Decreased abundance of F aecalibacterium prausnitzii in the gut microbiota of C rohn's disease
Abstract
Background and Aims: Dysbiosis is thought to be relevant to the etiology and pathogenesis of C rohn's disease ( CD ). In this study, we investigated the abundance of F aecalibacterium prausnitzii , as well as B ilophila wadsworthia , in the gut microbiota of J apanese CD patients. Methods: Forty‐seven CD patients and 20 healthy controls were enrolled. Abundance of F . prausnitzii in fecal samples was quantified by real‐time polymerase chain reaction. The gut microbiota profile was evaluated by terminal restriction fragment length polymorphisms. Results: The abundance of F . prausnitzii significantly decreased in CD patients compared with healthy subjects. B . wadsworthia was scarcely detected in the same samples. Among CD patients, the C rohn's D isease A ctivity I ndex, C ‐reactive protein levels, and erythrocyte sedimentation rate were significantly lower, and serum albumin levels were significantly higher in the high F . prausnitzii group compared with the low group. Terminal restriction fragment length polymorphisms analysis showed that fecal bacterial communities of CD patients differed from those of healthy individuals. The changes in simulated bacterial composition indicated that class C lostridia, including genus F aecalibacterium, was significantly less abundant in CD patients as compared with healthy individuals. The bacterial diversity measured by the S hannon D iversity I ndex was significantly reduced in CD patients compared with healthy individuals. Conclusion: The decreased abundance of class C lostridia, including F . prausnitzii , may translate into a reduction of commensal bacteria‐mediated, anti‐inflammatory activities in the mucosa, which are relevant to the pathophysiology of CD . In contrast, the role of B . wadsworthia was suspected to be minimal.
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Saccharolytic organisms such as Ruminococcaceae and Lachnospiraceae persist in fibrolytic gut communities and are considered an important component of a healthy gut microbiota, while their depletion has been observed in inflammatory bowel disease patients.
“These saccharolytic organisms persist in fibrolytic gut communities and are considered an important component of a healthy gut microbiota, while their depletion has been observed in inflammatory bowel disease patients [189, 190].”
From The athletic gut microbiota (2020) · cites this paper as [190]
Faecalibacterium prausnitzii is depleted in IBD patients, including ulcerative colitis.
“The depletion of F prausnitzii in IBD patients3,41,42, including ulcerative colitis43”
From Cholestasis induced by bile duct ligation promotes changes in the intestinal microbiome in mice (2019) · cites this paper as [42]
Cites
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Induction of Colonic Regulatory T Cells by Indigenous <i>Clostridium</i> Species
Atarashi, K., Tanoue, T., Shima, T., Imaoka, A., Kuwahara, T., Momose, Y., Cheng, G., Yamasaki, S., Saito, T., Ohba, Y., et al. (2011) · Science · doi:10.1126/science.1198469 · Cited by 3,752 · see citing works
Podolsky, D. K. (2002) · New England Journal of Medicine · doi:10.1056/nejmra020831 · Cited by 3,183 · see citing works
Development of a Crohn's Disease Activity Index
Best, W. R., Becktel, J. M., Singleton, J. W., & Kern, F. (1976) · Gastroenterology · doi:10.1016/s0016-5085(76)80163-1 · Cited by 3,152 · see citing works
Development of a Crohn's disease activity index. National Cooperative Crohn's Disease Study.
Best, W. R., Becktel, J. M., Singleton, J. W., & Kern, F. (1976) · PubMed · Cited by 3,147 · see citing works
Review article: the role of butyrate on colonic function
HAMER, H. M., JONKERS, D., VENEMA, K., VANHOUTVIN, S., TROOST, F. J., & BRUMMER, R. ‐. (2008) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2007.03562.x · Cited by 2,721 · see citing works
Microbial Influences in Inflammatory Bowel Diseases
Sartor, R. B. (2008) · Gastroenterology · doi:10.1053/j.gastro.2007.11.059 · Cited by 1,927 · see citing works
Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10-/- mice
Devkota, S., Wang, Y., Musch, M. W., Leone, V., Fehlner-Peach, H., Nadimpalli, A., Antonopoulos, D. A., Jabri, B., & Chang, E. B. (2012) · Nature · doi:10.1038/nature11225 · Cited by 1,904 · see citing works
Mechanisms of Disease: pathogenesis of Crohn's disease and ulcerative colitis
Sartor, R. B. (2006) · Nature Clinical Practice Gastroenterology & Hepatology · doi:10.1038/ncpgasthep0528 · Cited by 1,763 · see citing works
A key role for autophagy and the autophagy gene Atg16l1 in mouse and human intestinal Paneth cells
Cadwell, K., Liu, J. Y., Brown, S. L., Miyoshi, H., Loh, J., Lennerz, J. K., Kishi, C., Kc, W., Carrero, J. A., Hunt, S., et al. (2008) · Nature · doi:10.1038/nature07416 · Cited by 1,542 · see citing works
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 · see citing works
Comparative Analysis of Human Gut Microbiota by Barcoded Pyrosequencing
Andersson, A. F., Lindberg, M., Jakobsson, H. E., Bäckhed, F., Nyrén, P., & Engstrand, L. G. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002836 · Cited by 1,037 · see citing works
Using ecological diversity measures with bacterial communities
Hill, T. C. J., Walsh, K. A., Harris, J. A., & Moffett, B. F. (2003) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2003.tb01040.x · Cited by 1,016 · see citing works
Comparative metagenomics revealed commonly enriched gene sets in human gut microbiomes
Kurokawa, K., Itoh, T., Kuwahara, T., Oshima, K., Toh, H., Toyoda, A., Takami, H., Morita, H., Sharma, V. K., Srivastava, T. P., et al. (2007) · DNA Research · doi:10.1093/dnares/dsm018 · Cited by 869 · see citing works
Ramirez-Farias, C., Slezak, K., Fuller, Z., Duncan, A., Holtrop, G., & Louis, P. (2008) · British Journal of Nutrition · doi:10.1017/s0007114508019880 · Cited by 822 · see citing works
Denman, S. E., & McSweeney, C. S. (2006) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2006.00190.x · Cited by 753 · see citing works
Duncan, S. H., Hold, G. L., Harmsen, H. J. M., Stewart, C. S., & Flint, H. J. (2002) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-52-6-2141 · Cited by 735 · see citing works
Walker, A. W., Sanderson, J. D., Churcher, C. M., Parkes, G. C., Hudspith, B. N., Rayment, N. B., Brostoff, J., Parkhill, J., Dougan, G., & Petrovska, L. (2011) · BMC Microbiology · doi:10.1186/1471-2180-11-7 · Cited by 727 · see citing works
Frank, D. N., Robertson, C. E., Hamm, C. M., Kpadeh, Z. Z., Zhang, T., Chen, H., Zhu, W., Sartor, R. B., Boedeker, E. C., Harpaz, N., et al. (2010) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21339 · Cited by 594 · see citing works
Feller, M., Huwiler, K., Stephan, R., Altpeter, E., Shang, A., Furrer, H., Pfyffer, G. E., Jemmi, T., Baumgartner, A., & Egger, M. (2007) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(07)70211-6 · Cited by 526 · see citing works
Mouse models of inflammatory bowel disease☆
Wirtz, S. J., & Neurath, M. F. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.07.003 · Cited by 508 · see citing works
Hall, J. A., Bouladoux, N. J., Sun, C., Wohlfert, E. A., Blank, R. B., Zhu, Q., Grigg, M. E., Berzofsky, J. A., & Belkaid, Y. (2008) · Immunity · doi:10.1016/j.immuni.2008.08.009 · Cited by 490 · see citing works
Lopez-Siles, M., Khan, T. M., Duncan, S. H., Harmsen, H. J. M., Garcia-Gil, L. J., & Flint, H. J. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.06858-11 · Cited by 433 · see citing works
Kang, S., Denman, S. E., Morrison, M., Yu, Z., Dore, J. M., Leclerc, M., & McSweeney, C. S. (2010) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21319 · Cited by 365 · see citing works
Scanlan, P. D., Shanahan, F., O'Mahony, C., & Marchesi, J. R. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.00312-06 · Cited by 330 · see citing works
Role of the microbiota in inflammatory bowel diseases
Nagalingam, N. A., & Lynch, S. V. (2012) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21866 · Cited by 315 · see citing works
Marsh, T. L., Saxman, P., Cole, J. R., & Tiedje, J. M. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.8.3616-3620.2000 · Cited by 306 · see citing works
Nagashima, K., Hisada, T., Sato, M., & Mochizuki, J. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.2.1251-1262.2003 · Cited by 233 · see citing works
Andoh, A., Imaeda, H., Aomatsu, T., Inatomi, O., Bamba, S., Sasaki, M., Saito, Y., Tsujikawa, T., & Fujiyama, Y. (2011) · Journal of Gastroenterology · doi:10.1007/s00535-010-0368-4 · Cited by 220 · see citing works
Self-citationDuncan, S. H. (2002) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.02241-0 · Cited by 184 · see citing works
Evolving paradigms in the pathogenesis of IBD
Mayer, L. (2009) · Journal of Gastroenterology · doi:10.1007/s00535-009-0138-3 · Cited by 175 · see citing works
Multicenter analysis of fecal microbiota profiles in Japanese patients with Crohn’s disease
Andoh, A., Kuzuoka, H., Tsujikawa, T., Nakamura, S., Hirai, F., Suzuki, Y., Matsui, T., Fujiyama, Y., & Matsumoto, T. (2012) · Journal of Gastroenterology · doi:10.1007/s00535-012-0605-0 · Cited by 163 · see citing works
Self-citationAdherent-invasive Escherichia coli and Crohnʼs disease
Barnich, N., & Darfeuille–Michaud, A. (2006) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e3280105a38 · Cited by 155 · see citing works
Inflammatory bowel disease, past, present and future: lessons from animal models
Mizoguchi, A., & Mizoguchi, E. (2008) · Journal of Gastroenterology · doi:10.1007/s00535-007-2111-3 · Cited by 146 · see citing works
Diversity of mucosa-associated microbiota in active and inactive ulcerative colitis
Nishikawa, J., Kudo, T., Sakata, S., Benno, Y., & Sugiyama, T. (2008) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365520802433231 · Cited by 129 · see citing works
Sakamoto, M., Takeuchi, Y., Umeda, M., et al. (2002) · Journal of Medical Microbiology · doi:10.1099/jmm.0.04991-0 · Cited by 119 · see citing works
Nagashima, K., Mochizuki, J., Hisada, T., Suzuki, S., & Shimomura, K. (2006) · Bioscience and Microflora · doi:10.12938/bifidus.25.99 · Cited by 104 · see citing works
Andoh, A., Fujiyama, Y., Hata, K., Araki, Y., Takaya, H., Shimada, M., & Bamba, T. (1999) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.1999.01038.x · Cited by 89 · see citing works
Self-citationMatsumoto, M., Sakamoto, M., Hayashi, H., et al. (2005) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2004.12.009 · Cited by 81 · see citing works
Digesting the genetics of inflammatory bowel disease: Insights from studies of autophagy risk genes
Kabi, A., Nickerson, K. P., Homer, C. R., & McDonald, C. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21868 · Cited by 56 · see citing works
Update on biologic pathways in inflammatory bowel disease and their therapeutic relevance
Hamilton, M. J., Snapper, S. B., & Blumberg, R. S. (2012) · Journal of Gastroenterology · doi:10.1007/s00535-011-0521-8 · Cited by 49 · see citing works
Recent Advances in Molecular Approaches to Gut Microbiota in Inflammatory Bowel Disease
Andoh, A., Benno, Y., Kanauchi, O., & Fujiyama, Y. (2009) · Current Pharmaceutical Design · doi:10.2174/138161209788489186 · Cited by 41 · see citing works
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Pittayanon, R., Lau, J. T., Leontiadis, G. I., Tse, F., Yuan, Y., Surette, M., & Moayyedi, P. (2020) · Gastroenterology · doi:10.1053/j.gastro.2019.11.294 · Cited by 623 · see citing works
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Cignarella, F., Cantoni, C., Ghezzi, L., Salter, A., Dorsett, Y., Chen, L., Phillips, D., Weinstock, G. M., Fontana, L., Cross, A. H., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.05.006 · Cited by 568 · see citing works
Estaki, M., Pither, J., Baumeister, P., Little, J. P., Gill, S. K., Ghosh, S., Ahmadi-Vand, Z., Marsden, K. R., & Gibson, D. L. (2016) · Microbiome · doi:10.1186/s40168-016-0189-7 · Cited by 476 · see citing works
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Zimmermann, P., & Curtis, N. (2019) · Journal of Infection · doi:10.1016/j.jinf.2019.10.008 · Cited by 383 · 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
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Vindigni, S. M., & Surawicz, C. M. (2017) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2016.09.012 · Cited by 283 · see citing works
Suskind, D. L., Brittnacher, M. J., Wahbeh, G., Shaffer, M. L., Hayden, H. S., Qin, X., Singh, N., Damman, C. J., Hager, K. R., Nielson, H., et al. (2015) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000307 · Cited by 243 · see citing works
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Carlsson, A. H., Yakymenko, O., Olivier, I., Håkansson, F., Postma, E., Keita, Å. V., & Söderholm, J. D. (2013) · Scandinavian Journal of Gastroenterology · doi:10.3109/00365521.2013.828773 · Cited by 219 · see citing works
Ganesan, K., Chung, S. K., Vanamala, J., & Xu, B. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19123720 · Cited by 221 · see citing works
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- Authors
- Fujimoto, T., Imaeda, H., Takahashi, K., Kasumi, E., Bamba, S., Fujiyama, Y., & Andoh, A.
- Affiliations
- Division of Mucosal Immunology Graduate School
- Shiga University of Medical Science (JP)
- Corresponding author
- Andoh, Akira
- Venue
- Journal of Gastroenterology and Hepatology
- Publisher
- Wiley
- Published
- 2013-03-25
- Volume
- 28
- Issue
- 4
- Pages
- 613-619
- ISSN
- 0815-9319 (ISSN-L)
- 1440-1746
- OpenAlex
- W1569647046
- Cited by
- 304
- References
- 45
- Citations by year
- 2026: 12 · 2025: 23 · 2024: 25 · 2023: 25 · 2022: 30 · 2021: 25 · 2020: 20 · 2019: 31 · 2018: 24 · 2017: 20 · 2016: 20 · 2015: 19 · 2014: 14 · 2013: 15
- FWCI
- 6.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Gastroenterology and Hepatology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- TechnoSuruga Laboratory Co., Ltd.
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Health Sciences › Medicine › Infectious Diseases › Clostridium difficile and Clostridium perfringens research
- Keywords
- Crohn's disease, Faecalibacterium prausnitzii, gut microbiota, dysbiosis, Bilophila wadsworthia, Clostridia, bacterial diversity, CDAI, serum albumin, Japanese patients
- MeSH terms
- Adult, Clostridium, Crohn Disease, DNA, Bacterial, Feces, Female, Humans, Male, Middle Aged, Polymorphism, Restriction Fragment Length, Severity of Illness Index, Case-Control Studies, DNA Primers, Gastrointestinal Tract, Bilophila, Metagenome, Real-Time Polymerase Chain Reaction
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