Utilization of amino acids by bacteria from the pig small intestine

Basic local alignment search tool

Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669 · see citing works

Ecological and Evolutionary Forces Shaping Microbial Diversity in the Human Intestine

Ley, R. E., Peterson, D. A., & Gordon, J. I. (2006) · Cell · doi:10.1016/j.cell.2006.02.017 · Cited by 3,358 · see citing works

Amino acids: Metabolism, functions, and nutrition

Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-009-0269-0 · Cited by 3,004 · see citing works

Amino acids and immune function

Li, P., Yin, Y., Li, D., Kim, S. W., & Wu, G. (2007) · British Journal Of Nutrition · doi:10.1017/s000711450769936x · Cited by 1,588 · see citing works

Arginine metabolism and nutrition in growth, health and disease

Wu, G., Bazer, F. W., Davis, T. A., Kim, S. W., Li, P., Marc Rhoads, J., Carey Satterfield, M., Smith, S. B., Spencer, T. E., & Yin, Y. (2009) · Amino Acids · doi:10.1007/s00726-008-0210-y · Cited by 1,362 · see citing works

Sequence heterogeneities of genes encoding 16S rRNAs in Paenibacillus polymyxa detected by temperature gradient gel electrophoresis

Nübel, U., Engelen, B., Felske, A., Snaidr, J., Wieshuber, A., Amann, R., Ludwig, W., & Backhaus, H. (1996) · Journal of Bacteriology · doi:10.1128/jb.178.19.5636-5643.1996 · Cited by 1,356 · see citing works

Rapid silver staining and recovery of PCR products separated on polyacrylamide gels.

Cj, S., Neto, E. D., & Aj, S. (1994) · PubMed · Cited by 1,179 · see citing works

Symbiotic gut microbes modulate human metabolic phenotypes

Li, M., Wang, B., Zhang, M., Rantalainen, M., Wang, S., Zhou, H., Zhang, Y., Shen, J., Pang, X., Zhang, M., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712038105 · Cited by 1,144 · see citing works

Lactate-Utilizing Bacteria, Isolated from Human Feces, That Produce Butyrate as a Major Fermentation Product

Duncan, S. H., Louis, P., & Flint, H. J. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.10.5810-5817.2004 · Cited by 1,124 · see citing works

Factors That Alter Rumen Microbial Ecology

Russell, J. B., & Rychlik, J. L. (2001) · Science · doi:10.1126/science.1058830 · Cited by 954 · see citing works

Culture-Independent Analysis of Gut Bacteria: the Pig Gastrointestinal Tract Microbiota Revisited

Leser, T. D., Amenuvor, J. Z., Jensen, T. K., Lindecrona, R. H., Boyé, M., & Møller, K. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.2.673-690.2002 · Cited by 868 · see citing works

Molecular Monitoring of Succession of Bacterial Communities in Human Neonates

Favier, C. F., Vaughan, E. E., de Vos, W. M., & Akkermans, A. D. L. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.1.219-226.2002 · Cited by 859 · see citing works

Intestinal mucosal amino acid catabolism.

Wu, G.-Y. (1998) · Journal of NutriLife · doi:10.1093/jn/128.8.1249 · Cited by 855 · see citing works

Interactions and competition within the microbial community of the human colon: links between diet and health

Flint, H. J., Duncan, S. H., Scott, K. P., & Louis, P. (2007) · Environmental Microbiology · doi:10.1111/j.1462-2920.2007.01281.x · Cited by 632 · see citing works

Catabolism dominates the first-pass intestinal metabolism of dietary essential amino acids in milk protein-fed piglets.

Stoll, B., Henry, J., Reeds, P., Yu, H., Jahoor, F., & Burrin, D. (1998) · Journal of NutriLife · doi:10.1093/jn/128.3.606 · Cited by 534 · see citing works

Fermentation in the large intestine of single-stomached animals and its relationship to animal health

Williams, B. A., Verstegen, M. W. A., & Tamminga, S. (2001) · Nutrition Research Reviews · doi:10.1079/nrr200127 · Cited by 467 · see citing works

Effects of amino acid-derived luminal metabolites on the colonic epithelium and physiopathological consequences

Blachier, F., Mariotti, F., Huneau, J. F., & Tomé, D. (2007) · Amino Acids · doi:10.1007/s00726-006-0477-9 · Cited by 452 · see citing works

Probiotic modulation of symbiotic gut microbial–host metabolic interactions in a humanized microbiome mouse model

Martin, F. J., Wang, Y., Sprenger, N., Yap, I. K. S., Lundstedt, T., Lek, P., Rezzi, S., Ramadan, Z., van Bladeren, P., Fay, L. B., et al. (2008) · Molecular Systems Biology · doi:10.1038/msb4100190 · Cited by 421 · see citing works

Contribution of microbial amino acids to amino acid homeostasis of the host

Metges, C. C. (2000) · The Journal of Nutrition · doi:10.1093/jn/130.7.1857s · Cited by 391 · see citing works

Dissimilatory Amino Acid Metabolism in Human Colonic Bacteria

Smith, E. A., & Macfarlane, G. T. (1997) · Anaerobe · doi:10.1006/anae.1997.0121 · Cited by 388 · see citing works

Glutamine, arginine, and leucine signaling in the intestine

Rhoads, J. M., & Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-008-0225-4 · Cited by 362 · see citing works

Post‐natal development of the porcine microbiota composition and activities

Konstantinov, S. R., Awati, A., Williams, B. A., Miller, B. G., Jones, P., Stokes, C., Akkermans, A. D. L., Smidt, H., & de Vos, W. M. (2006) · Environmental Microbiology · doi:10.1111/j.1462-2920.2006.01009.x · Cited by 350 · see citing works

Advances in protein–amino acid nutrition of poultry

Baker, D. H. (2008) · Amino Acids · doi:10.1007/s00726-008-0198-3 · Cited by 343 · see citing works

Dietary l-arginine supplementation increases muscle gain and reduces body fat mass in growing-finishing pigs

Tan, B., Yin, Y., Liu, Z., Xin-guo, L., Xu, H.-J., Kong, X., Huang, R., Tang, W., Shinzato, I., Smith, S. B., et al. (2008) · Amino Acids · doi:10.1007/s00726-008-0148-0 · Cited by 309 · see citing works

Amino acids and gut function

Wang, W. W., Qiao, S. Y., & Li, D. F. (2008) · Amino Acids · doi:10.1007/s00726-008-0152-4 · Cited by 292 · see citing works

Enumeration of amino acid fermenting bacteria in the human large intestine: effects of pH and starch on peptide metabolism and dissimilation of amino acids

Smith, E. A., & Macfarlane, G. T. (1998) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.1998.tb00487.x · Cited by 277 · see citing works

An in vitro batch culture method to assess potential fermentability of feed ingredients for monogastric diets

Williams, B. A., Bosch, M. W., Boer, H., Verstegen, M. W. A., & Tamminga, S. (2005) · Animal Feed Science and Technology · doi:10.1016/j.anifeedsci.2005.04.031 · Cited by 231 · see citing works

l-Arginine stimulates proliferation and prevents endotoxin-induced death of intestinal cells

Tan, B., Yin, Y., Kong, X., Li, P., Li, X., Gao, H., Li, X., Huang, R., & Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-009-0334-8 · Cited by 225 · see citing works

NITROGEN CYCLING IN THE GUT

Fuller, M. F., & Reeds, P. J. (1998) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.18.1.385 · Cited by 225 · see citing works

Isolation of DNA from bacterial samples of the human gastrointestinal tract

Zoetendal, E. G., Heilig, H. G. H. J., Klaassens, E. S., Booijink, C. C., Kleerebezem, M., Smidt, H., & de Vos, W. M. (2006) · Nature Protocols · doi:10.1038/nprot.2006.142 · Cited by 224 · see citing works

Dietary l-arginine supplementation enhances the immune status in early-weaned piglets

Tan, B., Li, X. G., Kong, X., Huang, R., Ruan, Z., Kang, Y., Deng, Z., Xie, M., Shinzato, I., Yin, Y., et al. (2008) · Amino Acids · doi:10.1007/s00726-008-0155-1 · Cited by 191 · see citing works

l-Glutamine or l-alanyl-l-glutamine prevents oxidant- or endotoxin-induced death of neonatal enterocytes

Haynes, T. E., Li, P., Li, X., Shimotori, K., Sato, H., Flynn, N. E., Wang, J., Knabe, D. A., & Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-009-0243-x · Cited by 183 · see citing works

Metabolomic analysis of the response of growing pigs to dietary l-arginine supplementation

He, Q., Kong, X., Wu, G., Ren, P., Tang, H., Hao, F., Huang, R., Li, T., Tan, B., Li, P., et al. (2008) · Amino Acids · doi:10.1007/s00726-008-0192-9 · Cited by 183 · see citing works

Intestinal nitrogen recycling and utilization in health and disease

Bergen, W. G., & Wu, G. (2009) · The Journal of Nutrition · doi:10.3945/jn.109.104497 · Cited by 183 · see citing works

Effect of fermentable carbohydrates on piglet faecal bacterial communities as revealed by denaturing gradient gel electrophoresis analysis of 16S ribosomal DNA

Konstantinov, S. R., Zhu, W., Williams, B. A., Tamminga, S., de Vos, W. M., & Akkermans, A. D. L. (2003) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2003.tb01062.x · Cited by 179 · see citing works

Stimulation of Butyrate Production by Gluconic Acid in Batch Culture of Pig Cecal Digesta and Identification of Butyrate-Producing Bacteria

Tsukahara, T., Koyama, H., Okada, M., & Ushida, K. (2002) · Journal of Nutrition · doi:10.1093/jn/132.8.2229 · Cited by 174 · see citing works

Amino Acid Composition of the Fetal Pig

Wu, G., OTT, T. L., Knabe, D. A., & Bazer, F. W. (1999) · Journal of Nutrition · doi:10.1093/jn/129.5.1031 · Cited by 174 · see citing works

Microbial Communities in the Human Small Intestine: Coupling Diversity to Metagenomics

Booijink, C. C., Zoetendal, E. G., Kleerebezem, M., & de Vos, W. M. (2007) · Future Microbiology · doi:10.2217/17460913.2.3.285 · Cited by 164 · see citing works

Histamine–cytokine connection in immunity and hematopoiesis

Dy, M., & Schneider, E. (2004) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2004.06.003 · Cited by 162 · see citing works

Panorganismal Gut Microbiome−Host Metabolic Crosstalk

Martin, F., Sprenger, N., Yap, I. K. S., Wang, Y., Bibiloni, R., Rochat, F., Rezzi, S., Cherbut, C., Kochhar, S., Lindon, J. C., et al. (2009) · Journal of Proteome Research · doi:10.1021/pr801068x · Cited by 161 · see citing works

Adaptive regulation of intestinal lysine metabolism

van Goudoever, J. B., Stoll, B., Henry, J. F., Burrin, D. G., & Reeds, P. J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.200371497 · Cited by 159 · see citing works

Ruminal Microbial Metabolism of Peptides and Amino Acids

Wallace, R. J. (1996) · Journal of Nutrition · doi:10.1093/jn/126.suppl_4.1326s · Cited by 159 · see citing works

Amino acids and gaseous signaling

Li, X., Bazer, F. W., Gao, H., Jobgen, W. S., Johnson, G. A., Li, P., McKnight, J. R., Satterfield, M. C., Spencer, T. E., & Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-009-0264-5 · Cited by 141 · see citing works

Pigs' Gastrointestinal Microflora Provide Them with Essential Amino Acids

Torrallardona, D., Harris, C. I., & Fuller, M. F. (2003) · Journal of Nutrition · doi:10.1093/jn/133.4.1127 · Cited by 140 · see citing works

Amino acid requirements in humans: with a special emphasis on the metabolic availability of amino acids

Elango, R., Ball, R. O., & Pencharz, P. B. (2009) · Amino Acids · doi:10.1007/s00726-009-0234-y · Cited by 139 · see citing works

Dietary supplementation with Astragalus polysaccharide enhances ileal digestibilities and serum concentrations of amino acids in early weaned piglets

Yin, F., Liu, Y., Yin, Y., Kong, X., Huang, R., Li, T. J., Wu, G., & Hou, Y. (2008) · Amino Acids · doi:10.1007/s00726-008-0142-6 · Cited by 133 · see citing works

Measuring splanchnic amino acid metabolism in vivo using stable isotopic tracers1,2

Stoll, B., & Burrin, D. G. (2006) · Journal of Animal Science · doi:10.2527/2006.8413_supple60x · Cited by 132 · see citing works

The high metabolic cost of a functional gut

van der Schoor, S. R. D., Reeds, P. J., Stoll, B., Henry, J. F., Rosenberger, J. N., Burrin, D. G., & van Goudoever, J. B. (2002) · Gastroenterology · doi:10.1053/gast.2002.37062 · Cited by 129 · see citing works

Catabolism of nutritionally essential amino acids in developing porcine enterocytes

Chen, L., Li, P., Wang, J., Li, X., Gao, H., Yin, Y., Hou, Y., & Wu, G. (2009) · Amino Acids · doi:10.1007/s00726-009-0268-1 · Cited by 127 · see citing works

16S rDNA analysis reveals low microbial diversity in community level physiological profile assays

Ros, M., Goberna, M., Pascual, J. A., Klammer, S. H., & Insam, H. (2008) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2008.01.003 · Cited by 121 · see citing works

The Uptake of Glutamine and Release of Arginine, Citruline and Proline by the Small Intestine of Developing Pigs ,

Wu, G., Borbolla, A. G., & Knabe, D. A. (1994) · Journal of Nutrition · doi:10.1093/jn/124.12.2437 · Cited by 120 · see citing works

Acidaminococcus gen. n., Acidaminococcus fermentans sp. n., Anaerobic Gram-negative Diplococci Using Amino Acids as the Sole Energy Source for Growth

Rogosa, M. (1969) · Journal of Bacteriology · doi:10.1128/jb.98.2.756-766.1969 · Cited by 113 · see citing works

Proteomic analysis reveals altered expression of proteins related to glutathione metabolism and apoptosis in the small intestine of zinc oxide-supplemented piglets

Wang, X., Ou, D., Yin, J., Wu, G., & Wang, J. (2009) · Amino Acids · doi:10.1007/s00726-009-0242-y · Cited by 111 · see citing works

A nutritive view on the host–pathogen interplay

Schaible, U. E., & Kaufmann, S. H. E. (2005) · Trends in Microbiology · doi:10.1016/j.tim.2005.06.009 · Cited by 106 · see citing works

Availability of intestinal microbial lysine for whole body lysine homeostasis in human subjects

Metges, C. C., El-Khoury, A. E., Henneman, L., Petzke, K. J., Grant, I., Bedri, S., Pereira, P. P., Ajami, A. M., Fuller, M. F., & Young, V. R. (1999) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1999.277.4.e597 · Cited by 100 · see citing works

Lysine synthesized by the gastrointestinal microflora of pigs is absorbed, mostly in the small intestine

Torrallardona, D., Harris, C. I., & Fuller, M. F. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00465.2002 · Cited by 80 · see citing works

Dietary supplementation with Chinese herbal powder enhances ileal digestibilities and serum concentrations of amino acids in young pigs

Kong, X., Yin, Y., He, Q. H., Yin, F., Liu, H. J., Li, T. J., Huang, R., Geng, M., Ruan, Z., Deng, Z., et al. (2008) · Amino Acids · doi:10.1007/s00726-008-0176-9 · Cited by 76 · see citing works

Amino acid use by the gastrointestinal tract of sheep given lucerne forage

Macrae, J., Bruce, L. A., Brown, D. S., & Calder, A. G. (1997) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1997.273.6.g1200 · Cited by 74 · see citing works

Degradation of Amino Acids by Pure Cultures of Rumen Bacteria

Scheifinger, C. C., Russell, N., & Chalupa, W. (1976) · Journal of Animal Science · doi:10.2527/jas1976.434821x · Cited by 71 · see citing works

Dietary supplementation with cholesterol and docosahexaenoic acid affects concentrations of amino acids in tissues of young pigs

Li, P., Kim, S. W., Li, X., Datta, S., Pond, W. G., & Wu, G. (2008) · Amino Acids · doi:10.1007/s00726-008-0196-5 · Cited by 67 · see citing works

In vitro oxidation of essential amino acids by jejunal mucosal cells of growing pigs

Chen, L., Yin, Y., Jobgen, W. S., Jobgen, S. C., Knabe, D. A., Hu, W., & Wu, G. (2007) · Livestock Science · doi:10.1016/j.livsci.2007.01.027 · Cited by 66 · see citing works

Studies on Amine Production in the Human Colon: Enumeration of Amine forming Bacteria and Physiological Effects of Carbohydrate and pH

Smith, E. A., & Macfarlane, G. T. (1996) · Anaerobe · doi:10.1006/anae.1996.0037 · Cited by 63 · see citing works

Colonic luminal ammonia and portal blood l-glutamine and l-arginine concentrations: a possible link between colon mucosa and liver ureagenesis

Eklou-Lawson, M., Bernard, F., Neveux, N., Chaumontet, C., Bos, C., Davila, A., Tomé, D., Cynober, L., & Blachier, F. (2008) · Amino Acids · doi:10.1007/s00726-008-0218-3 · Cited by 55 · see citing works

The in vitro uptake and metabolism of peptides and amino acids by five species of rumen bacteria

Ling, J. R., & Armstead, I. (1995) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1995.tb02831.x · Cited by 54 · see citing works

Effect of Microflora on the Free Amino Acid Distribution in Various Regions of the Mouse Gastrointestinal Tract

Whitt, D. D., & Demoss, R. D. (1975) · Applied Microbiology · doi:10.1128/am.30.4.609-615.1975 · Cited by 51 · see citing works

Assessment of metabolic diversity within the intestinal microbiota from healthy humans using combined molecular and cultural approaches

Chassard, C., Scott, K. P., Marquet, P., Martin, J. C., Del’Homme, C., Dapoigny, M. C., Flint, H. J., & Bernalier‐Donadille, A. (2008) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2008.00595.x · Cited by 51 · see citing works

Alternative fuels in the gastrointestinal tract

Burrin, D. G., & Reeds, P. J. (1997) · Current Opinion in Gastroenterology · doi:10.1097/00001574-199703000-00015 · Cited by 51 · see citing works

Catabolism of Amino Acids by Megasphaera elsdenii LC1

Wallace, R. J. (1986) · Applied and Environmental Microbiology · doi:10.1128/aem.51.5.1141-1143.1986 · Cited by 43 · see citing works

Alimentary proteins, amino acids and cholesterolemia

Blachier, F., Lancha, A. H., Boutry, C., & Tomé, D. (2009) · Amino Acids · doi:10.1007/s00726-009-0239-6 · Cited by 36 · see citing works

Amino Acid Deamination by Ruminal Megasphaera elsdenii Strains

Rychlik, J. L., LaVera, R., & Russell, J. B. (2002) · Current Microbiology · doi:10.1007/s00284-002-3743-4 · Cited by 31 · see citing works

Peptide and amino acid transport in Streptococcus bovis

Westlake, K., & Mackie, R. (1990) · Applied Microbiology and Biotechnology · doi:10.1007/bf00170931 · Cited by 24 · see citing works

Coarse structured feed stimulates members of the genera Lactobacillus and Mitsuokella as well as propionate and butyrate producers in the pig stomach

Mikkelsen, L. L., Højberg, O., & Jensen, B. B. (2007) · Livestock Science · doi:10.1016/j.livsci.2007.01.130 · Cited by 18 · see citing works

Analysis of diversity and function of the human small intestinal microbiota

Booijink, C. C. (2009) · doi:10.18174/4065 · Cited by 17 · see citing works

Effect of Microflora on the Free Amino Acid Distribution in Various Regions of the Mouse Gastrointestinal Tract

Whitt, D. D., & Demoss, R. D. (1975) · Applied Microbiology · doi:10.1128/aem.30.4.609-615.1975 · Cited by 17 · see citing works

Gut microbiota functions: metabolism of nutrients and other food components

Rowland, I., Gibson, G., Heinken, A., Scott, K., Swann, J., Thiele, I., & Tuohy, K. (2018) · European Journal of Nutrition · doi:10.1007/s00394-017-1445-8 · Cited by 2,878 · see citing works

The role of microbial amino acid metabolism in host metabolism

Neis, E., Dejong, C., & Rensen, S. (2015) · Nutrients · doi:10.3390/nu7042930 · Cited by 920 · see citing works

Functional Amino Acids in Growth, Reproduction, and Health

Wu, G. (2010) · Advances in Nutrition · doi:10.3945/an.110.1008 · Cited by 791 · see citing works

Glycine metabolism in animals and humans: implications for nutrition and health

Wang, W., Wu, Z., Dai, Z., Yang, Y., Wang, J., & Wu, G. (2013) · Amino Acids · doi:10.1007/s00726-013-1493-1 · Cited by 766 · see citing works

Proline and hydroxyproline metabolism: implications for animal and human nutrition

Wu, G., Bazer, F. W., Burghardt, R. C., Johnson, G. A., Kim, S. W., Knabe, D. A., Li, P., Li, X., McKnight, J. R., Satterfield, M. C., et al. (2010) · Amino Acids · doi:10.1007/s00726-010-0715-z · Cited by 688 · see citing works

Novel metabolic and physiological functions of branched chain amino acids: a review

Zhang, S., Zeng, X., Ren, M., Mao, X., & Qiao, S. (2017) · Journal of Animal Science and Biotechnology · doi:10.1186/s40104-016-0139-z · Cited by 639 · see citing works

Amino acid metabolism in intestinal bacteria: links between gut ecology and host health

Dai, Z. (2010) · Frontiers in bioscience · doi:10.2741/3820 · Cited by 563 · see citing works

Microbial Fermentation of Dietary Protein: An Important Factor in Diet–Microbe–Host Interaction

Diether, N. E., & Willing, B. P. (2019) · Microorganisms · doi:10.3390/microorganisms7010019 · Cited by 574 · see citing works

Intestinal luminal nitrogen metabolism: Role of the gut microbiota and consequences for the host

Davila, A.-M., Blachier, F., Gotteland, M., Andriamihaja, M., Benetti, P.-H., Sanz, Y., & Tomé, D. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2012.11.005 · Cited by 548 · see citing works

Diet, Gut Microbiota, and Obesity: Links with Host Genetics and Epigenetics and Potential Applications

Cuevas-Sierra, A., Ramos-Lopez, O., Riezu-Boj, J. I., Milagro, F. I., & Martinez, J. A. (2019) · Advances in Nutrition · doi:10.1093/advances/nmy078 · Cited by 523 · see citing works

Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis

Rusch, J. A., Layden, B. T., & Dugas, L. R. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1130689 · Cited by 415 · see citing works

Dietary requirements of “nutritionally non-essential amino acids” by animals and humans

Wu, G., Wu, Z., Dai, Z., Yang, Y., Wang, W., Liu, C., Wang, B., Wang, J., & Yin, Y. (2012) · Amino Acids · doi:10.1007/s00726-012-1444-2 · Cited by 393 · see citing works

Glycine Metabolism and Its Alterations in Obesity and Metabolic Diseases

Alves, A., Bassot, A., Bulteau, A., Pirola, L., & Morio, B. (2019) · Nutrients · doi:10.3390/nu11061356 · Cited by 371 · see citing works

Gut microbiota role in dietary protein metabolism and health-related outcomes: The two sides of the coin

Portune, K. J., Beaumont, M., Davila, A.-M., Tomé, D., Blachier, F., & Sanz, Y. (2016) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2016.08.011 · Cited by 356 · see citing works

Early microbial and metabolomic signatures predict later onset of necrotizing enterocolitis in preterm infants

Morrow, A. L., Lagomarcino, A. J., Schibler, K. R., Taft, D. H., Yu, Z., Wang, B., Altaye, M., Wagner, M., Gevers, D., Ward, D. V., et al. (2013) · Microbiome · doi:10.1186/2049-2618-1-13 · Cited by 341 · see citing works

Multifarious Beneficial Effect of Nonessential Amino Acid, Glycine: A Review

Razak, M. A., Begum, P. S., Viswanath, B., & Rajagopal, S. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/1716701 · Cited by 327 · see citing works

Advances in low-protein diets for swine

Wang, Y., Zhou, J., Wang, G., Cai, S., Zeng, X., & Qiao, S. (2018) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-018-0276-7 · Cited by 292 · see citing works

A review of metabolic potential of human gut microbiome in human nutrition

Yadav, M., Verma, M. K., & Chauhan, N. S. (2017) · Archives of Microbiology · doi:10.1007/s00203-017-1459-x · Cited by 288 · see citing works

Dietary Amino Acids and the Gut‐Microbiome‐Immune Axis: Physiological Metabolism and Therapeutic Prospects

Ma, N., & Ma, X. (2018) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/1541-4337.12401 · Cited by 278 · see citing works

Glutamine and intestinal barrier function

Wang, B., Wu, G., Zhou, Z., Dai, Z., Sun, Y., Ji, Y. S., Li, W., Wang, W., Liu, C., Han, F. X., et al. (2014) · Amino Acids · doi:10.1007/s00726-014-1773-4 · Cited by 267 · see citing works

Nutrients Mediate Intestinal Bacteria–Mucosal Immune Crosstalk

Ma, N., Guo, P., Zhang, J., He, T., Kim, S. W., Zhang, G., & Ma, X. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00005 · Cited by 248 · see citing works

TRIENNIAL GROWTH SYMPOSIUM: Important roles for L-glutamine in swine nutrition and production1,2

Wu, G., Bazer, F. W., Johnson, G. A., Knabe, D. A., Burghardt, R. C., Spencer, T. E., Li, X., & Wang, J. (2010) · Journal of Animal Science · doi:10.2527/jas.2010-3614 · Cited by 246 · see citing works

Re-print of “Intestinal luminal nitrogen metabolism: Role of the gut microbiota and consequences for the host”

Davila, A.-M., Blachier, F., Gotteland, M., Andriamihaja, M., Benetti, P.-H., Sanz, Y., & Tomé, D. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2013.01.003 · Cited by 231 · see citing works

Microbiota alterations in proline metabolism impact depression

Mayneris‐Perxachs, J., Castells‐Nobau, A., Arnoriaga‐Rodríguez, M., Martín, M., de la Vega-Correa, L., Zapata, C., Burokas, A., Blasco, G., Coll, C., Escrichs, A., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.04.001 · Cited by 229 · see citing works

Amino acid metabolism in intestinal bacteria and its potential implications for mammalian reproduction

Dai, Z., Wu, Z., Hang, S., Zhu, W., & Wu, G. (2015) · Molecular Human Reproduction · doi:10.1093/molehr/gav003 · Cited by 228 · see citing works

Mechanisms Linking the Gut Microbiome and Glucose Metabolism

Utzschneider, K. M., Kratz, M., Damman, C. J., & Hullarg, M. (2016) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2015-4251 · Cited by 223 · see citing works

Dietary Arginine Supplementation of Mice Alters the Microbial Population and Activates Intestinal Innate Immunity

Ren, W., Chen, S., Yin, J., Duan, J., Li, T., Liu, G., Feng, Z., Tan, B., Yin, Y., & Wu, G. (2014) · Journal of Nutrition · doi:10.3945/jn.114.192120 · Cited by 189 · see citing works

Comparison of adhesive gut bacteria composition, immunity, and disease resistance in juvenile hybrid tilapia fed two different Lactobacillus strains

Liu, W., Ren, P., He, S., Xu, L., Yang, Y., Gu, Z., & Zhou, Z. (2013) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2013.04.010 · Cited by 173 · see citing works

Alpha-ketoglutarate inhibits glutamine degradation and enhances protein synthesis in intestinal porcine epithelial cells

Kang, Y., Yin, Y., Li, X., Xi, P., Wang, J., Lei, J., Hou, Y., & Wu, G. (2011) · Amino Acids · doi:10.1007/s00726-011-1060-6 · Cited by 166 · see citing works

l-Arginine stimulates the mTOR signaling pathway and protein synthesis in porcine trophectoderm cells

Kong, X., Tan, B., Yin, Y., Gao, H., Li, X., Jaeger, L. A., Bazer, F. W., & Wu, G. (2011) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2011.06.012 · Cited by 166 · see citing works

Dietary supplementation with monosodium glutamate is safe and improves growth performance in postweaning pigs

Rezaei, R., Knabe, D. A., Tekwe, C. D., DAHANAYAKA, S. A., Ficken, M. D., Fielder, S. E., Eide, S. J., Lovering, S. L., & Wu, G. (2012) · Amino Acids · doi:10.1007/s00726-012-1420-x · Cited by 164 · see citing works

Glycine Stimulates Protein Synthesis and Inhibits Oxidative Stress in Pig Small Intestinal Epithelial Cells

Wang, W., Wu, Z., Lin, G., Hu, S., Wang, B., Dai, Z., & Wu, G. (2014) · Journal of Nutrition · doi:10.3945/jn.114.194001 · Cited by 155 · see citing works

The Colonic Microbiome and Epithelial Transcriptome Are Altered in Rats Fed a High-Protein Diet Compared with a Normal-Protein Diet

Mu, C., Yang, Y., Luo, Z., Guan, L. L., & Zhu, W. (2016) · Journal of Nutrition · doi:10.3945/jn.115.223990 · Cited by 146 · see citing works

Supplementation with branched-chain amino acids to a low-protein diet regulates intestinal expression of amino acid and peptide transporters in weanling pigs

Zhang, S., Qiao, S., Ren, M., Zeng, X., Ma, X., Wu, Z., Thacker, P. A., & Wu, G. (2013) · Amino Acids · doi:10.1007/s00726-013-1577-y · Cited by 143 · see citing works

l-Glutamine regulates amino acid utilization by intestinal bacteria

Dai, Z., Li, X.-L., Xi, P., Zhang, J., Wu, G., & Zhu, W. (2012) · Amino Acids · doi:10.1007/s00726-012-1264-4 · Cited by 135 · see citing works

Intestinal microbiota and its interaction to intestinal health in nursery pigs

Duarte, M. E., & Kim, S. W. (2021) · Animal nutrition · doi:10.1016/j.aninu.2021.05.001 · Cited by 137 · see citing works

Metabolism of select amino acids in bacteria from the pig small intestine

Dai, Z., Li, X.-L., Xi, P., Zhang, J., Wu, G., & Zhu, W. (2011) · Amino Acids · doi:10.1007/s00726-011-0846-x · Cited by 130 · see citing works

L-Tryptophan Activates Mammalian Target of Rapamycin and Enhances Expression of Tight Junction Proteins in Intestinal Porcine Epithelial Cells ,

Wang, H., Ji, Y. S., Wu, G., Sun, K., Sun, Y., Li, W., Wang, B., He, B., Zhang, Q., Dai, Z., et al. (2015) · Journal of Nutrition · doi:10.3945/jn.114.209817 · Cited by 127 · see citing works

Antibiotics-induced modulation of large intestinal microbiota altered aromatic amino acid profile and expression of neurotransmitters in the hypothalamus of piglets

Gao, K., Pi, Y., Mu, C., Peng, Y., Huang, Z., & Zhu, W. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14333 · Cited by 119 · see citing works

Differences in Microbiota Membership along the Gastrointestinal Tract of Piglets and Their Differential Alterations Following an Early-Life Antibiotic Intervention

Mu, C., Yang, Y., Su, Y., Zoetendal, E. G., & Zhu, W. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00797 · Cited by 115 · see citing works

Methionine Nutrition and Metabolism:Insights from Animal Studies to Inform Human Nutrition

Elango, R. (2020) · Journal of Nutrition · doi:10.1093/jn/nxaa155 · Cited by 112 · see citing works

Functional Amino Acids in Pigs and Chickens: Implication for Gut Health

Chalvon‐Demersay, T., Luise, D., Floc'H, N. L., Tesseraud, S., Lambert, W., Bosi, P., Trevisi, P., Beaumont, M., & Corrent, E. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.663727 · Cited by 115 · see citing works

Microbial osteoporosis: The interplay between the gut microbiota and bones via host metabolism and immunity

Li, L., Rao, S., Cheng, Y., Zhuo, X., Deng, C., Xu, N., Zhang, H., & Yang, L. (2019) · MicrobiologyOpen · doi:10.1002/mbo3.810 · Cited by 109 · see citing works

Dietary l-glutamine supplementation modulates microbial community and activates innate immunity in the mouse intestine

Ren, W., Duan, J., Yin, J., Liu, G., Cao, Z. Y., Xiong, X., Chen, S., Li, T., Yin, Y., Hou, Y., et al. (2014) · Amino Acids · doi:10.1007/s00726-014-1793-0 · Cited by 106 · see citing works

Swine gut microbiota and its interaction with host nutrient metabolism

Wang, H., Xu, R., Zhang, H., Su, Y., & Zhu, W. (2020) · Animal nutrition · doi:10.1016/j.aninu.2020.10.002 · Cited by 109 · see citing works

Characteristics and nutrient function of intestinal bacterial communities in black soldier fly ( Hermetia illucens L.) larvae in livestock manure conversion

Ao, Y., Yang, C., Wang, S., Hu, Q., Li, Y., Zhang, J., Yu, Z., Cai, M., & Yu, C. (2020) · Microbial Biotechnology · doi:10.1111/1751-7915.13595 · Cited by 107 · see citing works

Resistant starch: Implications of dietary inclusion on gut health and growth in pigs: a review

Tan, F., Beltranena, E., & Zijlstra, R. T. (2021) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-021-00644-5 · Cited by 110 · see citing works

Evaluating the profound effect of gut microbiome on host appetite in pigs

Yang, H., Yang, M. J., Fang, S., Huang, X., He, M., Ke, S., Gao, J., Wu, J., Zhou, Y., Fu, H., et al. (2018) · BMC Microbiology · doi:10.1186/s12866-018-1364-8 · Cited by 108 · see citing works

Amino Acid Catabolism: An Overlooked Area of Metabolism

Torres, N., Tobón‐Cornejo, S., Velázquez‐Villegas, L. A., Noriega, L. G., Alemán, G., & Tovar, A. R. (2023) · Nutrients · doi:10.3390/nu15153378 · Cited by 104 · see citing works

Functional role of branched chain amino acids in poultry: a review

Kim, W. K., Singh, A. K., Wang, J., & Applegate, T. J. (2022) · Poultry Science · doi:10.1016/j.psj.2022.101715 · Cited by 102 · see citing works

Dietary supplementation of sodium butyrate may benefit growth performance and intestinal function in juvenile grass carp ( Ctenopharyngodon idellus )

Liu, M., Guo, W., Wu, F., Qu, Q., Tan, Q., & Gong, W. (2016) · Aquaculture Research · doi:10.1111/are.13230 · Cited by 99 · see citing works

Necrotizing enterocolitis: The intestinal microbiome, metabolome and inflammatory mediators

Neu, J., & Pammi, M. (2018) · Seminars in Fetal and Neonatal Medicine · doi:10.1016/j.siny.2018.08.001 · Cited by 97 · see citing works

Amino Acids in Intestinal Physiology and Health

Beaumont, M., & Blachier, F. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-45328-2_1 · Cited by 98 · see citing works

Monensin and Nisin Affect Rumen Fermentation and Microbiota Differently In Vitro

Shen, J., Liu, Z., Yu, Z., & Zhu, W. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01111 · Cited by 94 · see citing works

Functional amino acids in the development of the pig placenta

Wu, G., Bazer, F. W., Johnson, G. A., Herring, C. M., Seo, H., Dai, Z., Wang, J., Wu, Z., & Wang, X. (2017) · Molecular Reproduction and Development · doi:10.1002/mrd.22809 · Cited by 93 · see citing works

Protective effect of glutamine and arginine against soybean meal-induced enteritis in the juvenile turbot (Scophthalmus maximus)

Gu, M., Bai, N., Xu, B., Xu, X., Jia, Q., & Zhang, Z. (2017) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2017.08.048 · Cited by 90 · see citing works

Putrescine Stimulates the mTOR Signaling Pathway and Protein Synthesis in Porcine Trophectoderm Cells1

Kong, X., Wang, X., Yin, Y., Li, X., Gao, H., Bazer, F. W., & Wu, G. (2014) · Biology of Reproduction · doi:10.1095/biolreprod.113.113977 · Cited by 87 · see citing works

Nutritional and regulatory role of branched-chain amino acids in lactation

Lei, J. (2012) · Frontiers in bioscience · doi:10.2741/4082 · Cited by 86 · see citing works

Dietary l-leucine supplementation enhances intestinal development in suckling piglets

Sun, Y., Wu, Z., Li, W., Zhang, C., Sun, K., Ji, Y. S., Bin, W., Jiao, N., He, B., Wang, W., et al. (2015) · Amino Acids · doi:10.1007/s00726-015-1985-2 · Cited by 85 · see citing works

Effects of dietary l-lysine intake on the intestinal mucosa and expression of CAT genes in weaned piglets

He, L., Yang, H., Hou, Y., Li, T., Fang, J. Q., Zhou, X., Yin, Y., Wu, L., Nyachoti, C. M., & Wu, G. (2013) · Amino Acids · doi:10.1007/s00726-013-1514-0 · Cited by 83 · see citing works

Regulatory role for l-arginine in the utilization of amino acids by pig small-intestinal bacteria

Dai, Z., Li, X.-L., Xi, P., Zhang, J., Wu, G., & Zhu, W. (2011) · Amino Acids · doi:10.1007/s00726-011-1067-z · Cited by 82 · see citing works

Mediterranean Diet to Prevent the Development of Colon Diseases: A Meta-Analysis of Gut Microbiota Studies

Illescas, O., Rodríguez‐Sosa, M., & Gariboldi, M. (2021) · Nutrients · doi:10.3390/nu13072234 · Cited by 80 · see citing works

Regulation of intestinal health by branched‐chain amino acids

Zhou, H. W., Yu, B., Gao, J. L., Htoo, J. K. K., & Chen, D. (2017) · Animal Science Journal · doi:10.1111/asj.12937 · Cited by 74 · see citing works

Regulation of protein turnover by l-glutamine in porcine intestinal epithelial cells

Xi, P., Jiang, Z., Dai, Z., Li, X., Kang, Y., Zheng, C., Lin, Y., Wang, J., & Wu, G. (2011) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2011.05.009 · Cited by 74 · see citing works

Dietary Nutrients Mediate Intestinal Host Defense Peptide Expression

Wu, J., Ma, N., Johnston, L. J., & Ma, X. (2019) · Advances in Nutrition · doi:10.1093/advances/nmz057 · Cited by 74 · see citing works

Metagenomics Reveals Seasonal Functional Adaptation of the Gut Microbiome to Host Feeding and Fasting in the Chinese Alligator

Tang, K., Wang, Z., Wan, Q., & Fang, S. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02409 · Cited by 67 · see citing works

Multiomics Approach to Explore the Amelioration Mechanisms of Glucomannans on the Metabolic Disorder of Type 2 Diabetic Rats

Chen, H., Nie, Q., Hu, J., Huang, X., Yin, J., & Nie, S. (2021) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c07871 · Cited by 68 · see citing works

Amino acid utilization allows intestinal dominance of Lactobacillus amylovorus

Jing, Y., Mu, C., Wang, H., Shen, J., Zoetendal, E. G., & Zhu, W. (2022) · The ISME Journal · doi:10.1038/s41396-022-01287-8 · Cited by 68 · see citing works

Effect of very low-protein diets supplemented with branched-chain amino acids on energy balance, plasma metabolomics and fecal microbiome of pigs

Spring, S., Premathilake, H., Bradway, C., Shili, C. N., DeSilva, U., Carter, S., & Pezeshki, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-72816-8 · Cited by 67 · see citing works

The small intestine: dining table of host–microbiota meetings

Delbaere, K., Roegiers, I. H., Bron, A., Durif, C., de Wiele, T. V., Blanquet‐Diot, S., & Marinelli, L. (2023) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuad022 · Cited by 69 · see citing works

Amino acid metabolism in the portal-drained viscera of young pigs: effects of dietary supplementation with chitosan and pea hull

Yin, Y., Huang, R., Li, T., Ruan, Z., Xie, M., Deng, Z., Hou, Y., & Wu, G. (2010) · Amino Acids · doi:10.1007/s00726-010-0577-4 · Cited by 63 · see citing works

Alteration of metabolomic markers of amino-acid metabolism in piglets with in-feed antibiotics

Mu, C., Yang, Y., Yu, K., Yu, M., Zhang, C., Su, Y., & Zhu, W. (2017) · Amino Acids · doi:10.1007/s00726-017-2379-4 · Cited by 59 · see citing works

Gastrointestinal interaction between dietary amino acids and gut microbiota: with special emphasis on host nutrition

Abdallah, A., Elemba, E., Zhong, Q., & Sun, Z. (2020) · Current Protein & Peptide Science · doi:10.2174/1389203721666200212095503 · Cited by 59 · see citing works

Increases in circulating amino acids with in-feed antibiotics correlated with gene expression of intestinal amino acid transporters in piglets

Yu, M., Mu, C., Yang, Y., Zhang, C., Su, Y., Huang, Z., Yu, K., & Zhu, W. (2017) · Amino Acids · doi:10.1007/s00726-017-2451-0 · Cited by 56 · see citing works

Amino Acid Nutrition and Reproductive Performance in Ruminants

Gilbreath, K. R., Bazer, F. W., Satterfield, M. C., & Wu, G. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-54462-1_4 · Cited by 56 · see citing works

Host-microbiota interaction in intestinal stem cell homeostasis

Wu, H., Mu, C., Xu, L., Yu, K., Shen, L., & Zhu, W. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2353399 · Cited by 57 · see citing works

Dietary l-glutamine supplementation increases Pasteurella multocida burden and the expression of its major virulence factors in mice

Ren, W., Liu, S., Chen, S., Zhang, F., Li, N., Yin, J., Peng, Y., Wu, L., Liu, G., Yin, Y., et al. (2013) · Amino Acids · doi:10.1007/s00726-013-1551-8 · Cited by 54 · see citing works

Time-course responses of ileal and fecal microbiota and metabolite profiles to antibiotics in cannulated pigs

Gao, K., Pi, Y., Peng, Y., Mu, C., & Zhu, W. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-8774-2 · Cited by 53 · see citing works

Succinate signaling attenuates high-fat diet-induced metabolic disturbance and intestinal barrier dysfunction

Li, X., Huang, G., Zhang, Y., Ren, Y., Zhang, R., Zhu, W., & Yu, K. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106865 · Cited by 51 · see citing works

Host transcriptome and microbiome interaction modulates physiology of full-sibs broilers with divergent feed conversion ratio

Shah, T. M., Patel, J. G., Gohil, T. P., Blake, D. P., & Joshi, C. G. (2019) · npj Biofilms and Microbiomes · doi:10.1038/s41522-019-0096-3 · Cited by 50 · see citing works

Antibiotic-induced alterations of the gut microbiota and microbial fermentation in protein parallel the changes in host nitrogen metabolism of growing pigs

Pi, Y., Gao, K., Peng, Y., Mu, C., & Zhu, W. (2018) · animal · doi:10.1017/s1751731118001416 · Cited by 49 · see citing works

Dietary influences on the Dahl SS rat gut microbiota and its effects on salt‐sensitive hypertension and renal damage

Abais‐Battad, J. M., Saravia, F. L., Lund, H., Dasinger, J. H., Fehrenbach, D. J., Alsheikh, A. J., Zemaj, J., Kirby, J. R., & Mattson, D. L. (2021) · Acta Physiologica · doi:10.1111/apha.13662 · Cited by 49 · see citing works

Important roles of amino acids in immune responses

Li, P., & Wu, G. (2021) · British Journal Of Nutrition · doi:10.1017/s0007114521004566 · Cited by 49 · see citing works

Amino Acids in Microbial Metabolism and Function

Dai, Z., Wu, Z., Zhu, W., & Wu, G. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-85686-1_7 · Cited by 48 · see citing works

Selective nourishing of gut microbiota with amino acids: A novel prebiotic approach?

Beaumont, M., Roura, E., Lambert, W., Turni, C., Michiels, J., & Chalvon‐Demersay, T. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1066898 · Cited by 48 · see citing works

Important impacts of intestinal bacteria on utilization of dietary amino acids in pigs

Yang, Y., Dai, Z., & Zhu, W. (2014) · Amino Acids · doi:10.1007/s00726-014-1807-y · Cited by 48 · see citing works

The biological functions and metabolic pathways of valine in swine

Wang, C., Peng, Y., Zhang, Y., Xu, J., Jiang, S., Wang, L., & Yin, Y. (2023) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-023-00927-z · Cited by 46 · see citing works

Effect of added dietary threonine on growth performance, health, immunity and gastrointestinal function of weaning pigs with differing genetic susceptibility to E scherichia coli infection and challenged with E . coli K88ac

Trevisi, P., Corrent, E., Mazzoni, M., Messori, S., Priori, D., Gherpelli, Y., Simongiovanni, A., & Bosi, P. (2014) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.12216 · Cited by 45 · see citing works

Alpha-Ketoglutarate in Low-Protein Diets for Growing Pigs: Effects on Cecal Microbial Communities and Parameters of Microbial Metabolism

Chen, J., Kang, B., Jiang, Q., Han, M., Zhao, Y., Long, L., Fu, C., & Kang, Y. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01057 · Cited by 45 · see citing works

NAD+ and its possible role in gut microbiota: Insights on the mechanisms by which gut microbes influence host metabolism

Ren, Z., Xu, Y., Li, T., Sun, W., Tang, Z., Wang, Y., Zhou, K., Li, J., Ding, Q., Liang, K., et al. (2022) · Animal Nutrition · doi:10.1016/j.aninu.2022.06.009 · Cited by 44 · see citing works

Unveiling the role of gut-brain axis in regulating neurodegenerative diseases: A comprehensive review

Yadav, H., Jaldhi, Bhardwaj, R., Anamika, A., Bakshi, A., Gupta, S., & Maurya, S. K. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122022 · Cited by 46 · see citing works

Single amino acid utilization for bacterial categorization

Liu, Y., Kuo, H.-C., Lai, C., & Chou, C. (2020) · Scientific Reports · doi:10.1038/s41598-020-69686-5 · Cited by 44 · see citing works

Swine Gastrointestinal Microbiota and the Effects of Dietary Amino Acids on Its Composition and Metabolism

Liao, S. F., Ji, F., Fan, P. F., & Denryter, K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021237 · Cited by 46 · see citing works

Effect of susceptibility to enterotoxigenic Escherichia coli F4 and of dietary tryptophan on gut microbiota diversity observed in healthy young pigs

Messori, S., Trevisi, P., Simongiovanni, A., Priori, D., & Bosi, P. (2012) · Veterinary Microbiology · doi:10.1016/j.vetmic.2012.09.001 · Cited by 41 · see citing works

Functional roles of xylanase enhancing intestinal health and growth performance of nursery pigs by reducing the digesta viscosity and modulating the mucosa-associated microbiota in the jejunum

Moita, V. H. C., Duarte, M. E., & Kim, S. W. (2022) · Journal of Animal Science · doi:10.1093/jas/skac116 · Cited by 40 · see citing works

Effects of dietary scFOS and lactobacilli on survival, growth, and disease resistance of hybrid tilapia

Liu, W., Wang, W., Ran, C., He, S., Yang, Y., & Zhou, Z. (2016) · Aquaculture · doi:10.1016/j.aquaculture.2016.12.013 · Cited by 40 · see citing works

The inhibition of high ammonia to in vitro rumen fermentation is pH dependent

Shen, J., Zheng, W., Xu, Y., & Yu, Z. (2023) · Frontiers in Veterinary Science · doi:10.3389/fvets.2023.1163021 · Cited by 39 · see citing works

Changes in the Ileal, but Not Fecal, Microbiome in Response to Increased Dietary Protein Level and Enterotoxigenic Escherichia coli Exposure in Pigs

Pollock, J., Hutchings, M. R., Hutchings, K. E. K., Gally, D. L., & Houdijk, J. G. M. (2019) · Applied and Environmental Microbiology · doi:10.1128/aem.01252-19 · Cited by 39 · see citing works

Dietary supplementation with monosodium l-glutamate modifies lipid composition and gene expression related to lipid metabolism in growing pigs fed a normal- or high-fat diet

Kong, X. F., Zhou, X. L., Feng, Z., Li, F. N., Ji, Y., Tan, B., Liu, Y. Y., Geng, M., Wu, G., Blachier, F., et al. (2015) · Livestock Science · doi:10.1016/j.livsci.2015.06.023 · Cited by 38 · see citing works

Low-protein diets supplemented with casein hydrolysate favor the microbiota and enhance the mucosal humoral immunity in the colon of pigs

Wang, H., Shen, J., Pi, Y., Gao, K., & Zhu, W. (2019) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-019-0387-9 · Cited by 37 · see citing works

Metabolism of select amino acids in bacteria from the pig small intestine

Dai, Z., Li, X.-L., Xi, P., Zhang, J., Wu, G., & Zhu, W. (2011) · Amino Acids · doi:10.1007/s00726-011-0846-x · Cited by 130 · see citing works

Important impacts of intestinal bacteria on utilization of dietary amino acids in pigs

Yang, Y., Dai, Z., & Zhu, W. (2014) · Amino Acids · doi:10.1007/s00726-014-1807-y · Cited by 48 · see citing works

Regulatory role for l-arginine in the utilization of amino acids by pig small-intestinal bacteria

Dai, Z., Li, X.-L., Xi, P., Zhang, J., Wu, G., & Zhu, W. (2011) · Amino Acids · doi:10.1007/s00726-011-1067-z · Cited by 82 · see citing works

[Metabolic pattern of pig hindgut bacteria on aromatic amino acids by an in vitro fermentation method].

Ma, M., He, X., & Zhu, W. (2016) · PubMed · Cited by 3 · see citing works

Amino acid metabolism by pig intestinal bacteria and consequences for intestinal health and environment: current knowledge and future directions

Blachier, F., Tang, M., & Wu, T. (2026) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-026-01491-y