Microbial endocrinology and infectious disease in the 21st century

Bacteria–host communication: the language of hormones

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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

Substantial Production of Dopamine in the Human Gastrointestinal Tract

Eisenhofer, G., Åneman, A., Friberg, P., Hooper, D., Fåndriks, L., Lonroth, H., Hunyady, B., & Mezey, E. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.82.11.4339 · Cited by 394 · see citing works

Anatomy and physiology of the enteric nervous system

Costa, M., Brookes, S., & Hennig, G. (2000) · Gut · doi:10.1136/gut.47.suppl_4.iv15 · Cited by 364 · see citing works

Chronic stress induces mast cell-dependent bacterial adherence and initiates mucosal inflammation in rat intestine

Söderholm, J. D., Yang, P., Ceponis, P., Vohra, A., Riddell, R., Sherman, P. M., & Perdue, M. H. (2002) · Gastroenterology · doi:10.1053/gast.2002.36019 · Cited by 362 · see citing works

Fundamentals of neurogastroenterology

Wood, J. D., Alpers, D. H., & Andrews, P. L. R. (1999) · Gut · doi:10.1136/gut.45.2008.ii6 · Cited by 311 · see citing works

Growth Stimulation of Intestinal Commensal Escherichia coli by Catecholamines: A Possible Contributory Factor in Trauma-Induced Sepsis

Freestone, P. P. E., WILLIAMS, P. H., Haigh, R., Maggs, A. F., Neal, C. P., & Lyte, M. (2002) · Shock · doi:10.1097/00024382-200211000-00014 · Cited by 227 · see citing works

The Mammalian Neuroendocrine Hormone Norepinephrine Supplies Iron for Bacterial Growth in the Presence of Transferrin or Lactoferrin

Freestone, P. P. E., Lyte, M., Neal, C. P., Maggs, A. F., Haigh, R., & WILLIAMS, P. H. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.21.6091-6098.2000 · Cited by 210 · see citing works

Gut-Derived Sepsis Occurs When the Right Pathogen With the Right Virulence Genes Meets the Right Host: Evidence for In Vivo Virulence Expression in Pseudomonas aeruginosa

Alverdy, J., Holbrook, C., Rocha, F., Seiden, L., Licheng, R., Wu, Musch, M., Chang, E., Ohman, D., & Suh, S. (2000) · Annals of Surgery · doi:10.1097/00000658-200010000-00003 · Cited by 207 · see citing works

Stimulation of Staphylococcus epidermidis growth and biofilm formation by catecholamine inotropes

Lyte, M., Freestone, P. P. E., Neal, C. P., Olson, B. A., Haigh, R., Bayston, R., & WILLIAMS, P. H. (2003) · The Lancet · doi:10.1016/s0140-6736(03)12231-3 · Cited by 205 · see citing works

Transmitter substances in insects: A review

Pitman, R. M. (1971) · Comparative and General Pharmacology · doi:10.1016/0010-4035(71)90060-7 · Cited by 200 · see citing works

Microflora modulates endocrine cells in the gastrointestinal mucosa of the rat

Uribe, A., Alam, M., Johansson, O., Midtvedt, T., & Theodorsson, E. (1994) · Gastroenterology · doi:10.1016/0016-5085(94)90526-6 · Cited by 171 · 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

The role of microbial endocrinology in infectious disease

Lyte, M. (1993) · Journal of Endocrinology · doi:10.1677/joe.0.1370343 · Cited by 168 · see citing works

Resuscitation of Salmonella enterica Serovar Typhimurium and Enterohemorrhagic Escherichia coli from the Viable but Nonculturable State by Heat-Stable Enterobacterial Autoinducer

Reissbrodt, R., Rienäcker, I., Romanova, J. M., Freestone, P. P. E., Haigh, R., Lyte, M., Tschäpe, H., & WILLIAMS, P. H. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.10.4788-4794.2002 · Cited by 142 · see citing works

Production of Shiga-like toxins by Escherichia coli O157:H7 can be influenced by the neuroendocrine hormone norepinephrine

Lyte, M., Arulanandam, B. P., & Frank, C. D. (1996) · Journal of Laboratory and Clinical Medicine · doi:10.1016/s0022-2143(96)80011-4 · Cited by 142 · see citing works

Insulin or a closely related molecule is native to Escherichia coli.

LeRoith, D., Shiloach, J., Roth, J., & Lesniak, M. A. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)69020-4 · Cited by 135 · see citing works

Catecholamines Modulate Escherichia coli O157:H7 Adherence to Murine Cecal Mucosa

Chen, C., Brown, D. R., Xie, Y., Green, B. T., & Lyte, M. (2003) · Shock · doi:10.1097/01.shk.0000073867.66587.e0 · Cited by 118 · see citing works

Degeneration and Regrowth of Adrenergic Nerve Fibers in the Rat Peripheral Tissues after 6-Hydroxydopamine

de Champlain, J. (1971) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y71-038 · Cited by 116 · 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

Involvement of enterobactin in norepinephrine-mediated iron supply from transferrin to enterohaemorrhagicEscherichia coli

Freestone, P. P. E., Haigh, R., WILLIAMS, P. H., & Lyte, M. (2003) · FEMS Microbiology Letters · doi:10.1016/s0378-1097(03)00243-x · Cited by 112 · see citing works

Production of an autoinducer of growth by norepinephrine culturedEscherichia coliO157:H7

Lyte, M., Frank, C. D., & Green, B. T. (1996) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1996.tb08196.x · Cited by 111 · see citing works

The Growth Response of Escherichia coli to Neurotransmitters and Related Catecholamine Drugs Requires a Functional Enterobactin Biosynthesis and Uptake System

Burton, C. L., Chhabra, S. R., Swift, S., Baldwin, T. J., Withers, H. L., Hill, S. J., & Williams, P. M. (2002) · Infection and Immunity · doi:10.1128/iai.70.11.5913-5923.2002 · Cited by 111 · see citing works

Stress and Pathogenesis of Infectious Disease

Peterson, P. K., Chao, C., Molitor, T. W., Murtaugh, M. P., Strgar, F., & Sharp, B. M. (1991) · Clinical Infectious Diseases · doi:10.1093/clinids/13.4.710 · Cited by 105 · see citing works

Plasma Catechofamines in Patients with Serious Postoperative Infection

GROVES, A. C., GRIFFITHS, J., LEUNC, F., & Meek, R. N. (1973) · Annals of Surgery · doi:10.1097/00000658-197307000-00020 · Cited by 101 · see citing works

Alpha and Beta Adrenergic Receptor Involvement in Catecholamine-Induced Growth of Gram-Negative Bacteria

Lyte, M., & Ernst, S. (1993) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1993.1068 · Cited by 100 · see citing works

Mammalian hormones in microbial cells

Lenard, J. (1992) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(92)90323-2 · Cited by 98 · see citing works

Beta adrenoceptor mediation of the enhancing effect of norepinephrine on the murine primary antibody response in vitro.

Sanders, V. M., & Munson, A. E. (1984) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)21378-7 · Cited by 94 · see citing works

Sympathetic discharge to mesenteric organs and the liver. Evidence for substantial mesenteric organ norepinephrine spillover.

Åneman, A., Eisenhofer, G., Olbe, L. C., Dalenbäck, J., Nitescu, P. V., Fändriks, L., & Friberg, P. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118590 · Cited by 84 · see citing works

α1-Adrenoceptor stimulation directly induces growth of vascular wall in vivo

Erami, C., Zhang, H., Ho, J. G., French, D. M., & Faber, J. E. (2002) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00218.2002 · Cited by 82 · see citing works

Gut bacteria provide precursors of benzodiazepine receptor ligands in a rat model of hepatic encephalopathy

Yurdaydın, C., Walsh, T. J., Engler, H. D., Ha, J., Li, Y., Jones, E. A., & Basile, A. S. (1995) · Brain Research · doi:10.1016/0006-8993(95)00241-h · Cited by 82 · see citing works

Interaction of insulin with Pseudomonas pseudomallei

Woods, D. E., Jones, A. L., & Hill, P. J. (1993) · Infection and Immunity · doi:10.1128/iai.61.10.4045-4050.1993 · Cited by 81 · see citing works

Morphological classifications of enteric neurons -- 100 years after Dogiel

Brehmer, A., Schroedl, F., & Neuhuber, W. (1999) · Anatomy and Embryology · doi:10.1007/s004290050267 · Cited by 80 · see citing works

Gut-derived norepinephrine plays a critical role in producing hepatocellular dysfunction during early sepsis

Yang, S., Koo, D. J., Zhou, M., Chaudry, I. H., & Wang, P. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.279.6.g1274 · Cited by 80 · see citing works

Innate and adaptive immune responses in a social conflict paradigm

Lyte, M., Nelson, S. G., & Thompson, M. L. (1990) · Clinical Immunology and Immunopathology · doi:10.1016/0090-1229(90)90029-p · Cited by 72 · see citing works

Estimation of intrasynaptic norepinephrine concentrations at vascular neuroeffector junctions in vivo

Kopin, I. J., Żukowska-Grójec, Z., Bayorh, M. A., & Goldstein, D. S. (1984) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00504372 · Cited by 71 · see citing works

The enhancement of bacterial infections by adrenaline.

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Evidence for widespread effects of noradrenaline on axon terminals in the rat frontal cortex.

Mobley, P. L., & Greengard, P. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.3.945 · Cited by 67 · see citing works

gamma-Aminobutyric acid uptake by a bacterial system with neurotransmitter binding characteristics.

Guthrie, G. D., & Nicholson-Guthrie, C. S. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.19.7378 · Cited by 61 · see citing works

Anthrax lethal factor represses glucocorticoid and progesterone receptor activity

Webster, J. I., Tonelli, L. H., Moayeri, M., Simons, S. S., Leppla, S. H., & STERNBERG, E. M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1036973100 · Cited by 59 · see citing works

Catecholamine Activity and Infectious Disease Episodes

Gruchow, H. W. (1979) · Journal of Human Stress · doi:10.1080/0097840x.1979.9934523 · Cited by 54 · see citing works

Catecholamines and in vitro growth of pathogenic bacteria: enhancement of growth varies greatly among bacterial species

Belay, T., Avilés, H., Vance, M., Fountain, K., & Sonnenfeld, G. (2003) · Life Sciences · doi:10.1016/s0024-3205(03)00472-7 · Cited by 52 · see citing works

Stress and neuroimmune regulation of gut mucosal function

Santos, J. (2000) · Gut · doi:10.1136/gut.47.suppl_4.iv49 · Cited by 47 · see citing works

Increased Type 1 Fimbrial Expression among CommensalEscherichia coliIsolates in the Murine Cecum following Catabolic Stress

Hendrickson, B. A., Guo, J., Laughlin, R. S., Chen, Y., & Alverdy, J. C. (1999) · Infection and Immunity · doi:10.1128/iai.67.2.745-753.1999 · Cited by 47 · see citing works

Jokichi Takamine (1854–1922), The Samurai Chemist, and His Work on Adrenalin

Yamashima, T. (2003) · Journal of Medical Biography · doi:10.1177/096777200301100211 · Cited by 46 · see citing works

Plasma catecholamines following cecal ligation and puncture in the rat.

Kovarik, M. F., Jones, S. B., & Romano, F. D. (1987) · PubMed · Cited by 41 · see citing works

Plasma NE concentrations do not accurately reflect sympathetic nervous system activity in human sepsis

Leinhardt, D., Arnold, J., Shipley, K., Mughal, M. M., Little, R., & Irving, M. H. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.265.2.e284 · Cited by 40 · see citing works

Gamma-aminobutyric Acid (GABA) Production by Eight Common Bacterial Pathogens

Minuk, G. Y. (1986) · Scandinavian Journal of Infectious Diseases · doi:10.3109/00365548609032366 · Cited by 40 · see citing works

GAS-GANGRENE FOLLOWING INJECTION OF ADRENALINE

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Plasma catecholamines during E. coli bacteremia in conscious rats

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Bacillus subtilis contains multiple forms of somatostatin-like material

LeRoith, D., Pickens, W. L., Vinik, A. I., & Shiloach, J. (1985) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(85)80001-2 · Cited by 37 · see citing works

Role of the Enteric Nervous System in the Pathophysiology of Secretory Diarrhea

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Activity of phenolsulfotransferases in the human gastrointestinal tract

Harris, R. M., Picton, R., Singh, S., & Waring, R. H. (2000) · Life Sciences · doi:10.1016/s0024-3205(00)00791-8 · Cited by 30 · see citing works

Inhibition of gamma interferon synthesis by catecholamines

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Norepinephrine Stimulates in Vitro Growth but does not Increase Pathogenicity of Salmonella Choleraesuis in an in Vivo Model

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Presence of a highly efficient ?binding? to bacterial contamination can distort data from binding studies

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Virulence of Clinical and Fecal Isolates of Clostridium perfringens Type A for Outbred NMRI Mice

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Pharmacological analysis of the adrenergic receptor for lipopolysaccharide-I of Shigella sonnei.

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Gut/brain axis and the microbiota

Mayer, E. A., Tillisch, K., & Gupta, A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci76304 · Cited by 1,503 · see citing works

Impact of Heat Stress on Poultry Production

Lara, L. J. C., & Rostagno, M. H. (2013) · Animals · doi:10.3390/ani3020356 · Cited by 1,276 · see citing works

Minireview: Gut microbiota: The neglected endocrine organ

Clarke, G., Stilling, R. M., Kennedy, P. J., Stanton, C., Cryan, J. F., & Dinan, T. G. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1108 · Cited by 1,192 · see citing works

Exposure to a social stressor alters the structure of the intestinal microbiota: Implications for stressor-induced immunomodulation

Bailey, M. T., Dowd, S. E., Galley, J. D., Hufnagle, A. R., Allen, R. G., & Lyte, M. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2010.10.023 · Cited by 1,123 · 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 Gut Microbiome and the Brain

Galland, L. (2014) · Journal of Medicinal Food · doi:10.1089/jmf.2014.7000 · Cited by 648 · see citing works

Neurotransmitters: The Critical Modulators Regulating Gut–Brain Axis

Mittal, R., Debs, L. H., Patel, A. P., Nguyen, D., Patel, K. V., O’Connor, G., Grati, M., Mittal, J., Yan, D. L. S., Eshraghi, A. A., et al. (2016) · Journal of Cellular Physiology · doi:10.1002/jcp.25518 · Cited by 644 · see citing works

Probiotics function mechanistically as delivery vehicles for neuroactive compounds: microbial endocrinology in the design, and use of probiotics.

Lyte, M. (2011) · BioEssays · doi:10.1002/bies.201100024 · Cited by 549 · see citing works

Brain gut microbiome interactions and functional bowel disorders

Mayer, E. A., Savidge, T., & Shulman, R. J. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.02.037 · Cited by 496 · see citing works

Sympathetic Overstimulation During Critical Illness: Adverse Effects of Adrenergic Stress

Dünser, M. W., & Hasibeder, W. R. (2009) · Journal of Intensive Care Medicine · doi:10.1177/0885066609340519 · Cited by 485 · see citing works

Mechanisms of Action of Probiotics and the Gastrointestinal Microbiota on Gut Motility and Constipation

Dimidi, E., Christodoulides, S., Scott, S. M., & Whelan, K. (2017) · Advances in Nutrition · doi:10.3945/an.116.014407 · Cited by 468 · see citing works

Brain injury induces specific changes in the caecal microbiota of mice via altered autonomic activity and mucoprotein production

Houlden, A., Goldrick, M., Brough, D., Vizi, E. S., Lénárt, N., Martinecz, B., Roberts, I. S., & Dénes, Á. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.04.003 · Cited by 369 · see citing works

Stressor Exposure Disrupts Commensal Microbial Populations in the Intestines and Leads to Increased Colonization by <i>Citrobacter rodentium</i>

Bailey, M. T., Dowd, S. E., Parry, N. M. A., Galley, J. D., Schauer, D. B., & Lyte, M. (2010) · Infection and Immunity · doi:10.1128/iai.00862-09 · Cited by 335 · see citing works

Interactions Between Commensal Bacteria and Gut Sensorimotor Function in Health and Disease

Barbara, G., Stanghellini, V., Brandi, G., Cremon, C., Nardo, G. D., De Giorgio, R., & Corinaldesi, R. (2005) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2005.00230.x · Cited by 325 · see citing works

Microbial endocrinology: how stress influences susceptibility to infection

Freestone, P. P. E., Sandrini, S. M., Haigh, R. D., & Lyte, M. (2008) · Trends in Microbiology · doi:10.1016/j.tim.2007.11.005 · Cited by 299 · see citing works

Intestinal permeability and systemic infections in critically ill patients: Effect of glutamine*

De-Souza, D. A., & Greene, L. J. (2005) · Critical Care Medicine · doi:10.1097/01.ccm.0000162680.52397.97 · Cited by 285 · see citing works

Stress at the intestinal surface: catecholamines and mucosa–bacteria interactions

Lyte, M., Vulchanova, L., & Brown, D. R. (2011) · Cell and Tissue Research · doi:10.1007/s00441-010-1050-0 · Cited by 281 · see citing works

Probiotics, Prebiotics, and Synbiotics: Gut and Beyond

Vyas, U., & Ranganathan, N. (2012) · Gastroenterology Research and Practice · doi:10.1155/2012/872716 · Cited by 258 · see citing works

Microbiome disturbances and autism spectrum disorders

Rosenfeld, C. S. (2015) · Drug Metabolism and Disposition · doi:10.1124/dmd.115.063826 · Cited by 229 · 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

Microbial endocrinology

Lyte, M. (2014) · Gut Microbes · doi:10.4161/gmic.28682 · Cited by 225 · see citing works

Dynorphin activates quorum sensing quinolone signaling in Pseudomonas aeruginosa

Zaborina, O., Lepine, F., Xiao, G., Valuckaite, V., Chen, Y., Li, T., Ciancio, M., Zaborin, A., Petroff, E., Turner, J. R., et al. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030035 · Cited by 207 · see citing works

Influence of photoperiod on hormones, behavior, and immune function

Walton, J. C., Weil, Z. M., & Nelson, R. J. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.12.003 · Cited by 207 · see citing works

Gut Dysbiosis in Animals Due to Environmental Chemical Exposures

Rosenfeld, C. S. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00396 · Cited by 207 · see citing works

Peptides as Quorum Sensing Molecules: Measurement Techniques and Obtained Levels In vitro and In vivo

Verbeke, F., Craemer, S. D., Debunne, N., Janssens, Y., Wynendaele, E., de Wiele, C. V., & Spiegeleer, B. M. J. D. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00183 · Cited by 199 · see citing works

Gut microbiome composition is associated with temperament during early childhood

Christian, L. M., Galley, J. D., Hade, E. M., Schoppe-Sullivan, S., Kamp Dush, C., & Bailey, M. T. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.10.018 · Cited by 191 · see citing works

Perception and Degradation of N-Acyl Homoserine Lactone Quorum Sensing Signals by Mammalian and Plant Cells

Teplitski, M., Mathesius, U., & Rumbaugh, K. P. (2010) · Chemical Reviews · doi:10.1021/cr100045m · Cited by 184 · see citing works

Crosstalk at the mucosal border: importance of the gut microenvironment in IBS

Öhman, L., Törnblom, H., & Simrén, M. (2014) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2014.200 · Cited by 181 · see citing works

Microbiome, HPA Axis and Production of Endocrine Hormones in the Gut

Sudo, N. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-0897-4_8 · Cited by 167 · see citing works

Pathogenesis, virulence factors and virulence regulation of vibrios belonging to the Harveyi clade

Ruwandeepika, H. A. D., Jayaweera, T. S. P., Bhowmick, P. P., Karunasagar, I., Bossier, P., & Defoirdt, T. (2012) · Reviews in Aquaculture · doi:10.1111/j.1753-5131.2012.01061.x · Cited by 166 · see citing works

The changing face of pathogen discovery and surveillance

Lipkin, W. I. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2949 · Cited by 166 · see citing works

On the translocation of bacteria and their lipopolysaccharides between blood and peripheral locations in chronic, inflammatory diseases: the central roles of LPS and LPS-induced cell death

Kell, D. B., & Pretorius, E. (2015) · Integrative Biology · doi:10.1039/c5ib00158g · Cited by 160 · see citing works

Dietary Capsaicin Improves Glucose Homeostasis and Alters the Gut Microbiota in Obese Diabetic ob/ob Mice

Song, J.-X., Ren, H., Gao, Y., Lee, C., Li, S., Zhang, F., Li, L., & Chen, H. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00602 · Cited by 156 · see citing works

The complex interplay between stress and bacterial infections in animals

Verbrugghe, E., Boyen, F., Gaastra, W., Bekhuis, L., Leyman, B., Parys, A. V., Haesebrouck, F., & Pasmans, F. (2011) · Veterinary Microbiology · doi:10.1016/j.vetmic.2011.09.012 · Cited by 152 · see citing works

Self-engineering capabilities of bacteria

Ben‐Jacob, E., & Levine, H. (2005) · Journal of The Royal Society Interface · doi:10.1098/rsif.2005.0089 · Cited by 150 · see citing works

Gut microbiota and host metabolism in liver cirrhosis

Usami, M. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i41.11597 · Cited by 148 · see citing works

New trends and perspectives in the evolution of neurotransmitters in microbial, plant, and animal cells

Roshchina, V. V. (2016) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-20215-0_2 · Cited by 143 · see citing works

Role of the Gut Microbiome in Autism Spectrum Disorders

Pulikkan, J., Mazumder, A., & Grace, T. (2019) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-030-05542-4_13 · Cited by 142 · see citing works

Host Responses to Biofilm

Watters, C., Fleming, D. F., Bishop, D. K., & Rumbaugh, K. P. (2016) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2016.05.007 · Cited by 140 · see citing works

Microbial endocrinology: Host-bacteria communication within the gut microbiome

Sandrini, S., Aldriwesh, M., Alruways, M., & Freestone, P. (2015) · Journal of Endocrinology · doi:10.1530/joe-14-0615 · Cited by 130 · see citing works

Biogenic Amines: Signals Between Commensal Microbiota and Gut Physiology

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