Gut microbiota functions: metabolism of nutrients and other food components
Open accessAbstract
The diverse microbial community that inhabits the human gut has an extensive metabolic repertoire that is distinct from, but complements the activity of mammalian enzymes in the liver and gut mucosa and includes functions essential for host digestion. As such, the gut microbiota is a key factor in shaping the biochemical profile of the diet and, therefore, its impact on host health and disease. The important role that the gut microbiota appears to play in human metabolism and health has stimulated research into the identification of specific microorganisms involved in different processes, and the elucidation of metabolic pathways, particularly those associated with metabolism of dietary components and some host-generated substances. In the first part of the review, we discuss the main gut microorganisms, particularly bacteria, and microbial pathways associated with the metabolism of dietary carbohydrates (to short chain fatty acids and gases), proteins, plant polyphenols, bile acids, and vitamins. The second part of the review focuses on the methodologies, existing and novel, that can be employed to explore gut microbial pathways of metabolism. These include mathematical models, omics techniques, isolated microbes, and enzyme assays.
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
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 gut microbiota's role in breaking down complex carbohydrates, proteins, and lipids enhances the digestive process, facilitating absorption of essential nutrients.
“The intricate role of the gut microbiota in breaking down complex carbohydrates, proteins, and lipids enhances the digestive process, facilitating the absorption of essential nutrients.”
From Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony (2024) · cites this paper as [15]
The Introduction and Proteins sections describe microbial breakdown of polysaccharides and proteins. The Bile acids section links microbial activity to lipid digestion and nutrient absorption indirectly, but says bacterial deconjugation can reduce the efficiency of bile acids in emulsifying dietary lipids. It does not establish that microbial breakdown of all three food groups enhances digestion and absorption as claimed. (LLM, conf=0.88)
Experimental — accuracy not yet measuredThe gut microbiota shapes both energy harvest and storage through metabolism of proteins and production of several metabolites including SCFAs, ammonia, sulfur-containing metabolites, and neuroactive compounds.
“The gut microbiota is an important factor that shapes both energy harvest and storage through metabolism of proteins and production of several metabolites including SCFAs, ammonia, sulfur-containing metabolites such as hydrogen sulfide and methanethiol, and neuroactive compounds such as tryptamine, serotonin, phenethylamine, tryptophan, and histamine [137, 138].”
From The athletic gut microbiota (2020) · cites this paper as [138]
The gut microbiota can synthesize certain vitamins, most notably vitamin K and B-group vitamins, some of which might be directly absorbed.
“It is well appreciated that the gut microbiota can synthesize certain vitamins, most notably vitamin K and B-group vitamins [e.g., cobalamin (B 12 ), folate, and riboflavin (144, 145)], some of which might be directly absorbed.”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [145]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
1 retracted
Kaoutari, A. E., Armougom, F., Leroy, Q., Vialettes, B., Million, M., Raoult, D., & Henrissat, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0084033 · Cited by 55 · see citing works
RetractedPolyphenols: Food sources and bioavailability
Manach, C., Scalbert, A., Morand, C., Rémésy, C., & Jiménez, L. (2004) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/79.5.727 · Cited by 8,175 · see citing works
A core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823 · see citing works
Gut 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 · see citing works
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 · see citing works
Circulating mitochondrial DAMPs cause inflammatory responses to injury
Zhang, Q., Raoof, M., Chen, Y., Sumi, Y., Sursal, T., Junger, W., Brohi, K., Itagaki, K., & Hauser, C. J. (2010) · Nature · doi:10.1038/nature08780 · Cited by 3,812 · see citing works
Formation of propionate and butyrate by the human colonic microbiota
Louis, P., & Flint, H. J. (2017) · Environmental Microbiology · doi:10.1111/1462-2920.13589 · Cited by 3,028 · see citing works
The gut microbiota, bacterial metabolites and colorectal cancer
Louis, P., Hold, G. L., & Flint, H. J. (2014) · Nature Reviews Microbiology · doi:10.1038/nrmicro3344 · Cited by 2,836 · see citing works
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 · see citing works
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677 · see citing works
Brown, A. J., Goldsworthy, S. M., Barnes, A. A., Eilert, M. M., Tcheang, L., Daniels, D., Muir, A. I., Wigglesworth, M. J., Kinghorn, I., Fraser, N. J., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211609200 · Cited by 2,409 · see citing works
The gut microbiota and host health: a new clinical frontier
Marchesi, J. R., Adams, D. H., Fava, F., Hermes, G. D. A., Hirschfield, G. M., Hold, G., Quraishi, M. N., Kinross, J., Smidt, H., Tuohy, K. M., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-309990 · Cited by 2,302 · cited 1× · see citing works
“More recently evidence has been accumulating that the microbiota may also be involved in obesity and diabetes [4, 5].”
BackgroundBile acids induce energy expenditure by promoting intracellular thyroid hormone activation
Watanabe, M., Houten, S. M., Mataki, C., Christoffolete, M. A., Kim, B. W., Sato, H., Messaddeq, N., Harney, J. W., Ezaki, O., Kodama, T., et al. (2006) · Nature · doi:10.1038/nature04330 · Cited by 2,220 · see citing works
Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits
De Vadder, F., Kovatcheva-Datchary, P., Goncalves, D., Vinera, J., Zitoun, C., Duchampt, A., Bäckhed, F., & Mithieux, G. (2014) · Cell · doi:10.1016/j.cell.2013.12.016 · Cited by 2,200 · see citing works
A regulatory cascade of the nuclear receptors FXR, SHP-1, and LRH-1 represses bile acid biosynthesis
Goodwin, B., Jones, S. A., Price, R. R., Watson, M. A., McKee, D. D., Moore, L. B., Galardi, C., Wilson, J. G., Lewis, M. C., Roth, M. E., et al. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00051-4 · Cited by 1,940 · see citing works
The interaction between bacteria and bile
Begley, M., Gahan, C. G. M., & Hill, C. (2004) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2004.09.003 · Cited by 1,793 · see citing works
The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism
Frost, G., Sleeth, M. L., Sahuri-Arisoylu, M., Lizarbe, B., Cerdan, S., Brody, L., Anastasovska, J., Ghourab, S., Hankir, M., Zhang, S., et al. (2014) · Nature Communications · doi:10.1038/ncomms4611 · Cited by 1,771 · see citing works
Dominant and diet-responsive groups of bacteria within the human colonic microbiota
Walker, A. W., Ince, J., Duncan, S. H., Webster, L. M., Holtrop, G., Ze, X., Brown, D., Stares, M. D., Scott, P., Bergerat, A., et al. (2011) · The ISME Journal · doi:10.1038/ismej.2010.118 · Cited by 1,632 · see citing works
Bacteria as vitamin suppliers to their host: A gut microbiota perspective
LeBlanc, J. G., Milani, C., de Giori, G. S., Sesma, F., van Sinderen, D., & Ventura, M. (2013) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2012.08.005 · Cited by 1,613 · cited 1× · see citing works
“[55] explored the metabolic potential of gut microbial sequences from two subjects and found that their microbiomes were enriched for a variety of clustered orthologous groups (COGs) involved in the synthesis of deoxyxylulose-5-phosphate, a precursor of thiamine and pyridoxal.”
BackgroundThe control and consequences of bacterial fermentation in the human colon
Cummings, J. H., & Macfarlane, G. T. (1991) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1991.tb02739.x · Cited by 1,499 · see citing works
Bile acids lower triglyceride levels via a pathway involving FXR, SHP, and SREBP-1c
渡辺, 光., Houten, S. M., Wang, L., Moschetta, A., Mangelsdorf, D. J., Heyman, R. A., Moore, D. D., & Auwerx, J. H. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21025 · Cited by 1,398 · see citing works
Reichardt, N., Duncan, S. H., Young, P., Belenguer, Á., Leitch, E. C. M., Scott, K. P., Flint, H. J., & Louis, P. (2014) · The ISME Journal · doi:10.1038/ismej.2014.14 · Cited by 1,302 · see citing works
Trygg, J., Holmes, E. C., & Lundstedt, T. (2006) · Journal of Proteome Research · doi:10.1021/pr060594q · Cited by 1,276 · see citing works
Revealing the Bacterial Butyrate Synthesis Pathways by Analyzing (Meta)genomic Data
Vital, M., Howe, A. C., & Tiedje, J. M. (2014) · mBio · doi:10.1128/mbio.00889-14 · Cited by 1,189 · see citing works
The first 1000 cultured species of the human gastrointestinal microbiota
Rajilić-Stojanović, M., & de Vos, W. M. (2014) · FEMS Microbiology Reviews · doi:10.1111/1574-6976.12075 · Cited by 1,182 · see citing works
Jones, B. V., Begley, M., Hill, C., Gahan, C. G. M., & Marchesi, J. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804437105 · Cited by 1,098 · see citing works
Duncan, S. H., Belenguer, A., Holtrop, G., Johnstone, A. M., Flint, H. J., & Lobley, G. E. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.02340-06 · Cited by 941 · see citing works
Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes
Magnúsdóttir, S., Ravcheev, D., de Crécy-Lagard, V., & Thiele, I. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00148 · Cited by 876 · see citing works
Belenguer, A., Duncan, S. H., Calder, A. G., Holtrop, G., Louis, P., Lobley, G. E., & Flint, H. J. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.72.5.3593-3599.2006 · Cited by 856 · see citing works
Greenblum, S., Turnbaugh, P. J., & Borenstein, E. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1116053109 · Cited by 821 · see citing works
Constraint-based models predict metabolic and associated cellular functions
Bordbar, A., Monk, J. M., King, Z. A., & Palsson, B. Ø. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3643 · Cited by 818 · see citing works
Katsuma, S., Hirasawa, A., & Tsujimoto, G. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.01.139 · Cited by 789 · see citing works
Louis, P., Young, P., Holtrop, G., & Flint, H. J. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.02066.x · Cited by 783 · see citing works
Constraining the metabolic genotype–phenotype relationship using a phylogeny of in silico methods
Lewis, N. E., Nagarajan, H., & Palsson, B. O. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2737 · Cited by 779 · see citing works
Bioavailability of Dietary Polyphenols and Gut Microbiota Metabolism: Antimicrobial Properties
Marín, L., Miguélez, E. M., Villar, C. J., & Lombó, F. (2015) · BioMed Research International · doi:10.1155/2015/905215 · Cited by 778 · see citing works
Sequencing and beyond: integrating molecular 'omics' for microbial community profiling
Franzosa, E. A., Hsu, T. Y., Sirota‐Madi, A., Shafquat, A., Abu-Ali, G., Morgan, X. C., & Huttenhower, C. (2015) · Nature Reviews Microbiology · doi:10.1038/nrmicro3451 · Cited by 725 · see citing works
Analytical Methods in Untargeted Metabolomics: State of the Art in 2015
Alonso, A., Marsal, S., & Julià, A. (2015) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2015.00023 · Cited by 685 · see citing works
Systems biology properties of reconstructed networks
Palsson, B. Ø. (2006) · Cited by 684 · see citing works
Diets that differ in their FODMAP content alter the colonic luminal microenvironment
Halmos, E. P., Christophersen, C. T., Bird, A. R., Shepherd, S. J., Gibson, P. R., & Muir, J. G. (2015) · Gut · doi:10.1136/gutjnl-2014-307264 · Cited by 681 · see citing works
Comparison of fermentation reactions in different regions of the human colon
Macfarlane, G. T., Gibson, G. R., & Cummings, J. H. (1992) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1992.tb04882.x · Cited by 676 · see citing works
Emwas, A.-H. M. (2015) · Methods in molecular biology · doi:10.1007/978-1-4939-2377-9_13 · Cited by 628 · see citing works
Systems Biology: Properties of Reconstructed Networks
Palsson, B. Ø. (2006) · doi:10.1017/cbo9780511790515 · Cited by 617 · see citing works
Regulation of host weight gain and lipid metabolism by bacterial bile acid modification in the gut
Joyce, S. A., MacSharry, J., Casey, P. G., Kinsella, M., Murphy, E. F., Shanahan, F., Hill, C., & Gahan, C. G. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323599111 · Cited by 604 · see citing works
Interaction of dietary compounds, especially polyphenols, with the intestinal microbiota: a review
Duda-Chodak, A., Tarko, T., Satora, P., & Sroka, P. (2015) · European Journal of Nutrition · doi:10.1007/s00394-015-0852-y · Cited by 599 · see citing works
Endocrine functions of bile acids
Houten, S. M., 渡辺, 光., & Auwerx, J. H. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601049 · Cited by 583 · see citing works
Chemometrics in metabolomics—A review in human disease diagnosis
Madsen, R., Lundstedt, T., & Trygg, J. (2009) · Analytica Chimica Acta · doi:10.1016/j.aca.2009.11.042 · Cited by 559 · see citing works
Intestinal flora and endogenous vitamin synthesis
Hill, M. J. (1997) · European Journal of Cancer Prevention · doi:10.1097/00008469-199703001-00009 · Cited by 551 · see citing works
Intestinal luminal nitrogen metabolism: Role of the gut microbiota and consequences for the host
Davila, A.-M., Blachier, F., Gotteland, M., Andriamihaja, M., Benetti, P.-H., Sanz, Y., & Tomé, D. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2012.11.005 · Cited by 548 · see citing works
Shotgun metaproteomics of the human distal gut microbiota
VerBerkmoes, N. C., Russell, A. L., Shah, M. B., Godzik, A., Rosenquist, M., Halfvarson, J., Lefsrud, M. G., Apajalahti, J., Tysk, C., Hettich, R. L., et al. (2008) · The ISME Journal · doi:10.1038/ismej.2008.108 · Cited by 544 · see citing works
Analytical Strategies in Metabonomics
Lenz, E. M., & Wilson, I. D. (2006) · Journal of Proteome Research · doi:10.1021/pr0605217 · Cited by 530 · see citing works
Louis, P., Duncan, S. H., McCrae, S. I., Millar, J., Jackson, M. S., & Flint, H. J. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.7.2099-2106.2004 · Cited by 517 · see citing works
Bacterial species involved in the conversion of dietary flavonoids in the human gut
Braune, A., & Blaut, M. (2016) · Gut Microbes · doi:10.1080/19490976.2016.1158395 · Cited by 514 · see citing works
Colonic metabolism of dietary polyphenols: influence of structure on microbial fermentation products
Rechner, A. R., Smith, M. A., Kuhnle, G., Gibson, G. R., Debnam, E. S., Srai, S. K., Moore, K. P., & Rice-Evans, C. A. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2003.09.022 · Cited by 512 · see citing works
Hooper, L. V., Xu, J., Falk, P. G., Midtvedt, T., & Gordon, J. I. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.17.9833 · Cited by 500 · see citing works
Contribution of acetate to butyrate formation by human faecal bacteria
Duncan, S. H., Holtrop, G., Lobley, G. E., Calder, A. G., Stewart, C. S., & Flint, H. J. (2004) · British Journal Of Nutrition · doi:10.1079/bjn20041150 · Cited by 494 · see citing works
Smith, E. A., & Macfarlane, G. T. (1996) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1996.tb04331.x · Cited by 481 · see citing works
Tomás‐Barberán, F. A., González‐Sarrías, A., García‐Villalba, R., Núñez‐Sánchez, M. A., Selma, M. V., García‐Conesa, M. T., & Espín, J. C. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500901 · Cited by 465 · see citing works
Protein Degradation by Human Intestinal Bacteria
Macfarlane, G. T., Cummings, J. H., & Allison, C. (1986) · Microbiology · doi:10.1099/00221287-132-6-1647 · Cited by 455 · see citing works
Dietary intake of 337 polyphenols in French adults
Pérez‐Jiménez, J., Fezeu, L., Touvier, M., Arnault, N., Manach, C., Herçberg, S., Galan, P., & Scalbert, A. (2011) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.110.007096 · Cited by 425 · see citing works
Tomás-Barberán, F. A., García-Villalba, R., González-Sarrías, A., Selma, M. V., & Espín, J. C. (2014) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf5024615 · Cited by 419 · see citing works
Russell, W. R., Duncan, S. H., Scobbie, L., Duncan, G., Cantlay, L., Calder, A. G., Anderson, S. E., & Flint, H. J. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201200594 · Cited by 417 · see citing works
Roles of short-chain fatty acids receptors, GPR41 and GPR43 on colonic functions.
Tazoe, H., Otomo, Y., Kaji, I., Tanaka, R., Si, K., & Kuwahara, A. (2008) · PubMed · Cited by 406 · see citing works
Application of metagenomics in the human gut microbiome
Wang, W., Xu, S., Ren, Z., Tao, L., Jiang, J., & Zheng, S. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i3.803 · Cited by 400 · see citing works
Bioavailability of phyto-oestrogens
Rowland, I. R., Faughnan, M. S., Hoey, L., Wähälä, K., Williamson, G., & Cassidy, A. (2003) · British Journal Of Nutrition · doi:10.1079/bjn2002796 · Cited by 397 · see citing works
Dietary requirements of “nutritionally non-essential amino acids” by animals and humans
Wu, G., Wu, Z., Dai, Z., Yang, Y., Wang, W., Liu, C., Wang, B., Wang, J., & Yin, Y. (2012) · Amino Acids · doi:10.1007/s00726-012-1444-2 · Cited by 393 · see citing works
Metatranscriptomic Approach to Analyze the Functional Human Gut Microbiota
Gosalbes, M. J., Durbán, A., Pignatelli, M., Abellan, J. J., Jiménez‐Hernández, N., Pérez‐Cobas, A. E., Latorre, A., & Moyá, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017447 · Cited by 379 · see citing works
Mechanism of growth inhibition by free bile acids in lactobacilli and bifidobacteria
Kurdi, P., Kawanishi, K., Mizutani, K., & Yokota, A. (2006) · Journal of Bacteriology · doi:10.1128/jb.188.5.1979-1986.2006 · Cited by 364 · see citing works
Falony, G., Vlachou, A., Verbrugghe, K., & Vuyst, L. D. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.01296-06 · Cited by 362 · see citing works
Dabek, M., McCrae, S. I., Stevens, V. J., Duncan, S. H., & Louis, P. (2008) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2008.00520.x · Cited by 332 · see citing works
Taurocholic acid metabolism by gut microbes and colon cancer
Ridlon, J. M., Wolf, P. G., & Gaskins, H. R. (2016) · Gut Microbes · doi:10.1080/19490976.2016.1150414 · Cited by 327 · see citing works
Isolation and characterization of human colonic bacteria able to hydrolyse chlorogenic acid
Couteau, D., McCartney, A. L., Gibson, G. R., Williamson, G., & Faulds, C. B. (2001) · Journal of Applied Microbiology · doi:10.1046/j.1365-2672.2001.01316.x · Cited by 305 · see citing works
Selma, M. V., Beltrán, D., García-Villalba, R., Espín, J. C., & Tomás-Barberán, F. A. (2014) · Food Funct. · doi:10.1039/c4fo00092g · Cited by 304 · see citing works
Production, metabolism, and excretion of hydrogen in the large intestine
Christl, S. U., Murgatroyd, P. R., Gibson, G. R., & Cummings, J. H. (1992) · Gastroenterology · doi:10.1016/0016-5085(92)90765-q · Cited by 300 · see citing works
Regulation of Carbohydrate Metabolism by the Farnesoid X Receptor
Stayrook, K. R., Bramlett, K. S., Savkur, R. S., FICORILLI, J. V., Cook, T. G., Christe, M. E., Michael, L. F., & Burris, T. P. (2004) · Endocrinology · doi:10.1210/en.2004-0965 · Cited by 288 · see citing works
Gibson, G. R., Cummings, J. H., & Macfarlane, G. T. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.11.2750-2755.1988 · Cited by 286 · see citing works
Scott, K. P., Martin, J. C., Campbell, G. P., Mayer, C., & Flint, H. J. (2006) · Journal of Bacteriology · doi:10.1128/jb.00137-06 · Cited by 282 · see citing works
García‐Cañaveras, J. C., Donato, M. T., Castell, J. V., & Lahoz, A. (2012) · Journal of Lipid Research · doi:10.1194/jlr.d028803 · Cited by 276 · see citing works
Functional metagenomics to mine the human gut microbiome for dietary fiber catabolic enzymesPreprint
Tasse, L., Bercovici, J., Pizzut‐Serin, S., Robe, P., Tap, J., Klopp, C., Cantarel, B. L., Coutinho, P. M., Henrissat, B., Leclerc, M., et al. (2010) · Genome Research · doi:10.1101/gr.108332.110 · Cited by 276 · see citing works
Detoxification of Lithocholic Acid, A Toxic Bile Acid: Relevance to Drug Hepatotoxicity
Hofmann, A. F. (2004) · Drug Metabolism Reviews · doi:10.1081/dmr-200033475 · Cited by 268 · see citing works
Utilization of amino acids by bacteria from the pig small intestine
Dai, Z.-L., Zhang, J., Wu, G., & Zhu, W.-Y. (2010) · Amino Acids · doi:10.1007/s00726-010-0556-9 · Cited by 246 · see citing works
Bjerrum, J. T., Wang, Y., Hao, F., Coskun, M., Ludwig, C., Günther, U. L., & Nielsen, O. H. (2014) · Metabolomics · doi:10.1007/s11306-014-0677-3 · Cited by 241 · see citing works
Functional Metabolic Map of Faecalibacterium prausnitzii, a Beneficial Human Gut Microbe
Heinken, A., Khan, M. T., Paglia, G., Rodionov, D. A., Harmsen, H. J. M., & Thiele, I. (2014) · Journal of Bacteriology · doi:10.1128/jb.01780-14 · Cited by 236 · see citing works
Physiology and ecology of the sulphate‐reducing bacteria
Gibson, G. R. (1990) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1990.tb01575.x · Cited by 234 · see citing works
Decroos, K., Vanhemmens, S., Cattoir, S., Boon, N., & Verstraete, W. (2004) · Archives of Microbiology · doi:10.1007/s00203-004-0747-4 · Cited by 234 · see citing works
Corona, G., Tzounis, X., Dessì, M., Deiana, M., Debnam, E. S., Visioli, F., & Spencer, J. P. E. (2006) · Free Radical Research · doi:10.1080/10715760500373000 · Cited by 231 · see citing works
Systems-level characterization of a host-microbe metabolic symbiosis in the mammalian gut
Heinken, A., Sahoo, S., Fleming, R. M. T., & Thiele, I. (2013) · Gut Microbes · doi:10.4161/gmic.22370 · Cited by 219 · see citing works
Synthetic Ecology of Microbes: Mathematical Models and Applications
Zomorrodi, A. R., & Segrè, D. (2015) · Journal of Molecular Biology · doi:10.1016/j.jmb.2015.10.019 · Cited by 212 · see citing works
Noecker, C. A., Eng, A., Srinivasan, S., Theriot, C. M., Young, V. B., Jansson, J. K., Fredricks, D. N., & Borenstein, E. (2016) · mSystems · doi:10.1128/msystems.00013-15 · Cited by 212 · see citing works
Clavel, T., Henderson, G., Engst, W., Dore, J. M., & Blaut, M. (2006) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2005.00057.x · Cited by 209 · see citing works
Butyrate Histone Deacetylase Inhibitors
Steliou, K., Boosalis, M. S., Perrine, S. P., Sangerman, J., & Faller, D. V. (2012) · BioResearch open access · doi:10.1089/biores.2012.0223 · Cited by 209 · see citing works
Dehydroepiandrosterone Sulfotransferase Gene Induction by Bile Acid Activated Farnesoid X Receptor
Song, C. S., Echchgadda, I., Baek, B. S., Ahn, S., Oh, T., Roy, A. K., & Chatterjee, B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m107557200 · Cited by 208 · see citing works
Bioactivation of Phytoestrogens: Intestinal Bacteria and Health
Landete, J. M., Arqués, J. L., Médina, M., Gaya, P., Rivas, B. D. L., & Múñoz, R. (2015) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2013.789823 · Cited by 204 · see citing works
In vitro transformation of chlorogenic acid by human gut microbiota
Tomás-Barberán, F. A., Garcı́a-Villalba, R., Quartieri, A., Raimondi, S., Amaretti, A., Leonardi, A., & Rossi, M. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201300441 · Cited by 202 · see citing works
Sulphate-reducing bacteria and hydrogen sulphide in the aetiology of ulcerative colitis
Rowan, F. E., Docherty, N. G., Coffey, J. C., & O'Connell, P. R. (2009) · British Journal of Surgery · doi:10.1002/bjs.6454 · Cited by 201 · see citing works
Volume, Composition, and Source of Intestinal Gas
Levitt, M. D., & Bond, J. H. (1970) · Gastroenterology · doi:10.1016/s0016-5085(19)33654-6 · Cited by 199 · see citing works
Kolmeder, C. A., de Been, M., Nikkilä, J., Ritamo, I., Mättö, J., Valmu, L., Salojärvi, J., Palva, A., Salonen, A., & de Vos, W. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029913 · Cited by 199 · see citing works
Farnesoid X Receptor Regulates Bile Acid-Amino Acid Conjugation
Pircher, P. C., Kitto, J. L., Petrowski, M. L., Tangirala, R. K., Bischoff, E. D., Schulman, I. G., & Westin, S. K. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302128200 · Cited by 197 · see citing works
Microbial regulation of host hydrogen sulfide bioavailability and metabolism
Shen, X., Carlström, M., Borniquel, S., Jädert, C., Kevil, C. G., & Lundberg, J. O. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.02.024 · Cited by 194 · see citing works
Hirokane, H., Nakahara, M., Tachibana, S., Shimizu, M., & Sato, R. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m404255200 · Cited by 189 · see citing works
Dose response and minimal daily requirement for vitamin K in man.
Frick, P. G., Riedler, G., & Brögli, H. (1967) · Journal of Applied Physiology · doi:10.1152/jappl.1967.23.3.387 · Cited by 184 · see citing works
Muñoz‐Tamayo, R., Laroche, B., Walter, É., Dore, J. M., Duncan, S. H., Flint, H. J., & Leclerc, M. (2011) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2011.01085.x · Cited by 164 · see citing works
Isolation of a human intestinal bacterium capable of daidzein and genistein conversion
Matthies, A., Blaut, M., & Braune, A. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01795-08 · Cited by 161 · see citing works
Is equol the key to the efficacy of soy foods?
Lampe, J. W. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.26736t · Cited by 158 · see citing works
Wei, X., Yan, X., Zou, D., Yang, Z., Wang, X., Liu, W., Wang, S., Li, X., Han, J., Huang, L., et al. (2013) · BMC Gastroenterology · doi:10.1186/1471-230x-13-175 · Cited by 157 · see citing works
Gut Bacteria and Hydrogen Sulfide: The New Old Players in Circulatory System Homeostasis
Tomášová, L., Konopelski, P., & Ufnal, M. (2016) · Molecules · doi:10.3390/molecules21111558 · Cited by 156 · see citing works
H2metabolism is widespread and diverse among human colonic microbes
Wolf, P. G., Biswas, A., Morales, S. E., Greening, C., & Gaskins, H. R. (2016) · Gut Microbes · doi:10.1080/19490976.2016.1182288 · Cited by 153 · see citing works
Modelling the emergent dynamics and major metabolites of the human colonic microbiota
Kettle, H., Louis, P., Holtrop, G., Duncan, S. H., & Flint, H. J. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12599 · Cited by 149 · see citing works
Significance of microflora in proteolysis in the colon
Gibson, S. A., McFarlan, C., Hay, S., & Macfarlane, G. T. (1989) · Applied and Environmental Microbiology · doi:10.1128/aem.55.3.679-683.1989 · Cited by 147 · see citing works
Transformation of Flavonoids by Intestinal Microorganisms
Blaut, M., Schoefer, & Braune, A. (2003) · International Journal for Vitamin and Nutrition Research · doi:10.1024/0300-9831.73.2.79 · Cited by 146 · see citing works
Clavel, T., Lippman, R., Gavini, F., Dore, J. M., & Blaut, M. (2006) · Systematic and Applied Microbiology · doi:10.1016/j.syapm.2006.02.003 · Cited by 145 · see citing works
François, I., Lescroart, O., Veraverbeke, W. S., Marzorati, M., Possemiers, S., Evenepoel, P., Hamer, H. M., Houben, E., Windey, K., Welling, G. W., et al. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512000372 · Cited by 144 · see citing works
Insights into human colonic physiology obtained from the study of flatus composition
Suarez, F. L., Furne, J. K., Springfield, J. R., & Levitt, M. D. (1997) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1997.272.5.g1028 · Cited by 141 · see citing works
The Bioavailability of Apigenin-7-Glucoside Is Influenced by Human Intestinal Microbiota in Rats
Hanske, L., Loh, G., Sczesny, S., Blaut, M., & Braune, A. (2009) · Journal of Nutrition · doi:10.3945/jn.108.102814 · Cited by 140 · see citing works
Bernstein, H. (1999) · Toxicology Letters · doi:10.1016/s0378-4274(99)00113-7 · Cited by 137 · see citing works
Matthies, A., Loh, G., Blaut, M., & Braune, A. (2011) · Journal of Nutrition · doi:10.3945/jn.111.148247 · Cited by 137 · see citing works
Acetate production from hydrogen and [13C]carbon dioxide by the microflora of human feces
Lajoie, S. F., Bank, S., Miller, T. L., & Wolin, M. J. (1988) · Applied and Environmental Microbiology · doi:10.1128/aem.54.11.2723-2727.1988 · Cited by 136 · see citing works
l-Glutamine regulates amino acid utilization by intestinal bacteria
Dai, Z., Li, X.-L., Xi, P., Zhang, J., Wu, G., & Zhu, W. (2012) · Amino Acids · doi:10.1007/s00726-012-1264-4 · Cited by 135 · see citing works
Xiong, W., Abraham, P. E., Li, Z., Pan, C., & Hettich, R. L. (2015) · PROTEOMICS · doi:10.1002/pmic.201400571 · Cited by 133 · see citing works
McIntosh, F. M., Maison, N., Holtrop, G., Young, P., Stevens, V. J., Ince, J., Johnstone, A. M., Lobley, G. E., Flint, H. J., & Louis, P. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02711.x · Cited by 132 · see citing works
Inference of Network Dynamics and Metabolic Interactions in the Gut Microbiome
Steinway, S. N., Biggs, M. B., Loughran, T. P., Papin, J. A., & Albert, R. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004338 · Cited by 127 · see citing works
Swann, J. R., Tuohy, K. M., Lindfors, P., Brown, D. T., Gibson, G. R., Wilson, I. D., Sidaway, J. E., Nicholson, J. K., & Holmes, E. C. (2011) · Journal of Proteome Research · doi:10.1021/pr200243t · Cited by 125 · see citing works
Metabolic network modeling of microbial communities
Biggs, M. B., Medlock, G. L., Kolling, G. L., & Papin, J. A. (2015) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1308 · Cited by 124 · see citing works
Anoxic Conditions Promote Species-Specific Mutualism between Gut Microbes <i>In Silico</i>
Heinken, A., & Thiele, I. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.00101-15 · Cited by 123 · cited 3× · see citing works
“The model predicted that the need to regenerate reducing equivalents enforced mutualism in certain pairs under anoxic conditions [153].”
BackgroundMethodInfluentialPossemiers, S., Rabot, S., Espı́n, J. C., Bruneau, A., Philippe, C., González‐Sarrías, A., Heyerick, A., Tomás-Barberán, F. A., Keukeleire, D. D., & Verstraete, W. (2008) · Journal of Nutrition · doi:10.1093/jn/138.7.1310 · Cited by 120 · see citing works
Kandell, R. L., & Bernstein, C. (1991) · Nutrition and Cancer · doi:10.1080/01635589109514161 · Cited by 120 · see citing works
The Role of FXR in Disorders of Bile Acid Homeostasis
Eloranta, J. J., & Kullak-Ublick, G. A. (2008) · Physiology · doi:10.1152/physiol.00020.2008 · Cited by 120 · see citing works
Wang, Y., Liu, S., Yuanjia, H., Li, P., & Wan, J. (2015) · RSC Advances · doi:10.1039/c5ra14058g · Cited by 112 · see citing works
Kolmeder, C. A., & de Vos, W. M. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2013.05.018 · Cited by 106 · see citing works
Heinken, A., & Thiele, I. (2015) · Gut Microbes · doi:10.1080/19490976.2015.1023494 · Cited by 105 · see citing works
Hanske, L., Engst, W., Loh, G., Sczesny, S., Blaut, M., & Braune, A. (2012) · British Journal Of Nutrition · doi:10.1017/s0007114512003376 · Cited by 105 · see citing works
Gustafsson, B. E., Daft, F. S., McDaniel, E. G., Smith, J. C., & FITZGERALD, R. J. (1962) · Journal of Nutrition · doi:10.1093/jn/78.4.461 · Cited by 102 · see citing works
Systems-based approaches to unravel multi-species microbial community functioning
Abram, F. (2014) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2014.11.009 · Cited by 102 · see citing works
A biomolecular isolation framework for eco-systems biology
Roume, H., Muller, E. E. L., Cordes, T., Renaut, J., Hiller, K., & Wilmes, P. (2012) · The ISME Journal · doi:10.1038/ismej.2012.72 · Cited by 98 · see citing works
Mallonee, D. H., & Hylemon, P. B. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.24.7053-7058.1996 · Cited by 97 · see citing works
Systems biology of host–microbe metabolomics
Heinken, A., & Thiele, I. (2015) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1301 · Cited by 96 · see citing works
Said, H. M. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00231.2013 · Cited by 94 · see citing works
Lockyer, S., Corona, G., Yaqoob, P., Spencer, J. P. E., & Rowland, I. R. (2015) · British Journal Of Nutrition · doi:10.1017/s0007114515001269 · Cited by 90 · see citing works
Cole, C. B., Fuller, R., Mallet, A., & Rowland, I. R. (1985) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1985.tb03359.x · Cited by 88 · see citing works
Hussaini, S. H., Pereira, S. P., Murphy, G. M., & Dowling, R. H. (1995) · Hepatology · doi:10.1002/hep.1840220619 · Cited by 87 · see citing works
Impaired hydrogen metabolism in pneumatosis cystoides intestinalis
Christl, S. U., Gibson, G. R., Murgatroyd, P. R., Scheppach, W. M., & Cummings, J. H. (1993) · Gastroenterology · doi:10.1016/0016-5085(93)90406-3 · Cited by 86 · see citing works
Anti-Inflammatory Implications of the Microbial Transformation of Dietary Phenolic Compounds
Russell, W. R., Scobbie, L., Chesson, A., Richardson, A. J., Stewart, C. S., Duncan, S. H., Drew, J. E., & Duthie, G. G. (2008) · Nutrition and Cancer · doi:10.1080/01635580801987498 · Cited by 86 · see citing works
Tauroconjugation of cholic acid stimulates 7 alpha-dehydroxylation by fecal bacteria
Eldere, J. V., Celis, P., Pauw, G. D., Lesaffre, E., & Eyssen, H. (1996) · Applied and Environmental Microbiology · doi:10.1128/aem.62.2.656-661.1996 · Cited by 86 · see citing works
Ziemer, C. J. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.03016-13 · Cited by 82 · see citing works
Manor, O., Levy, R., & Borenstein, E. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.07.021 · Cited by 81 · see citing works
Amino Acids in Human and Animal Nutrition
Karau, A., & Grayson, I. (2014) · Advances in biochemical engineering, biotechnology · doi:10.1007/10_2014_269 · Cited by 79 · see citing works
Intestinal colonization: How key microbial players become established in this dynamic process
Aidy, S. E., den Abbeele, P. V., de Wiele, T. V., Louis, P., & Kleerebezem, M. (2013) · BioEssays · doi:10.1002/bies.201300073 · Cited by 72 · see citing works
Braune, A., Engst, W., & Blaut, M. (2015) · Environmental Microbiology · doi:10.1111/1462-2920.12864 · Cited by 64 · see citing works
Detection of novel metabolites of flaxseed lignans in vitro and in vivo
Quartieri, A., Garcı́a-Villalba, R., Amaretti, A., Raimondi, S., Leonardi, A., Rossi, M., & Tomás-Barberán, F. A. (2016) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201500773 · Cited by 64 · see citing works
Human lymphocyte repertoires in ageing
Boyd, S. D., Liu, Y., Wang, C., Martin, V., & Dunn‐Walters, D. K. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.07.007 · Cited by 61 · see citing works
Profiling of Phenols in Human Fecal Water after Raspberry Supplementation
Gill, C. I. R., McDougall, G. J., Glidewell, S. M., Stewart, D., Shen, Q., Tuohy, K. M., Dobbin, A., Boyd, A., Brown, E. M., Haldar, S., et al. (2010) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf1017143 · Cited by 61 · see citing works
Young, J. C., Pan, C., Adams, R. M., Brooks, B., Banfield, J. F., Morowitz, M. J., & Hettich, R. L. (2015) · PROTEOMICS · doi:10.1002/pmic.201400563 · Cited by 61 · see citing works
Agent Based Modeling of Human Gut Microbiome Interactions and Perturbations
Shashkova, T., Popenko, A., Tyakht, A., Peskov, K. V., Kosinsky, Y., Bogolubsky, L. I., Raigorodskii, A. M., Ischenko, D. S., Alexeev, D. G., & Govorun, V. M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148386 · Cited by 56 · see citing works
Bauer, E., Laczny, C. C., Magnúsdóttir, S., Wilmes, P., & Thiele, I. (2015) · Microbiome · doi:10.1186/s40168-015-0121-6 · Cited by 44 · see citing works
Kok, M. G. M., Ruijken, M., Swann, J. R., Wilson, I. D., Somsen, G. W., & de Jong, G. J. (2013) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-012-6701-4 · Cited by 42 · see citing works
Tannock, G. W., Lawley, B., Munro, K., Sims, I. M., Lee, J., Butts, C. A., & Roy, N. C. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.03799-13 · Cited by 39 · see citing works
Gustafsson, B. E., Angelin, B., Einarsson, K., & Gustafsson, J.-Α. (1977) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)41589-5 · Cited by 34 · see citing works
Effect of ursodeoxycholic acid on cholesterol absorption and metabolism in humans
Woollett, L. A., Buckley, D. D., Yao, L., Jones, P. J. H., Granholm, N. A., Tolley, E. A., & Heubi, J. E. (2003) · Journal of Lipid Research · doi:10.1194/jlr.m200478-jlr200 · Cited by 33 · see citing works
Microbiological aspects of enterohepatic neutral sterol and bile acid metabolism.
Kellogg, T. F. (1972) · PubMed · Cited by 33 · see citing works
Metabolome progression during early gut microbial colonization of gnotobiotic mice
Marcobal, A. M., Yusufaly, T., Higginbottom, S. K., Snyder, M. P., Sonnenburg, J. L., & Mias, G. I. (2015) · Scientific Reports · doi:10.1038/srep11589 · Cited by 29 · see citing works
Mohammed, A., & Guda, C. (2015) · BMC Genomics · doi:10.1186/1471-2164-16-s7-s16 · Cited by 28 · see citing works
Bastos, F. S., Bessa, J., Pacheco, C. C., Marco, P. D., Castro, P. M. L., SILVA, M. N. A., & Jorge, R. F. (2002) · Biodegradation · doi:10.1023/a:1020834603785 · Cited by 27 · see citing works
Bacterial Enzymes: Their Role in the Formation of Mutagens and Carcinogens in the Intestine
Mallett, A. K., & Rowland, I. R. (2008) · Digestive Diseases · doi:10.1159/000171241 · Cited by 22 · see citing works
Hermanussen, M., Gonder, U., Jakobs, C., Stegemann, D., & Hoffmann, G. F. (2009) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2009.116 · Cited by 17 · see citing works
pH feedback and phenotypic diversity within bacterial functional groups of the human gut
Kettle, H., Donnelly, R., Flint, H. J., & Marion, G. (2013) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2013.10.015 · Cited by 13 · see citing works
Methane excretion and experimental colonic carcinogenesis
Flick, J. A., Hamilton, S. R., Rosales, F. J., & Perman, J. A. (1990) · Digestive Diseases and Sciences · doi:10.1007/bf01536766 · Cited by 9 · see citing works
[Clinical significance of sulfate-reducing bacteria for ulcerative colitis].
Watanabe, K., Mikamo, H., & Tanaka, K. Y. (2007) · PubMed · Cited by 4 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [115]Walker AW Duncan SH Louis P Flint HJ Phylogeny, culturing, and metagenomics of the approaches to unravel multi-species microbial community functioning. Comput Struct Biotechnol J 2014 13 24 32 PMC4348430 25750697
Cited by
Sorted by citations
Probiotics and prebiotics in intestinal health and disease: from biology to the clinic
Sanders, M. E., Merenstein, D. J., Reid, G., Gibson, G. R., & Rastall, R. A. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0173-3 · Cited by 2,059 · see citing works
Stojanov, S., Berlec, A., & Štrukelj, B. (2020) · Microorganisms · doi:10.3390/microorganisms8111715 · Cited by 1,903 · see citing works
Flavonoids as Anticancer Agents
Kopustinskienė, D. M., Jakštas, V., Savickas, A., & Bernatonienė, J. (2020) · Nutrients · doi:10.3390/nu12020457 · Cited by 1,313 · see citing works
Fassarella, M., Blaak, E. E., Penders, J., Nauta, A., Smidt, H., & Zoetendal, E. G. (2020) · Gut · doi:10.1136/gutjnl-2020-321747 · Cited by 781 · see citing works
Human gut microbiota in health and disease: Unveiling the relationship
Afzaal, M., Saeed, F., Shah, Y. A., Hussain, M., Rabail, R., Socol, C. T., Hassoun, A., Pateiro, M., Lorenzo, J. M., Rusu, A. V., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.999001 · Cited by 762 · see citing works
Impact of antibiotics on the human microbiome and consequences for host health
Patangia, D. V., Ryan, C. A., Dempsey, E. M., Ross, R. P., & Stanton, C. (2022) · MicrobiologyOpen · doi:10.1002/mbo3.1260 · Cited by 806 · see citing works
Gut Microbiota as a Trigger for Metabolic Inflammation in Obesity and Type 2 Diabetes
Scheithauer, T. P. M., Rampanelli, E., Nieuwdorp, M., Vallance, B. A., Verchere, C. B., van Raalte, D. H., & Herrema, H. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.571731 · Cited by 694 · see citing works
Tanase, D. M., Gosav, E. M., Costea, C. F., Ciocoiu, M., Lacatusu, C. M., Maranduca, M. A., Ouatu, A., & Floria, M. (2020) · Journal of Diabetes Research · doi:10.1155/2020/3920196 · Cited by 627 · see citing works
Impact of Diet-Modulated Butyrate Production on Intestinal Barrier Function and Inflammation
Bach Knudsen, K. E., Lærke, H. N., Hedemann, M. S., Nielsen, T. S., Ingerslev, A. K., Gundelund Nielsen, D. S., Theil, P. K., Purup, S., Hald, S., Schioldan, A. G., et al. (2018) · Nutrients · doi:10.3390/nu10101499 · Cited by 572 · see citing works
Wang, A., Zhang, Z., Ding, Q., Yang, Y., Bindelle, J., Ran, C., & Zhou, Z. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1900996 · Cited by 479 · see citing works
Cuevas-Sierra, A., Ramos-Lopez, O., Riezu-Boj, J. I., Milagro, F. I., & Martinez, J. A. (2019) · Advances in Nutrition · doi:10.1093/advances/nmy078 · Cited by 523 · see citing works
Mycotoxin: Its Impact on Gut Health and Microbiota
Liew, W.-P.-P., & Sabran, M. R. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00060 · Cited by 472 · see citing works
Role of Dietary Nutrients in the Modulation of Gut Microbiota: A Narrative Review
Yang, Q., Liang, Q., Balakrishnan, B., Belobrajdic, D. P., Feng, Q.-J., & Zhang, W. Y. (2020) · Nutrients · doi:10.3390/nu12020381 · Cited by 475 · see citing works
Hosomi, K., Saito, M., Park, J., Murakami, H., Shibata, N., Ando, M., Nagatake, T., Konishi, K., Ohno, H., Tanisawa, K., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32015-7 · Cited by 467 · see citing works
Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health
Berding, K., Vlckova, K., Marx, W., Schellekens, H., Stanton, C., Clarke, G., Jacka, F., Dinan, T. G., & Cryan, J. F. (2021) · Advances in Nutrition · doi:10.1093/advances/nmaa181 · Cited by 451 · see citing works
Montero, C. G., Fraile‐Μartinez, O., Gomez-Lahoz, A. M., Pekarek, L., Castellanos, A. J., Noguerales-Fraguas, F., Coca, S., Guijarro, L. G., García‐Honduvilla, N., Asúnsolo, Á., et al. (2021) · Nutrients · doi:10.3390/nu13020699 · Cited by 452 · see citing works
The Interactions between Polyphenols and Microorganisms, Especially Gut Microbiota
Makarewicz, M., Drożdż, I., Tarko, T., & Duda‐Chodak, A. (2021) · Antioxidants · doi:10.3390/antiox10020188 · Cited by 444 · see citing works
Polyphenols—Gut Microbiota Interrelationship: A Transition to a New Generation of Prebiotics
Plamada, D., & Vodnar, D. C. (2021) · Nutrients · doi:10.3390/nu14010137 · Cited by 432 · see citing works
The interaction among gut microbes, the intestinal barrier and short chain fatty acids
Ma, J., Piao, X., Mahfuz, S. U., Long, S., & Wang, J. (2021) · Animal nutrition · doi:10.1016/j.aninu.2021.09.012 · Cited by 409 · see citing works
Recent advances in the application of metabolomics for food safety control and food quality analyses
Li, S., Tian, Y., Jiang, P., Lin, Y., Liu, X., & Yang, H. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1761287 · Cited by 395 · see citing works
Uterine Microbiota: Residents, Tourists, or Invaders?
Baker, J. M., Chase, D. M., & Herbst‐Kralovetz, M. M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00208 · Cited by 390 · see citing works
Gut microbial molecules in behavioural and neurodegenerative conditions
Needham, B. D., Kaddurah-Daouk, R., & Mazmanian, S. K. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-00381-0 · Cited by 379 · see citing works
Microbiota and metabolic diseases
Pascale, A., Marchesi, N., Marelli, C., Coppola, A., Luzi, L., Govoni, S., Giustina, A., & Gazzaruso, C. (2018) · Endocrine · doi:10.1007/s12020-018-1605-5 · Cited by 423 · see citing works
Pathogenesis of allergic diseases and implications for therapeutic interventions
Wang, J., Zhou, Y., Zhang, H., Hu, L., Liu, J., Wang, L., Wang, T., Zhang, H., Cong, L., & Wang, Q. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01344-4 · Cited by 415 · see citing works
Mohr, A. E., Jäger, R., Carpenter, K. C., Kerksick, C. M., Purpura, M., Townsend, J. R., West, N. P., Black, K., Gleeson, M., Pyne, D. B., et al. (2020) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-020-00353-w · Cited by 378 · see citing works
“The gut microbiota is an important factor that shapes both energy harvest and storage through metabolism of proteins and production of several metabolites including SCFAs, ammonia, sulfur-containing metabolites such as hydrogen sulfide and methanethiol, and neuroactive compounds such as tryptamine, serotonin, phenethy…”
BackgroundBrain–gut–microbiota axis in depression: A historical overview and future directions
Chang, L., Wei, Y., & Hashimoto, K. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.02.004 · Cited by 395 · see citing works
Immune regulation by microbiome metabolites
Kim, C. H. (2018) · Immunology · doi:10.1111/imm.12930 · Cited by 375 · see citing works
Gut–organ axis: a microbial outreach and networking
Ahlawat, S., Asha, A., & Sharma, K. K. (2020) · Letters in Applied Microbiology · doi:10.1111/lam.13333 · Cited by 363 · see citing works
Gut Microbiome Dysbiosis and Immunometabolism: New Frontiers for Treatment of Metabolic Diseases
Belizário, J. E., Faintuch, J., & Garay-Malpartida, M. (2018) · Mediators of Inflammation · doi:10.1155/2018/2037838 · Cited by 341 · see citing works
Insulin resistance in obesity: an overview of fundamental alterations
Barazzoni, R., Cappellari, G. G., Ragni, M., & Nisoli, E. (2018) · Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity · doi:10.1007/s40519-018-0481-6 · Cited by 375 · see citing works
Effects of Synbiotic Supplement on Human Gut Microbiota, Body Composition and Weight Loss in Obesity
Sergeev, I. N., Aljutaily, T., Walton, G., & Huarte, E. (2020) · Nutrients · doi:10.3390/nu12010222 · Cited by 331 · see citing works
Inflammation in Renal Diseases: New and Old Players
Andrade‐Oliveira, V., Foresto‐Neto, O., Watanabe, I. K. M., Zatz, R., & Câmara, N. O. S. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01192 · Cited by 330 · see citing works
Glutamatergic Signaling Along The Microbiota-Gut-Brain Axis
Baj, A., Moro, E., Bistoletti, M., Orlandi, V. T., Crema, F., & Giaroni, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20061482 · Cited by 330 · see citing works
Çatalkaya, G., Venema, K., Lucini, L., Rocchetti, G., Delmas, D., Daglia, M., Filippis, A. D., Xiao, H., Quiles, J. L., Xiao, J., et al. (2020) · Food Frontiers · doi:10.1002/fft2.25 · Cited by 339 · see citing works
The Microbiota–Gut–Brain Axis and Alzheimer’s Disease: Neuroinflammation Is to Blame?
Megur, A., Baltriukienė, D., Bukelskienė, V., & Burokas, A. (2020) · Nutrients · doi:10.3390/nu13010037 · Cited by 323 · see citing works
Bioactive potential of fruit and vegetable wastes
Coman, V., Teleky, B., Mitrea, L., Martău, G. A., Szabo, K., Călinoiu, L. F., & Vodnar, D. C. (2019) · Advances in food and nutrition research · doi:10.1016/bs.afnr.2019.07.001 · Cited by 328 · see citing works
Corrêa, T. A. F., Rogero, M. M., Hassimotto, N. M. A., & Lajolo, F. M. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00188 · Cited by 320 · see citing works
Microbiota, Inflammation and Colorectal Cancer
Lucas, C., Barnich, N., & Nguyen, H. T. T. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18061310 · Cited by 318 · see citing works
Pérez-Burillo, S., Molino, S., Navajas-Porras, B., Valverde-Moya, Á. J., Hinojosa-Nogueira, D., López-Maldonado, A., Pastoriza, S., & Rufián‐Henares, J. Á. (2021) · Nature Protocols · doi:10.1038/s41596-021-00537-x · Cited by 314 · see citing works
Cholesterol Metabolism by Uncultured Human Gut Bacteria Influences Host Cholesterol Level
Kenny, D. J., Plichta, D. R., Shungin, D., Koppel, N., Hall, A. B., Fu, B., Vasan, R. S., Shaw, S. Y., Vlamakis, H. C., Balskus, E. P., et al. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.05.013 · Cited by 311 · see citing works
Oral microbial biofilms: an update
Mosaddad, S. A., Tahmasebi, E., Yazdanian, A., Rezvani, M. B., Seifalian, A. M., Yazdanıan, M., & Tebyanian, H. (2019) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-019-03641-9 · Cited by 306 · see citing works
Human gut microbiome aging clock based on taxonomic profiling and deep learning
Galkin, F., Mamoshina, P., Aliper, A., Lane, E., Moskalev, V., Gladyshev, V. N., & Zhavoronkov, A. (2020) · iScience · doi:10.1016/j.isci.2020.101199 · Cited by 292 · see citing works
Dietary polyphenols to combat the metabolic diseases via altering gut microbiota
Gowd, V., Karim, N., Shishir, M. R. I., Xie, L., & Chen, W. (2019) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2019.09.005 · Cited by 294 · see citing works
Intestinal mucus and their glycans: A habitat for thriving microbiota
Luis, A. S., & Hansson, G. C. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2023.05.026 · Cited by 290 · see citing works
Pirsaheb, M., Hossini, H., & Makhdoumi, P. (2020) · Process Safety and Environmental Protection · doi:10.1016/j.psep.2020.05.050 · Cited by 276 · see citing works
Gut microbiota of aquatic organisms: A key endpoint for ecotoxicological studies
Evariste, L., Barret, M., Mottier, A., Mouchet, F., Gauthier, L., & Pinelli, É. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.02.101 · Cited by 262 · see citing works
Ketogenic Diet and Microbiota: Friends or Enemies?
Paoli, A., Mancin, L., Bianco, A., Thomas, E., Mota, J. F., & Piccini, F. (2019) · Genes · doi:10.3390/genes10070534 · Cited by 265 · see citing works
Effectiveness of probiotics, prebiotics, and prebiotic‐like components in common functional foods
Peng, M., Tabashsum, Z., Anderson, M., Truong, A., Houser, A., Padilla, J., Akmel, A., Bhatti, J., Rahaman, S. O., & Biswas, D. (2020) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12565 · Cited by 258 · see citing works
Intestinal microbiota-derived tryptophan metabolites are predictive of Ah receptor activity
Dong, F., Hao, F., Murray, I. A., Smith, P. B. W., Koo, I., Tindall, A. M., Kris‐Etherton, P. M., Gowda, K., Amin, S., Patterson, A. D., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1788899 · Cited by 252 · see citing works
Benedé-Ubieto, R., Cubero, F. J., & Nevzorova, Y. A. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2331460 · Cited by 242 · see citing works
Chakrabarti, A., Geurts, L., Hoyles, L., Iozzo, P., Kraneveld, A. D., Fata, G. L., Miani, M., Patterson, E., Pot, B., Shortt, C., et al. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-04060-w · Cited by 252 · see citing works
Plasma metabolites to profile pathways in noncommunicable disease multimorbidity
Pietzner, M., Stewart, I. D., Raffler, J., Khaw, K., Michelotti, G. A., Kastenmüller, G., Wareham, N. J., & Langenberg, C. (2021) · Nature Medicine · doi:10.1038/s41591-021-01266-0 · Cited by 238 · see citing works
Possible Side Effects of Polyphenols and Their Interactions with Medicines
Duda‐Chodak, A., & Tarko, T. (2023) · Molecules · doi:10.3390/molecules28062536 · Cited by 244 · see citing works
Impact of Fecal Microbiota Transplantation on Obesity and Metabolic Syndrome—A Systematic Review
Zhang, Z., Mocanu, V., Cai, C., Dang, J. T., Slater, L., Deehan, E. C., Walter, J., & Madsen, K. L. (2019) · Nutrients · doi:10.3390/nu11102291 · Cited by 235 · see citing works
Wegierska, A. E., Charitos, I. A., Topi, S., Potenza, M. A., Montagnani, M., & Santacroce, L. (2022) · Sports Medicine · doi:10.1007/s40279-022-01696-x · Cited by 239 · see citing works
Update of probiotics in human world: A nonstop source of benefactions till the end of time
Zommiti, M., Feuilloley, M. G. J., & Connil, N. (2020) · Microorganisms · doi:10.3390/microorganisms8121907 · Cited by 225 · see citing works
Bosi, A., Banfi, D., Bistoletti, M., Giaroni, C., & Baj, A. (2020) · International Journal of Tryptophan Research · doi:10.1177/1178646920928984 · Cited by 221 · see citing works
Vaiserman, A. M., Romanenko, M., Півень, Л. В., Moseiko, V., Lushchak, O. V., Kryzhanovska, N., Gurianov, V. G., & Koliada, A. K. (2020) · BMC Microbiology · doi:10.1186/s12866-020-01903-7 · Cited by 216 · see citing works
Effects of Polyphenol Intake on Metabolic Syndrome: Current Evidences from Human Trials
Chiva‐Blanch, G., & Badimón, L. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/5812401 · Cited by 211 · see citing works
Dey, P. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.104367 · Cited by 215 · see citing works
Microbial-derived metabolites as a risk factor of age-related cognitive decline and dementia
Connell, E., Le Gall, G., Pontifex, M. G., Sami, S., Cryan, J. F., Clarke, G., Müller, M., & Vauzour, D. (2022) · Molecular Neurodegeneration · doi:10.1186/s13024-022-00548-6 · Cited by 208 · see citing works
Bioactive compounds produced by probiotics in food products
Chugh, B., & Kamal‐Eldin, A. (2020) · Current Opinion in Food Science · doi:10.1016/j.cofs.2020.02.003 · Cited by 208 · see citing works
Engevik, M. A., Morra, C. N., Röth, D., Engevik, K. A., Spinler, J. K., Devaraj, S., Crawford, S. E., Estes, M. K., Kalkum, M., & Versalovic, J. A. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02305 · Cited by 206 · see citing works
Williams, B. A., Mikkelsen, D., Flanagan, B. M., & Gidley, M. J. (2019) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-019-0350-9 · Cited by 204 · see citing works
Dietary Factors Modulating Colorectal Carcinogenesis
Vernia, F., Longo, S. A., Stefanelli, G., Viscido, A., & Latella, G. (2021) · Nutrients · doi:10.3390/nu13010143 · Cited by 198 · see citing works
Arias, N., Arboleya, S., Allison, J., Kaliszewska, A., Higarza, S. G., Gueimonde, M., & Arias, J. L. (2020) · Nutrients · doi:10.3390/nu12082340 · Cited by 200 · see citing works
Macrofungi: A review of cultivation strategies, bioactivity, and application of mushrooms
Lu, H., Lou, H., Hu, J., Liu, Z., & Chen, Q. (2020) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12602 · Cited by 202 · see citing works
Stevia Leaf to Stevia Sweetener: Exploring Its Science, Benefits, and Future Potential
Samuel, P., Ayoob, K. T., Magnuson, B. A., Wölwer‐Rieck, U., Jeppesen, P. B., Rogers, P. J., Rowland, I. R., & Mathews, R. (2018) · Journal of Nutrition · doi:10.1093/jn/nxy102 · Cited by 202 · see citing works
Role of Physiology, Immunity, Microbiota, and Infectious Diseases in the Gut Health of Poultry
Wickramasuriya, S. S., Park, I., Lee, K.-W., Lee, Y., Kim, W. H., Nam, H., & Lillehoj, H. S. (2022) · Vaccines · doi:10.3390/vaccines10020172 · Cited by 189 · see citing works
Unveiling the therapeutic symphony of probiotics, prebiotics, and postbiotics in gut-immune harmony
Zhou, P., Chen, C., Patil, S., & Dong, S. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1355542 · Cited by 193 · see citing works
“This microbial activity optimizes the utilization of vitamins, minerals, and nutrients by the body (15).”
BackgroundMicrobiota and Lifestyle: A Special Focus on Diet
Redondo-Useros, N., Nova, E., González-Zancada, N., Díaz, L. E., Gómez-Martínez, S., & Marcos, A. (2020) · Nutrients · doi:10.3390/nu12061776 · Cited by 189 · see citing works
Kabir, M. T., Rahman, M. H., Shah, M., Jamiruddin, M. R., Basak, D., Al‐Harrasi, A., Bhatia, S., Ashraf, G. M., Najda, A., El-kott, A. F., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112610 · Cited by 184 · see citing works
Chavda, V. P., Patel, A., Mistry, K. J., Suthar, S. F., Wu, Z., Chen, Z., & Hou, K. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.867655 · Cited by 190 · see citing works
Kong, H. G., Kim, H. H., Chung, J.-H., Jun, J., Lee, S., Kim, H., Jeon, S., Park, S. G., Bhak, J., & Ryu, C. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.02.018 · Cited by 181 · see citing works
Postbiotics: From emerging concept to application
Aggarwal, S., Sabharwal, V., Kaushik, P., Joshi, A., Aayushi, A., & Suri, M. (2022) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2022.887642 · Cited by 181 · see citing works
Nutraceutical Value of Citrus Flavanones and Their Implications in Cardiovascular Disease
Testai, L., & Calderone, V. (2017) · Nutrients · doi:10.3390/nu9050502 · Cited by 179 · see citing works
Cowan, C. S. M., Dinan, T. G., & Cryan, J. F. (2020) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.13156 · Cited by 176 · see citing works
Liu, C., Du, P., Cheng, Y., Guo, Y., Hu, B., Yao, W., Zhu, X., & Qian, H. (2021) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.117571 · Cited by 178 · see citing works
Postbiotics as potential new therapeutic agents for metabolic disorders management
Bourebaba, Y., Marycz, K., Mularczyk, M., & Bourebaba, L. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113138 · Cited by 185 · see citing works
Felizardo, R. J. F., Watanabe, I. K. M., Dardi, P., Rossoni, L. V., & Câmara, N. O. S. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.01.019 · Cited by 176 · see citing works
Nutritional Status and the Influence of the Vegan Diet on the Gut Microbiota and Human Health
Sakkas, H., Bozidis, P., Touzios, C., Kolios, D., Αθανασίου, Γ., Athanasopoulou, E., Gerou, I., & Gartzonika, C. (2020) · Medicina · doi:10.3390/medicina56020088 · Cited by 175 · see citing works
Disturbances of the Gut Microbiota and Microbiota-Derived Metabolites in Inflammatory Bowel Disease
Hu, Y., Chen, Z., Xu, C., Kan, S., & Chen, D. (2022) · Nutrients · doi:10.3390/nu14235140 · Cited by 175 · see citing works
The Preterm Gut Microbiota: An Inconspicuous Challenge in Nutritional Neonatal Care
Henderickx, J. G. E., Zwittink, R. D., van Lingen, R. A., Knol, J., & Belzer, C. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00085 · Cited by 173 · see citing works
Mapping Interactions of Microbial Metabolites with Human G-Protein-Coupled Receptors
Colosimo, D. A., Kohn, J. A., Luo, P. M., Piscotta, F. J., Han, S. M., Pickard, A. J., Rao, A., Cross, J. R., Cohen, L. J., & Brady, S. F. (2019) · Cell Host & Microbe · doi:10.1016/j.chom.2019.07.002 · Cited by 173 · see citing works
The Impact of Plant Phytochemicals on the Gut Microbiota of Humans for a Balanced Life
Santhiravel, S., Bekhit, A. E. A., Mendis, E., Jacobs, J. L., Dunshea, F. R., Rajapakse, N., & Ponnampalam, E. N. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158124 · Cited by 171 · see citing works
Plant Prebiotics and Their Role in the Amelioration of Diseases
Kaur, A. P., Bhardwaj, S., Dhanjal, D. S., Nepovimová, E., Martins, N. A., Kuča, K., Chopra, C., Singh, R., Kumar, H., Şen, F., et al. (2021) · Biomolecules · doi:10.3390/biom11030440 · Cited by 169 · see citing works
How Diet and Physical Activity Modulate Gut Microbiota: Evidence, and Perspectives
Campaniello, D., Corbo, M. R., Sinigaglia, M., Speranza, B., Racioppo, A., Altieri, C., & Bevilacqua, A. (2022) · Nutrients · doi:10.3390/nu14122456 · Cited by 168 · see citing works
Promising bioactivities of postbiotics: A comprehensive review
Rafique, N., Jan, S. Y., Dar, A. H., Dash, K. K., Sarkar, A., Shams, R., Pandey, V. K., Khan, S. A., Amin, Q. A., & Hussain, S. Z. (2023) · Journal of Agriculture and Food Research · doi:10.1016/j.jafr.2023.100708 · Cited by 168 · see citing works
Hydrogen cross-feeders of the human gastrointestinal tract
Smith, N. W., Shorten, P. R., Altermann, E., Roy, N. C., & McNabb, W. C. (2018) · Gut Microbes · doi:10.1080/19490976.2018.1546522 · Cited by 165 · see citing works
Health promoting microbial metabolites produced by gut microbiota after prebiotics metabolism
Peredo-Lovillo, A. G., Romero‐Luna, H. E., & Jiménez‐Fernández, M. (2020) · Food Research International · doi:10.1016/j.foodres.2020.109473 · Cited by 168 · see citing works
Postbiotic production: harnessing the power of microbial metabolites for health applications
Prajapati, N., Patel, J., Singh, S., Yadav, V. K., Joshi, C., Patani, A., Prajapati, D., Sahoo, D. K., & Patel, A. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1306192 · Cited by 167 · see citing works
Association between gut microbiota and bone health: Potential mechanisms and prospective
Chen, Y.-C., Greenbaum, J., Shen, H., & Deng, H.-W. (2017) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-00513 · Cited by 165 · see citing works
Influence of Maternal Milk on the Neonatal Intestinal Microbiome
Gopalakrishna, K. P., & Hand, T. W. (2020) · Nutrients · doi:10.3390/nu12030823 · Cited by 166 · see citing works
Lucas, L. N., Barrett, K., Kerby, R. L., Zhang, Q., Cattaneo, L. E., Stevenson, D., Rey, F. E., & Amador-Noguez, D. (2021) · mSystems · doi:10.1128/msystems.00805-21 · Cited by 168 · see citing works
Cross-Domain and Viral Interactions in the Microbiome
Rowan-Nash, A. D., Korry, B. J., Mylonakis, E. E., & Belenky, P. A. (2019) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00044-18 · Cited by 164 · see citing works
Dual role of microbiota-derived short-chain fatty acids on host and pathogen
Mirzaei, R., Dehkhodaie, E., Bouzari, B., Rahimi, M., Gholestani, A., Hosseini‐Fard, S. R., Keyvani, H., Teimoori, A., & Karampoor, S. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112352 · Cited by 165 · see citing works
Kandpal, M., Indari, O., Baral, B., Jakhmola, S., Tiwari, D., Bhandari, V., Pandey, R. K., Bala, K., Sonawane, A., & Jha, H. C. (2022) · Metabolites · doi:10.3390/metabo12111064 · Cited by 172 · see citing works
Role of dietary fiber in promoting immune health—An EAACI position paper
Venter, C., Meyer, R. W., Greenhawt, M., Pali‐Schöll, I., Nwaru, B. I., Roduit, C., Untersmayr, E., Adel‐Patient, K., Agache, I. O., Agostoni, C. V., et al. (2022) · Allergy · doi:10.1111/all.15430 · Cited by 161 · see citing works
Barone, M., D’Amico, F., Brigidi, P., & Turroni, S. (2022) · BioFactors · doi:10.1002/biof.1835 · Cited by 161 · see citing works
Kim, I.-S., Kim, C., & Yang, W. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084054 · Cited by 170 · see citing works
- Authors
- Rowland, I., Gibson, G., Heinken, A., Scott, K., Swann, J., Thiele, I., & Tuohy, K.
- Affiliations
- University of Reading (GB)
- University of Luxembourg (LU)
- University of Aberdeen (GB)
- Imperial College London (GB)
- Fondazione Edmund Mach (IT)
- Corresponding author
- Rowland, Ian
- Venue
- European Journal of Nutrition
- Published
- 2017-04-09
- Volume
- 57
- Issue
- 1
- Pages
- 1-24
- ISSN
- 1436-6207 (ISSN-L)
- 1436-6215
- PMC
- PMC5847071
- OpenAlex
- W2604323123
- Cited by
- 2,878
- References
- 166
- Citations by year
- 2026: 317 · 2025: 393 · 2024: 431 · 2023: 382 · 2022: 424 · 2021: 365 · 2020: 305 · 2019: 173 · 2018: 65 · 2017: 17 · 2016: 1
- FWCI
- 14.34
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- European Journal of Nutrition (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- CentAUR (University of Reading) (acceptedVersion, other-oa)
- ePrints Soton (University of Southampton) (acceptedVersion)
- Aberdeen University Research Archive (Aberdeen University) (submittedVersion, other-oa)
- CINECA IRIS Institutional Research Information System (Fondazione Edmund Mach) (submittedVersion, cc-by)
- Open Repository and Bibliography (University of Luxembourg) (submittedVersion, cc-by-nc-sa)
- Spiral (Imperial College London) (submittedVersion, cc-by)
- Funders
- International Life Sciences Institute Europe
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
- Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
- Keywords
- gut microbiota, host-microbe interactions, nutrient metabolism, dietary carbohydrates, short-chain fatty acids, protein metabolism, plant polyphenols, bile acids, vitamin metabolism, microbial metabolic pathways, enzyme activity assay
- MeSH terms
- Gastrointestinal Microbiome, Bacteria, Bile Acids and Salts, Diet, Dietary Carbohydrates, Dietary Proteins, Fatty Acids, Food, Health Promotion, Humans, Models, Theoretical, Plants, Edible, Vitamins, Proteomics, Metagenomics, Polyphenols, Phytochemicals
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