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Dysbiosis of the faecal microbiota in patients with Crohn’s disease and their unaffected relatives
Abstract
BACKGROUND AND AIMS: A general dysbiosis of the intestinal microbiota has been established in patients with Crohn's disease (CD), but a systematic characterisation of this dysbiosis is lacking. Therefore the composition of the predominant faecal microbiota of patients with CD was studied in comparison with the predominant composition in unaffected controls. Whether dysbiosis is present in relatives of patients CD was also examined. METHODS: Focusing on families with at least three members affected with CD, faecal samples of 68 patients with CD, 84 of their unaffected relatives and 55 matched controls were subjected to community fingerprinting of the predominant microbiota using denaturing gradient gel electrophoresis (DGGE). To analyse the DGGE profiles, BioNumerics software and non-parametric statistical analyses (SPSS V.17.0) were used. Observed differences in the predominant microbiota were subsequently confirmed and quantified with real-time PCR. RESULTS: Five bacterial species characterised dysbiosis in CD, namely a decrease in Dialister invisus (p=0.04), an uncharacterised species of Clostridium cluster XIVa (p = 0.03), Faecalibacterium prausnitzii (p < 1.3 × 10⁻⁵) and Bifidobacterium adolescentis (p = 5.4 × 10⁻⁶), and an increase in Ruminococcus gnavus (p = 2.1 × 10⁻⁷). Unaffected relatives of patients with CD had less Collinsella aerofaciens (p = 0.004) and a member of the Escherichia coli-Shigella group (p = 0.01) and more Ruminococcus torques (p = 0.02) in their predominant microbiota as compared with healthy subjects. CONCLUSION: Unaffected relatives of patients with CD have a different composition of their microbiota compared with healthy controls. This dysbiosis is not characterised by lack of butyrate producing-bacteria as observed in CD but suggests a role for microorganisms with mucin degradation capacity.
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“Although dysbiosis is associated with chronic inflammation and production of carcinogenic metabolites, 175, 176 there is limited evidence to support a direct link between specific intestinal bacteria, their virulence factors, and sporadic CRC.”
From Influence of the Gut Microbiome, Diet, and Environment on Risk of Colorectal Cancer (2020) · cites this paper as [175]
Citations
Cites
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
Hugot, J.-P., Chamaillard, M., Zouali, H., Lesage, S., Cézard, J.-P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C. A., Gassull, M., et al. (2001) · Nature · doi:10.1038/35079107 · Cited by 5,591
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
Ogura, Y., Bonen, D. K., Inohara, N., Nicolae, D. L., Chen, F. F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R. H., et al. (2001) · Nature · doi:10.1038/35079114 · Cited by 5,030
Frank, D. N., St. Amand, A. L., Feldman, R. A., Boedeker, E. C., Harpaz, N., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706625104 · Cited by 4,611
Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413
Reduced diversity of faecal microbiota in Crohn’s disease revealed by a metagenomic approach
Manichanh, C., Rigottier-Gois, L., Bonnaud, E., Gloux, K., Pelletier, E., Frangeul, L., Nalin, R., Jarrin, C., Chardon, P., Marteau, P., et al. (2006) · Gut · doi:10.1136/gut.2005.073817 · Cited by 2,277
Hampe, J., Franke, A., Rosenstiel, P. C., Till, A., Teuber, M., Huse, K., Albrecht, M., Mayr, G., Vega, F. M. D. L., Briggs, J. C., et al. (2006) · Nature Genetics · doi:10.1038/ng1954 · Cited by 1,951
Microbial Influences in Inflammatory Bowel Diseases
Sartor, R. B. (2008) · Gastroenterology · doi:10.1053/j.gastro.2007.11.059 · Cited by 1,927
Low counts of Faecalibacterium prausnitzii in colitis microbiota
Sokol, H., Seksik, P., Furet, J. P., Firmesse, O., Nion-Larmurier, I., Beaugerie, L., Cosnes, J., Corthier, G., Marteau, P., & Doré, J. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20903 · Cited by 1,275
Parkes, M., Barrett, J. C., Prescott, N. J., Tremelling, M., Anderson, C. A., Fisher, S. A., Roberts, R. G., Nimmo, E. R., Cummings, F. J. R., Soars, D., et al. (2007) · Nature Genetics · doi:10.1038/ng2061 · Cited by 1,175
D’Haens, G., Geboes, K., Peeters, M., Baert, F., PENNINCKX, F. M., & Rutgeerts, P. (1998) · Gastroenterology · doi:10.1016/s0016-5085(98)70476-7 · Cited by 866
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Li, M., Zhu, L., Xie, A., & Yuan, J. (2014) · Inflammation · doi:10.1007/s10753-014-0019-7 · Cited by 43
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Banaszkiewicz, A., Kadzielska, J., Gawrońska, A., Pituch, H. M., Obuch-Woszczatyński, P., Albrecht, P., Młynarczyk, G., & Radzikowski, A. (2013) · Journal of Crohn s and Colitis · doi:10.1016/j.crohns.2013.08.018 · Cited by 43
Kovatcheva‐Datchary, P., Tremaroli, V., & Bäckhed, F. (2013) · Springer eBooks · doi:10.1007/978-3-642-30144-5_87 · Cited by 46
He, Q., Wang, L., Wang, F., & Li, Q. (2014) · Zebrafish · doi:10.1089/zeb.2013.0917 · Cited by 42
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Oh, B. S., Choi, W. J., Kim, J., Ryu, S. W., Yu, S. Y., Lee, J., Park, S., Kang, S. W., Lee, J., Jung, W. Y., et al. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.736343 · Cited by 41
Al-Amrah, H., Saadah, O. I., Mosli, M. H., Annese, V., Al-Hindi, R. R., Edris, S., Alshehri, D., Alatawi, H. A., Alatawy, M., & Bahieldin, A. (2023) · Saudi Journal of Gastroenterology · doi:10.4103/sjg.sjg_368_22 · Cited by 41
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Kwon, J., Bae, M., Szamosvári, D., Cassilly, C. D., Bolze, A. S., Jackson, D. R., Xavier, R. J., & Clardy, J. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.3c00250 · Cited by 40
Hedin, C. R. H., Stagg, A. J., Whelan, K., & Lindsay, J. O. (2011) · Gut · doi:10.1136/gut.2011.238568 · Cited by 40
Cook, L. E., Lisko, D. J., Wong, M. Q., García, R., Himmel, M. E., Seidman, E. G., Bressler, B. L., Levings, M. K., & Steiner, T. S. (2019) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2019.11.012 · Cited by 42
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Melton, S. L., Taylor, K. M., Gibson, P. R., & Halmos, E. P. (2023) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.17451 · Cited by 39
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Li, Q., Wang, C., Zhang, Q., Tang, C. X., Li, N., Ruan, B., & Li, J. (2012) · Human Pathology · doi:10.1016/j.humpath.2011.09.017 · Cited by 39
Strain, C., Collins, K. C., Naughton, V. R., McSorley, E. M., Stanton, C., Smyth, T. J., Soler‐Vila, A., Rea, M. C., Ross, R. P., Cherry, P., et al. (2019) · European Journal of Nutrition · doi:10.1007/s00394-019-01909-6 · Cited by 43
Paola, M. D., Rizzetto, L., Stefanini, I., Vitali, F., Massi-Benedetti, C., Tocci, N., Romani, L. R., Ramazzotti, M., Lionetti, P., Filippo, C. D., et al. (2020) · Journal of Translational Autoimmunity · doi:10.1016/j.jtauto.2020.100036 · Cited by 39
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Palmieri, O., Castellana, S., Biscaglia, G., Panza, A., Latiano, A., Fontana, R., Guerra, M., Corritore, G., Latiano, T. P., Martino, G., et al. (2021) · Cells · doi:10.3390/cells10113243 · Cited by 37
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Xu, Y., Zhu, W., & Guo, Z. (2022) · World Journal of Gastroenterology · doi:10.3748/wjg.v28.i48.6888 · Cited by 40
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Noğay, N. H., & Nahikian-Nelms, M. L. (2019) · Nutritional Neuroscience · doi:10.1080/1028415x.2019.1630894 · Cited by 39
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Lacroix, V., Cassard, A., Mas, E., & Barreau, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011255 · Cited by 36
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Li, J., Liu, F., Luo, Y., Wijeyesekera, A., Wang, S., Chen, X., Lv, Y., Jin, J., Sheng, H.-F., Wang, G., et al. (2025) · BMC Medicine · doi:10.1186/s12916-025-04189-6 · Cited by 39
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Dunn, K. A., Moore-Connors, J., MacIntyre, B., Stadnyk, A. W., Thomas, N. A., Noble, A. J., Mahdi, G., Rashid, M., Otley, A. R., Bielawski, J. P., et al. (2016) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000949 · Cited by 36
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Labourel, A., Parrou, J., Deraison, C., Mercier‐Bonin, M., Lajus, S., & Potocki-Véronèse, G. (2023) · Essays in Biochemistry · doi:10.1042/ebc20220153 · Cited by 36
Context-Dependent Regulation of Type17 Immunity by Microbiota at the Intestinal Barrier
Akuzum, B., & Lee, J. (2022) · Immune Network · doi:10.4110/in.2022.22.e46 · Cited by 36
The gut microbiome in systemic lupus erythematosus: lessons from rheumatic fever
Silverman, G. J., Azzouz, D. F., Gisch, N., & Amarnani, A. (2024) · Nature Reviews Rheumatology · doi:10.1038/s41584-023-01071-8 · Cited by 39
Olteanu, G., Pană, M.-A., Busnatu, Ș., Lupuliasa, D., Neacșu, S. M., Mititelu, M., Musuc, A. M., Ioniță-Mîndrican, C.-B., & Boroghină, S. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105561 · Cited by 36
Zachos, K. A., Gamboa, J. A., Dewji, A. S., Lee, J., Brijbassi, S., & Andreazza, A. C. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1428242 · Cited by 35
Perturbation of the Human Microbiome as a Contributor to Inflammatory Bowel Disease
Missaghi, B., Barkema, H. W., Madsen, K., & Ghosh, S. K. (2014) · Pathogens · doi:10.3390/pathogens3030510 · Cited by 35
Swafford, D., Shanmugam, A., Ranganathan, P. V., Hussein, M. S., Koni, P. A., Prasad, P. D., Thangaraju, M., & Manicassamy, S. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701086 · Cited by 34
Liu, F., Wang, T. T. Y., Tang, Q., Xue, C., Li, R. W., & Wu, V. C. H. (2019) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900455 · Cited by 34
Sarrabayrouse, G., Elías, A. D., Yáñez, F., Mayorga, L., Varela, E., Bartoli, C., Casellas, F., Borruel, N., Guise, C. H.-D., Machiels, K., et al. (2021) · mSystems · doi:10.1128/msystems.01277-20 · Cited by 35
Self-citationShort chain fatty acids (SCFAs) improves TNBS-induced colitis in zebrafish
Morales, C., do Amaral, M. A., Xavier, I. K., Padovani, B. N., Paredes, L. C., Takiishi, T., Lopes‐Ferreira, M., Lima, C., Colombo, A., & Câmara, N. O. S. (2021) · Current Research in Immunology · doi:10.1016/j.crimmu.2021.08.003 · Cited by 37
Basile, A., Heinken, A., Hertel, J., Smarr, L. L., Li, W., Treu, L., Valle, G., Campanaro, S., & Thiele, I. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2226921 · Cited by 32
Zeamer, A. L., Salive, M.-C., An, X., Beaudoin, F. L., House, S. L., Stevens, J. S., Zeng, D., Neylan, T. C., Clifford, G. D., Linnstaedt, S. D., et al. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02643-8 · Cited by 34
Zhang, J., Huang, Y.-J., Trapečar, M., Wright, C. W., Schneider, K., Kemmitt, J., Hernandez‐Gordillo, V., Yoon, J. Y., Poyet, M., Alm, E. J., et al. (2024) · npj Biofilms and Microbiomes · doi:10.1038/s41522-024-00501-z · Cited by 33
The role of goblet cells in Crohn’ s disease
Wang, Z., & Shen, J. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01220-w · Cited by 35
Host–pathobiont interactions in Crohn’s disease
Caruso, R., Lo, B. C., Chen, G., & Núñez, G. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-024-00997-y · Cited by 35
Uncovering a novel molecular mechanism for scavenging sialic acids in bacteria
Bell, A., Severi, E., Lee, M., Monaco, S., Latousakis, D., Angulo, J., Thomas, G. H., Naismith, J. H., & Juge, N. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.014454 · Cited by 35
Impact of bacterial infection and intestinal microbiome on colorectal cancer development
Sun, J. (2022) · Chinese Medical Journal · doi:10.1097/cm9.0000000000001979 · Cited by 35
Matrix metalloproteinase 9 contributes to gut microbe homeostasis in a model of infectious colitis
Rodrigues, D. M., Sousa, A. J., Hawley, S. P., Vong, L., Gareau, M. G., Kumar, S. A., Johnson‐Henry, K. C., & Sherman, P. M. (2012) · BMC Microbiology · doi:10.1186/1471-2180-12-105 · Cited by 33
Metabolic independence drives gut microbial colonization and resilience in health and diseasePreprint
Watson, A. R., Füssel, J., Veseli, I., DeLongchamp, J. Z., Silva, M., Trigodet, F., Lolans, K., Shaiber, A., Fogarty, E. C., Runde, J., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.02.433653 · Cited by 33
Park, J., Song, W., Lee, J., Jo, S.-H., Lee, J., Jeon, H., Kwon, J.-E., Kim, Y., Baek, J., Kim, M. G., et al. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.825399 · Cited by 34
Ghosal, S., Bag, S., Rao, S. R., & Bhowmik, S. (2024) · RSC Advances · doi:10.1039/d4ra04544k · Cited by 37
Lu, H., Zhang, C., Qian, G., Hu, X., Zhang, H., Chen, C., Liang, W., Gao, H., Yang, Y., & Li, L. (2014) · BMC Infectious Diseases · doi:10.1186/1471-2334-14-359 · Cited by 32
Impact of Obesity on the Management of Inflammatory Bowel Disease.
Johnson, A. M., & Loftus, E. V. (2020) · PubMed Central · Cited by 32
Watanabe, S., Kameoka, S., Shinozaki, N. O., Ryuichi, K. U. B. O., Nishida, A., Kuriyama, M., & Takeda, A. (2021) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.2020-038 · Cited by 37
Metadata
- Authors
- Joossens, M., Huys, G., Cnockaert, M., De Preter, V., Verbeke, K., Rutgeerts, P., Vandamme, P., & Vermeire, S.
- Affiliations
- Universitair Ziekenhuis Leuven (BE)
- Ghent University (BE)
- Venue
- Gut
- Publisher
- BMJ
- Published
- 2011-01-05
- Volume
- 60
- Issue
- 5
- Pages
- 631-637
- ISSN
- 0017-5749 (ISSN-L)
- OpenAlex
- W2139327060
- Semantic Scholar
- 3c76b951197740ae02ffa2ef816767ede9de1b85
- Cited by
- 1,063
- References
- 47
- Citations by year
- 2026: 30 · 2025: 67 · 2024: 88 · 2023: 91 · 2022: 73 · 2021: 103 · 2020: 95 · 2019: 81 · 2018: 65 · 2017: 60 · 2016: 74 · 2015: 56 · 2014: 68 · 2013: 57 · 2012: 34
- FWCI
- 23.48
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Gut (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- HighWire Press Open Archive (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Inflammatory Bowel Disease
- Health Sciences › Medicine › Infectious Diseases › Clostridium difficile and Clostridium perfringens research
- Keywords
- Crohn's disease, fecal microbiota, dysbiosis, gut microbiota composition, unaffected relatives, Dialister invisus, Faecalibacterium prausnitzii, Bifidobacterium adolescentis, Ruminococcus gnavus, Ruminococcus torques, Collinsella aerofaciens, Clostridium cluster XIVa, mucin degradation, butyrate-producing bacteria, familial aggregation
- MeSH terms
- Adolescent, Adult, Aged, Aged, 80 and over, Bacteria, Crohn Disease, DNA, Bacterial, Feces, Female, Humans, Male, Middle Aged, Symbiosis, Case-Control Studies, Reverse Transcriptase Polymerase Chain Reaction, Metagenome, Young Adult, Denaturing Gradient Gel Electrophoresis
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