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Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10-/- mice
Open accessAbstract
The composite human microbiome of Western populations has probably changed over the past century, brought on by new environmental triggers that often have a negative impact on human health. Here we show that consumption of a diet high in saturated (milk-derived) fat, but not polyunsaturated (safflower oil) fat, changes the conditions for microbial assemblage and promotes the expansion of a low-abundance, sulphite-reducing pathobiont, Bilophila wadsworthia. This was associated with a pro-inflammatory T helper type 1 (T(H)1) immune response and increased incidence of colitis in genetically susceptible Il10(−/−), but not wild-type mice. These effects are mediated by milk-derived-fat-promoted taurine conjugation of hepatic bile acids, which increases the availability of organic sulphur used by sulphite-reducing microorganisms like B. wadsworthia. When mice were fed a low-fat diet supplemented with taurocholic acid, but not with glycocholic acid, for example, a bloom of B. wadsworthia and development of colitis were observed in Il10(−/−) mice. Together these data show that dietary fats, by promoting changes in host bile acid composition, can markedly alter conditions for gut microbial assemblage, resulting in dysbiosis that can perturb immune homeostasis. The data provide a plausible mechanistic basis by which Western-type diets high in certain saturated fats might increase the prevalence of complex immune-mediated diseases like inflammatory bowel disease in genetically susceptible hosts.
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In the citing paper
“Bacteria with BSH activity have benefited from enhanced tolerance against bile and better survival in the gut environment (Begley et al., 2006;Devkota et al., 2012).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Devkota et al., 2012
Experimental — accuracy not yet measuredIn the citing paper
“In Il10−/− mice and mice without disruption of this gene, a diet high in saturated (milk-derived) fat (MF) promoted expansion of the immunogenic sulfite-reducing pathobiont Bilophila wadsworthia, a member of the Deltaproteobacteria.174”
From Influence of the Gut Microbiome, Diet, and Environment on Risk of Colorectal Cancer (2020) · cites this paper as [174]
In the citing paper
“Bilophila wadsworthia, a sulphite-reducing bacteria, has been associated with an increased incidence of colitis [52], and emerges under pathological conditions such as appendicitis and other intestinal inflammatory disorders [52].”
From Intestinal Microbiota Is Influenced by Gender and Body Mass Index (2016) · cites this paper as [52]
In the citing paper
“Consumption of milk fat has been shown to alter bile acid composition, promoting expansion of the sulphite-reducing pathobiont Bilophila wadsworthia and exacerbating colitis in IL10 knockout mice69.”
From Diet and the Intestinal Microbiome: Associations, Functions, and Implications for Health and Disease (2014) · cites this paper as [69]
In the citing paper
“B. wadsworthia increases gut inflammation in mice that lack in the anti-inflammatory cytokine interleukin (IL)-10.”
From Diet–microbiota interactions as moderators of human metabolism (2016) · cites this paper as [111]
In the citing paper
“Levels of the bacterium Bilophila wadsworthia increase when mice are fed a diet rich in milk fat or supplemented with the bile acid taurocholic acid111.”
From Diet–microbiota interactions as moderators of human metabolism (2016) · cites this paper as [111]
In the citing paper
“This is in line with the suggestion that SRB are linked to an inflammatory state of the gut 41, 42.”
From The composition of the gut microbiota shapes the colon mucus barrier (2015) · cites this paper as [42]
In the citing paper
“This pathobiont promotes Th1 type immune responses and increases susceptibility to colitis in IL10–/– mice.137”
From Interaction between microbiota and immunity in health and disease (2020) · cites this paper as [137]
In the citing paper
“The gut microbiota has been shown to differ between mice fed diets that are high or low in fat and between diets that contain equal amounts of fat but from different sources [10–13] (Fig. 1).”
From Dietary lipids, gut microbiota and lipid metabolism (2019) · cites this paper as [13]
In the citing paper
“Milk fat promoted taurine-conjugation of bile acids, which increases the availability of sulfur used by B. wadsworthia.”
From Dietary lipids, gut microbiota and lipid metabolism (2019) · cites this paper as [13]
In the citing paper
“The increased levels of B. wadsworthia were associated with a pro-inflammatory immune response and increased incidence of colitis in genetically susceptible mice.”
From Dietary lipids, gut microbiota and lipid metabolism (2019) · cites this paper as [13]
In the citing paper
“Devkota et al showed that a diet with milk fat, but not diets with lard or safflower oil, increased expansion of Bilophila wadsworthia in mice [13].”
From Dietary lipids, gut microbiota and lipid metabolism (2019) · cites this paper as [13]
In the citing paper
“This phyla has been shown to be intimately tied to a pro-inflammatory state.11,60,61”
From Using Corticosteroids to Reshape the Gut Microbiome: Implications for Inflammatory Bowel Diseases (2015) · cites this paper as [11]
In the citing paper
“For example, high SFA intake has been shown to be associated with reduction in total bacterial abundance in humans (95) and in microbial diversity and richness (95,96), as well as an increase in proinflammatory bacteria (e.g., Bilophila wadsworthia) (96)(97)(98) in mice.”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [96]
In the citing paper
“animals fed with a diet rich in animal-derived saturated fats demonstrated a significant increase in Proteobacteria (Bilophila wadsworthia) abundance (Devkota et al., 2012).”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Devkota et al., 2012
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Molodecky, N. A., Soon, I. S., Rabi, D. M., Ghali, W. A., Ferris, M., Chernoff, G., Benchimol, E. I., Panaccione, R., Ghosh, S., Barkema, H. W., et al. (2012) · Gastroenterology · doi:10.1053/j.gastro.2011.10.001 · Cited by 4,833
Turnbaugh, P. J., Bäckhed, F., Fulton, L., & Gordon, J. I. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.02.015 · Cited by 2,915
High-Fat Diet Determines the Composition of the Murine Gut Microbiome Independently of Obesity
Hildebrandt, M. A., Hoffmann, C., Sherrill–Mix, S. A., Keilbaugh, S. A., Hamady, M., Chen, Y., Knight, R., Ahima, R. S., Bushman, F., & Wu, G. D. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.08.042 · Cited by 1,576
Diet, gut microbiota and immune responses
Maslowski, K. M., & Mackay, C. R. (2011) · Nature Immunology · doi:10.1038/ni0111-5 · Cited by 1,261
Berg, D., Davidson, N. M., Kühn, R., Müller, W., Menon, S., Holland, G., Thompson-Snipes, L., Leach, M. W., & Rennick, D. M. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118861 · Cited by 1,125
The human gut microbiome: ecology and recent evolutionary changes
Walter, J., & Ley, R. (2011) · Annual Review of Microbiology · doi:10.1146/annurev-micro-090110-102830 · Cited by 720
Wang, Y., Hoenig, J. D., Malin, K. J., Qamar, S., Petrof, E. O., Sun, J., Antonopoulos, D. A., Chang, E. B., & Claud, E. C. (2009) · The ISME Journal · doi:10.1038/ismej.2009.37 · Cited by 600
Sulfate-reducing bacteria in human feces and their association with inflammatory bowel diseases
Loubinoux, J., Bronowicki, J., Pereira, I. A. C., Mougenel, J.-L., & Faou, A. L. (2002) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2002.tb00942.x · Cited by 404
Evidence That Hydrogen Sulfide Is a Genotoxic Agent
Attene‐Ramos, M. S., Wagner, E. D., Plewa, M. J., & Gaskins, H. R. (2006) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-05-0126 · Cited by 367
Dussurget, O., Cabanes, D., Dehoux, P., Lecuit, M., Buchrieser, C., Glaser, P., & Cossart, P. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03080.x · Cited by 356
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Li, N., Zhan, S., Tian, Z., Liu, C., Xie, Z., Zhang, S., Chen, M., Zeng, Z., & Zhuang, X. (2021) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izaa342 · Cited by 60
Liu, X., Xi, X., Jia, A., Zhang, M., Cui, T., Bai, X., Shi, Y., & Liu, C. (2021) · Food Chemistry · doi:10.1016/j.foodchem.2021.129908 · Cited by 57
Teofani, A., Marafini, I., Laudisi, F., Pietrucci, D., Salvatori, S., Unida, V., Biocca, S., Monteleone, G., & Desideri, A. (2022) · Nutrients · doi:10.3390/nu14020260 · Cited by 60
Alexander, J. L., Mullish, B. H., Danckert, N. P., Liu, Z., Olbei, M. L., Saifuddin, A., Torkizadeh, M., Ibraheim, H., Blanco, J. M., Roberts, L. A., et al. (2023) · EBioMedicine · doi:10.1016/j.ebiom.2022.104430 · Cited by 58
Yu, J., Liu, T., Guo, Q., Wang, Z., Chen, Y., & Dong, Y. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.04698-22 · Cited by 62
The role of bile acid receptor TGR5 in regulating inflammatory signalling
Ye, D., He, J., & He, X. (2024) · Scandinavian Journal of Immunology · doi:10.1111/sji.13361 · Cited by 61
Changing views on diverticular disease: impact of aging, obesity, diet, and microbiota
Spiller, R. (2015) · Neurogastroenterology and Motility · doi:10.1111/nmo.12526 · Cited by 56
Zhao, J., Zhang, Q., Shen, J., Wang, K., & Liu, J. (2018) · Acta Pharmacologica Sinica · doi:10.1038/s41401-018-0029-3 · Cited by 56
n-6 High Fat Diet Induces Gut Microbiome Dysbiosis and Colonic Inflammation
Selmin, O. I., Papoutsis, A. J., Hazan, S. C., Smith, C., Greenfield, N., Donovan, M. G., Wren, S. N., Doetschman, T., Snider, J. M., Snider, A. J., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136919 · Cited by 57
Association between Microbiota and Nasal Mucosal Diseases in terms of Immunity
Tai, J., Han, M. S., Kwak, J., & Kim, T. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094744 · Cited by 60
Fecal microbiota transplantation in clinical practice: Present controversies and future prospects
Tian, H., Wang, X., Fang, Z., Li, L., Wu, C., Bi, D., Li, N., Chen, Q., & Qin, H. (2024) · hLife · doi:10.1016/j.hlife.2024.01.006 · Cited by 56
Kashyap, P., Moayyedi, P., Quigley, E. M. M., Simrén, M., & Vanner, S. J. (2024) · Neurogastroenterology & Motility · doi:10.1111/nmo.14817 · Cited by 66
Diet, Microbiome, and the Intestinal Epithelium: An Essential Triumvirate?
Guzman, J. R., Conlin, V. S., & Jobin, C. (2013) · BioMed Research International · doi:10.1155/2013/425146 · Cited by 61
Andersen, V. C. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i41.11862 · Cited by 57
European Crohn's and Colitis Organisation Topical Review on environmental factors in IBD
Maaser, C., Langholz, E., Gordon, H., Burisch, J. M., Ellul, P., Ramirez, V. H., Karakan, T., Katsanos, K. H., Krustiņš, E., Levine, A., et al. (2016) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjw223 · Cited by 57
Food, microbiome and colorectal cancer
Niederreiter, L., Adolph, T. E., & Tilg, H. (2018) · Digestive and Liver Disease · doi:10.1016/j.dld.2018.03.030 · Cited by 56
Small intestinal microbiota: the neglected stepchild needed for fat digestion and absorption
Chang, E. B., & Martinez, K. (2018) · Gut Microbes · doi:10.1080/19490976.2018.1502539 · Cited by 58
Gargari, G., Deon, V., Taverniti, V., Gardana, C., Denina, M., Riso, P., Guardamagna, O., & Guglielmetti, S. (2018) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiy045 · Cited by 57
Predictability and persistence of prebiotic dietary supplementation in a healthy human cohort
Gurry, T., Dannenberg, P. H., Finlayson, S. G., Hughes, T. K., Macias-Treviño, C., Owusu-Boaitey, K. E., Shomorony, A., Tuang, S. L., Valenstein, M. L., Wang, K. K., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-30783-1 · Cited by 57
Nutritional modulators of ulcerative colitis: Clinical efficacies and mechanistic view
Sung, M. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i7.994 · Cited by 56
Fecal Microbiota and Metabolome in a Mouse Model of Spontaneous Chronic Colitis
Robinson, A. M., Gondalia, S. V., Karpe, A. V., Eri, R. D., Beale, D. J., Morrison, P. D., Palombo, E. A., & Nurgali, K. (2016) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000970 · Cited by 55
Towards an Integrative Understanding of Diet–Host–Gut Microbiome Interactions
Read, M. N., & Holmes, A. J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00538 · Cited by 56
Exploring the microbiome in health and disease
Scotti, E., Boué, S., Sasso, G. L., Zanetti, F., Belcastro, V., Poussin, C., Sierro, N., Battey, J. N. D., Gimalac, A., Ivanov, N. V., et al. (2017) · Toxicology Research and Application · doi:10.1177/2397847317741884 · Cited by 56
Regulation of bile acid metabolism-related signaling pathways by gut microbiota in diseases
Jia, E., Liu, Z.-Y., Pan, M., Lu, J., & Ge, Q. (2019) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1900073 · Cited by 55
Xie, Z., Bai, Y., Chen, G., Rui, Y., Chen, D., Sun, Y., Zeng, X., & Liu, Z. (2020) · Food & Function · doi:10.1039/d0fo02272a · Cited by 55
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Chen, Y., & Chen, Y. (2021) · Cancers · doi:10.3390/cancers13164054 · Cited by 54
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Druszczyńska, M., Sadowska, B., Kulesza, J., Gąsienica-Gliwa, N., Kulesza, E., & Fol, M. (2024) · Pathogens · doi:10.3390/pathogens13111005 · Cited by 62
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Bernard, H., Desseyn, J., Bartke, N., Kleinjans, L., Stahl, B., Belzer, C., Knol, J., Gottrand, F., & Husson, M.-O. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu391 · Cited by 55
Gastrointestinal immune and microbiome changes during parenteral nutrition
Pierre, J. F. (2017) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00321.2016 · Cited by 57
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Martin, G., Kolida, S., Marchesi, J. R., Want, E. J., Sidaway, J. E., & Swann, J. R. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01153 · Cited by 55
Gut microbiota in children and altered profiles in juvenile idiopathic arthritis
Filippo, C. D., Paola, M. D., Giani, T., Tirelli, F., & Cimaz, R. (2019) · Journal of Autoimmunity · doi:10.1016/j.jaut.2019.01.001 · Cited by 58
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Frazier, K., Manzoor, S. S., Carroll, K., DeLeon, O., Miyoshi, S., Miyoshi, J., George, M. S., Tan, A., Chrisler, E. A., Izumo, M., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci162515 · Cited by 58
Ray, A., & Dittel, B. N. (2015) · Immunology · doi:10.1111/imm.12511 · Cited by 52
Obesity and the gut microbiome: pathophysiological aspects
Bradlow, H. L. (2014) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2013-0063 · Cited by 53
Garrett, W. S., & Onderdonk, A. B. (2015) · Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases · doi:10.1016/b978-1-4557-4801-3.00249-6 · Cited by 53
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Wang, L., & Wan, Y. Y. (2019) · Liver Research · doi:10.1016/j.livres.2019.02.001 · Cited by 53
Ocvirk, S., Sava, I. G., Lengfelder, I., Lagkouvardos, I., Steck, N., Roh, J. H., Tchaptchet, S., Bao, Y., Hansen, J. J., Hüebner, J., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1004911 · Cited by 53
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Chassaing, B., Vijay-Kumar, M., & Gewirtz, A. T. (2017) · Current Opinion in Gastroenterology · doi:10.1097/mog.0000000000000401 · Cited by 52
Li, X., Wang, H., Wang, T., Zheng, F., Wang, H., & Wang, C. (2019) · Food & Function · doi:10.1039/c8fo02271b · Cited by 52
Ellermann, M., Gharaibeh, R. Z., Maharshak, N., Peréz-Chanona, E., Jobin, C., Carroll, I. M., Arthur, J. C., Plevy, S. E., Fodor, A. A., Brouwer, C., et al. (2019) · Gut Microbes · doi:10.1080/19490976.2019.1599794 · Cited by 54
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Sauvaitre, T., Etienne‐Mesmin, L., Sivignon, A., Mosoni, P., Courtin, C. M., de Wiele, T. V., & Blanquet‐Diot, S. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa052 · Cited by 53
Martin, A., Ecklu-Mensah, G., Ha, C. W. Y., Hendrick, G., Layman, D. K., Gilbert, J. A., & Devkota, S. (2021) · Nature Communications · doi:10.1038/s41467-021-24074-z · Cited by 52
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Shabat, C. S., Albenberg, L. G., Limbergen, J. V., Pressman, N., Otley, A. R., Yaakov, M., Wine, E., Weiner, D., & Levine, A. (2021) · Nutrients · doi:10.3390/nu13113736 · Cited by 51
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García-Vega, Á. S., Corrales-Agudelo, V., Reyes, A., & Escobar, J. S. (2020) · Nutrients · doi:10.3390/nu12102938 · Cited by 52
Patrone, V., Minuti, A., Lizier, M., Miragoli, F., Lucchini, F., Trevisi, E., Rossi, F., & Callegari, M. L. (2018) · BMC Genomics · doi:10.1186/s12864-018-5202-z · Cited by 47
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Si, W., Zhao, X., Li, R., Li, Y., Ma, C., Zhao, X., Bugno, J., Qin, Y., Zhang, J., Liu, H., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci174910 · Cited by 52
Kashima, S., Fujiya, M., Konishi, H., Ueno, N., Inaba, Y., Moriichi, K., Tanabe, H., Ikuta, K., Ohtake, T., & Kohgo, Y. (2015) · Translational research · doi:10.1016/j.trsl.2015.02.002 · Cited by 49
Kloos, D., Lingeman, H., Mayboroda, O. A., Deelder, A. M., Niessen, W. M. A., & Giera, M. A. (2014) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2014.05.008 · Cited by 49
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Luo, W., Zhao, M., Dwidar, M., Gao, Y., Xiang, L., Wu, X., Medema, M. H., Xu, S., Li, X., Schäfer, H., et al. (2024) · Microbiome · doi:10.1186/s40168-024-01873-2 · Cited by 51
Farzaei, M. H., Bahramsoltani, R., Abdolghaffari, A. H., Sodagari, H. R., Esfahani, S. A., & Rezaei, N. (2016) · Expert Review of Gastroenterology & Hepatology · doi:10.1586/17474124.2016.1145546 · Cited by 50
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Lin, D. M., & Lin, H. C. (2019) · F1000Research · doi:10.12688/f1000research.18480.1 · Cited by 49
Gut microbiota and inflammatory bowel disease: the role of antibiotics in disease management
Kerman, D. H., & Deshpande, A. R. (2014) · Postgraduate Medicine · doi:10.3810/pgm.2014.07.2779 · Cited by 47
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Khan, S. S., Sebastian, S. A., Parmar, M. P., Ghadge, N. M., Padda, I., Keshta, A. S., Minhaz, N., & Patel, A. (2023) · Disease-a-Month · doi:10.1016/j.disamonth.2023.101672 · Cited by 47
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Fanizzi, F., D’Amico, F., Bombassaro, I., Zilli, A., Furfaro, F., Parigi, T. L., Cicerone, C., Fiorino, G., Peyrin‐Biroulet, L., Danese, S., et al. (2024) · Microorganisms · doi:10.3390/microorganisms12091755 · Cited by 49
Behera, S. K., Praharaj, A. B., Dehury, B., & Negi, S. (2015) · Glycoconjugate Journal · doi:10.1007/s10719-015-9606-6 · Cited by 47
Lu, S., Zuo, T., Zhang, N., Shi, H., Liu, F., Wu, J., Wang, Y., Xue, C., & Tang, Q. (2015) · Journal of Functional Foods · doi:10.1016/j.jff.2015.11.017 · Cited by 46
Martinez, K., Pierre, J. F., & Chang, E. B. (2016) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2016.07.001 · Cited by 51
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Pero, R., Brancaccio, M., Laneri, S., Biasi, M.-G. D., Lombardo, B., & Scudiero, O. (2019) · Biomolecules · doi:10.3390/biom9060237 · Cited by 47
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Zeng, C., Yang, P., Cao, T., Gu, Y., Li, N., Zhang, B., Xu, P., Liu, Y., Luo, Z., & Cai, H. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110097 · Cited by 54
Tong, L., Xiao, T., Wang, L., Lü, C., Liu, L., Zhou, X., Wang, A., Qin, W., & Wang, F. (2021) · iScience · doi:10.1016/j.isci.2021.103435 · Cited by 51
Long, W., Xue, Z., Zhang, Q., Zhou, F., Bridgewater, L. C., Wang, L., Zhao, L., & Pang, X. (2015) · Scientific Reports · doi:10.1038/srep13469 · Cited by 47
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Roussel, C., Guebara, S. A. B., Plante, P.-L., Desjardins, Y., Marzo, V. D., & Silvestri, C. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2120344 · Cited by 44
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Gibson, D., Gill, S. K., Brown, K., Tasnim, N., Ghosh, S., Innis, S. M., & Jacobson, K. (2015) · Gut Microbes · doi:10.1080/19490976.2014.997610 · Cited by 45
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Ji, Y., Sun, S., Goodrich, J. K., Kim, H., Poole, A. C., Duhamel, G. E., Ley, R. E., & Qi, L. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.05.040 · Cited by 46
Gyires, K., Toth, E., & Zadori, S. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113199990417 · Cited by 47
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Metadata
- Authors
- Devkota, S., Wang, Y., Musch, M. W., Leone, V., Fehlner-Peach, H., Nadimpalli, A., Antonopoulos, D. A., Jabri, B., & Chang, E. B.
- Affiliations
- University of Chicago (US)
- Argonne National Laboratory (US)
- Corresponding author
- Chang, Eugene B.
- ORCID
- Venue
- Nature
- Published
- 2012-06-13
- Volume
- 487
- Issue
- 7405
- Pages
- 104-108
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3393783
- OpenAlex
- W2151798187
- Cited by
- 1,904
- References
- 27
- Citations by year
- 2026: 106 · 2025: 137 · 2024: 144 · 2023: 140 · 2022: 164 · 2021: 162 · 2020: 139 · 2019: 144 · 2018: 133 · 2017: 144 · 2016: 125 · 2015: 115 · 2014: 118 · 2013: 103 · 2012: 26
- FWCI
- 46.57
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK047722, DK-47722, R37DK047722, R01DK097268, T32DK007074, UH3DK083993, DK42086, P30DK042086)
- National Center for Complementary and Integrative Health (F31AT006073)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Health Sciences › Medicine › Gastroenterology › Microscopic Colitis
- Keywords
- taurocholate, milk fat, saturated fatty acids, Bilophila wadsworthia, colitis, IL-10-deficient mice, bile acid conjugation, taurine, gut dysbiosis, inflammatory bowel disease, Th1 response, Western diet, unsaturated fatty acids, safflower oil, gut microbiota
- MeSH terms
- Animals, Bile Acids and Salts, Colitis, Dietary Fats, Inflammation, Mice, Inbred C57BL, Milk, Molecular Sequence Data, Safflower Oil, Sulfites, Taurine, Taurocholic Acid, Inflammatory Bowel Diseases, Interleukin-10, Th1 Cells, Diet, Fat-Restricted, Bilophila, Mice, Metagenome
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