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PLoS Pathogens, ISSN 1553-7366, 06/2018, Volume 14, Issue 6, p. e1007133
While infectious agents have typical host preferences, the noninvasive enteric bacterium Vibrio cholerae is remarkable for its ability to survive in many... 
GM1 GANGLIOSIDE | TOXIN | ESCHERICHIA-COLI | GASTROINTESTINAL-TRACT | N-GLYCOLYLNEURAMINIC ACID | SMALL-INTESTINE | MICROBIOLOGY | VIBRIO-CHOLERAE | VIROLOGY | MOUSE MODEL | VERTEBRATE AMINO-SUGARS | THROUGHPUT SUBSTRATE-SPECIFICITY | PARASITOLOGY | Disease Susceptibility | Epithelial Cells - metabolism | Intestine, Small - pathology | Species Specificity | Humans | Intestine, Small - microbiology | Mice, Inbred C57BL | Vibrio cholerae - pathogenicity | Cholera - metabolism | Cholera - pathology | Epithelial Cells - pathology | Male | Vibrio cholerae - classification | Mice, Knockout | Biological Evolution | Animals | Neuraminic Acids - metabolism | Female | Mice | Intestine, Small - metabolism | Mixed Function Oxygenases - physiology | Cholera - microbiology | Vibrio cholerae | Development and progression | Genetic aspects | Cholera | Research | Adaptation (Biology) | Gene expression | Water-borne diseases | Pediatrics | Pathogenesis | Epithelial cells | Biological evolution | Virulence | Biology | Infections | Ganglioside GM1 | Small intestine | Optimization | Training | Exo-a-sialidase | Gastroenterology | Evolution | Host preferences | Cholera toxin | Public health | Binding | Departments | Nutrition | Secretion | Research & development--R&D | Ion transport | Diarrhea | Glycoproteins | Sodium chloride | Mammals | Sialic acids | Medicine | Acids | Intoxication | Gangliosides | N-Acetylneuraminic acid | Vibrio | Research & development | R&D
Journal Article
The Journal of Infectious Diseases, ISSN 0022-1899, 7/2012, Volume 206, Issue 1, pp. 99 - 109
Journal Article
Gut, ISSN 0017-5749, 03/2011, Volume 60, Issue 3, pp. 307 - 317
BackgroundThe brain–gut axis is a key regulator of normal intestinal physiology; for example, psychological stress is linked to altered gut barrier function,... 
MATERNAL SEPARATION | MURINE COLONIC HYPERPLASIA | C-FOS | ESCHERICHIA-COLI | CHRONIC PSYCHOLOGICAL STRESS | CITROBACTER-RODENTIUM INFECTION | SPATIAL MEMORY | GASTROENTEROLOGY & HEPATOLOGY | SYNAPTIC PLASTICITY | IRRITABLE-BOWEL-SYNDROME | INTESTINAL BARRIER FUNCTION | Anxiety - microbiology | Stress, Psychological - psychology | Hyperplasia - microbiology | Behavior, Animal | Feces - microbiology | Inflammation Mediators - metabolism | Female | Brain-Derived Neurotrophic Factor - metabolism | Memory Disorders - microbiology | Corticosterone - blood | Enterobacteriaceae Infections - psychology | Hyperplasia - prevention & control | Colon - pathology | Enterobacteriaceae Infections - metabolism | Stress, Psychological - blood | Mice, Inbred C57BL | Proto-Oncogene Proteins c-fos - metabolism | Hippocampus - metabolism | Memory Disorders - prevention & control | Animals | Memory Disorders - etiology | Germ-Free Life | Probiotics - therapeutic use | Mice | Citrobacter rodentium | Hippocampus - physiopathology | Cytokines - biosynthesis | Complications and side effects | Enterobacteriaceae infections | Microbiota (Symbiotic organisms) | Development and progression | Models | Research | Stress (Psychology) | Memory, Disorders of | Studies | Inflammatory bowel disease | Probiotics | Bacterial infections | Rodents | Memory | Irritable bowel syndrome | Infections | Behavior
Journal Article
Immunity, ISSN 1074-7613, 08/2011, Volume 35, Issue 2, pp. 223 - 235
Thymic stromal lymphopoetin (TSLP) influences numerous immune functions, including those in the colonic mucosa. Here we report that TSLP-deficient ( ) mice did... 
SECRETORY LEUKOPROTEASE INHIBITOR | DENDRITIC CELLS | EPITHELIAL-CELLS | EXPERIMENTAL COLITIS | TSLP | MICE | IMMUNOLOGY | PRIMARY CULTURES | NF-KAPPA-B | T-CELLS | INTESTINAL IMMUNE HOMEOSTASIS | Leukocyte Elastase - metabolism | Intestinal Mucosa - metabolism | Colitis - genetics | Colon - drug effects | Immunity, Mucosal | Intestinal Mucosa - drug effects | Secretory Leukocyte Peptidase Inhibitor - administration & dosage | Immunoglobulins - metabolism | Signal Transduction - immunology | Intestinal Mucosa - immunology | Colitis - chemically induced | Receptors, Cytokine - metabolism | Colitis - immunology | Secretory Leukocyte Peptidase Inhibitor - metabolism | Colon - pathology | Down-Regulation | Cells, Cultured | Leukocyte Elastase - genetics | Inflammation | Recombinant Proteins - genetics | Signal Transduction - genetics | Enzyme Activation - drug effects | Mice, Knockout | Animals | Signal Transduction - drug effects | Colitis - metabolism | Mice | Dextran Sulfate - administration & dosage | Secretory Leukocyte Peptidase Inhibitor - genetics | Enzyme Activation - genetics | Leukocyte Elastase - immunology | Intestinal Mucosa - pathology | Dextran | Enzymes | Children's hospitals | Oncology, Experimental | Research | Colitis | Sulfates | Cancer | Inflammatory bowel disease | Medical research | Disease | Rodents | Collagen | Mortality | Colon
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2017, Volume 12, Issue 7, p. e0182416
The nervous system plays a profound regulatory role in maintaining appropriate immune responses by signaling to immune cells. These immune cells, including B-... 
VAGUS | VOLUME TRANSMISSION | NERVE | IMMUNE INTERACTIONS | STIMULATION | EXPERIMENTAL COLITIS | DENDRITIC CELLS | LYMPHOID ORGANS | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | STROMAL CELLS | Lymphocytes - metabolism | B-Lymphocytes - cytology | Receptors, CXCR5 - metabolism | Spleen - innervation | Sympathetic Nervous System - cytology | Axons - metabolism | Male | Spleen - cytology | Sympathetic Nervous System - metabolism | Microscopy, Confocal | Animals | Flow Cytometry | Spleen - metabolism | T-Lymphocytes - cytology | T-Lymphocytes - metabolism | Chemokine CXCL13 - metabolism | Polymerase Chain Reaction | Female | Mice | Neurons - metabolism | B-Lymphocytes - metabolism | Spleen | Immune response | Lymphocytes | Neurons | Neuroanatomy | Research | Diagnosis | Health aspects | Veterinary colleges | Trafficking | Innervation | CXCL13 protein | Confocal microscopy | Nervous system | Lymphocytes T | Biology | Choline O-acetyltransferase | Confocal | Veterinary medicine | Pulp | Fibers | Immunology | CXCR5 protein | Rodents | Physiology | Acetyltransferase | Localization | Immune system | Nerve endings | Tyrosine | Lymphatic system | Dendritic cells | Hydroxylase | Septic shock | T cell receptors | Anatomy & physiology | Gene expression | Sympathetic nervous system | Anatomy | Axons | Signaling | Lymphocytes B | Microscopy | Stromal cells | Choline | Relative abundance | Sympathetic nerves | Adrenergic receptors | Acetylcholine | Norepinephrine | Chemokines
Journal Article
Journal Article