The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
A metabolic pathway for bile acid dehydroxylation by the gut microbiome
Open accessPublished version of a preprint
Abstract
The gut microbiota synthesize hundreds of molecules, many of which influence host physiology. Among the most abundant metabolites are the secondary bile acids deoxycholic acid (DCA) and lithocholic acid (LCA), which accumulate at concentrations of around 500 μM and are known to block the growth of Clostridium difficile 1, promote hepatocellular carcinoma 2 and modulate host metabolism via the G-protein-coupled receptor TGR5 (ref. 3). More broadly, DCA, LCA and their derivatives are major components of the recirculating pool of bile acids 4; the size and composition of this pool are a target of therapies for primary biliary cholangitis and nonalcoholic steatohepatitis. Nonetheless, despite the clear impact of DCA and LCA on host physiology, an incomplete knowledge of their biosynthetic genes and a lack of genetic tools to enable modification of their native microbial producers limit our ability to modulate secondary bile acid levels in the host. Here we complete the pathway to DCA and LCA by assigning and characterizing enzymes for each of the steps in its reductive arm, revealing a strategy in which the A-B rings of the steroid core are transiently converted into an electron acceptor for two reductive steps carried out by Fe-S flavoenzymes. Using anaerobic in vitro reconstitution, we establish that a set of six enzymes is necessary and sufficient for the eight-step conversion of cholic acid to DCA. We then engineer the pathway into Clostridium sporogenes, conferring production of DCA and LCA on a nonproducing commensal and demonstrating that a microbiome-derived pathway can be expressed and controlled heterologously. These data establish a complete pathway to two central components of the bile acid pool.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Bacteria in the gastrointestinal tract produce amino acid bile acid amidates that can affect host-mediated metabolic processes1–6; however, the bacterial gene(s) responsible for their production remain unknown.”
From Bile Acids Are Substrates for Amine N-Acyl Transferase Activity by Bile Salt Hydrolase (2022) · cites this paper as [5]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells
Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549
The Microbial Metabolites, Short-Chain Fatty Acids, Regulate Colonic T reg Cell Homeostasis
Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413
Host-gut microbiota metabolic interactions
Nicholson, J. K., Holmes, E., Kinross, J., Burcelin, R., Gibson, G., Jia, W., & Pettersson, S. (2012) · Science · doi:10.1126/science.1223813 · Cited by 4,760
Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43
Maslowski, K. M., Vieira, A. T., Ng, A., Kranich, J., Sierro, F., Yu, D., Schilter, H. C., Rolph, M. S., Mackay, F., Artis, D., et al. (2009) · Nature · doi:10.1038/nature08530 · Cited by 3,241
Intestinal Crosstalk between Bile Acids and Microbiota and Its Impact on Host Metabolism
Wahlstrom, A. M., Sayin, S. I., Marschall, H., & Bäckhed, F. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.005 · Cited by 2,969
Bile salt biotransformations by human intestinal bacteria
Ridlon, J. M., Kang, D.-J., & Hylemon, P. B. (2006) · Journal of Lipid Research · doi:10.1194/jlr.r500013-jlr200 · Cited by 2,829
Obesity-induced gut microbial metabolite promotes liver cancer through senescence secretome
Yoshimoto, S., Loo, T. M., Atarashi, K., Kanda, H., Sato, S., Oyadomari, S., Iwakura, Y., Oshima, K., Morita, H., Hattori, M., et al. (2013) · Nature · doi:10.1038/nature12347 · Cited by 2,219
Precision microbiome reconstitution restores bile acid mediated resistance to Clostridium difficile
Buffie, C. G., Bucci, V., Stein, R. R., McKenney, P. T., Ling, L., Gobourne, A., No, D., Liu, H., Kinnebrew, M., Viale, A., et al. (2015) · Nature · doi:10.1038/nature13828 · Cited by 1,872
Bouatra, S., Aziat, F., Mandal, R., Guo, A. C., Wilson, M. R., Knox, C., Bjorndahl, T. C., Krishnamurthy, R., Saleem, F., Liu, P., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073076 · Cited by 1,457
Bile acid metabolites control TH17 and Treg cell differentiation
Hang, S., Paik, D., Yao, L., Kim, E., Trinath, J., Lu, J., Ha, S., Nelson, B. N., Kelly, S. P., Wu, L., et al. (2019) · Nature · doi:10.1038/s41586-019-1785-z · Cited by 1,457
Self-citation
Cited by
Sorted by citations
Items 301–400 of 597
Bile acid and microbiome interactions in the developing child
Tessier, M. E. M., Shneider, B. L., Petrosino, J. F., & Preidis, G. A. (2025) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1002/jpn3.70014 · Cited by 13
Wang, Y., Zheng, L., Zhou, Z., Yao, D., Huang, Y., Liu, B., Duan, Y., & Li, Y. (2021) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.16676 · Cited by 12
Microbial metabolites and heart failure: Friends or enemies?
Lu, X., Liu, J., Zhou, B., Wang, S., Liu, Z., Mei, F., Luo, J., & Cui, Y. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.956516 · Cited by 11
Yang, R., Yang, L., Long, M., Wu, F., Shi, Y., Ran, X., Lv, J., Zhang, Y., Lei, Y., Jiao, Y., et al. (2023) · Oncogene · doi:10.1038/s41388-023-02660-3 · Cited by 12
Geiger, M. A., Oppi, S., Nusser‐Stein, S., Costantino, S., Mohammed, S. A., Gorica, E., Hoogerland, J. A., Matter, C. M., Guillaumon, A. T., Ruschitzka, F. T., et al. (2023) · Cardiovascular Diabetology · doi:10.1186/s12933-023-01865-w · Cited by 11
Insights into vitamin A in bladder cancer, lack of attention to gut microbiota?
Luo, P., Zheng, L., Zou, J., Chen, T., Zou, J., Li, W., Chen, Q., & Qian, B. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1252616 · Cited by 12
Potential role of bile acids in the pathogenesis of necrotizing enterocolitis
Yang, J., Chen, X., Liu, T., & Shi, Y. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122279 · Cited by 11
Deng, Z.-L., Pieper, D. H., Stallmach, A., Steube, A., Vital, M., Reck, M., & Wagner-Döbler, I. (2023) · Microbiome · doi:10.1186/s40168-023-01713-9 · Cited by 13
Xiao, P., Hua, Z., Kang, X., Lu, B., Li, M., Wu, J., Dong, W., Zhang, J., & Cheng, C. (2022) · Journal of Cancer · doi:10.7150/jca.67068 · Cited by 10
Urinary Antibiotics and Bile Acid Homeostasis in Chinese Adults
Wang, H., Zhao, Q., Jiang, Y., Liu, X., Wang, Y., Han, M., Yang, Z., Wang, Y., Yang, D., Huang, M., et al. (2023) · Environmental Science & Technology Letters · doi:10.1021/acs.estlett.3c00350 · Cited by 10
Firrman, J., Friedman, E. S., Hecht, A. L., Strange, W. C., Narrowe, A. B., Mahalak, K. K., Wu, G. D., & Liu, L. (2024) · mBio · doi:10.1128/mbio.00943-24 · Cited by 10
Wang, X., Zhu, B., Hua, Y., Sun, R., Tan, X., Chang, X., Tang, D., & Gu, J. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1395634 · Cited by 10
Chen, H., Zhang, L., Li, Y., Meng, X., Chi, Y., & Liu, M. (2024) · Aging and Disease · doi:10.14336/ad.2024.0538 · Cited by 11
Ageing, proteostasis, and the gut: Insights into neurological health and disease
Akbar, M., Toppo, P., & Nazir, A. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102504 · Cited by 13
The role of the gut microbial metabolism of sterols and bile acids in human health
Tang, J., Xu, W., Yu, Y., Yin, S., Ye, B.-C., & Zhou, Y. (2024) · Biochimie · doi:10.1016/j.biochi.2024.11.003 · Cited by 12
Gu, M., Hong, Q., Cui, J., Li, W., Zhang, J., Sun, Y., Jiang, J., & Hu, Y. (2025) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2025.2504162 · Cited by 10
Bile Acids in Control of the Gut-Liver-Axis
Hild, B., Heinzow, H. S., Schmidt, H., & Maschmeier, M. (2021) · Zeitschrift für Gastroenterologie · doi:10.1055/a-1330-9644 · Cited by 10
Systematic dissection of a complex gut bacterial communityPreprint
Cheng, A. G., Aranda-Díaz, A., Jain, S., Yu, F. B., Iakiviak, M., Meng, X., Weakley, A. M., Patil, A., Shiver, A. L., Deutschbauer, A. M., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.15.448618 · Cited by 9
Self-citationChen, J., Malhi, K. K., Li, X., Li, X., Kang, J., Zhao, B., Xu, Y., Li, X., & Li, X. (2024) · Animal nutrition · doi:10.1016/j.aninu.2024.09.003 · Cited by 9
Genomic insights into probiotic metabolism of dietary carbohydrates, proteins, and fats
Li, B., Ye, L., Chen, Y., & Zhang, H. (2024) · Current Opinion in Food Science · doi:10.1016/j.cofs.2024.101241 · Cited by 9
Depletion of key gut bacteria predicts disrupted bile acid metabolism in inflammatory bowel disease
Peterson, D., Weidenmaier, C., Timberlake, S. C., & Sadovsky, R. G. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.01999-24 · Cited by 12
Exploring the etiology of colitis: insights from gut microbiota research
Qian, G., Chen, X., Liu, G., Yu, J., Zhong, S.-J., Yang, J., Sun, Y., & Zhou, J. (2025) · Gut Microbes · doi:10.1080/19490976.2025.2512010 · Cited by 11
From Dysbiosis to Prediction: AI-Powered Microbiome Insights into IBD and CRC
Kim, M., Gim, D. H., Kim, S., Park, S., Eom, T. P., Seol, J., Yeo, J., Jo, C., Seo, G., Ku, H., et al. (2025) · Gastroenterology Insights · doi:10.3390/gastroent16030034 · Cited by 11
Distinguishing diet- and microbe-derived metabolites in the human gut
Tanes, C., Hu, W., Friedman, E. S., Hecht, A. L., Daniel, S. G., Clish, C. B., Lewis, J. D., Wu, G. D., & Bittinger, K. L. (2025) · Microbiome · doi:10.1186/s40168-025-02258-9 · Cited by 11
A host-centric view of the microbiota metabolome
Yamada, T., & Palm, N. W. (2025) · Immunity · doi:10.1016/j.immuni.2025.11.006 · Cited by 12
The interplay mechanisms between gut microbiota and ferroptosis in inflammatory bowel disease
Shi, Z., Zhang, S., Zhai, H., Wu, Q., Li, Y., Xu, H., & Zhang, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1753617 · Cited by 9
Li, N., Zhang, X., Cui, Y., Wu, H. C., Yu, Y., & Yu, S. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1229407 · Cited by 9
Gui, L., Wu, Q., Hu, Y., Zeng, W., Tan, X., Zhu, P., Li, X., Yang, L., Jia, W. P., Liu, C., et al. (2021) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.1c00052 · Cited by 9
Diet, Microbiota and the Gut-Brain Axis
García-Gutiérrez, E., & Sayavedra, L. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819265-8.00089-9 · Cited by 10
Kuang, J., Zheng, X., & Jia, W. P. (2024) · Protein & Cell · doi:10.1093/procel/pwae058 · Cited by 10
Pu, Y., Qi, X., Huang, L., Wu, W., Zhou, X., Li, W., Zheng, Y., Kong, M., Shen, J., Qi, W., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116297 · Cited by 8
Leng, L., Zhou, G., Liu, A., Wang, H., & Ni, Y. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311530 · Cited by 8
Pharmacology and therapeutics of bile acid synthesis and modification enzymes in metabolic diseases
Ding, L., Jin, L., & Huang, W. (2026) · Pharmacological Reviews · doi:10.1016/j.pharmr.2026.100115 · Cited by 9
Liao, J., Zhou, Z., Lv, Y., Zhang, Y., Liu, S., Tang, H., Qv, F., Wang, S., Yang, L., Lu, Y., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1667180 · Cited by 8
Microbial transformation of secondary bile acids: roles in gut ecology and autoimmune diseases
Ren, L., Li, M., Wu, L., Lin, Z. M., & Chen, A. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1769792 · Cited by 7
Gu, Y., Wang, M., & Mao, Y. (2026) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2026.101247 · Cited by 9
Self-citationThe microbiome regulates host metabolic health and diseases through microbial enzymes
Ding, Y., Zhang, Z., Wang, K., & Jiang, C. (2026) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-026-01195-8 · Cited by 14
Teng, M., Zhao, X., Zhou, L., Yan, H. Y., Zhao, L., Sun, J., Li, Y., Zhu, W., & Wu, F. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.167287 · Cited by 9
Zhuang, K., Shu, X., Meng, W., & Zhang, D. (2024) · European Journal of Nutrition · doi:10.1007/s00394-024-03359-1 · Cited by 8
He, S., Li, L., Lei, S., Su, J., Zhang, Y., & Zeng, H. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.131174 · Cited by 8
Wang, Y., Wang, Y., Zhao, Q., Cong, W., Wang, N., Zhao, K., Liu, J., Liu, X., Zhao, G., Lambert, H., et al. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.116451 · Cited by 8
Zahn, L. E., Gannon, P. M., & Rajakovich, L. J. (2024) · Metallomics · doi:10.1093/mtomcs/mfae049 · Cited by 9
Intestinal Production of Alpha-Glucosidase Inhibitor by Bacillus coagulans Spores
Kim, H.-W., Choi, S., Lee, D., & Rhee, H.-I. (2023) · Microorganisms · doi:10.3390/microorganisms11061462 · Cited by 8
Rashid, H., Anwar, H., Baig, F. M., Mukhtar, I., Muhammad, T., & Zaidi, A. (2025) · BMC Biotechnology · doi:10.1186/s12896-024-00943-5 · Cited by 7
Qiu, X., Gao, Q., Wang, J., Zhang, Z., & Tao, L. (2025) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2025.189317 · Cited by 8
BioMGCore: A toolkit for detection of biological metabolites in microbiome
Yang, G., Yu, G., Cui, Q., Huang, X., Guo, K., & Jia, S. (2025) · iMetaOmics. · doi:10.1002/imo2.70036 · Cited by 7
He, T., Wang, Y., Zhao, L., Che, Y., Zhang, L., Zeng, Y., Shen, H., Hao, H., & Cao, L. (2025) · The FASEB Journal · doi:10.1096/fj.202501078r · Cited by 7
Chen, Y., Huo, R., Melo, B., Shen, J. X., Ogasawara, K., & Xue, Y. (2025) · Drug Metabolism and Disposition · doi:10.1016/j.dmd.2025.100141 · Cited by 7
Aznou, A., Drenth, J. P. H., Nieuwdorp, M., & Meijnikman, A. S. (2025) · Yearbook of pediatric endocrinology · doi:10.1210/jendso/bvaf130 · Cited by 8
Huang, X., Yang, Y., Li, X., Zhu, X., Lin, D., Ma, Y., Zhou, M., Cui, X., Zhang, B., Dang, D., et al. (2023) · Frontiers in Nutrition · doi:10.3389/fnut.2023.1089909 · Cited by 7
Potent Bile Acid Microbial Metabolites Modulate Clostridium perfringens Virulence
Alenezi, T., Fu, Y., Alrubaye, B., Alanazi, T., Almansour, A. M., Wang, H., & Sun, X. (2023) · Pathogens · doi:10.3390/pathogens12101202 · Cited by 7
Zeng, Y., Gan, D., Zhang, K., Long, T., He, Y., Zhou, R., Liu, S., & Xiong, M. (2024) · Hepatology International · doi:10.1007/s12072-024-10712-3 · Cited by 8
Patho‐immunological mechanisms of atopic dermatitis: The role of the three major human microbiomes
Zhou, Z., Yang, J., Liu, Q., Gao, J., & Ji, W. (2024) · Scandinavian Journal of Immunology · doi:10.1111/sji.13403 · Cited by 6
Effect of Cichorium glandulosum on intestinal microbiota and bile acid metabolism in db/db mice
Yan, J., Zhang, R., Kang, J., Zhong, Y., Abudurexiti, A., Tan, H., Yi, L., & Ma, X. (2023) · Food Science & Nutrition · doi:10.1002/fsn3.3694 · Cited by 7
Gut Bacteria Encode Reductases that Biotransform Steroid HormonesPreprint
Arp, G., Jiang, A., Dufault‐Thompson, K., Levy, S., Zhong, A., Wassan, J. T., Grant, M., Li, Y., Hall, B., & Jiang, X. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.04.616736 · Cited by 7
Peng, Z., Deng, J., Xu, Z.-J., Niu, Q.-J., Lamesgen, D., Refaie, A., Sun, L., Feng, Y., & Liu, M. (2025) · Toxicon · doi:10.1016/j.toxicon.2025.108419 · Cited by 6
Li, T., & Jing, W. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1565778 · Cited by 7
Cha, Q., Zhao, W., Ran, L., Wang, Y., Wang, X., Xu, F., Yu, Z., & Wu, Y. (2025) · Metabolism Open · doi:10.1016/j.metop.2025.100412 · Cited by 6
Wu, W., Wang, S., Xue, C., & Dong, N. (2026) · Animal nutrition · doi:10.1016/j.aninu.2025.10.004 · Cited by 6
Bile acids and gut microbiota: interactions and impacts on polycystic ovary syndrome
Qian, H., Tao, J., Shi, L., Haiyan, S., Yang, L., Cui, L. J., Xu, W., & Wang, L. (2026) · Frontiers in Microbiomes · doi:10.3389/frmbi.2025.1702198 · Cited by 7
Zhou, S., Su, F., Gao, Q., Wang, M., Duan, J., & Li, J. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.158007 · Cited by 6
Self-citationFeller, F. M., Richtsmeier, P., Wege, M., & Philipp, B. (2021) · Applied and Environmental Microbiology · doi:10.1128/aem.01453-21 · Cited by 6
Zhou, X., Sun, H. J., Ren, J., Yan, G., Yang, L., Zhang, H., Lu, H., Li, X., Makino, T., Yin, F., et al. (2024) · MedComm · doi:10.1002/mco2.556 · Cited by 7
Alenezi, T., Alrubaye, B., Fu, Y., Shrestha, J., Algehani, S., Wang, H., Liyanage, R., & Sun, X. (2024) · Pathogens · doi:10.3390/pathogens13060464 · Cited by 6
Aoi, W., Koyama, T., Honda, A., Takagi, T., & Naito, Y. (2024) · Nutrients · doi:10.3390/nu16193381 · Cited by 8
Wang, L., Wang, Z., Zhao, Y., Yang, B., Huang, G., Li, J., Zhou, X., Jiang, H., Lan, P., & Chen, Z. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113413 · Cited by 6
Li, J.-X., Liu, C., & Chen, J. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00775-x · Cited by 5
Feller, F. M., Marke, G., Drees, S. L., Wöhlbrand, L., Rabus, R., & Philipp, B. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.655312 · Cited by 7
A versatile tailoring tool for pentacyclic triterpenes of Penicillium griseofulvum CICC 40293
Zhu, Y., Shen, P., Zhou, X., Fei, Y., Wang, W., Raj, R., Du, Z., Ge, H., Wang, W., Xu, S., et al. (2021) · Phytochemistry Letters · doi:10.1016/j.phytol.2021.06.027 · Cited by 6
BSH-TRAP: Bile salt hydrolase tagging and retrieval with activity-based probes
Parasar, B., & Chang, P. V. (2022) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2021.12.002 · Cited by 6
Analysis of metabolites in human gut: illuminating the design of gut-targeted drugs
Gil-Pichardo, A., Sánchez-Ruiz, A., & Colmenarejo, G. (2023) · Journal of Cheminformatics · doi:10.1186/s13321-023-00768-y · Cited by 7
Wang, L., Yang, L., Cheng, X., Qin, X.-M., Chai, Z., & Li, Z.-Y. (2024) · Journal of Medicinal Food · doi:10.1089/jmf.2023.k.0091 · Cited by 4
Translating the human microbiome: a path to improving health
Xavier, R. J. (2021) · Genome Medicine · doi:10.1186/s13073-021-00896-w · Cited by 7
Linking bacterial androgen production and prostate cancer
Arp, G., Levy, S., & Hall, B. (2025) · Nature Microbiology · doi:10.1038/s41564-025-01996-8 · Cited by 5
Microbiota-derived secondary bile acids promote STING activation and antitumor activityPreprint
Yang, X., Zhang, X., Li, W., Gharpure, A., Hansel-Harris, A., Hsieh, Y.-Z., Dikiy, S., Tillack, A. F., Wu, C., Sulpizio, A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.16.649255 · Cited by 6
De, T., Ma, T., Wang, Y., An, X., Liu, D., Yin, H., Wang, Q., Zhao, T., & Wang, H. (2025) · BMC Gastroenterology · doi:10.1186/s12876-025-04096-3 · Cited by 6
Gut microbiota-derived metabolites in keloid and hypertrophic scarring
Jin, J., & ZHENG, Z. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1644758 · Cited by 6
Wu, J. H., Zheng, W., Ding, X., Jin, Q.-P., & Ding, M. (2025) · Metabolism Open · doi:10.1016/j.metop.2025.100420 · Cited by 5
Bile acids as gatekeepers: Orchestrating gut-liver axis for metabolic and immune balance
Chen, Q., Xin, L. I. U., & Jiang, Z.-H. (2026) · Hepatobiliary & pancreatic diseases international · doi:10.1016/j.hbpd.2026.01.001 · Cited by 6
Bracken, A. K., Malarney, K. P., & Chang, P. V. (2026) · Journal of the American Chemical Society · doi:10.1021/jacs.5c18912 · Cited by 5
Gut microbial bile salt hydrolase as a metabolic gatekeeper in digestive homeostasis and disease
Chu, H., Song, X., Liu, C., Ma, T., & Cui, W. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1870619 · Cited by 7
Wang, C., Cheng, B., Wei, W., Gui, L., Zeng, W., Wang, Y., Wang, Y., Chen, Q., Xu, L., Miao, J., et al. (2023) · Drug Metabolism and Disposition · doi:10.1124/dmd.123.001513 · Cited by 5
Impact of the Gut Microbiota–Metabolite Axis on Intestinal Fatty Acid Absorption in Huainan Pigs
Wang, J., Zhu, L., Wang, Y., Ma, Q., Yan, X., Li, M., & Xing, B. (2025) · Microorganisms · doi:10.3390/microorganisms13071609 · Cited by 5
Evaluation of gut dysbiosis using serum and fecal bile acid profiles
Monma, T., Iwamoto, J., Ueda, H., Tamamushi, M., Kakizaki, F., Konishi, N., Yara, S., Miyazaki, T., Hirayama, T. T., Ikegami, T., et al. (2022) · World Journal of Clinical Cases · doi:10.12998/wjcc.v10.i34.12484 · Cited by 5
Manipulating the Microbiome: An Alternative Treatment for Bile Acid Diarrhoea
Hillman, E. B. M., Rijpkema, S. G. T., Carson, D., Arasaradnam, R. P., Wellington, E. M. H., & Amos, G. C. A. (2021) · Microbiology Research · doi:10.3390/microbiolres12020023 · Cited by 5
Calton, C. M., Carothers, K. E., Ramamurthy, S., Jagadish, N., Phanindra, B., Garcia, A., Viswanathan, V. K., & Halpern, M. D. (2023) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00102.2023 · Cited by 6
Strain-dependent induction of primary bile acid 7-dehydroxylation by cholic acidPreprint
Oton, E. V., Volet, C., Jacquemin, N., Dong, Y., Hapfelmeier, S., Meibom, K. L., & Bernier‐Latmani, R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.15.480494 · Cited by 5
Hillman, E. B. M., Carson, D., Walters, J. R. F., Fritzsche, M., Mate, R., Chappell, K. E., Chekmeneva, E., Romero, M. G., Lewis, S. J., Rijpkema, S. G. T., et al. (2025) · Gastro Hep Advances · doi:10.1016/j.gastha.2025.100712 · Cited by 5
Yue, S. R., Tan, Y. L., Gong, L., & Liao, F. (2026) · iScience · doi:10.1016/j.isci.2026.114961 · Cited by 5
Qi, D., Zheng, T., Yang, M., Huang, Z., Wang, T., Wang, Q., & Chen, B. (2024) · Metabolites · doi:10.3390/metabo14080451 · Cited by 4
Zhang, Y., Zhou, Z., Li, Y., Xu, M., Li, Y., Yang, Y., Hu, X., Wang, X., Yi, H., & Wu, X. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.152565 · Cited by 4
Wen, J., Liang, H., Zhao, M., Xuan, B., Meng, X., Liu, Y., Wang, L., He, L., Zhou, T., Tao, Y., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1703964 · Cited by 4
Luo, X., Mao, T., Wang, X., Cheng, P., Liu, M., Tao, R., Wang, F., Zhao, L., Shan, Y., Lu, Y., et al. (2025) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00862-z · Cited by 4
Sun, R., Chen, Y., & Tang, X. (2026) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5c01353 · Cited by 4
Han, Z., Sun, Z., Liu, X., Zhen, D., Guo, Q., Zheng, L., Jiang, S., Zhang, Z., Shen, S., & Zhang, J. (2026) · Nature Communications · doi:10.1038/s41467-026-69823-0 · Cited by 4
Targeting the gut-lung axis in COPD: from microbial metabolites to fecal microbiota transplantation
Yu, Z., Qian, W., & Chu, Y. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1798150 · Cited by 5
The role of intestinal bacteria in promoting tolerance to food
Ionescu, E., & Nagler‐Anderson, C. (2024) · Current Opinion in Immunology · doi:10.1016/j.coi.2024.102492 · Cited by 4
How Do Microbial Metabolites Interact with Their Protein Targets?
Astigarraga, M., Sánchez-Ruiz, A., Diop-Aw, A., Quintero, R., & Colmenarejo, G. (2025) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.4c01875 · Cited by 4
Gut-brain connection in schizophrenia: A narrative review
Iqbal, A., Bokhari, S. F. H., Rehman, M. U., Sattar, S. M. F., Bakht, D., Dost, W., & Basit, A. (2025) · World Journal of Psychiatry · doi:10.5498/wjp.v15.i5.103751 · Cited by 6
Zhou, Y., Song, W., Wang, Y., Li, S., Shan, C., Dong, J., Xu, Z., Zou, H., Pan, Y., Chen, X., et al. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177707 · Cited by 4
Metadata
- Authors
- Funabashi, M., Grove, T. L., Wang, M., Varma, Y., McFadden, M. E., Brown, L. C., Guo, C., Higginbottom, S., Almo, S. C., & Fischbach, M. A.
- Affiliations
- Daiichi Sankyo RD Novare (Japan) (JP)
- Albert Einstein College of Medicine (US)
- Stanford University (US)
- Indiana University Bloomington (US)
- Stanford Medicine (US)
- Chan Zuckerberg Biohub San Francisco (US)
- Corresponding author
- Almo, Steven C.
- Fischbach, Michael A.
- ORCID
- Venue
- Nature
- Published
- 2020-06-17
- Volume
- 582
- Issue
- 7813
- Pages
- 566-570
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC7319900
- OpenAlex
- W3036012425
- Cited by
- 590
- References
- 46
- Citations by year
- 2026: 125 · 2025: 108 · 2024: 123 · 2023: 89 · 2022: 78 · 2021: 53 · 2020: 13
- FWCI
- 18.90
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Nature (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Price Family Foundation
- National Institutes of Health (1dp2hd101401-01, GM093342, DK113598, DK110174, GM094662)
- National Heart, Lung, and Blood Institute (P01HL147823)
- National Institute of General Medical Sciences (U54GM093342, U54GM094662, P01GM118303)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK110174, DP1DK113598, R01DK101674)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (DP2 HD101401)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Steroid Chemistry and Biochemistry
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Microbial Natural Products and Biosynthesis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
- Keywords
- secondary bile acids, deoxycholic acid, lithocholic acid, gut microbiota, reductive dehydroxylation, cholic acid, Clostridium sporogenes, heterologous pathway expression, germ-free mice, primary biliary cirrhosis, nonalcoholic steatohepatitis, TGR5
- MeSH terms
- Gastrointestinal Microbiome, Animals, Bile Acids and Salts, Clostridium, Deoxycholic Acid, Hydroxylation, Lithocholic Acid, Male, Operon, Symbiosis, Mice, Metabolic Networks and Pathways, Metabolic Engineering
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review