Glycan Foraging in Vivo by an Intestine-Adapted Bacterial Symbiont

The gut microbiota as an environmental factor that regulates fat storage

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Biodiversity and ecosystem productivity in a fluctuating environment: The insurance hypothesis

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MICROBIAL ECOLOGY OF THE GASTROINTESTINAL TRACT

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H OW H OST -M ICROBIAL I NTERACTIONS S HAPE THE N UTRIENT E NVIRONMENT OF THE M AMMALIAN I NTESTINE

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A Genomic View of the Human- Bacteroides thetaiotaomicron Symbiosis

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Human Fecal Flora: The Normal Flora of 20 Japanese-Hawaiians

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Honor thy symbionts

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A Model of Host-Microbial Interactions in an Open Mammalian Ecosystem

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Carbon nutrition of Escherichia coli in the mouse intestine

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Prior exposure to microcystin alters host gut resistome and is associated with dysregulated immune homeostasis in translatable mouse models

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Ecological Interactions of Bacteria in the Human Gut

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Mucin Production and Mucous Cell Metaplasia in Otitis Media

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The genomics of probiotic intestinal microorganisms.

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Effects of antimicrobial peptides from dietary Hermetia illucens larvae on the growth, immunity, gene expression, intestinal microbiota and resistance to Aeromonas hydrophila of juvenile red claw crayfish (Cherax quadricarinatus)

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Human gut microbes express functionally distinct endoglycosidases to metabolize the same N-glycan substrate

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Intestinal Population in Host with Metabolic Syndrome during Administration of Chitosan and Its Derivatives

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Fibra dietaria y microbiota, revisión narrativa de un grupo de expertos de la Asociación Mexicana de Gastroenterología

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Comparison of the Intestinal Microbiota During the Different Growth Stages of Red Swamp Crayfish (Procambarus clarkii)

Xie, M., Zhang, S., Xu, L., Wu, Z., Yuan, J., & Chen, X. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.696281 · Cited by 23

Starvation responses impact interaction dynamics of human gut bacteriaBacteroides thetaiotaomicronandRoseburia intestinalis

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A Mesocosm of Lactobacillus johnsonii , Bifidobacterium longum , and Escherichia coli in the Mouse Gut

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FUT1genetic variants impact protein glycosylation of porcine intestinal mucosa

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Unraveling the Substrate Recognition Mechanism and Specificity of the Unusual Glycosyl Hydrolase Family 29 BT2192 from Bacteroides thetaiotaomicron

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Interleukin-10 is Differentially Expressed in the Small Intestine and the Colon Experiencing Chronic Inflammation and Ulcerative Colitis Induced by Dextran Sodium Sulfate in Young Pigs

Lackeyram, D., Young, D. D., KIM, C. J., Yang, C., Archbold, T. L., Mine, Y., & Fan, M. Z. (2017) · Physiological Research · doi:10.33549/physiolres.933259 · Cited by 23

Metabolism of Dietary Polyphenols by Human Gut Microbiota and Their Health Benefits

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In Vitro Communities Derived from Oral and Gut Microbial Floras Inhibit the Growth of Bacteria of Foreign Origins

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The case for microbial intervention at weaning

Flores, J. N., Lubin, J., & Silverman, M. A. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2414798 · Cited by 23

Are the gut microbial systems of giant pandas unstable?

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Dietary Influence on the Dynamics of the Human Gut Microbiome: Prospective Implications in Interventional Therapies

Adithya, K. K., Rajeev, R., Selvin, J., & Kiran, G. S. (2021) · ACS Food Science & Technology · doi:10.1021/acsfoodscitech.0c00075 · Cited by 23

GH20 and GH84 β-N-acetylglucosaminidases with different linkage specificities underpin mucin O-glycan breakdown capability of Bifidobacterium bifidum

Takada, H., Katoh, T., Sakanaka, M., Odamaki, T., & Katayama, T. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104781 · Cited by 22

Phage Interactions with the Nervous System in Health and Disease

Jędrusiak, A., Fortuna, W., Majewska, J., Górski, A., & Jończyk‐Matysiak, E. (2023) · Cells · doi:10.3390/cells12131720 · Cited by 25

Understanding the factors regulating host–microbiome interactions using Caenorhabditis elegans

Singh, A., & Luallen, R. J. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0059 · Cited by 21

Characterisation and in vitro fermentation of resistant maltodextrins using human faecal inoculum and analysis of bacterial enzymes present

Rösch, C., Venema, K., Gruppen, H., & Schols, H. A. (2015) · Bioactive Carbohydrates and Dietary Fibre · doi:10.1016/j.bcdf.2015.07.002 · Cited by 22

A Single Host-Derived Glycan Impacts Key Regulatory Nodes of Symbiont Metabolism in a Coevolved Mutualism

Pan, M., Schwartzman, J. A., Dunn, A. K., Lu, Z., & Ruby, E. G. (2015) · mBio · doi:10.1128/mbio.00811-15 · Cited by 22

Les fonctions majeures du microbiote intestinal

Gérard, P., & Bernalier‐Donadille, A. (2007) · Cahiers de Nutrition et de Diététique · doi:10.1016/s0007-9960(07)91318-8 · Cited by 22

UDP-Glucuronic Acid Decarboxylases of Bacteroides fragilis and Their Prevalence in Bacteria

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Response of Germfree Mice to Colonization by Oxalobacter formigenes and Altered Schaedler Flora

Li, X., Ellis, M. L., Dowell, A. E., Kumar, R., Morrow, C. D., Schoeb, T. R., & Knight, J. L. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.02381-16 · Cited by 22

Analyzing global gene expression of Lactobacillus plantarum in the human gastrointestinal tract

de Vries, M. C. (2006) · doi:10.18174/33094 · Cited by 22

Nutrition of Escherichia coli within the intestinal microbiome

Doranga, S., Krogfelt, K. A., Cohen, P. S., & Conway, T. (2024) · EcoSal Plus · doi:10.1128/ecosalplus.esp-0006-2023 · Cited by 23

Effect of diet on the evolution of gut commensal bacteria

Đapa, T., & Xavier, K. B. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2369337 · Cited by 23

The global RNA-binding protein RbpB is a regulator of polysaccharide utilization in Bacteroides thetaiotaomicron

Rüttiger, A.-S., Ryan, D., Spiga, L., Lamm‐Schmidt, V., Prezza, G., Reichardt, S., Langford, M., Barquist, L., Faber, F., Zhu, W., et al. (2025) · Nature Communications · doi:10.1038/s41467-024-55383-8 · Cited by 23

A Novel Family of RNA-Binding Proteins Regulate Polysaccharide Metabolism in Bacteroides thetaiotaomicron

Adams, A. N. D., Azam, M. S., Costliow, Z. A., Ma, X., Degnan, P. H., & Vanderpool, C. K. (2021) · Journal of Bacteriology · doi:10.1128/jb.00217-21 · Cited by 22

Bacterial Metabolism Shapes the Host-Pathogen Interface

Passalacqua, K. D., Charbonneau, M., & O’Riordan, M. X. (2016) · ASM Press eBooks · doi:10.1128/9781555819286.ch2 · Cited by 21

Technical note: Intraobserver, interobserver, and test-retest reliabilities of an assessment of vaginal discharge from cows with and without acute puerperal metritis

Sannmann, I., & Heuwieser, W. (2015) · Journal of Dairy Science · doi:10.3168/jds.2014-9169 · Cited by 21

Close association between intestinal microbiota and irritable bowel syndrome

Fan, W.-T., Ding, C., Xu, N., Zong, S., Ma, P., & Gu, B. (2017) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-017-3060-2 · Cited by 24

3-Sulfogalactosyl–dependent adhesion of Escherichia coli HS multivalent adhesion molecule is attenuated by sulfatase activity

Al-Saedi, F., Vaz, D. P., Stones, D. H., & Krachler, A. M. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.817908 · Cited by 23

Structure of RagB, a major immunodominant outer‐membrane surface receptor antigen of Porphyromonas gingivalis

Goulas, T., Garcia-Ferrer, I., Hutcherson, J. A., Potempa, B. A., Potempa, J., Scott, D. A., & Gomis‐Rüth, F. X. (2015) · Molecular Oral Microbiology · doi:10.1111/omi.12140 · Cited by 22

Effects of Probiotic Bacillus subtilis on Intestinal Microbial Diversity and Immunity of Orange Spotted Grouper Epinephelus coioides

Purwandari, A. R., & Chen, H. Y. (2013) · Journal of Applied Biotechnology · doi:10.5296/jab.v1i1.3714 · Cited by 21

The gut mucin-microbiota interactions: a missing key to optimizing endurance performance

Clark, A. P., & Mach, N. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1284423 · Cited by 22

The gastrointestinal tract of farmed mink (Neovison vison) maintains a diverse mucosa‐associated microbiota following a 3‐day fasting period

Bahl, M. I., Hammer, A. S., Clausen, T. N., Jakobsen, A., Skov, S., & Andresen, L. O. (2017) · MicrobiologyOpen · doi:10.1002/mbo3.434 · Cited by 21

Comparison of the Gut Microbiota Between Pulsatilla Decoction and Levofloxacin Hydrochloride Therapy on Escherichia coli Infection

Liu, X., He, S., Li, Q., Mu, X., Hu, G., & Dong, H. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00319 · Cited by 20

Alteration of Gut Microbiota of a Food-Storing Hibernator, Siberian Chipmunk Tamias sibiricus

Zhou, J., Wang, M., & Yi, X. (2021) · Microbial Ecology · doi:10.1007/s00248-021-01877-7 · Cited by 19

Crystal structures of apparent saccharide sensors from histidine kinase receptors prevalent in a human gut symbiont

Zhang, Z., Liu, Q., & Hendrickson, W. A. (2014) · FEBS Journal · doi:10.1111/febs.12904 · Cited by 19

Dietary Fibers: A Way to a Healthy Microbiome

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Bacterial adaptation to the gut environment favors successful colonization

Rezzonico, E., Mestdagh, R., Delley, M., Combremont, S., Dumas, M., Holmes, E. C., Nicholson, J. K., & Bibiloni, R. (2011) · Gut Microbes · doi:10.4161/gmic.18754 · Cited by 18

The gut microbial metabolite indole-3-aldehyde alleviates impaired intestinal development by promoting intestinal stem cell expansion in weaned piglets

Zhang, J., Chen, Y., Guo, X., Li, X., Zhang, R., Wang, M., Zhu, W., & Yu, K. (2024) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-024-01111-7 · Cited by 19

Xylan Prebiotics and the Gut Microbiome Promote Health and Wellbeing: Potential Novel Roles for Pentosan Polysulfate

Smith, M. M., & Melrose, J. (2022) · Pharmaceuticals · doi:10.3390/ph15091151 · Cited by 18

A one month high fat diet disrupts the gut microbiome and integrity of the colon inducing adiposity and behavioral despair in male Sprague Dawley rats

Chompré, G., Sambolin‐Escobales, L., Cruz, M. L., Sanchez, R., Rodriguez, Y., Rodríguez-Santiago, R. E., Yamamura, Y., & Appleyard, C. B. (2022) · Heliyon · doi:10.1016/j.heliyon.2022.e11194 · Cited by 17

The importance of host physical niches for the stability of gut microbiome composition

Ludington, W. B. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0066 · Cited by 18

Obesity, dysbiosis and inflammation: interactions that modulate the efficacy of immunotherapy

Yende, A. S., & Sharma, D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1444589 · Cited by 19

Rodent models to study the relationships between mammals and their bacterial inhabitants

Bibiloni, R. (2012) · Gut Microbes · doi:10.4161/gmic.21905 · Cited by 18

Control of host inflammatory responsiveness by indigenous microbiota reveals an adaptive component of the innate immune system

Fagundes, C. T., Souza, D. G., Nicoli, J. R., & Teixeira, M. M. (2011) · Microbes and Infection · doi:10.1016/j.micinf.2011.07.012 · Cited by 18

Microbial Metabolism of Polyphenols and Health

Celep, G. S., Rastmanesh, R., & Marotta, F. (2013) · Polyphenols in Human Health and Disease · doi:10.1016/b978-0-12-398456-2.00043-8 · Cited by 18

Tissue macrophages as mediators of a healthy relationship with gut commensal microbiota

Nakagaki, B. N., Vieira, A. T., Rezende, R. M., David, B. A., & Menezes, G. B. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.01.017 · Cited by 18

Differential Responses to Dietary Protein and Carbohydrate Ratio on Gut Microbiome in Obese vs. Lean Cats

Li, Q., & Pan, Y. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.591462 · Cited by 21

Gut microbiome responses in the metabolism of human dietary components: Implications in health and homeostasis

Rajeev, R., Seethalakshmi, P. S., Jena, P. K., Prathiviraj, R., Kiran, G. S., & Selvin, J. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1916429 · Cited by 18

Aga1, the first alpha-Galactosidase from the human bacteria Ruminococcus gnavus E1, efficiently transcribed in gut conditions

Aguilera, J., Rakotoarivonina, H., Brutus, A., Giardina, T., Simon, G., & Fons, M. (2011) · Research in Microbiology · doi:10.1016/j.resmic.2011.10.005 · Cited by 18

Characterizing Kiwifruit Carbohydrate Utilization in vitro and its Consequences for Human Faecal Microbiota

Rosendale, D., Blatchford, P. A., Sims, I. M., Parkar, S. G., Carnachan, S., HEDDERLEY, D. I., & Ansell, J. (2012) · Journal of Proteome Research · doi:10.1021/pr300646m · Cited by 18

Influence of habitual dietary fibre intake on the responsiveness of the gut microbiota to a prebiotic: protocol for a randomised, double-blind, placebo-controlled, cross-over, single-centre study

Lunken, G., Brough, L., Butts, C. A., Murphy, R., Whelan, K., & Coad, J. (2016) · BMJ Open · doi:10.1136/bmjopen-2016-012504 · Cited by 17

The Yin and Yang of host-commensal mutualism

Tchaptchet, S., & Hansen, J. J. (2011) · Gut Microbes · doi:10.4161/gmic.19089 · Cited by 22

Genome analysis of Bifidobacterium adolescentis and investigation of its effects on inflammation and intestinal barrier function

Li, B., Wang, H., Wang, M., Liang, H., Hu, T., Yang, J., Li, S., You, X., Xia, B., Yuan, Y., et al. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1496280 · Cited by 19

The interaction between various food components and intestinal microbiota improves human health through the gut–X axis: independently or synergistically

Li, F. N., Peng, X., & Li, W. (2025) · Food & Function · doi:10.1039/d4fo04430d · Cited by 17

Composition and Function of the Gut Microbiome

Blaut, M. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_2 · Cited by 20

Deciphering the Role of Colicins during Colonization of the Mammalian Gut by Commensal E. coli

Samuels, A. N., Roggiani, M., Smith, K. A., Zhu, J., Goulian, M., & Kohli, R. M. (2020) · Microorganisms · doi:10.3390/microorganisms8050664 · Cited by 17

Lessons from the diet: Captivity and sex shape the gut microbiota in an oviparous lizard (Calotes versicolor)

Zhang, L., Yang, F., Li, T., Dayananda, B., Lin, L., & Lin, C.-X. (2022) · Ecology and Evolution · doi:10.1002/ece3.8586 · Cited by 17

Comparative Analysis of Gut Microbial Community Structure of Three Tropical Sea Cucumber Species

Wang, Y., Zhang, Y., Jia, C., Xu, Q., Rong, Y., Xu, Z., Wang, Y., & Gao, F. (2023) · Diversity · doi:10.3390/d15070855 · Cited by 17

Gut microbiota of the small intestine as an antimicrobial barrier against foodborne pathogens: Impact of diet on the survival of S. Typhimurium and L. monocytogenes during in vitro digestion

Akritidou, T., Akkermans, S., Smet, C., Gaspari, S., Sharma, C., Matthews, E., & van Impe, J. F. M. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113292 · Cited by 19

Role of Gut Microbiota in Statin-Associated New-Onset Diabetes—A Cross-Sectional and Prospective Analysis of the FINRISK 2002 Cohort

Koponen, K., Kambur, O., Joseph, B., Ruuskanen, M. O., Jousilahti, P., Salido, R. A., Brennan, C., Jain, M., Méric, G., Inouye, M., et al. (2023) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.123.319458 · Cited by 17

Unexpected effect of a Bacteroides conjugative transposon, CTnDOT, on chromosomal gene expression in its bacterial host

Moon, K., Sonnenburg, J. L., & Salyers, A. A. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05756.x · Cited by 17

Probiotics as Pathogen Control Agents for Organic Meat Production

Siragusa, G. R., & Ricke, S. C. (2012) · Wiley eBooks · doi:10.1002/9781118229088.ch20 · Cited by 17

Identification of carbohydrate gene clusters obtained from in vitro fermentations as predictive biomarkers of prebiotic responses

Kok, C. R., Rose, D. J., Cui, J., Whisenhunt, L. A., & Hutkins, R. L. (2024) · BMC Microbiology · doi:10.1186/s12866-024-03344-y · Cited by 19

Trust Your Gut: The Human Gut Microbiome in Health and Disease

AboNahas, H. H., Darwish, A. M. G., El-Kareem, H. F. A., AboNahas, Y. H., Mansour, S. A., Korra, Y. H., Sayyed, R. Z., Abdel-Azeem, A. M., & Saied, E. M. (2022) · Springer eBooks · doi:10.1007/978-981-16-1626-6_3 · Cited by 16

Tutorial: Microbiome studies in drug metabolism

Dodd, D., & Cann, I. (2022) · Clinical and Translational Science · doi:10.1111/cts.13416 · Cited by 17

Subchronic Oral Cylindrospermopsin Exposure Alters the Host Gut Microbiome and Is Associated with Progressive Hepatic Inflammation, Stellate Cell Activation, and Mild Fibrosis in a Preclinical Study

Saha, P., Upright, M., Bose, D., Roy, S., Trivedi, A., More, M., Scott, G., Brooks, B. W., & Chatterjee, S. (2022) · Toxins · doi:10.3390/toxins14120835 · Cited by 17

Multiple TonB homologs are important for carbohydrate utilization by Bacteroides thetaiotaomicron

Pollet, R. M., Foley, M. H., Kumar, S. S., Elmore, A. G., Jabara, N. T., Venkatesh, S., Pereira, G. V., Martens, E. C., & Koropatkin, N. M. (2023) · Journal of Bacteriology · doi:10.1128/jb.00218-23 · Cited by 16

Early life exposure to broccoli sprouts confers stronger protection against enterocolitis development in an immunological mouse model of inflammatory bowel disease

Holcomb, L. E., Holman, J. M., Hurd, M., Lavoie, B. A., Colucci, L., Hunt, B., Hunt, T., Kinney, M. S., Pathak, J., Mawe, G. M., et al. (2023) · mSystems · doi:10.1128/msystems.00688-23 · Cited by 20

Metagenomic analysis demonstrates distinct changes in the gut microbiome of Kawasaki diseases children

Han, L., Liu, X., Lan, Y., Hua, Y., Fan, Z.-X., & Li, Y.-F. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1416185 · Cited by 19

Intrinsic association between diet and the gut microbiome: current evidence

Fodor, A. A., & Winglee, K. (2015) · Nutrition and Dietary Supplements · doi:10.2147/nds.s62362 · Cited by 16

Mice Overexpressing β-1,4-Galactosyltransferase I Are Resistant to TNF-Induced Inflammation and DSS-Induced Colitis

Vanhooren, V., Vandenbroucke, R. E., Dewaele, S., Hamme, E. V., Haigh, J. J., Hochepied, T., & Libert, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0079883 · Cited by 16

Maintenance of Distal Intestinal Structure in the Face of Prolonged Fasting: A Comparative Examination of Species From Five Vertebrate Classes

McCue, M. D., Passement, C. A., & Meyerholz, D. K. (2017) · The Anatomical Record · doi:10.1002/ar.23691 · Cited by 16

Prebiotics, Probiotics, and Synbiotics

Chen, L. A., & Sears, C. L. (2015) · Elsevier eBooks · doi:10.1016/b978-1-4557-4801-3.00003-5 · Cited by 18

Identification and characterization of the lipoprotein N -acyltransferase in Bacteroides

Armbruster, K. M., Jiang, J., Sartorio, M. G., Scott, N. E., Peterson, J. M., Sexton, J. Z., Feldman, M. F., & Koropatkin, N. M. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2410909121 · Cited by 15

Gut Microbiota and Alzheimer’s Disease: Pathophysiology and Therapeutic Perspectives

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Comparison of intestinal flora between patients with chronic and advanced Schistosoma japonicum infection

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In vitro fermentation and isolation of heparin-degrading bacteria from human gut microbiota

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Natural polysaccharides: Types, basic structure and suitability for forming hydrogels

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Microbiota and the human nature: know thyself

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The Hypothesis on Function of Glycosphingolipids and ABO Blood Groups Revisited

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Impact of Hibernation on Gut Microbiota and Intestinal Barrier Function in Ground Squirrels

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How Bacterial Communities Expand Functional Repertoires

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Large-scale computational analyses of gut microbial CAZyme repertoires enabled by CaymanPreprint

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Morphine and high-fat diet differentially alter the gut microbiota composition and metabolic function in lean versus obese mice

Blakeley‐Ruiz, J. A., McClintock, C. S., Shrestha, H. K., Poudel, S., Yang, Z. K., Giannone, R. J., Choo, J. J., Podar, M., Baghdoyan, H. A., Lydic, R., et al. (2022) · ISME Communications · doi:10.1038/s43705-022-00131-6 · Cited by 13

The immune interactions of gut glycans and microbiota in health and disease

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New approaches to secondary metabolite discovery from anaerobic gut microbes

Butkovich, L. V., Vining, O. B., & O’Malley, M. (2025) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-024-13393-y · Cited by 14

Remodeling the intestinal ecosystem toward better performance and intestinal health

Pedroso, A. A., Maurer, J. J., Cheng, Y., & Lee, M. D. (2012) · The Journal of Applied Poultry Research · doi:10.3382/japr.2011-00401 · Cited by 14

Bacterial colonization and TH17 immunity are shaped by intestinal sialylation in neonatal mice

Irons, E. E., Gomez, E. C., Andersen, V. L., & Lau, J. T. Y. (2022) · Glycobiology · doi:10.1093/glycob/cwac005 · Cited by 14

Entamoeba histolytica adaptation to glucose starvation: a matter of life and death

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Host-microbial interaction in the mammalian intestine and their metabolic role inside

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In vitro Fermentation of Digested Milk Fat Globule Membrane From Ruminant Milk Modulates Piglet Ileal and Caecal Microbiota

Thum, C., Young, W., Montoya, C. A., Roy, N. C., & McNabb, W. C. (2020) · Frontiers in Nutrition · doi:10.3389/fnut.2020.00091 · Cited by 14

In vitro ileal and caecal fermentation of fibre substrates in the growing pig given a human-type diet

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Adaptive foraging of a prominent human intestinal symbiont in gnotobiotic mice

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Mucosal Glycan Foraging Enhances Fitness and Transmission of a Saccharolytic Human Gut Bacterial Symbiont

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A Continuous Battle for Host-Derived Glycans Between a Mucus Specialist and a Glycan Generalist in vitro and in vivo

Kostopoulos, I., Aalvink, S., Kovatcheva‐Datchary, P., Nijsse, B., Bäckhed, F., Knol, J., de Vos, W. M., & Belzer, C. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.632454 · Cited by 40

Symbiotic Human Gut Bacteria with Variable Metabolic Priorities for Host Mucosal Glycans

Pudlo, N. A., Urs, K., Kumar, S. S., German, J. B., Mills, D. A., & Martens, E. C. (2015) · mBio · doi:10.1128/mbio.01282-15 · Cited by 187

Symbiotic Human Gut Bacteria with Variable Metabolic Priorities for

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