Symposium review: microbial endocrinology—why the integration of microbes, epithelial cells, and neurochemical signals in the digestive tract matters to ruminant health

Evolution of mammals and their gut microbes

Ley, R. E., Hamady, M., Lozupone, C., Turnbaugh, P. J., Ramey, R. R., Bircher, J. S., Schlegel, M. L., Tucker, T. A., Schrenzel, M. D., Knight, R., et al. (2008) · Science · doi:10.1126/science.1155725 · Cited by 3,747 · see citing works

Gut microbiota composition correlates with diet and health in the elderly

Claesson, M. J., Jeffery, I. B., Conde, S., Power, S. E., O’Connor, E. M., Cusack, S., Harris, H. M. B., Coakley, M., Lakshminarayanan, B., O’Sullivan, O., et al. (2012) · Nature · doi:10.1038/nature11319 · Cited by 3,314 · see citing works

Biogenic amines: their importance in foods.

Santos, M. H. S. (1996) · International Journal of Food Microbiology · doi:10.1016/0168-1605(95)00032-1 · Cited by 1,516 · see citing works

Signals from the gut microbiota to distant organs in physiology and disease

Schroeder, B. O., & Bäckhed, F. (2016) · Nature Medicine · doi:10.1038/nm.4185 · Cited by 1,409 · see citing works

Anti-virulence strategies to combat bacteria-mediated disease

Rasko, D. A., & Sperandio, V. (2010) · Nature Reviews Drug Discovery · doi:10.1038/nrd3013 · Cited by 1,383 · see citing works

The adherent gastrointestinal mucus gel layer: thickness and physical state in vivo

Atuma, C., Strugala, V., Allen, A., & Holm, L. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.280.5.g922 · Cited by 1,083 · see citing works

Decreased Diversity of the Fecal Microbiome in Recurrent<i>Clostridium difficile</i>–Associated Diarrhea

Chang, J. Y., Antonopoulos, D. A., Kalra, A., Tonelli, A., Khalife, W. T., Schmidt, T. M., & Young, V. B. (2008) · The Journal of Infectious Diseases · doi:10.1086/525047 · Cited by 1,010 · see citing works

Metabolic and hormonal acclimation to heat stress in domesticated ruminants

Bernabucci, U., Lacetera, N., Baumgard, L. H., Rhoads, R. P., Ronchi, B., & Nardone, A. (2010) · animal · doi:10.1017/s175173111000090x · Cited by 966 · see citing works

Effects of Heat Stress on Postabsorptive Metabolism and Energetics

Baumgard, L. H., & Rhoads, R. P. (2012) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-031412-103644 · Cited by 909 · see citing works

Inter-kingdom signalling: Communication between bacteria and their hosts

Hughes, D. T., & Sperandio, V. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1836 · Cited by 761 · see citing works

Major Advances Associated with Environmental Effects on Dairy Cattle

Collier, R. J., Dahl, G. E., & VanBaale, M. J. (2006) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(06)72193-2 · Cited by 681 · see citing works

Critical role of gut microbiota in the production of biologically active, free catecholamines in the gut lumen of mice

Asano, Y., Hiramoto, T., Nishino, R., Aiba, Y., Kimura, T., Yoshihara, K., Koga, Y., & Sudo, N. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00341.2012 · Cited by 659 · see citing works

The QseC sensor kinase: A bacterial adrenergic receptor

Clarke, M. B., Hughes, D. T., Zhu, C., Boedeker, E. C., & Sperandio, V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604343103 · Cited by 621 · see citing works

The gut as a sensory organ

Furness, J. B., Rivera, L. R., Cho, H., Bravo, D. M., & Callaghan, B. P. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.180 · Cited by 549 · see citing works

Specialized metabolites from the microbiome in health and disease

Sharon, G., Garg, N., Debelius, J., Knight, R., Dorrestein, P. C., & Mazmanian, S. K. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.10.016 · Cited by 544 · see citing works

Characterising the bacterial microbiota across the gastrointestinal tracts of dairy cattle: membership and potential function

Mao, S., Zhang, M., Liu, J., & Zhu, W. (2015) · Scientific Reports · doi:10.1038/srep16116 · Cited by 532 · see citing works

Invited review: Inflammation during the transition to lactation: New adventures with an old flame

Bradford, B. J., Yuan, K., Farney, J. K., Mamedova, L. K., & Carpenter, A. J. (2015) · Journal of Dairy Science · doi:10.3168/jds.2015-9683 · Cited by 480 · see citing works

Catecholamine induced growth of gram negative bacteria

Lyte, M., & Ernst, S. (1992) · Life Sciences · doi:10.1016/0024-3205(92)90273-r · Cited by 396 · see citing works

Livestock metabolomics and the livestock metabolome: A systematic review

Goldansaz, S. A., Guo, A. C., Sajed, T., Steele, M. A., Plastow, G. S., & Wishart, D. S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177675 · Cited by 379 · see citing works

Bioactive Molecules Released in Food by Lactic Acid Bacteria: Encrypted Peptides and Biogenic Amines

Pessione, E., & Cirrincione, S. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00876 · Cited by 333 · see citing works

Development and physiology of the rumen and the lower gut: Targets for improving gut health

Steele, M. A., Penner, G. B., Chaucheyras‐Durand, F., & Guan, L. L. (2016) · Journal of Dairy Science · doi:10.3168/jds.2015-10351 · Cited by 302 · see citing works

RUMINANT NUTRITION SYMPOSIUM: Ruminant Production and Metabolic Responses to Heat Stress1,2

Baumgard, L. H., & Rhoads, R. P. (2011) · Journal of Animal Science · doi:10.2527/jas.2011-4675 · Cited by 235 · see citing works

Functional organization of the bovine rumen epithelium

Graham, C., & Simmons, N. L. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00425.2004 · Cited by 233 · see citing works

Microbial Endocrinology and the Microbiota-Gut-Brain Axis

Lyte, M. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-0897-4_1 · Cited by 227 · see citing works

Understanding host-microbial interactions in rumen: searching the best opportunity for microbiota manipulation

Malmuthuge, N., & Guan, L. L. (2017) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-016-0135-3 · Cited by 204 · see citing works

Siderophore-mediated iron acquisition and modulation of host-bacterial interactions

Ellermann, M., & Arthur, J. C. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.10.489 · Cited by 186 · see citing works

Neuroendocrine–Bacterial Interactions in a Neurotoxin-Induced Model of Trauma

Lyte, M., & Bailey, M. T. (1997) · Journal of Surgical Research · doi:10.1006/jsre.1997.5130 · Cited by 168 · see citing works

From pre- to postweaning: transformation of the young calf's gastrointestinal tract

Meale, S. J., Chaucheyras-Durand, F., Berends, H., Guan, L. L., & Steele, M. A. (2017) · Journal of Dairy Science · doi:10.3168/jds.2016-12474 · Cited by 163 · see citing works

Bacterial Adrenergic Sensors Regulate Virulence of Enteric Pathogens in the Gut

Moreira, C. G., Russell, R., Mishra, A. A., Narayanan, S., Ritchie, J. M., Waldor, M. K., Curtis, M. M., Winter, S. E., Weinshenker, D., & Sperandio, V. (2016) · mBio · doi:10.1128/mbio.00826-16 · Cited by 157 · see citing works

Challenges of metabolomics in human gut microbiota research

Smirnov, K. S., Maier, T. V., Walker, A., Heinzmann, S. S., Forcisi, S., Martínez, I., Walter, J., & Schmitt‐Kopplin, P. (2016) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2016.03.006 · Cited by 153 · see citing works

Elucidation of the Mechanism by Which Catecholamine Stress Hormones Liberate Iron from the Innate Immune Defense Proteins Transferrin and Lactoferrin

Sandrini, S. M., Shergill, R., Woodward, J., Muralikuttan, R., Haigh, R. D., Lyte, M., & Freestone, P. P. (2010) · Journal of Bacteriology · doi:10.1128/jb.01028-09 · Cited by 143 · see citing works

QseC Inhibitors as an Antivirulence Approach for Gram-Negative Pathogens

Curtis, M. M., Russell, R., Moreira, C. G., Adebesin, A. M., Wang, C., Williams, N. S., Taussig, R., Stewart, D., Zimmern, P., Lu, B., et al. (2014) · mBio · doi:10.1128/mbio.02165-14 · Cited by 136 · see citing works

Rumen Function and Development

Baldwin, R. L., & Connor, E. E. (2017) · Veterinary Clinics of North America Food Animal Practice · doi:10.1016/j.cvfa.2017.06.001 · Cited by 119 · see citing works

The Neuroendocrine Stress Hormone Norepinephrine Augments Escherichia coli O157:H7-Induced Enteritis and Adherence in a Bovine Ligated Ileal Loop Model of Infection

Vlisidou, I., Lyte, M., van Diemen, P. M., Hawes, P. C., Monaghan, P., Wallis, T. S., & Stevens, M. P. (2004) · Infection and Immunity · doi:10.1128/iai.72.9.5446-5451.2004 · Cited by 117 · see citing works

An rRNA-based analysis for evaluating the effect of heat stress on the rumen microbial composition of Holstein heifers

Uyeno, Y., Sekiguchi, Y., Tajima, K., Takénaka, A., KURIHARA, M., & Kamagata, Y. (2009) · Anaerobe · doi:10.1016/j.anaerobe.2009.04.006 · Cited by 115 · see citing works

Fostering of advanced mutualism with gut microbiota by Immunoglobulin A

Sutherland, D. B., Suzuki, K., & Fagarasan, S. (2016) · Immunological Reviews · doi:10.1111/imr.12384 · Cited by 115 · see citing works

Norepinephrine-Induced Expression of the K99 Pilus Adhesin of EnterotoxigenicEscherichia coli

Lyte, M., Erickson, A. K., Arulanandam, B. P., Frank, C. D., Crawford, M., & Francis, D. H. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6356 · Cited by 114 · see citing works

Intentionally induced intestinal barrier dysfunction causes inflammation, affects metabolism, and reduces productivity in lactating Holstein cows

Kvidera, S. K., Dickson, M. J., Abuajamieh, M., Snider, D. B., Sanz-Fernandez, M. V., Johnson, J. S., Keating, A. F., Gorden, P. J., Green, H. B., Schoenberg, K. M., et al. (2017) · Journal of Dairy Science · doi:10.3168/jds.2016-12349 · Cited by 109 · see citing works

Pseudomonas aeruginosa -Catecholamine Inotrope Interactions

Freestone, P. P., Hirst, R. A., Sandrini, S. M., Sharaff, F., Fry, H., Hyman, S., & O'Callaghan, C. (2012) · Chest · doi:10.1378/chest.11-2614 · Cited by 107 · see citing works

Symposium review: Host–rumen microbe interactions may be leveraged to improve the productivity of dairy cows

Bickhart, D. M., & Weimer, P. J. (2017) · Journal of Dairy Science · doi:10.3168/jds.2017-13328 · Cited by 105 · see citing works

Adhesion of bacteria to epithelial cell surfaces within the reticulo-rumen of cattle

McCowan, R. P., Cheng, K.-J., Bailey, C. B., & Costerton, J. W. (1978) · Applied and Environmental Microbiology · doi:10.1128/aem.35.1.149-155.1978 · Cited by 99 · see citing works

Neuromodulation of enteropathogen internalization in Peyer's patches from porcine jejunum

Green, B. T., Lyte, M., Kulkarni, A. P., & Brown, D. R. (2003) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(03)00225-x · Cited by 98 · see citing works

Adrenergic modulation of Escherichia coli O157:H7 adherence to the colonic mucosa

Green, B. T., Lyte, M., Chen, C., Xie, Y., Casey, M. A., Kulkarni, A. P., Vulchanova, L., & Brown, D. R. (2004) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00471.2003 · Cited by 90 · see citing works

Integrated neural and endocrine control of gastrointestinal function

Furness, J. B. (2016) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-27592-5_16 · Cited by 87 · see citing works

Alterations in ruminal bacterial populations at induction and recovery from diet-induced milk fat depression in dairy cows

Pitta, D. W., Indugu, N., Vecchiarelli, B., Rico, D. E., & Harvatine, K. J. (2018) · Journal of Dairy Science · doi:10.3168/jds.2016-12514 · Cited by 73 · see citing works

Norepinephrine Augments Salmonella enterica -Induced Enteritis in a Manner Associated with Increased Net Replication but Independent of the Putative Adrenergic Sensor Kinases QseC and QseE

Pullinger, G. D., Carnell, S. C., Sharaff, F., van Diemen, P. M., Dziva, F., Morgan, E., Lyte, M., Freestone, P. P. E., & Stevens, M. P. (2009) · Infection and Immunity · doi:10.1128/iai.01203-09 · Cited by 71 · see citing works

Anatomical evidence for ileal Peyer’s patches innervation by enteric nervous system: a potential route for prion neuroinvasion?

Chiocchetti, R., Mazzuoli‐Weber, G., Albanese, V., Mazzoni, M., Clavenzani, P., Lalatta‐Costerbosa, G., Lucchi, M. L., Guardo, G. D., Marruchella, G., & Furness, J. B. (2008) · Cell and Tissue Research · doi:10.1007/s00441-008-0583-y · Cited by 69 · see citing works

Chemotaxis of Escherichia coli to Norepinephrine (NE) Requires Conversion of NE to 3,4-Dihydroxymandelic Acid

Pasupuleti, S., Sule, N., Cohn, W. B., MacKenzie, D. S., Jayaraman, A., & Manson, M. D. (2014) · Journal of Bacteriology · doi:10.1128/jb.02065-14 · Cited by 65 · see citing works

The role of the commensal microbiota in adaptive and maladaptive stressor-induced immunomodulation

Mackos, A. R., Maltz, R. M., & Bailey, M. T. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2016.10.006 · Cited by 63 · see citing works

Evidence for PMAT- and OCT-like biogenic amine transporters in a probiotic strain of Lactobacillus: Implications for interkingdom communication within the microbiota-gut-brain axis

Lyte, M., & Brown, D. R. (2018) · PLoS ONE · doi:10.1371/journal.pone.0191037 · Cited by 60 · see citing works

Mucosally-directed adrenergic nerves and sympathomimetic drugs enhance non-intimate adherence of Escherichia coli O157:H7 to porcine cecum and colon

Chen, C., Lyte, M., Stevens, M. P., Vulchanova, L., & Brown, D. R. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.03.081 · Cited by 54 · see citing works

Global Effects of Catecholamines on Actinobacillus pleuropneumoniae Gene Expression

Li, L., Xu, Z., Zhou, Y., Sun, L., Liu, Z., Chen, H., & Zhou, R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031121 · Cited by 48 · see citing works

Jejunal hemorrhage syndrome in dairy and beef cattle: 11 cases (2001 to 2003).

Abutarbush, S. M., & Radostits, O. M. (2005) · PubMed · Cited by 45 · see citing works

Epimural Indicator Phylotypes of Transiently-Induced Subacute Ruminal Acidosis in Dairy Cattle

Wetzels, S. U., Mann, E., Metzler-Zebeli, B. U., Pourazad, P., Qumar, M., Klevenhusen, F., Conrady, B., Wagner, M., Zebeli, Q., & Schmitz‐Esser, S. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00274 · Cited by 43 · see citing works

Microbial Endocrinology in the Pathogenesis of Infectious Disease

Lyte, M. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0021-2015 · Cited by 42 · see citing works

Autonomic neurotransmitters modulate immunoglobulin A secretion in porcine colonic mucosa

Schmidt, L. D., Xie, Y., Lyte, M., Vulchanova, L., & Brown, D. R. (2007) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.10.028 · Cited by 40 · see citing works

GAS-GANGRENE FOLLOWING INJECTION OF ADRENALINE

Cooper, E. (1946) · The Lancet · doi:10.1016/s0140-6736(46)91431-6 · Cited by 40 · see citing works

Intravenous lipopolysaccharide challenge alters ruminal bacterial microbiota and disrupts ruminal metabolism in dairy cattle

Jing, L., Zhang, R., Liu, Y., Zhu, W., & Mao, S. (2014) · British Journal Of Nutrition · doi:10.1017/s000711451400066x · Cited by 36 · see citing works

Regulation of Ion Transport in the Porcine Intestinal Tract by Enteric Neurotransmitters and Hormones

Brown, D. R., & O’Grady, S. M. (1997) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/s0300-9629(96)00311-8 · Cited by 35 · see citing works

Complex formation followed by internal electron transfer: the reaction between L-dopa and iron(III)

Linert, W., Jameson, R. F., & Herlinger, E. (1991) · Inorganica Chimica Acta · doi:10.1016/s0020-1693(00)90400-6 · Cited by 34 · see citing works

Fast acting nervous regulation of immunoglobulin A secretion from isolated perfused porcine ileum

Schmidt, P. T., Eriksen, L., Loftager, M., Rasmussen, T. N., & Holst, J. J. (1999) · Gut · doi:10.1136/gut.45.5.679 · Cited by 29 · see citing works

Structural differences of the enteric nervous system in the cattle forestomach revealed by whole mount immunohistochemistry

Teixeira, A. F., Wedel, T., Krammer, H.-J., & Kühnel, W. (1998) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/s0940-9602(98)80099-x · Cited by 28 · see citing works

Understanding jejunal hemorrhage syndrome

Elhanafy, M. M., French, D. D., & Braun, U. (2013) · Journal of the American Veterinary Medical Association · doi:10.2460/javma.243.3.352 · Cited by 28 · see citing works

The catecholamine neurotransmitter precursor tyrosine increases anger during exposure to severe psychological stress

Lieberman, H. R., Thompson, L., Caruso, C. M., Niro, P. J., Mahoney, C. R., McClung, J. P., & Caron, G. R. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3727-7 · Cited by 25 · see citing works

Dopamine stimulates Cl− absorption coupled with HCO3− secretion in rat late distal colon

Zhang, G. H., Zhu, J. X., Xue, H., Fan, J., Chen, X., Tsang, L. L., Chung, Y. W., Xing, Y., & Chan, H. C. (2007) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.05.038 · Cited by 23 · see citing works

The rumen and beyond: Nutritional physiology of the modern dairy cow

Bravo, D. M., & Wall, E. H. (2016) · Journal of Dairy Science · doi:10.3168/jds.2015-10191 · Cited by 19 · see citing works

Successive changes in the epimural bacterial community of young lambs as revealed by scanning electron microscopy

Mueller, R. E., Asplund, J. M., & Iannotti, E. L. (1984) · Applied and Environmental Microbiology · doi:10.1128/aem.47.4.715-723.1984 · Cited by 14 · see citing works

Substance P-Immunoreactive Neurons of the Bovine Forestomach Mucosa: Their Presumptive Role in a Sensory Mechanism.

Kitamura, N., Yamada, J., Yamamoto, Y., & YAMASHITA, T. (1993) · Archivum histologicum japonicum · doi:10.1679/aohc.56.399 · Cited by 14 · see citing works

Immunohistochemical study on the distribution of neuron‐specific enolase‐ and peptide‐containing nerves in the omasum of cattle

Kitamura, N., Yamada, J., & Yamashita, T. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902560411 · Cited by 13 · see citing works

Managing complexity: Dealing with systemic crosstalk in bovine physiology

Bradford, B. J., Yuan, K., & Ylioja, C. M. (2015) · Journal of Dairy Science · doi:10.3168/jds.2015-10271 · Cited by 11 · see citing works

Effects of Catecholamines on Gut Microflora and Potential for Beta- Adrenergic Agonists to Impact Ruminal Fermentation

Walker, C. E., & Drouillard, J. S. (2012) · The Open Agriculture Journal · doi:10.2174/1874331501206010057 · Cited by 8 · see citing works

The Microbiota-Gut-Brain Axis

Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works

Addressing global ruminant agricultural challenges through understanding the rumen microbiome: past, present, and future

Huws, S. A., Creevey, C. J., Oyama, L. B., Mizrahi, I., Denman, S. E., Popova, M., Muñoz-Tamayo, R., Forano, E., Waters, S. M., Hess, M., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02161 · Cited by 487 · see citing works

Intestinal serotonin and fluoxetine exposure modulate bacterial colonization in the gut

Fung, T. C., Vuong, H. E., Luna, C. G. G., Pronovost, G. N., Aleksandrova, A. A., Riley, N. G., Vavilina, A., McGinn, J., Rendon, T. K., Forrest, L. R., et al. (2019) · Nature Microbiology · doi:10.1038/s41564-019-0540-4 · Cited by 481 · see citing works

Gut Microbiota and Their Neuroinflammatory Implications in Alzheimer’s Disease

Giau, V. V., Wu, S., Jamerlan, A., An, S. S. A., Kim, S., & Hulme, J. (2018) · Nutrients · doi:10.3390/nu10111765 · Cited by 235 · see citing works

The microbiota-gut-brain axis: Focus on the fundamental communication pathways

Bistoletti, M., Bosi, A., Banfi, D., Giaroni, C., & Baj, A. (2020) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2020.08.012 · Cited by 88 · see citing works

Neutrophils in the periodontium: Interactions with pathogens and roles in tissue homeostasis and inflammation

Uriarte, S. M., & Hajishengallis, G. (2022) · Immunological Reviews · doi:10.1111/imr.13152 · Cited by 71 · see citing works

Targeting the microbiome-gut-brain axis for improving cognition in schizophrenia and major mood disorders: A narrative review

Bioque, M., González-Rodríguez, A., García‐Rizo, C., Cobo, J., Monreal, J. A., Usall, J., Soria, V., & Labad, J. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110130 · Cited by 58 · see citing works

Microbial endocrinology: the mechanisms by which the microbiota influences host sex steroids

Cotton, S., Clayton, C. A., & Tropini, C. (2023) · Trends in Microbiology · doi:10.1016/j.tim.2023.03.010 · Cited by 57 · see citing works

Gut microbiota-derived metabolites contribute negatively to hindgut barrier function development at the early weaning goat model

Zhang, K., Xu, Y., Yang, Y., Guo, M., Zhang, T., Zong, B., Huang, S., Suo, L., Ma, B., Wang, X., et al. (2022) · Animal nutrition · doi:10.1016/j.aninu.2022.04.004 · Cited by 39 · see citing works

Dialog between skin and its microbiota: Emergence of “Cutaneous Bacterial Endocrinology”

Racine, P., Janvier, X., Clabaut, M., Catovic, C., Souak, D., Boukerb, A. M., Groboillot, A., Konto‐Ghiorghi, Y., Poc, C. D., Lesouhaitier, O., et al. (2020) · Experimental Dermatology · doi:10.1111/exd.14158 · Cited by 38 · see citing works

Helminths, hosts, and their microbiota: new avenues for managing gastrointestinal helminthiases in ruminants

Cortés, A., Rooney, J., Bartley, D. J., Nisbet, A. J., & Cantacessi, C. (2020) · Expert Review of Anti-infective Therapy · doi:10.1080/14787210.2020.1782188 · Cited by 36 · see citing works

Influence of the Gut Microbiome on Feed Intake of Farm Animals

Wessels, A. G. (2022) · Microorganisms · doi:10.3390/microorganisms10071305 · Cited by 34 · see citing works

Editorial: Gut Microbiome Modulation in Ruminants: Enhancing Advantages and Minimizing Drawbacks

Belanche, A., Patra, A. K., Morgavi, D. P., Suen, G., Newbold, C. J., & Yáñez-Ruíz, D. R. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.622002 · Cited by 30 · see citing works

Functional profile of oral plaque microbiome: Further insight into the bidirectional relationship between type 2 diabetes and periodontitis

Favale, N., Fariña, R., Carrieri, A., Simonelli, A., Severi, M., Sabbioni, S., Trombelli, L., & Scapoli, C. (2023) · Molecular Oral Microbiology · doi:10.1111/omi.12418 · Cited by 28 · see citing works

Review: Microbial endocrinology: intersection of microbiology and neurobiology matters to swine health from infection to behavior

Lyte, J. M., & Lyte, M. (2019) · animal · doi:10.1017/s1751731119000284 · Cited by 28 · see citing works

Beyond classic concepts in thyroid homeostasis: Immune system and microbiota

Fernández-García, V., González-Ramos, S., Martín‐Sanz, P., Laparra, J. M., & Boscá, L. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111333 · Cited by 27 · see citing works

The Hunger Games: Aggregatibacter actinomycetemcomitans Exploits Human Neutrophils As an Epinephrine Source for Survival

Ozuna, H., Uriarte, S. M., & Demuth, D. R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.707096 · Cited by 26 · see citing works

Characterization of the Microbial Communities along the Gastrointestinal Tract in Crossbred Cattle

Wang, K., Zhang, H., Hu, L., Zhang, G., Lu, H., Luo, H., Zhao, S., Zhu, H., & Wang, Y. (2022) · Animals · doi:10.3390/ani12070825 · Cited by 23 · see citing works

Norepinephrine affects the interaction of adherent-invasive Escherichia coli with intestinal epithelial cells

Sobieszczańska, B., Turniak, M., Olbromski, M., Walczuk, U., Choroszy, M., Tukiendorf, A., & Dzięgiel, P. (2021) · Virulence · doi:10.1080/21505594.2021.1882780 · Cited by 18 · see citing works

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Animal Models Used for Studying the Benefits of Probiotics in Neurodegeneration

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Aggregatibacter actinomycetemcomitans exploits and modulates the immune response by human neutrophils for survival in the anaerobic environment.

Ozuna, H. (2022) · doi:10.18297/etd/3808

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Microbial Endocrinology: The Microbiota-Gut-Brain Axis in Health and Disease

(2014) · Thammasat University Digital Collections

Microbial Endocrinology in the Pathogenesis of Infectious Disease

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