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High temporal and inter‐individual variation detected in the human ileal microbiota
Open accessAbstract
Summary: The diversity and temporal stability of the predominant bacteria in the human ileum was studied with the use of ileal effluent samples of seven individuals with Brooke ileostomies. The total number of bacteria within the ileal effluent was in the range of 10 7 –10 8 bacteria per gram (wet weight). The diversity of the bacteria in the ileal effluent showed marked differences compared with that in faecal samples from age‐matched healthy adults. The ileal effluent had a higher relative abundance of species within the orders Lactobacillales and Clostridiales , mainly Streptococcus bovis ‐related species, and the Veillonella group, and a lower proportion of species related to Ruminococcus gnavus , R. obeum and Bacteroides plebeius . In addition, inter‐individual differences were found, indicative of a highly personal ileal microbiota profile. Furthermore, temporal profiles showed large fluctuations per individual over a period of 9–28 days (average similarity over a period of 9 days was as low as 44%), and differences between morning and afternoon profiles were observed. Parallel cloning and sequencing efforts revealed several phylotypes that were not identified in previous studies (12 out of 65 phylotypes showed less than 97% sequence similarity with previously reported sequences). Achaea were found to be below detection limit by quantitative PCR. Overall, the results indicate that the microbiota of the human ileum is relatively unstable, less complex and consisting of different dominating phylotypes when compared with the colonic microbiota.
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BackgroundThe role of the gut microbiome in gastrointestinal cancers
Mishra, Y., Ranjan, A., Mishra, V. K., Chattaraj, A., Aljabali, A. A. A., El‐Tanani, M., Hromić‐Jahjefendić, A., Uversky, V. N., & Tambuwala, M. M. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.111013 · Cited by 28
Deyaert, S., Moens, F., Pirovano, W., van den Bogert, B., Klaassens, E. S., Marzorati, M., de Wiele, T. V., Kleerebezem, M., & den Abbeele, P. V. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1054061 · Cited by 27
“Enrichment of these genera is in line with literature regarding microbial composition of ileostomy effluent which has often been used as a proxy for investigating the ileal community (Collado et al., 2007; Booijink et al., 2010; van den Bogert et al., 2011, 2013; Zoetendal et al., 2012; Dlugosz et al., 2015; El Aidy e…”
BackgroundResultInfluentialSelf-citationDjurić, Z., Bassis, C. M., Plegue, M. A., Sen, A., Turgeon, D. K., Herman, K., Young, V. B., Brenner, D. E., & Ruffin, M. T. (2019) · Journal of Nutrition · doi:10.1093/jn/nxy255 · Cited by 25
“The intestinal microbiota, however, do differ along the length of the intestine (37, 38).”
BackgroundThe cultivable microbiota of the human distal ileum
Villmones, H. C., Halland, A., Stenstad, T., Ulvestad, E., Weedon‐Fekjær, H., & Kommedal, Ø. (2020) · Clinical Microbiology and Infection · doi:10.1016/j.cmi.2020.08.021 · Cited by 22
van Trijp, M. P. H., Ríos-Morales, M., Witteman, B. J. M., Abegaz, F., Gerding, A., An, R., Koehorst, M., Evers, B., van Dongen, K. C. W., Zoetendal, E. G., et al. (2024) · iScience · doi:10.1016/j.isci.2024.109208 · Cited by 24
Self-citationSpatio-temporal dynamics of the human small intestinal microbiome and its response to a synbiotic
An, R., Wilms, E., Gerritsen, J., Kim, H. K., Segui‐Perez, C., der Vaart, I. B.-V., Jonkers, D. M. A. E., Rijkers, G. T., de Vos, W. M., Masclee, A., et al. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2350173 · Cited by 23
“11,12,16,42 Consistent with earlier studies, 2 the spatial and physiological differences between upper, mid and lower regions of the small intestine and feces, were reflected in their microbial and metabolomic composition.”
BackgroundSelf-citationKaindi, D. W. M., Kogi‐Makau, W., Lule, G. N., Kreikemeyer, B., Renault, P., Bonfoh, B., Otaru, N., Schmid, T., Meile, L., Hattendorf, J., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-27383-4 · Cited by 21
“However, profile-based analysis indicated the formation of a possible dairy CC-37 together with the Sgm type strain while EAH Sgm and PV1(1) represented singletons, suggesting possible diverging human and dairy lineages as for Sii but on a more global scale.”
BackgroundResultInfluentialImmunostimulation in the treatment for chronic fatigue syndrome/myalgic encephalomyelitis
Proal, A. D., Albert, P. J., Marshall, T. G., Blaney, G. P., & Lindseth, I. A. (2013) · Immunologic Research · doi:10.1007/s12026-013-8413-z · Cited by 20
Novel Strategies for Applied Metagenomics
Moore-Connors, J., Dunn, K. A., Bielawski, J. P., & Limbergen, J. V. (2016) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000717 · Cited by 24
Byrne, C., Preston, T., Brignardello, J., García‐Pérez, I., Holmes, E. C., Frost, G. S., & Morrison, D. J. (2018) · Journal of Breath Research · doi:10.1088/1752-7163/aad3f1 · Cited by 20
Itano, A. A., Maslin, D., Ramani, K., Mehraei, G., Carpenter, N., Cormack, T. A., Saghari, M., Moerland, M., Troy, E. B., Caffry, W., et al. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1070433 · Cited by 19
“We describe broad and potent anti-inflammatory effects of EDP1815 in preclinical studies which capture Th1, Th2 and Th17 biology and in three corresponding clinical studies that determined the safety and efficacy of EDP1815 in, (1) a T cell-mediated skin challenge model in healthy volunteers; (2) patients with atopic…”
Backgroundde Veen, H. V. B., Smelt, M. J., Wels, M., van Hijum, S. A. F. T., de Vos, P., Kleerebezem, M., & Bron, P. A. (2013) · Biotechnology Journal · doi:10.1002/biot.201200259 · Cited by 19
“This mechanism seems especially feasible in the small intestine, because this region of the GI tract contains a relatively large amount of the immunomodulatory capacity of the body, while the population size of the endogenous microbiota is relatively small, allowing transient dominance of dietary microorganisms, inclu…”
BackgroundSelf-citationStability of saliva microbiota during moderate consumption of red wine
Barroso, E., Martín, V., Martínez‐Cuesta, M. C., Peláez, C., & Requena, T. (2015) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2015.09.015 · Cited by 18
How stable is the human gut microbiota? And why this question matters
Brüssow, H. (2016) · Environmental Microbiology · doi:10.1111/1462-2920.13473 · Cited by 19
Salas‐Leiva, J. S., Mazón‐Suástegui, J. M., Teles, A., & Tovar‐Ramírez, D. (2020) · Molecular Biology Reports · doi:10.1007/s11033-020-05970-x · Cited by 19
“Amino acid fermenting bacteria, which belonged to Clostridium, Bacillus, Lactobacillus, Streptococcus and Proteobacteria groups commonly reported in humans [75], were found in S.”
BackgroundImpact of the ileal microbiota on colon cancer
Roberti, M. P., Rauber, C., Kroemer, G., & Zitvogel, L. (2021) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2021.09.016 · Cited by 18
Tutorial: Microbiome studies in drug metabolism
Dodd, D., & Cann, I. (2022) · Clinical and Translational Science · doi:10.1111/cts.13416 · Cited by 17
Pantophlet, A. J., Wopereis, S., Eelderink, C., Vonk, R. J., Stroeve, J. H. M., Bijlsma, S., van Stee, L., Bobeldijk, I., & Priebe, M. G. (2016) · Journal of Nutrition · doi:10.3945/jn.116.237404 · Cited by 17
“These GH families were associated with the Bacteroidales group (36), which was also identified to be present in the human small intestine in other studies (33, 35, 38, 39).”
BackgroundEfficacy of Probiotics in Prevention and Treatment of Infectious Diseases
Rostami, F., Mousavi, H., Mousavi, M. R. N., & Shahsafi, M. (2018) · Clinical Microbiology Newsletter · doi:10.1016/j.clinmicnews.2018.06.001 · Cited by 16
Composition and Function of the Gut Microbiome
Blaut, M. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_2 · Cited by 20
What happened to K och's postulates in diarrhoea?
Sultana, S., Sarker, S. A., & Brüssow, H. (2017) · Environmental Microbiology · doi:10.1111/1462-2920.13787 · Cited by 19
Singh, S. B., Meena, A. K., Sisodia, B. S., Sharma, S., Sharma, M., & Mansoria, P. (2023) · Journal of Drug Research in Ayurvedic Sciences · doi:10.4103/jdras.jdras_192_23 · Cited by 15
Coenzyme A metabolism: a key driver of gut microbiota dynamics and metabolic profiles
Böttcher, J., Sibon, O. C. M., & Aidy, S. E. (2025) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaf051 · Cited by 15
“While the small intestine is consistently inhabited by Streptococcus and Veillonella , which belong to the Bacillota phyla, the abundance of Clostridium and Escherichia can vary (Booijink et al. 2010 , El Aidy et al. 2015 ).”
Vitetta, L., Hall, S., & Linnane, A. W. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2014.00143 · Cited by 15
Metabolomics and metagenomics in mice reveal the role of the gut microbiota in tryptophan metabolism
Levé, M., Manghi, P., Bredon, M., Lefèvre, A., Manara, S., Armanini, F., Emond, P., Planchais, J., Rolhion, N., Segata, N., et al. (2025) · iScience · doi:10.1016/j.isci.2025.113751 · Cited by 16
Intestinal stem cells and gut microbiota therapeutics: hype or hope?
Sophien, A. N. A., Jusop, A. S., Tye, G. J., Tan, Y.-F., Zaman, W. S. W. K., & Nordin, F. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1195374 · Cited by 14
“Thereby, a study has revealed that facultative anaerobes such as gram-positive lactobacilli, enterococci, and streptococci, as well as gram-negative Bacteroides and Proteobacteria, were observed through molecular analysis to populate the jejunum and ileum region (65, 66).”
BackgroundHyun, D., Lee, J., Kim, M., Shin, N.-R., Whon, T. W., Kim, K. H., Kim, P. S., Tak, E. J., Jung, M., Lee, J., et al. (2021) · The Journal of Microbiology · doi:10.1007/s12275-021-1165-x · Cited by 13
Functional Intestinal Metagenomics
van den Bogert, B., Leimena, M. M., de Vos, W. M., Zoetendal, E. G., & Kleerebezem, M. (2011) · doi:10.1002/9781118010549.ch18 · Cited by 13
Self-citationLiu, L., Lei, S., Lin, X., Ji, J., Wang, Y., Zheng, B., Zhang, Y., & Zeng, H. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.123553 · Cited by 12
Draft Genome Sequence of Veillonella parvula HSIVP1, Isolated from the Human Small Intestine
van den Bogert, B., Boekhorst, J., Smid, E. J., Zoetendal, E. G., & Kleerebezem, M. (2013) · Genome Announcements · doi:10.1128/genomea.00977-13 · Cited by 12
Self-citation
Metadata
- Authors
- Booijink, C. C. G. M., El‐Aidy, S., Rajilić‐Stojanović, M., Heilig, H. G. H. J., Troost, F. J., Smidt, H., Kleerebezem, M., De Vos, W. M., & Zoetendal, E. G.
- Affiliations
- TiFN (NL)
- Wageningen University & Research (NL)
- Maastricht University Medical Centre (NL)
- Corresponding author
- Zoetendal, Erwin G.
- Venue
- Environmental Microbiology
- Publisher
- Wiley
- Published
- 2010-12
- Volume
- 12
- Issue
- 12
- Pages
- 3213-3227
- ISSN
- 1462-2912 (ISSN-L)
- 1462-2920
- OpenAlex
- W2130329894
- Cited by
- 324
- References
- 52
- Citations by year
- 2026: 9 · 2025: 13 · 2024: 17 · 2023: 27 · 2022: 22 · 2021: 23 · 2020: 30 · 2019: 29 · 2018: 24 · 2017: 17 · 2016: 10 · 2015: 15 · 2014: 24 · 2013: 28 · 2012: 18
- FWCI
- 8.31
- Type
- journal article
- Language
- en
- Open access
- green
- research.wur.nl
- Locations
- Environmental Microbiology (publishedVersion)
- PubMed (publishedVersion)
- TechnoRep (University of Belgrade – Faculty of Technology and Metallurgy) (publishedVersion)
- Research Publications (Maastricht University) (publishedVersion)
- Socio-Environmental Systems Modeling (acceptedVersion)
- Research Publications (Maastricht University) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Keywords
- ileal microbiota, ileostomy, temporal stability, interindividual variability, bacterial diversity, Lactobacillales, Clostridiales, Streptococcus bovis, Veillonella, Ruminococcus, Bacteroides plebeius, Achaea, novel phylotypes, human gut bacteria
- MeSH terms
- Adult, Aged, Bacteria, Feces, Female, Humans, Ileostomy, Ileum, Male, Middle Aged, Molecular Sequence Data, Phylogeny, Time Factors, Case-Control Studies, Polymerase Chain Reaction, Genes, rRNA, Metagenome
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