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Genetically dictated change in host mucus carbohydrate landscape exerts a diet-dependent effect on the gut microbiota
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Significance: Our data demonstrate that differences in host genotype that affect the carbohydrate landscape of the distal gut interact with diet to alter the composition and function of resident microbes in a diet-dependent manner.
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“differences in host genotype, which affect the carbohydrate landscape of the distal gut, interact with diet to alter the composition and function of resident microbes in a diet-dependent manner.103”
From The gut microbiota and host health: a new clinical frontier (2016) · cites this paper as [103]
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Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887
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Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815
Self-citationLinking 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
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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
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Xavier, R. J., & Podolsky, D. K. (2007) · Nature · doi:10.1038/nature06005 · Cited by 4,364
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Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173
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Turnbaugh, P. J., Ridaura, V. K., Faith, J. J., Rey, F. E., Knight, R., & Gordon, J. I. (2009) · Science Translational Medicine · doi:10.1126/scitranslmed.3000322 · Cited by 3,058 · cited 1×
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Yin, Y.-B., Mao, X., Yang, J., Chen, X., Mao, F., & Xu, Y. (2012) · Nucleic Acids Res. · doi:10.1093/nar/gks479 · Cited by 1,666
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Lozupone, C., Hamady, M., & Knight, R. D. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-371 · Cited by 1,454
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Dashnyam, P., Mudududdla, R., Hsieh, T.-J., Lin, T.-C., Lin, H.-Y., Chen, P.-Y., Hsu, C.-Y., & Lin, C.-H. (2018) · Scientific Reports · doi:10.1038/s41598-018-34678-z · Cited by 108
Hoek, M. J. A., & Merks, R. M. H. (2017) · BMC Systems Biology · doi:10.1186/s12918-017-0430-4 · Cited by 105
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Rodríguez‐Díaz, J., García‐Mantrana, I., Vila-Vicent, S., Gozalbo‐Rovira, R., Buesa, J., Monedero, V., & Collado, M. C. (2017) · Scientific Reports · doi:10.1038/srep45559 · Cited by 95
Bergstrom, K., & Xia, L. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2052699 · Cited by 100
Dill‐McFarland, K. A., Neil, K. L., Zeng, A., Sprenger, R. J., Kurtz, C. C., Suen, G., & Carey, H. V. (2014) · Molecular Ecology · doi:10.1111/mec.12884 · Cited by 91
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Mortzfeld, B. M., Urbanski, S., Reitzel, A. M., Künzel, S., Technau, U., & Fraune, S. (2015) · Environmental Microbiology · doi:10.1111/1462-2920.12926 · Cited by 86
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Zhou, Y., Ou, Z., Tang, X., Zhou, Y., Xu, H., Wang, X., Li, K., He, J., Du, Y., Wang, H., et al. (2018) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13508 · Cited by 81
Troll, J. V., Hamilton, M. K., Abel, M. L., Ganz, J., Bates, J. M., Stephens, W. Z., Melançon, E., van der Vaart, M., Meijer, A. H., Distel, M., et al. (2018) · Development · doi:10.1242/dev.155317 · Cited by 77
Becerra, J. E., Yebra, M. J., & Monedero, V. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.00260-15 · Cited by 82
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Metadata
- Authors
- Kashyap, P. C., Marcobal, A., Ursell, L. K., Smits, S. A., Sonnenburg, E. D., Costello, E. K., Higginbottom, S. K., Domino, S. E., Holmes, S. P., Relman, D. A., Knight, R., Gordon, J. I., & Sonnenburg, J. L.
- Affiliations
- Mayo Clinic (US)
- Stanford Medicine (US)
- Howard Hughes Medical Institute (US)
- University of Michigan (US)
- Stanford University (US)
- VA Palo Alto Health Care System (US)
- Washington University in St. Louis (US)
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2013-09-23
- Volume
- 110
- Issue
- 42
- Pages
- 17059-17064
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3800993
- OpenAlex
- W1989848555
- Cited by
- 285
- References
- 43
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 14 · 2023: 37 · 2022: 23 · 2021: 26 · 2020: 20 · 2019: 15 · 2018: 18 · 2017: 19 · 2016: 26 · 2015: 27 · 2014: 36 · 2013: 2
- FWCI
- 13.58
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Science Foundation
- Howard Hughes Medical Institute
- Crohn's and Colitis Foundation of America
- Crohn's and Colitis Foundation
- National Institutes of Health (DGE-114747, DP1OD000964)
- National Institute of General Medical Sciences (R01GM086884, GM86884, T32GM008759, T32GM142607)
- National Institute of Diabetes and Digestive and Kidney Diseases (R37DK030292, DK-30292, DK085025, P30DK084567, R01DK030292, R01DK085025)
- 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 › Infant Nutrition and Health
- Keywords
- gut microbiota, fucosyltransferase, Bacteroides thetaiotaomicron, host-microbe interactions, fecal metabolites
- MeSH terms
- Galactoside 2-alpha-L-fucosyltransferase, Animals, Bacteroides, Dietary Carbohydrates, Fucosyltransferases, Glucans, Humans, Intestinal Mucosa, Mice, Knockout, Mice, Microbiota
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