Cited by 397Gut microbiota and healthMicrobial Metabolites in Food BiotechnologyFood composition and properties

The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.

Gut microbiota richness promotes its stability upon increased dietary fibre intake in healthy adults

Open access

Tap, Julien, Furet, Jean‐Pierre, Bensaada, Martine, Philippe, Catherine, Roth, Hubert, Rabot, Sylvie, Lakhdari, Omar, Lombard, Vincent, Henrissat, Bernard, Corthier, Gérard, Fontaine, Eric, Doré, Joël, Leclerc, Marion·2015·Environmental Microbiology

DOI 10.1111/1462-2920.13006

Open this paper in CoChat — free account Open PDF

Abstract

Summary: Gut microbiota richness and stability are important parameters in host–microbe symbiosis. Diet modification, notably using dietary fibres, might be a way to restore a high richness and stability in the gut microbiota. In this work, during a 6‐week nutritional trial, 19 healthy adults consumed a basal diet supplemented with 10 or 40 g dietary fibre per day for 5 days, followed by 15‐day washout periods. Fecal samples were analysed by a combination of 16S r RNA gene pyrosequencing, intestinal cell genotoxicity assay, metatranscriptomics sequencing approach and short‐chain fatty analysis. This short‐term change in the dietary fibre level did not have the same impact for all individuals but remained significant within each individual gut microbiota at genus level. Higher microbiota richness was associated with higher microbiota stability upon increased dietary fibre intake. Increasing fibre modulated the expression of numerous microbiota metabolic pathways such as glycan metabolism, with genes encoding carbohydrate‐active enzymes active on fibre or host glycans. High microbial richness was also associated with high proportions of Prevotella and Coprococcus species and high levels of caproate and valerate. This study provides new insights on the role of gut microbial richness in healthy adults upon dietary changes and host microbes' interaction

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

Crossref · 10.1111/1462-2920.13006

Cites

51 of 51 references verified0 citation errors · 0 not checkable

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
Altschul, S. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.17.3389 · Cited by 73,302
A human gut microbial gene catalogue established by metagenomic sequencing
MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624
Self-citation
Diet rapidly and reproducibly alters the human gut microbiome
David, L. A., Maurice, C. F., Carmody, R. N., Gootenberg, D. B., Button, J. E., Wolfe, B. E., Ling, A. V., Devlin, A. S., Varma, Y., Fischbach, M. A., et al. (2014) · Nature · doi:10.1038/nature12820 · Cited by 10,100
Dietary Modulation of the Human Colonic Microbiota: Introducing the Concept of Prebiotics
Gibson, G. R., & Roberfroid, M. B. (1995) · Journal of Nutrition · doi:10.1093/jn/125.6.1401 · Cited by 7,659
Enterotypes of the human gut microbiome
MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548
Self-citation
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
Obesity alters gut microbial ecology
Ley, R. E., Bäckhed, F., Turnbaugh, P., Lozupone, C. A., Knight, R. D., & Gordon, J. I. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504978102 · Cited by 6,176
The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics
Cantarel, B. L., Coutinho, P. M., Rancurel, C., Bernard, T., Lombard, V., & Henrissat, B. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn663 · Cited by 6,108
Self-citation
Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa
De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579
CAP3: A DNA Sequence Assembly Program
Huang, X., & Madan, A. (1999) · Genome Research · doi:10.1101/gr.9.9.868 · Cited by 5,261

Show all 51 references

Sorted by citations

Items 301–396 of 396

Consumption of steam explosion and fermentation-pretreated corn stover affects the growth performance of sheep by shifting the rumen microbiota community structure
Wang, Y., Yin, X., Hao, K., Wang, C., Wei, W., Li, Y., Gao, S., Ji, Z., Wang, W., Xie, Y., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1532746 · Cited by 2
Determining the level of knowledge and consumption of probiotics and prebiotics among athletes in Jordan
Al-Maseimi, O. D., Ahmad, L., Elsahoryi, N. A., & Al-Maaitah, L. (2025) · Journal of Nutritional Science · doi:10.1017/jns.2025.10013 · Cited by 2
From the Laboratory to the Plate: How Gut Microbiome Science Is Reshaping Our Diet
Hiol, A. N., & Veiga, P. (2025) · Journal of Nutrition · doi:10.1016/j.tjnut.2025.08.032 · Cited by 4
Gut microbiome plasticity explains the altitudinal distribution pattern and adaptability in a small mammal species ( Apodemus draco )
Yun, Y., Duan, C. W., He, X., Tang, R., Lan, Y., Lu, M., Liu, T., Fan, X., Fan, Z., & Ran, J. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.02388-25 · Cited by 2
The Role of Diet and Physical Activity in Gut Microbiota Modulation in Type 2 Diabetes Management: A Systematic Review of Clinical Trials
Soares, R. D. C. S., Cândido, F. G., Fraiz, G. M., Alfenas, R. D. C. G., & Bressan, J. (2025) · Nutrition Reviews · doi:10.1093/nutrit/nuaf270 · Cited by 2
Fluoroscopic control of a magnetorobotic capsule for precision gastrointestinal sampling and delivery
Nguyen, S., Le, T. A., Guven, M. N., Lu, C., Alabay, H. H., & Ceylan, H. (2026) · iScience · doi:10.1016/j.isci.2026.115007 · Cited by 2
Impact of polyphenols on human gut microbiome and associated biomarkers
Costa, E. M., & Silva, S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85273-9.00005-3 · Cited by 2
The Microbiome, Metabolism, and Networks in Precision Nutrition
Mensah, G. E., Maseng, M. G., Allard, S., & Gilbert, J. A. (2024) · Precision Nutrition · doi:10.1016/b978-0-443-15315-0.00011-0 · Cited by 2
Nutrition in Cycling
Brooke, N. K., & Cosío-Lima, L. (2021) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2021.08.011 · Cited by 3
Food-gut microbiota interactions
Berding, K., Kaulmann, D., & Cryan, J. F. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85170-1.00011-7 · Cited by 2
Identifying the Role of Vasopressin and Oxytocin in the Microbiota-Gut-Brain-Behavior Axis
Peters, N. V. (2022) · Digital Archive @ GSU · doi:10.57709/14972899 · Cited by 2
The effect of various fiber types on the growth, digestibility and chemical elements exchange in broiler body
Grechkina, V. V., Lebedev, S. V., Ushakov, A. S., & Petrusha, Y. K. (2021) · Животноводство и кормопроизводство · doi:10.33284/2658-3135-104-4-136 · Cited by 2
Phylogenetic diversity analysis of shotgun metagenomic reads describes gut microbiome development and treatment effects in the post-weaned pigPreprint
Gaio, D., DeMaere, M. Z., Anantanawat, K., Eamens, G. J., Zingali, T., Falconer, L., Chapman, T. A., Djordjevic, S. P., & Darling, A. E. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.20.211326 · Cited by 2
Equibiotic-GI Consumption Improves Intestinal Microbiota in Subjects with Functional Dyspepsia
Palacios‐González, B., Meraz‐Cruz, N., Valdez-Palomares, F., & Nambo‐Venegas, R. (2019) · Current Drug Therapy · doi:10.2174/1574885514666190212114412 · Cited by 2
Effect of Artificial Sweetener Aspartame on Gut Microbiota - A Narrative Review
Sandhu, P. K. (2021) · International Journal for Research in Applied Science and Engineering Technology · doi:10.22214/ijraset.2021.37053 · Cited by 1
Maternal supplementation of functional fiber improves reproduction performance by modulating gut microbiota during pregnancy
Yin, S., Cheng, J., Wang, M., Zhou, Y., Wei, H., Jiang, S., & Peng, J. (2026) · Frontiers in Microbiology · doi:10.3389/fmicb.2026.1758091 · Cited by 1
Prebiotics Enhance Microbiome Recovery Following Antibiotic-Induced Dysbiosis
Ramkissoon, P., Ducasse, A., Berman, I., Sadanaga, J., O’Neill, I., & Gondek, D. C. (2026) · Microorganisms · doi:10.3390/microorganisms14051079 · Cited by 1
Resistant starch selectively depletes a putative pathobiont-enriched gut microbial module: evidence from multiple dietary fiber intervention cohorts
Dong, B., Ye, M., Xu, Z. Z., Huang, X., & Hu, Y. (2026) · Frontiers in Nutrition · doi:10.3389/fnut.2026.1845191 · Cited by 1
Lien entre les probiotiques et le microbiote : vision du clinicien
Joly, F., Nuzzo, A., Kapel, N., & Thomas, M. (2017) · Cahiers de Nutrition et de Diététique · doi:10.1016/s0007-9960(17)30193-1 · Cited by 1
Whole Plant Foods in Aging and Disease
Dreher, M. L. (2018) · Springer eBooks · doi:10.1007/978-3-319-59180-3_3 · Cited by 1
Prebiotic and probiotic knowledge and consumption in collegiate athletes
Kahn, H. (2021) · Cited by 1
Impact of selected nutritional components and lifestyle on human intestinal barrier function
Andrulewicz, M. (2021) · Medycyna Ogólna i Nauki o Zdrowiu · doi:10.26444/monz/139615 · Cited by 1
Gut Microbiota in Elderly’s Health
Bäuerl, C., Selma‐Royo, M., Mera-Balseca, A. G., Collado, M. C., & Pérez‐Martínez, G. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_163 · Cited by 1
Techniques for Studying the Microbiome
Zain, M., Saba, S., Hussain, A., Khalid, J., Janiad, S., Mahmood, S., & Cheema, M. T. (2024) · Springer eBooks · doi:10.1007/978-981-97-3790-1_3 · Cited by 1
Ecosystemic Approach to Understanding Gut Microbiome–Mediated Prevention of Colorectal Cancer
Lutsiv, T., Hussan, H., & Thompson, H. J. (2024) · The Cancer Journal · doi:10.1097/ppo.0000000000000743 · Cited by 2
Adaptive characteristics of the gut microbiota of the scaly-sided merganser (Mergus squamatus) in energy compensation at different developmental stages
Yu, Y., Wang, J., Shi, L., Sun, H., Cheng, B., & Sun, Y. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1614319 · Cited by 1
Gut Microbiota in Elderly’s Health
Bäuerl, C., Selma‐Royo, M., Mera-Balseca, A. G., Collado, M. C., & Pérez‐Martínez, G. (2017) · Springer eBooks · doi:10.1007/978-3-319-64597-1_163-1 · Cited by 1
Fiber-Rich Dietary Patterns and Colonic Microbiota in Aging and Disease
Dreher, M. L. (2018) · Springer eBooks · doi:10.1007/978-3-319-59180-3_4 · Cited by 1
Status of edible insects as an alternative source of food in Iran: A review
Talaei, B., Alizadeh, I., Afshar, A. A., Seyedi, F., & Gorouhi, M. A. (2022) · Journal of Entomological Research · doi:10.5958/0974-4576.2022.00075.5 · Cited by 1
Cohort Specific Effects of Cereal-bar Supplementation in Overweight Patients With or Without Type 2 Diabetes MellitusPreprint
Chou, C. J., Lauber, C., Chakrabarti, A., Siddharth, J., Chalut-Carpentier, A., Pataky, Z., Golay, A., & Parkinson, S. J. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/066704 · Cited by 1
The Role of Fibers and Bioactive Compounds in Gut Microbiota Composition and Health
Graham, É. A., Mallet, J., Jambi, M., Alsadi, N., & Matar, C. (2016) · Wiley eBooks · doi:10.1002/9781119138105.ch8 · Cited by 1
The role of hydrogenotrophic microbiota in the human gut
Wang, T. (2022) · doi:10.18174/569022 · Cited by 1
Effects of different foods and cooking methods on the gut microbiota: an in vitro approachPreprint
Lerma-Aguilera, A. M., Pérez-Burillo, S., Navajas-Porras, B., León, E. D., Ruiz, S. S., Pastoriza, S., Jiménez‐Hernández, N., Cämmerer, B., Rufián‐Henares, J. Á., Gosalbes, M. J., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-2405776/v1 · Cited by 1
The influence of the gut microbiota on influenza vaccine-induced immunity
Mooney, A. (2018) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17131847.v1
DYNAMICS OF THE GUT VIROME AND BACTERIAL MICROBIOME IN PEDIATRIC CROHN’S DISEASE PATIENTS
Jones, C. M. A. (2018) · DalSpace (Dalhousie University)
Diet and the microbiome in precision medicine
Toribio-Mateas, M. A., & Bester, A. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-819178-1.00043-5
Peer Review #3 of "Systematic evaluation of the gut microbiome of swamp eel (Monopterus albus) by 16S rRNA gene sequencing (v0.1)"
(2019) · PeerJ · doi:10.7287/peerj.8176v0.1/reviews/3
Peer Review #2 of "Systematic evaluation of the gut microbiome of swamp eel (Monopterus albus) by 16S rRNA gene sequencing (v0.1)"
(2019) · PeerJ · doi:10.7287/peerj.8176v0.1/reviews/2
Microbiome Diversity and Differential Abundances Associated with BMI, Immune Markers, and Fecal Short Chain Fatty Acids Before and After Synbiotic Supplementation
Sterrett, J. D., Clark, W. A., & Chandley, M. (2020) · Digital Commons - East Tennessee State University (East Tennessee State University)
Gut microbiome composition predicts summer core range size in a generalist and specialist ungulatePreprint
Wolf, J. F., Kriss, K. D., MacAulay, K. M., Munro, K., Patterson, B. R., & Shafer, A. B. A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.04.236638
Dietary changes and lifestyle shifts affect the gut microbiomes of giant pandasPreprint
Jin, L., Yang, S., Li, C., Wu, D., He, Y., Li, B., Zhang, G., Xiong, Y., Wei, R., Guo, L., et al. (2020) · doi:10.22541/au.158505225.57347715
High fiber, whole foods dietary intervention alters the human gut microbiome but not fecal short-chain fatty acidsPreprint
Oliver, A. S., Chase, A. B., Weihe, C., Orchanian, S. B., Riedel, S. F., Hendrickson, C. L., Lay, M., Sewall, J. M., Martiny, J. B. H., & Whiteson, K. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.04.429869
Excitation of the 4 1 S Level of Helium by Hydrogen Impact
Crothers, D. S. F. (1968)
軌道対称性の保存 : ウッドワード・ホフマン則
Woodward, R. B., Hoffmann, R., 伊東, 椒., & 遠藤, 勝. (1971) · 広川書店 eBooks
Efeitos da suplementação com prebiótico inulina na produção de butirato e imunorregulação do diabetes tipo 1 em modelo experimental
Guimarães, J. B. (2021) · doi:10.11606/d.17.2021.tde-06122021-150302
Growth limitation via chemically complex carbohydrates reduces sensitivity of synthetic human gut communities to perturbationsPreprint
Loss, E. O., Thompson, J. C., Cheung, K. P., Qian, Y., & Venturelli, O. S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.08.487701
The role of diet and physical activity in influencing the microbiota/microbiome
Murphy, E. A., & Velázquez, K. T. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822130-3.00017-x
Peer Review #1 of "Systematic evaluation of the gut microbiome of swamp eel (Monopterus albus) by 16S rRNA gene sequencing (v0.2)"
(2019) · PeerJ · doi:10.7287/peerj.8176v0.2/reviews/1
Peer Review #1 of "Systematic evaluation of the gut microbiome of swamp eel (Monopterus albus) by 16S rRNA gene sequencing (v0.1)"
(2019) · PeerJ · doi:10.7287/peerj.8176v0.1/reviews/1
The interplay between diet, gastrointestinal complaints and gut microbiota: more than a gut feeling?
Rijnaarts, I. (2022) · doi:10.18174/567948
Rhizomatous Plants: Curcuma longa and Zingiber officinale in Affording Immunity
Abdelkader, N. F., & Moustafa, P. E. (2022) · Springer eBooks · doi:10.1007/978-981-16-8117-2_12
Survey of the Intestinal Bacterial Compositions of Three Sympatric Passeriformes Species
Masuda, H., Zarabadi, F. N., & Rifai, L. B. (2022) · Journal of Advances in Microbiology · doi:10.9734/jamb/2022/v22i12689
The role of diet in modulating the intestinal microbiota in healthy adults: Is the evidence enough?
Ruţă, F. D., Mardale, E., Pintea, A., & Avram, C. (2023) · Acta Marisiensis. Seria Medica · doi:10.2478/amma-2023-0025
The manifestations and interdependence of social and physiological aging in wild female Assamese macaques (Macaca assamensis)
Sadoughi, B. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10248
Developmental Immunotoxicology Testing (DIT)
Dere, E., Prell, R. A., Comstock, S. S., Holsapple, M. P., & Burns‐Naas, L. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00092-9
Effects of Pelleted and Mashed Alfalfa Supplementation on Sow and Litter Performance, Constipation and Fecal Microbiome in Sows during Gestation
Lee, J. H., Kim, J.-E., Hong, J. S., Park, H. J., Choi, Y. H., Jeong, Y. D., Back, S. H., Jung, J. S., & Sa, S. J. (2025) · Han-guk choji josaryo hakoeji · doi:10.5333/kgfs.2025.45.2.89
Effects of dietary Vitamin A on growth performance, antioxidant and immune capacity of mandarin fish (Siniperca chuatsi)
Yan, X., Pan, L., Zhao, M., Ma, J., Wang, F., Zhai, X., Xue, Y., Liu, H., Chen, Y., He, Y., et al. (2025) · Aquaculture Reports · doi:10.1016/j.aqrep.2025.103039
Ernährung
Camirand, N. (2025) · Elsevier eBooks · doi:10.1016/b978-3-437-55312-7.00018-9
Ecologically robust gut environment associated with personalized metabolic responses in a Japanese cohort
Ishii, C., Suzuki, M., Murakami, S., Song, I., Soejima, Y., Kato, M., & Fukuda, S. (2025) · Gut microbes reports · doi:10.1080/29933935.2025.2574930 · Cited by 1
Additional file 3 of Altitude influences microbial diversity and herbage fermentation in the rumen of yaks
Fan, Q., Wanapat, M., Yan, T., & Hou, F. (2020) · Figshare · doi:10.6084/m9.figshare.13336453
Additional file 16 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053585
Additional file 2 of Metatranscriptomic analysis of colonic microbiota’s functional response to different dietary fibers in growing pigs
Xu, J., Xu, R., Jia, M., Su, Y., & Zhu, W. (2021) · Figshare · doi:10.6084/m9.figshare.14906052
Additional file 8 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053612
Additional file 10 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053567
Additional file 13 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053576
Additional file 2 of Aging gut microbiota of wild macaques are equally diverse, less stable, but progressively personalized
Sadoughi, B., Schneider, D., Daniel, R., Schülke, O., & Ostner, J. (2022) · Figshare · doi:10.6084/m9.figshare.20099721
Additional file 4 of Metatranscriptomic analysis of colonic microbiota’s functional response to different dietary fibers in growing pigs
Xu, J., Xu, R., Jia, M., Su, Y., & Zhu, W. (2021) · Figshare · doi:10.6084/m9.figshare.14906058
Additional file 14 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053579
Additional file 1 of Metatranscriptomic analysis of colonic microbiota’s functional response to different dietary fibers in growing pigs
Xu, J., Xu, R., Jia, M., Su, Y., & Zhu, W. (2021) · Figshare · doi:10.6084/m9.figshare.14906049
Additional file 5 of Altitude influences microbial diversity and herbage fermentation in the rumen of yaks
Fan, Q., Wanapat, M., Yan, T., & Hou, F. (2020) · Figshare · doi:10.6084/m9.figshare.13336465
Additional file 17 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053588
Additional file 4 of Altitude influences microbial diversity and herbage fermentation in the rumen of yaks
Fan, Q., Wanapat, M., Yan, T., & Hou, F. (2020) · Figshare · doi:10.6084/m9.figshare.13336459
Additional file 3 of Metatranscriptomic analysis of colonic microbiota’s functional response to different dietary fibers in growing pigs
Xu, J., Xu, R., Jia, M., Su, Y., & Zhu, W. (2021) · Figshare · doi:10.6084/m9.figshare.14906055
Additional file 4 of Seasonal responses and host uniqueness of gut microbiome of Japanese macaques in lowland Yakushima
Sawada, A., Hayakawa, T., Kurihara, Y., Lee, W., & Hanya, G. (2022) · Figshare · doi:10.6084/m9.figshare.21211310
Additional file 9 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053615
Additional file 5 of Seasonal responses and host uniqueness of gut microbiome of Japanese macaques in lowland Yakushima
Sawada, A., Hayakawa, T., Kurihara, Y., Lee, W., & Hanya, G. (2022) · Figshare · doi:10.6084/m9.figshare.21211313
Additional file 1 of Altitude influences microbial diversity and herbage fermentation in the rumen of yaks
Fan, Q., Wanapat, M., Yan, T., & Hou, F. (2020) · Figshare · doi:10.6084/m9.figshare.13336441
Additional file 2 of Altitude influences microbial diversity and herbage fermentation in the rumen of yaks
Fan, Q., Wanapat, M., Yan, T., & Hou, F. (2020) · Figshare · doi:10.6084/m9.figshare.13336447
Additional file 11 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053570
Additional file 15 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053582
Additional file 2 of Seasonal responses and host uniqueness of gut microbiome of Japanese macaques in lowland Yakushima
Sawada, A., Hayakawa, T., Kurihara, Y., Lee, W., & Hanya, G. (2022) · Figshare · doi:10.6084/m9.figshare.21211304
Additional file 12 of Limited effects of long-term daily cranberry consumption on the gut microbiome in a placebo-controlled study of women with recurrent urinary tract infections
Straub, T. J., Chou, W.-C., Manson, A. L., Schreiber, H. L., Walker, B. J., Desjardins, C. A., Chapman, S. B., Kaspar, K. L., Kahsai, O. J., Traylor, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14053573
Additional file 1 of Identification of robust and generalizable biomarkers for microbiome-based stratification in lifestyle interventions
Chen, J., Siliceo, S. L., Ni, Y., Nielsen, H. B., Xu, A., & Panagiotou, G. (2024) · Figshare · doi:10.6084/m9.figshare.26609145
Gut microbiota and metabolic status during pregnancy in captive Asian elephants
Zeng, F., Zhu, T., Chen, X., Huang, K., Liu, L., Wang, G., Mai, J., & Zhang, S. (2026) · Frontiers in Veterinary Science · doi:10.3389/fvets.2026.1749490
Du laboratoire à l’assiette comment les découvertes sur le microbiote intestinal ont changé notre alimentation
Veiga, P., & Hiol, A. N. (2024) · Histoire de la recherche contemporaine · doi:10.4000/15v9o
Health benefits of dietary live microbes: A narrative review
Shen, C., Wu, J., Sun, X., Fan, B., & Xiang, X. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108725 · Cited by 1
Microbiote intestinal, cancer du sein et métabolisme lipidique
Luu, T. H. (2018) · theses.fr (ABES) · doi:10.70675/5a95efcbzc6e9z41b8z84a5z058eda043638
Interactions between prebiotics and health-relevant commensal bacteria : impact on bacterial growth and metabolic activities
Bedu-Ferrari, C. (2022) · theses.fr (ABES) · doi:10.70675/17cf5e69z9e36z4daczb0b6z93f0767b79db
Étude du rôle fonctionnel du microbiote intestinal dans l'adaptation à un régime sous optimal et dans l'efficience alimentaire de la poule pondeuse en utilisant une approche multi-omique.
Bernard, M. (2024) · theses.fr (ABES) · doi:10.70675/566f36f5z4361z4a72z83f4z6abd401a4af9
Effects of environmental setting and diet on the gut microbial ecology of eastern hellbenders (Cryptobranchus alleganiensis alleganiensis)
Cummins, C., Sutton, W. B., McLeod, T., Dallas, J. W., Ghotbi, M., Vargas‐Gastélum, L., Alexander, N. R., Rurik, A. J., McGinnity, D., Reinsch, S. D., et al. (2026) · Animal Microbiome · doi:10.1186/s42523-026-00537-w
Functional fiber supplementation improves reproductive performance in sows by reshaping gut microbial functions related to immunity and metabolic health
Yin, S., Fu, S., Cheng, J., Wang, M., Zhou, Y. Q., Wei, H., & Peng, J. (2026) · Frontiers in Veterinary Science · doi:10.3389/fvets.2026.1834008
Phenological Changes in the Fecal Microbiota of Elaphurus davidianus in Inner Mongolia Daqingshan National Nature Reserve
Liu, C., Zhang, J., Dong, Y., Ju, H., HAOREN, T., He, L., Suritu, Ma, H., Liu, J., Hu, D., et al. (2026) · Animals · doi:10.3390/ani16111698
Influence of dietary patterns on gut microbiota metabolism in patients with type 2 diabetes mellitus
Demidova, T. Y., Teplova, A. S., Чернуха, П. А., Степанова, Е. В., & Moiseeva, E. Y. (2026) · Russian Journal of Evidence-Based Gastroenterology · doi:10.17116/dokgastro20261502123
The Bile Acid–Diet–Microbiome Axis in Clostridioides difficile Infection
Trofin, F., Buzilă, E. R., Iancu, I. R., Tuchiluş, C., Temneanu, O. R., Iancu, L. S., Vlad, M. A., Anton-Păduraru, D.-T., Armașu, I., Bădescu, A. C., et al. (2026) · Nutrients · doi:10.3390/nu18172872
Способ определения растворимых пищевых волокон (степени резистентности) в продуктах биоконверсии крахмала методом высокоэффективной жидкостной хроматографии
Kuzina, L. B., Семипятный, В. К., Климова, Д. В., Косарева, А. В., Ануфриев, К. Э., & Юрьевна, С. С. (2026) · Food processing industry · doi:10.52653/ppi.2026.9.9.009
Effects of anti-aging diets and exercise on age-related musculoskeletal diseases via gut microbiota modulation
Yu, M., Guo, P., Liu, Q., & Zhang, X. (2026) · Annals of Medicine · doi:10.1080/07853890.2026.2726635

Authors: Tap, J., Furet, J., Bensaada, M., Philippe, C., Roth, H., Rabot, S., Lakhdari, O., Lombard, V., Henrissat, B., Corthier, G., Fontaine, E., Doré, J., & Leclerc, M.
Affiliations: Microbiologie de l’alimentation au service de la santé (FR)
Inserm (FR)
Centre National de la Recherche Scientifique (FR)
INRA Micalis Institute UMR1319 Jouy‐en‐Josas 78350 France
Corresponding author: Leclerc, Marion
ORCID: Tap, Julien
Philippe, Catherine
Roth, Hubert
Rabot, Sylvie
Lakhdari, Omar
Lombard, Vincent
Henrissat, Bernard
Fontaine, Eric
Leclerc, Marion
Venue: Environmental Microbiology
Publisher: Wiley
Published: 2015-09-03
Volume: 17
Issue: 12
Pages: 4954-4964
ISSN: 1462-2912 (ISSN-L)
1462-2920
DOI: 10.1111/1462-2920.13006
OpenAlex: W1790787093
Cited by: 397
References: 51
Citations by year: 2026: 14 · 2025: 33 · 2024: 34 · 2023: 28 · 2022: 62 · 2021: 53 · 2020: 54 · 2019: 46 · 2018: 24 · 2017: 26 · 2016: 21
FWCI: 10.27
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-nd
creativecommons.org/licenses/by-nc-nd/4.0/ (vor)
Locations: Environmental Microbiology (publishedVersion, cc-by-nc-nd)
PubMed (publishedVersion)
HAL (submittedVersion, cc-by-nc-nd)
Funders: French National Agency for Research (ANR/DEDD/PNRA/PROJ/200206-01-01)
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
Health Sciences › Nursing › Nutrition and Dietetics › Food composition and properties
Keywords: microbiome stability, dietary fiber, short-chain fatty acids, host-microbe symbiosis, carbohydrate-active enzymes, glycan metabolism, Prevotella, Coprococcus, caproate, valerate, metatranscriptomics, healthy adults
MeSH terms: Eubacteriales, Gastrointestinal Microbiome, Adult, Diet, Dietary Fiber, Fatty Acids, Feces, Female, Humans, Male, RNA, Ribosomal, 16S, Symbiosis, Prevotella, Dietary Supplements, Young Adult

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

Gut microbiota richness promotes its stability upon increased dietary fibre intake in healthy adults

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks