fcimb.2013.00003

[58]

Fatkhullina, Aliia R., Iuliia O. Peshkova, Amiran Dzutsev, Turan Aghayev, John A. McCulloch, Vishal Thovarai, Jonathan H. Badger, et al. 2018. “An Interleukin-23-Interleukin-22 Axis Regulates Intestinal Microbial Homeostasis to Protect From Diet-Induced Atherosclerosis.” Immunity 49: 943-957. https://doi.org/10.1016/j.immuni.2018.09.011

[59]

Bleicher, Lucas, Patricia Ribeiro de Moura, Leandra Watanabe, Didier Colau, Laure Dumoutier, Jean-Christophe Renauld, and Igor Polikarpov. 2008. “Crystal Structure of the IL-22/IL-22R1 Complex and Its Implications for the IL-22 Signaling Mechanism.” FEBS Letters 582: 2985-2992. https://doi.org/10.1016/j.febslet.2008.07.046

[60]

Backert, Ingo, Sergei B. Koralov, Stefan Wirtz, Vera Kitowski, Ulrike Billmeier, Eva Martini, Katharina Hofmann, et al. 2014. “STAT3 Activation in Th17 and Th22 Cells Controls IL-22-Mediated Epithelial Host Defense during Infectious Colitis.” The Journal of Immunology 193: 3779-3791. https://doi.org/10.4049/jimmunol.1303076

[61]

Sonnenberg, Gregory F., and David Artis. 2015. “Innate Lymphoid Cells in the Initiation, Regulation and Resolution of Inflammation.” Nature Medicine 21: 698-708. https://doi.org/10.1038/nm.3892

[62]

Parrish, Amy, Marie Boudaud, Erica T. Grant, Stéphanie Willieme, Mareike Neumann, Mathis Wolter, Sophie Z. Craig, et al. 2023. “Akkermansia muciniphila Exacerbates Food Allergy in Fibre-Deprived Mice.” Nature Microbiology 8: 1863-1879. https://doi.org/10.1038/s41564-023-01464-1

[63]

Seregin, Sergey S., Natasha Golovchenko, Bryan Schaf, Jiachen Chen, Nicholas A. Pudlo, Jonathan Mitchell, Nielson T. Baxter, et al. 2017. “NLRP6 Protects IL-10−/− Mice from Colitis by Limiting Colonization of Akkermansia muciniphila.” Cell Reports 19: 733-745. https://doi.org/10.1016/j.celrep.2017.03.080

[64]

Wang, Wenyan, Na Li, Hongkai Xu, Siting Wei, Yiping Li, Jiayao Ou, Jiacheng Hao, et al. 2025. “ILC3s Regulate the Gut Microbiota via Host Intestinal Galactosylation to Limit Pathogen Infection in Mice.” Nature Microbiology 10: 654-666. https://doi.org/10.1038/s41564-025-01933-9

[65]

Li, Zhitao, Guoao Hu, Li Zhu, Zhenglong Sun, Yun Jiang, Min-jie Gao, and Xiaobei Zhan. 2021. “Study of Growth, Metabolism, and Morphology of Akkermansia muciniphila With an In Vitro Advanced Bionic Intestinal Reactor.” BMC Microbiology 21: 61. https://doi.org/10.1186/s12866-021-02111-7

[66]

Kittelberger, Reinhold, and Frans Hilbink. 1993. “Sensitive Silver-Staining Detection of Bacterial Lipopolysaccharides in Polyacrylamide Gels.” Journal of Biochemical and Biophysical Methods 26: 81-86. https://doi.org/10.1016/0165-022X(93)90024-I

[67]

De Castro, Cristina, Michelangelo Parrilli, Otto Holst, and Antonio Molinaro. 2010. “Microbe-Associated Molecular Patterns in Innate Immunity: Extraction and Chemical Analysis of Gram-Negative Bacterial Lipopolysaccharides.” Methods in Enzymology Academic Press 480: 89-115. https://doi.org/10.1016/S0076-6879(10)80005-9

[68]

Scortichini, Serena, Maria Chiara Boarelli, Stefania Silvi, and Dennis Fiorini. 2020. “Development and Validation of a GC-FID Method for the Analysis of Short Chain Fatty Acids in Rat and Human Faeces and in Fermentation Fluids.” Journal of Chromatography B 1143: 121972. https://doi.org/10.1016/j.jchromb.2020.121972

[69]

Pan, Wei, Jinxiu Zhao, Jiacheng Wu, Daxiang Xu, Xianran Meng, Pengfei Jiang, Hongli Shi, et al. 2023. “Dimethyl Itaconate Ameliorates Cognitive Impairment Induced by a High-Fat Diet Via the Gut-Brain Axis in Mice.” Microbiome 11: 30. https://doi.org/10.1186/s40168-023-01471-8

RIGHTS & PERMISSIONS

2025 The Author(s). iMeta published by John Wiley & Sons Australia, Ltd on behalf of iMeta Science.

PDF

0

Accesses

0

Citation

Detail

Sections
Recommended

/