The DOI matches its Crossref record; 155 of the 155 references it cites were found in a registry or an index.
Specialized Metabolites from the Microbiome in Health and Disease
Open accessAbstract
The microbiota, and the genes that comprise its microbiome, play key roles in human health. Host-microbe interactions affect immunity, metabolism, development, and behavior, and dysbiosis of gut bacteria contributes to disease. Despite advances in correlating changes in the microbiota with various conditions, specific mechanisms of host-microbiota signaling remain largely elusive. We discuss the synthesis of microbial metabolites, their absorption, and potential physiological effects on the host. We propose that the effects of specialized metabolites may explain present knowledge gaps in linking the gut microbiota to biological host mechanisms during initial colonization, and in health and disease.
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?
In the citing paper
“Beyond these general mechanisms, the gut microbiome affects atherogenesis more specifically through its degradation of phosphatidylcholine, which is abundant in eggs, cheese, seafood and red meat (Jonsson and Bäckhed, 2017; Sharon et al., 2014; Sonnenburg and Bäckhed, 2016).”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Sharon et al., 2014
In the citing paper
“The primary cause of cardiovascular disease is atherosclerosis, a process in which the microbiome has been implicated as well (Jonsson and Bäckhed, 2017; Sharon et al., 2014).”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Sharon et al., 2014
In the citing paper
“the gut microbiota appears to influence nearly every aspect of host physiology, including energy balance, cardiovascular health, chronic inflammation, development of adaptive immune cells and many more systems that fall outside of the scope of this review (Rooks and Garrett, 2016; Sharon et al., 2014).”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Sharon et al., 2014
In the citing paper
“changes in the microbiome often result in altered metabolic profiles, impacting the availability and diversity of nutrients and microbial metabolites (Dodd et al., 2017; Melnik et al., 2017; Sharon et al., 2014; Wikoff et al., 2009).”
From Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice (2019) · cites this paper as Sharon et al., 2014
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
Naive Bayesian Classifier for Rapid Assignment of rRNA Sequences into the New Bacterial Taxonomy
Wang, Q., Garrity, G. M., Tiedje, J. M., & Cole, J. R. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00062-07 · Cited by 20,145
Linking long-term dietary patterns with gut microbial enterotypes
Wu, G. D., Chen, J., Hoffmann, C., Bittinger, K., Chen, Y.-Y., Keilbaugh, S. A., Bewtra, M., Knights, D., Walters, W. A., Knight, R., et al. (2011) · Science · doi:10.1126/science.1208344 · Cited by 6,513
Self-citationTurnbaugh, P. J., Ley, R. E., Hamady, M., Fraser-Liggett, C. M., Knight, R., & Gordon, J. I. (2007) · Nature · doi:10.1038/nature06244 · Cited by 6,091
Self-citationGut flora metabolism of phosphatidylcholine promotes cardiovascular disease
Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597
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
den Besten, G., van Eunen, K., Groen, A. K., Venema, K., Reijngoud, D.-J., & Bakker, B. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r036012 · Cited by 5,048
The gut microbiota shapes intestinal immune responses during health and disease
Round, J. L., & Mazmanian, S. K. (2009) · Nature Reviews Immunology · doi:10.1038/nri2515 · Cited by 5,029
Self-citationMetabolites produced by commensal bacteria promote peripheral regulatory T-cell generation
Arpaia, N., Campbell, C., Fan, X., Dikiy, S., van der Veeken, J., deRoos, P., Liu, H., Cross, J. R., Pfeffer, K., Coffer, P. J., et al. (2013) · Nature · doi:10.1038/nature12726 · Cited by 4,838
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
Flagged first, then by citations
Cited by
Sorted by citations
Rivière, A., Selak, M., Lantin, D., Leroy, F., & Vuyst, L. D. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00979 · Cited by 1,810
Emerging Pathogenic Links Between Microbiota and the Gut-Lung Axis
Budden, K. F., Gellatly, S. L., Wood, D. L. A., Cooper, M. A., Morrison, M., Hugenholtz, P., & Hansbro, P. M. (2017) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.142 · Cited by 1,606
Human Gut Microbiota from Autism Spectrum Disorder Promote Behavioral Symptoms in Mice
Sharon, G., Cruz, N. J., Kang, D.-W., Gandal, M. J., Wang, B., Kim, Y.-M., Zink, E. M., Casey, C. P., Taylor, B. C., Lane, C. J., et al. (2019) · Cell · doi:10.1016/j.cell.2019.05.004 · Cited by 1,182
Self-citationControl of brain development, function, and behavior by the microbiome
Sampson, T. R., & Mazmanian, S. K. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.04.011 · Cited by 1,093
Self-citationChemical transformation of xenobiotics by the human gut microbiota
Koppel, N., Maini Rekdal, V., & Balskus, E. P. (2017) · Science · doi:10.1126/science.aag2770 · Cited by 1,080
Microbes, Metabolites, and the Gut-Lung Axis
Dang, A. T., & Marsland, B. J. (2019) · Mucosal Immunology · doi:10.1038/s41385-019-0160-6 · Cited by 1,028
Postler, T. S., & Ghosh, S. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.05.008 · Cited by 876
“…gut microbiota appears to influence nearly every aspect of host physiology, including energy balance, cardiovascular health, chronic inflammation, development of adaptive immune cells, andmany more systems that fall outside of the scope of this review (Rooks and Garrett, 2016; Sharon et al., 2014).”
BackgroundInfluentialTime for food: the intimate interplay between nutrition, metabolism, and the circadian clock
Asher, G., & Sassone-Corsi, P. (2015) · Cell · doi:10.1016/j.cell.2015.03.015 · Cited by 844
Gut microbiota induce IGF-1 and promote bone formation and growth
Yan, J., Herzog, J. W., Tsang, K., Brennan, C. A., Bower, M. A., Garrett, W. S., Sartor, B. R., Aliprantis, A. O., & Charles, J. F. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1607235113 · Cited by 750
Short chain fatty acids: Microbial metabolites for gut-brain axis signalling
O’Riordan, K. J., Collins, M., Moloney, G. M., Knox, E. G., Aburto, M. R., Fülling, C., Morley, S. J., Clarke, G. A., Schellekens, H., & Cryan, J. F. (2022) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2022.111572 · Cited by 788
Fröhlich, E. E., Farzi, A., Mayerhofer, R., Reichmann, F., Jačan, A., Wagner, B., Zinser, E., Bordag, N., Magnes, C., Fröhlich, E., et al. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.02.020 · Cited by 720
GPCR-Mediated Signaling of Metabolites
Husted, A. S., Trauelsen, M., Rudenko, O., Hjorth, S. A., & Schwartz, T. W. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.03.008 · Cited by 602
Deciphering microbial interactions in synthetic human gut microbiome communities
Venturelli, O. S., Carr, A. V., Fisher, G., Hsu, R. H., Lau, R., Bowen, B. P., Hromada, S. E., Northen, T. R., & Arkin, A. P. (2018) · Molecular Systems Biology · doi:10.15252/msb.20178157 · Cited by 572
The role of the microbiome in NAFLD and NASH
Kolodziejczyk, A. A., Zheng, D., Shibolet, O., & Elinav, E. (2019) · EMBO Molecular Medicine · doi:10.15252/emmm.201809302 · Cited by 523
A gut-derived metabolite alters brain activity and anxiety behaviour in mice
Needham, B. D., Funabashi, M., Adame, M. D., Wang, Z., Boktor, J. C., Haney, J., Wu, W.-L., Rabut, C., Ladinsky, M. S., Hwang, S.-J., et al. (2022) · Nature · doi:10.1038/s41586-022-04396-8 · Cited by 489
Self-citationMetagenomics, Metatranscriptomics, and Metabolomics Approaches for Microbiome Analysis
Aguiar‐Pulido, V., Huang, W., Suárez-Ulloa, V., Cickovski, T., Mathee, K., & Narasimhan, G. (2016) · Evolutionary Bioinformatics · doi:10.4137/ebo.s36436 · Cited by 549
Advances in pathogenesis and therapeutic strategies for osteoporosis
Song, S., Guo, Y., Yang, Y., & Fu, D. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108168 · Cited by 476
Elevated circulating levels of succinate in human obesity are linked to specific gut microbiota
Serena, C., Ceperuelo‐Mallafré, V., Keiran, N., Queipo‐Ortuño, M. I., Bernal, R., Gómez-Huelgas, R., Urpí-Sardà, M., Sabater, M., Pérez‐Brocal, V., Andrés‐Lacueva, C., et al. (2018) · The ISME Journal · doi:10.1038/s41396-018-0068-2 · Cited by 415
Diet, Microbiota and Gut-Lung Connection
Anand, S., & Mande, S. S. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02147 · Cited by 423
SpaceM reveals metabolic states of single cells
Rappez, L., Stadler, M., Triana, S., Gathungu, R. M., Ovchinnikova, K., Phapale, P. B., Heikenwälder, M. F., & Alexandrov, T. (2021) · Nature Methods · doi:10.1038/s41592-021-01198-0 · Cited by 400
Metagenomics of Parkinson’s disease implicates the gut microbiome in multiple disease mechanisms
Wallen, Z. D., Demirkan, A., Twa, G., Cohen, G., Dean, M. N., Standaert, D. G., Sampson, T. R., & Payami, H. (2022) · Nature Communications · doi:10.1038/s41467-022-34667-x · Cited by 346
Bioactive Molecules Released in Food by Lactic Acid Bacteria: Encrypted Peptides and Biogenic Amines
Pessione, E., & Cirrincione, S. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00876 · Cited by 333
Microbiome therapeutics — Advances and challenges
Mimee, M., Citorik, R. J., & Lu, T. K. (2016) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2016.04.032 · Cited by 324
Commensal bacteria and essential amino acids control food choice behavior and reproduction
Leitão-Gonçalves, R., Carvalho-Santos, Z., Francisco, A. P., Fioreze, G. T., Anjos, M., Baltazar, C., Elias, A. P., Itskov, P. M., Piper, M. D. W., & Ribeiro, C. (2017) · PLOS Biology · doi:10.1371/journal.pbio.2000862 · Cited by 315
The gut microbiota promotes hepatic fatty acid desaturation and elongation in mice
Kindt, A., Liebisch, G., Clavel, T., Haller, D., Hörmannsperger, G., Yoon, H., Kolmeder, D., Sigruener, A., Krautbauer, S., Seeliger, C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05767-4 · Cited by 311
Gut microbial metabolites in depression: understanding the biochemical mechanisms
Caspani, G., Kennedy, S. H., Foster, J. A., & Swann, J. R. (2019) · Microbial Cell · doi:10.15698/mic2019.10.693 · Cited by 289
Spatial Metabolomics and Imaging Mass Spectrometry in the Age of Artificial Intelligence
Alexandrov, T. (2020) · Annual Review of Biomedical Data Science · doi:10.1146/annurev-biodatasci-011420-031537 · Cited by 308
Chen, F., Dai, X., Zhou, C., Li, K.-X., Zhang, Y., Lou, X., Zhu, Y., Sun, Y., Peng, B.-X., & Cui, W. (2021) · Gut · doi:10.1136/gutjnl-2020-323476 · Cited by 295
Predictive metabolomic profiling of microbial communities using amplicon or metagenomic sequences
Mallick, H., Franzosa, E. A., Mclver, L. J., Banerjee, S., Sirota‐Madi, A., Kostic, A. D., Clish, C. B., Vlamakis, H. C., Xavier, R. J., & Huttenhower, C. (2019) · Nature Communications · doi:10.1038/s41467-019-10927-1 · Cited by 283
Association of Psoriasis With Inflammatory Bowel Disease
Fu, Y., Lee, C., & Chi, C. (2018) · JAMA Dermatology · doi:10.1001/jamadermatol.2018.3631 · Cited by 294
Jaglin, M., Rhimi, M., Philippe, C., Pons, N., Bruneau, A., Goustard, B., Daugé, V., Maguin, E., Naudon, L., & Rabot, S. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00216 · Cited by 269
Interplay between diet, gut microbiota, epigenetic events, and colorectal cancer
Bultman, S. J. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500902 · Cited by 275
Diez-Gutiérrez, L., Vicente, L. S., Barrón, L. J. R., Villarán, M. C., & Chávarri, M. (2019) · Journal of Functional Foods · doi:10.1016/j.jff.2019.103669 · Cited by 277
Metabolic regulation of macrophage phenotype and function
Saha, S., Shalova, I. N., & Biswas, S. K. (2017) · Immunological Reviews · doi:10.1111/imr.12603 · Cited by 260
Microbiome: Focus on Causation and Mechanism
Fischbach, M. A. (2018) · Cell · doi:10.1016/j.cell.2018.07.038 · Cited by 259
The colibactin warhead crosslinks DNA
Vizcaino, M. I., & Crawford, J. M. (2015) · Nature Chemistry · doi:10.1038/nchem.2221 · Cited by 247
The Microbiome–Estrogen Connection and Breast Cancer Risk
Parida, S., & Sharma, D. (2019) · Cells · doi:10.3390/cells8121642 · Cited by 248
Bharwani, A., Mian, M. F., Surette, M. G., Bienenstock, J., & Forsythe, P. (2017) · BMC Medicine · doi:10.1186/s12916-016-0771-7 · Cited by 236
Schistosoma “Eggs-Iting” the Host: Granuloma Formation and Egg Excretion
Schwartz, C., & Fallon, P. G. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02492 · Cited by 247
The Skin and Gut Microbiome and Its Role in Common Dermatologic Conditions
Ellis, S. R., Nguyen, M., Vaughn, A. R., Notay, M., Burney, W. A., Sandhu, S., & Sivamani, R. K. (2019) · Microorganisms · doi:10.3390/microorganisms7110550 · Cited by 242
Gut Microbiota Metabolism and Interaction with Food Components
Vernocchi, P., CHIERICO, F. D., & Putignani, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103688 · Cited by 242
Gamma-aminobutyric acid as a potential postbiotic mediator in the gut–brain axis
Braga, J. D., Thongngam, M., & Kumrungsee, T. (2024) · npj Science of Food · doi:10.1038/s41538-024-00253-2 · Cited by 250
Martínez-del Campo, A., Bodea, S., Hamer, H. A., Marks, J. A., Haiser, H. J., Turnbaugh, P. J., & Balskus, E. P. (2015) · mBio · doi:10.1128/mbio.00042-15 · Cited by 224
Rivière, A., Gagnon, M., Weckx, S., Roy, D., & Vuyst, L. D. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.02089-15 · Cited by 226
Gut Microbiota: The Conductor in the Orchestra of Immune–Neuroendocrine Communication
El Aidy, S., Dinan, T. G., & Cryan, J. F. (2015) · Clinical Therapeutics · doi:10.1016/j.clinthera.2015.03.002 · Cited by 215
Gut Microbiota, Host Organism, and Diet Trialogue in Diabetes and Obesity
Lazăr, V., Diţu, L.-M., Pîrcălăbioru, G. G., Picu, A. A., Petcu, L. M., Cucu, N., & Chifiriuc, M. C. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00021 · Cited by 211
Chidambaram, S. B., Essa, M. M., Rathipriya, A. G., Bishir, M., Ray, B., Mahalakshmi, A. M., Tousif, A. H., Sakharkar, M. K., Kashyap, R. S., Friedland, R. P., et al. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107988 · Cited by 204
Baumann-Dudenhoeffer, A. M., D’Souza, A. W., Tarr, P. I., Warner, B. B., & Dantas, G. A. (2018) · Nature Medicine · doi:10.1038/s41591-018-0216-2 · Cited by 203
Gut microbiota and colorectal cancer
Gao, R., Gao, Z., Huang, L., & Qin, H. (2017) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-016-2881-8 · Cited by 205
Oral Administration of Porphyromonas gingivalis Alters the Gut Microbiome and Serum Metabolome
Kato, T., Yamazaki, K., Nakajima, M., Date, Y., Kikuchi, J., Hase, K., Ohno, H., & Yamazaki, K. (2018) · mSphere · doi:10.1128/msphere.00460-18 · Cited by 210
Clos‐Garcia, M., Andrés, N., Fernández‐Eulate, G., Abecia, L., Lavín, J. L., Liempd, S. M. V., Cabrera, D., Royo, F., Valero, A., Errazquin, N., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.07.031 · Cited by 202
The Cellular and Molecular Basis of Translational Immunometabolism
Norata, G. D., Caligiuri, G., Chavakis, T., Matarese, G., Netea, M. G., Nicoletti, A., O'Neill, L. A. J., & Marelli‐Berg, F. M. (2015) · Immunity · doi:10.1016/j.immuni.2015.08.023 · Cited by 197
Epigenetic Regulation at the Interplay Between Gut Microbiota and Host Metabolism
Miro-Blanch, J., & Yanes, O. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00638 · Cited by 195
Gonzalez, A., Krieg, R. J., Massey, H. D., Carl, D. E., Ghosh, S., Gehr, T. W. B., & Ghosh, S. S. (2018) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfy238 · Cited by 203
Integrative Physiology of Fasting
Secor, S. M. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150013 · Cited by 183
Li, C., Huang, Q., Yang, R., Dai, Y., Zeng, Y., Tao, L., Li, X., Zeng, J., & Wang, Q. (2019) · Osteoporosis International · doi:10.1007/s00198-019-04855-5 · Cited by 186
Gut microbiota-derived metabolites in obesity: a systematic review
Ejtahed, H., Angoorani, P., Soroush, A., Hasani‐Ranjbar, S., Siadat, S. D., & Larijani, B. A. (2020) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.2019-026 · Cited by 196
Role of gut microbiota in identification of novel TCM-derived active metabolites
Lin, T., Lu, C., Lai, W.-F., Wu, T., Lu, J., Chen, Y.-M., Tzeng, C., Liu, H., Wei, H., & Lai, H. (2020) · Protein & Cell · doi:10.1007/s13238-020-00784-w · Cited by 175
Bacterial Signaling to the Nervous System through Toxins and Metabolites
Yang, N. J., & Chiu, I. M. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.12.023 · Cited by 167
Gut microbiota: a potential regulator of neurodevelopment
Tognini, P. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00025 · Cited by 163
Chemical language and warfare of bacterial natural products in bacteria–nematode–insect interactions
Shi, Y., & Bode, H. B. (2018) · Natural Product Reports · doi:10.1039/c7np00054e · Cited by 162
Disruption of maternal gut microbiota during gestation alters offspring microbiota and immunity
Nyangahu, D. D., Lennard, K. S., Brown, B. P., Darby, M., Wendoh, J. M., Havyarimana, E., Smith, P., Butcher, J., Stintzi, A., Mulder, N., et al. (2018) · Microbiome · doi:10.1186/s40168-018-0511-7 · Cited by 173
Murakami, M., Tognini, P., Liu, Y., Eckel‐Mahan, K. L., Baldi, P., & Sassone‐Corsi, P. (2016) · EMBO Reports · doi:10.15252/embr.201642463 · Cited by 160
Nastasi, C., Fredholm, S., Willerslev-Olsen, A., Hansen, M., Bonefeld, C. M., Geisler, C., Andersen, M. H., Ødum, N., & Woetmann, A. (2017) · Scientific Reports · doi:10.1038/s41598-017-15099-w · Cited by 166
Tochitani, S., Ikeno, T., Ito, T., Sakurai, A., Yamauchi, T., & Matsuzaki, H. (2016) · PLOS ONE · doi:10.1371/journal.pone.0138293 · Cited by 157
Reshaping the gut microbiota: Impact of low calorie sweeteners and the link to insulin resistance?
Nettleton, J. E., Reimer, R. A., & Shearer, J. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.04.029 · Cited by 158
Covington, B. C., MCLEAN, J. A. J., & Bachmann, B. O. (2016) · Natural Product Reports · doi:10.1039/c6np00048g · Cited by 154
Accessing Bioactive Natural Products from the Human Microbiome
Milshteyn, A., Colosimo, D. A., & Brady, S. F. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.05.013 · Cited by 150
Impact of prematurity and nutrition on the developing gut microbiome and preterm infant growth
Grier, A., Qiu, X., Bandyopadhyay, S., Holden‐Wiltse, J., Kessler, H. A., Gill, A. L., Hamilton, B., Huyck, H. L., Misra, S. K., Mariani, T. J., et al. (2017) · Microbiome · doi:10.1186/s40168-017-0377-0 · Cited by 154
Henriques, S. F., Dhakan, D. B., Serra, L., Francisco, A. P., Carvalho-Santos, Z., Baltazar, C., Elias, A. P., Anjos, M., Zhang, T., Maddocks, O. D. K., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18049-9 · Cited by 152
Gut Microbiota during Dietary Restrictions: New Insights in Non-Communicable Diseases
Rinninella, E., Cintoni, M., Raoul, P. C., Ianiro, G., Laterza, L., Lopetuso, L. R., Ponziani, F. R., Gasbarrini, A., & Mele, M. C. (2020) · Microorganisms · doi:10.3390/microorganisms8081140 · Cited by 153
Frye, R. E., Rose, S., Slattery, J. M., & MacFabe, D. F. (2015) · Microbial Ecology in Health and Disease · doi:10.3402/mehd.v26.27458 · Cited by 145
Abdollahi‐Roodsaz, S., Abramson, S. B., & Scher, J. U. (2016) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2016.68 · Cited by 142
Exploring and Understanding the Biochemical Diversity of the Human Microbiota
Koppel, N., & Balskus, E. P. (2016) · Cell chemical biology · doi:10.1016/j.chembiol.2015.12.008 · Cited by 140
Hepatic circadian clock oscillators and nuclear receptors integrate microbiome-derived signals
Montagner, A., Korecka, A., Polizzi, A., Lippi, Y., Blum, Y., Canlet, C., Tremblay-Franco, M., Gautier-Stein, A., Burcelin, R., Yen, Y.-C., et al. (2016) · Scientific Reports · doi:10.1038/srep20127 · Cited by 137
“Because the gut microbiome actively participates in gaining energy from food and in producing diet-derived products, the question of its impact on peripheral clock functions in metabolic organs is important 26 .”
Symbiosis-inspired approaches to antibiotic discovery
Adnani, N., Rajski, S. R., & Bugni, T. S. (2017) · Natural Product Reports · doi:10.1039/c7np00009j · Cited by 139
Gut Microbiome Toxicity: Connecting the Environment and Gut Microbiome-Associated Diseases
Tu, P., Chi, L., Bodnar, W. M., Zhang, Z., Gao, B., Bian, X., Stewart, J. R., Fry, R. C., & Lü, K. (2020) · Toxics · doi:10.3390/toxics8010019 · Cited by 136
Food Fight: Role of Itaconate and Other Metabolites in Antimicrobial Defense
Luan, H. H., & Medzhitov, R. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.08.013 · Cited by 130
“For example, two of the best-characterized microbial metabolism pathways influencing the immune system are short-chain fatty acid production and tryptophan metabolism (Sharon et al., 2014).”
BackgroundSpichak, S., Bastiaanssen, T. F. S., Berding, K., Vlckova, K., Clarke, G., Dinan, T. G., & Cryan, J. F. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.044 · Cited by 127
Hoffman, J. D., Yanckello, L. M., Chlipala, G. E., Hammond, T. C., McCulloch, S. D., Parikh, I. J., Sun, S., Morganti, J. M., Green, S. J., & Lin, A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0221828 · Cited by 137
Frame, L. A., Costa, E., & Jackson, S. A. (2019) · Nutrition Reviews · doi:10.1093/nutrit/nuz106 · Cited by 129
Let thy food be thy medicine….when possible
Witkamp, R. F., & van Norren, K. (2018) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2018.06.026 · Cited by 131
Mukherjee, S., Joardar, N., Sengupta, S., & Babu, S. P. S. (2018) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2018.07.010 · Cited by 129
Xie, R., Jiang, P., Li, L., Jiang, J. H., Yu, B., Rao, J., Liu, H., Wei, W., & Qiao, Y. (2019) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2019.12.013 · Cited by 128
Nutritional Correlates of Human Oral Microbiome
Kato, I., Vasquez, A. A., Moyerbrailean, G. A., Land, S. J., Djurić, Z., Sun, J., Lin, H.-S., & Ram, J. L. (2016) · Journal of the American College of Nutrition · doi:10.1080/07315724.2016.1185386 · Cited by 134
Blachier, F., Beaumont, M., Portune, K. J., Steuer, N., Lan, A., Audebert, M., Khodorova, N., Andriamihaja, M., Airinei, G., Benamouzig, R., et al. (2019) · Clinical Nutrition · doi:10.1016/j.clnu.2018.09.016 · Cited by 124
Toxicomicrobiomics: The Human Microbiome vs. Pharmaceutical, Dietary, and Environmental Xenobiotics
Abdelsalam, N. A., Ramadan, A. T., ElRakaiby, M. T., & Aziz, R. K. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00390 · Cited by 125
Yang, M. J., Qi, X., Li, N., Kaifi, J. T., Chen, S., Wheeler, A. A., Kimchi, E. T., Ericsson, A. C., Rector, R. S., Staveley-O’Carroll, K. F., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-35861-1 · Cited by 129
Bai, Y., Li, Y., Marion, T. N., Tong, Y., Zaiss, M. M., Tang, Z., Zhang, Q., Liu, Y., & Luo, Y. (2020) · Journal of Autoimmunity · doi:10.1016/j.jaut.2020.102564 · Cited by 121
Edible fungal polysaccharides, the gut microbiota, and host health
Liang, J., Zhang, M., Wang, X., Ren, Y., Yue, T., Wang, Z., & Gao, Z. (2021) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2021.118558 · Cited by 122
Diet and feeding pattern modulate diurnal dynamics of the ileal microbiome and transcriptome
Machado, A. C. D., Brown, S. D., Lingaraju, A., Sivaganesh, V., Martino, C., Chaix, A., Zhao, P., Pinto, A. F. M., Chang, M. W., Richter, R. A., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111008 · Cited by 114
Self-citationThe Microbiome in Cystic Fibrosis Pulmonary Disease
Françoise, A., & Héry-Arnaud, G. (2020) · Genes · doi:10.3390/genes11050536 · Cited by 129
Pedersen, H., Forslund, S. K., Guðmundsdóttir, V., Petersen, A. Ø., Hildebrand, F., Hyötyläinen, T., Nielsen, T., Hansen, T. F., Bork, P., Ehrlich, S. D., et al. (2018) · Nature Protocols · doi:10.1038/s41596-018-0064-z · Cited by 121
Ikeda-Ohtsubo, W., Brugman, S., Warden, C. H., Rebel, J. M. J., Folkerts, G., & Pieterse, C. M. J. (2018) · Frontiers in Nutrition · doi:10.3389/fnut.2018.00090 · Cited by 115
Sanguinetti, E., Collado, M. C., Marrachelli, V. G., Monleón, D., Selma‐Royo, M., Pardo-Tendero, M., Burchielli, S., & Iozzo, P. (2018) · Scientific Reports · doi:10.1038/s41598-018-23261-1 · Cited by 117
Ciarlo, E., Heinonen, T., Herderschee, J., Fenwick, C. W., Mombelli, M., Roy, D. L., & Roger, T. (2016) · Scientific Reports · doi:10.1038/srep37944 · Cited by 122
The Gut Microbiota, Food Science, and Human Nutrition: A Timely Marriage
Barratt, M. J., Lebrilla, C. B., Shapiro, H.-Y., & Gordon, J. I. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.07.006 · Cited by 117
Intestinal Sensing by Gut Microbiota: Targeting Gut Peptides
Covașă, M., Stephens, R. W., Toderean, R., & Cobuz, C. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00082 · Cited by 117
Rodríguez‐Carrio, J., López, P., Sánchez, B., González, S., Gueimonde, M., Margollés, A., Reyes‐Gavilán, C. G. D. L., & Suárez, A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00023 · Cited by 114
Dietary lipids from body to brain
Custers, Emma, E. M., Kiliaan, & Amanda, J. K. (2021) · Progress in Lipid Research · doi:10.1016/j.plipres.2021.101144 · Cited by 119
Metadata
- Authors
- Sharon, G., Garg, N., Debelius, J., Knight, R., Dorrestein, P. C., & Mazmanian, S. K.
- Affiliations
- California Institute of Technology (US)
- University of California San Diego (US)
- University of Colorado Boulder (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Mazmanian, Sarkis K.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2014-11
- Volume
- 20
- Issue
- 5
- Pages
- 719-730
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC4337795
- OpenAlex
- W2092725930
- Cited by
- 544
- References
- 155
- Citations by year
- 2026: 18 · 2025: 33 · 2024: 46 · 2023: 48 · 2022: 59 · 2021: 62 · 2020: 66 · 2019: 46 · 2018: 59 · 2017: 42 · 2016: 36 · 2015: 27
- FWCI
- 14.34
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (UL1TR000100)
- National Institute of Mental Health (R01MH100556, MH100556)
- National Institute of General Medical Sciences (GM099535, R01GM099535, GM095384, R01GM095384)
- National Institute of Allergy and Infectious Diseases (R01AI095125, AI095125)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 078938, R01DK078938, R56DK078938)
- National Institute of Neurological Disorders and Stroke (R01NS085910)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolomics and Mass Spectrometry Studies
- Keywords
- gut microbiota, microbial metabolites, secondary metabolites, host-microbe interactions, dysbiosis, host-microbe signaling, host immunity, host metabolism, microbial colonization, disease
- MeSH terms
- Bacteria, Cardiovascular Diseases, Cystic Fibrosis, Health, Humans, Neoplasms, Gastrointestinal Tract, Metagenome, Microbiota
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