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Microbiology of the Gastrointestinal Tract
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Introduction GI defenses Normal flora Mouth and Esophagus Dental infections Candida infection Stomach Helicobacter infection Intestine Food poisoning Non-food-related diarrhea LECTURE OUTLINE
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“The digestive system is a microbiologist’s paradise. In health or in disease, the digestive tract is a microbial garden of unsurpassed variety and complexity, and feces is the seed of its creation.” - Schaechter INTRODUCTION
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Introduction GI defenses Normal flora Mouth and Esophagus Dental infections Candida infection Stomach Helicobacter infection Intestine Food poisoning Non-food-related diarrhea LECTURE OUTLINE
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epithelial lining mucus peristalsis GI Tract Defenses | general defenses
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liquid flow lysozyme normal flora GI Tract Defenses | mouth defenses
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peristalsis liquid flow GI Tract Defenses | esophagus defenses
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acid GI Tract Defenses | stomach defenses
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peristalsis liquid flow epithelial shedding decoy binding sites bile Peyer’s patches, IgA, mucus normal flora GI Tract Defenses | intestine defenses
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Introduction GI defenses Normal flora Mouth and Esophagus Dental infections Candida infection Stomach Helicobacter infection Intestine Food poisoning Non-food-related diarrhea LECTURE OUTLINE
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Normal Flora | mouth anaerobes strep viridans other stuff
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Hemolysis: Alpha: Almost Beta: Best Gamma: Garbage
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Normal Flora | esophagus, stomach, small intestine sparse flora increasing distally
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Normal Flora | large intestine tons of bugs! anaerobes gram-negative rods enterococcus spirochetes
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Introduction GI defenses Normal flora Mouth and Esophagus Dental infections Candida infection Stomach Helicobacter infection Intestine Food poisoning Non-food-related diarrhea LECTURE OUTLINE
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Dental infections | clinical Infectious disease that causes tooth decay Untreated: pain, tooth loss, spread of infection Risk factors: high-sugar diet, poor oral hygiene, reduced amount of saliva, smoking, periodontal disease Dental Caries
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Caries
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Dental infections | clinical Infectious disease destroying supporting structures of teeth Most common form: gingivitis Other forms (affecting periodontal membrane and alveolar bone) are more serious Periodontal disease
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Healthy gums
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Gingivitis
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Dental infections | pathogenesis What causes tooth decay? Fermentable sugars Acid-producing bacteria Demineralization + enough time
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Plaque
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Dental infections | pathogenesis Bugs attach weakly to salivary glycoproteins adsorbed onto the surface of the tooth Bugs make “glucans” from dietary sugar Glucans attach bacteria to each other and to tooth, forming large aggregates How does plaque form?
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Weak attachment
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Aggregation and plaque formation
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Acid production and tooth decay
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Dental infections | bugs Streptococcus species mutans sanguis Anaerobes Bacteroides fragilis, melaninogenicus Porphyromonas gingivalis Spirochetes Treponema denticola
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Streptococcus mutans gram stain
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Dental infections | bugs Present normally in large numbers Produces lots of lactic acid quickly Tolerant to low pH, high sugar concentration Has glycosyl transferase (cell-surface protein) attaches to mucins on tooth surface converts sugar into glucans (part of plaque) Paves the way for entry by other organisms What’s so special about S. mutans?
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Dental infections | prevention Less sugar in diet Brush and floss frequently Fluoride Saliva Vaccine? Genetically altered bacteria?
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Introduction GI defenses Normal flora Mouth and Esophagus Dental infections Candida infection Stomach Helicobacter infection Intestine Food poisoning Non-food-related diarrhea LECTURE OUTLINE
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Candida | clinical newborns, immunocompromised white plaques with red bases oral cavity danger: spread to esophagus, blood
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Oral candidiasis
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Esophageal candidiasis
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Candida | pathogenesis Candida albicans part of normal flora break in host flora → candida takeover
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Candida
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Candida | diagnosis clinical culture useless smear will show hyphal forms
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Introduction GI defenses Normal flora Mouth and Esophagus Dental infections Candida infection Stomach Helicobacter infection Intestine Food poisoning Non-food-related diarrhea LECTURE OUTLINE
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Peptic ulcer disease: 500,000 new cases each year. 1 million hospitalized. 6000 die. Annual cost: $6 billion.
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Peptic ulcer disease: unfavorable balance between gastric acid secretion and mucosal resistance genes, smoking, stress - Harrison’s 10 th edition, 1983
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Robin Warren Barry Marshall noted unusual bug in stomach grew the bug (eventually) Marshall ingested the bug …and got gastritis The discovery of Helicobacter
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‘Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration’ - Warren and Marshall Lancet 1984 The discovery of Helicobacter
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Nobel Prize, 2005
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Bug characteristics STOMACH | H. pylori small, curved rod gram-negative related to Campylobacter
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www.giantmicrobes.com ulcer plush doll: $5.95
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Helicobacter | epidemiology Fecal-oral transmission US: 50% of adults are infected Third world: virtually all adults infected
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Helicobacter | features microaerophilic corkscrew motility mucinase urease
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C O NH 2 urease urea NH 3 CO 2 ammonia carbon dioxide
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Helicobacter | even more features cagA vacA
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TFSS* CagA protein cytokines * Type IV Secretion System free radicals VacA protein holes immobilized T-helper cells
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Bugs hide in mucous and attract inflammatory cells Inflammatory cells release toxins but can’t kill bugs easily Host causes damage by continual, ineffective immune response! How does Helicobacter cause ulcers?
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Helicobacter infection gastritis ulcergastritiscarcinomalymphoma What happens after infection?
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Helicobacter infection gastritis ulcergastritiscarcinomalymphoma What happens after infection?
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Gastritis
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Helicobacter infection gastritis ulcer gastritis carcinomalymphoma What happens after infection?
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Helicobacter infection gastritis ulcer gastritiscarcinomalymphoma What happens after infection?
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Ulcer
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Helicobacter infection gastritis ulcergastritis carcinoma lymphoma What happens after infection?
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Gastric carcinoma
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Helicobacter infection gastritis atrophy intestinal metaplasia carcinoma dysplasia
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Helicobacter infection gastritis ulcergastritiscarcinoma lymphoma What happens after infection?
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MALT lymphoma
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Helicobacter | diagnosis lots of tests for H. pylori! consider: purpose (diagnosis or follow-up) invasiveness cost
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Endoscopy gold standard guided biopsy three tests: rapid urease testing histology culture
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Normal gastric mucosa
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Gastric ulcer
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C O NH 2 urease urea NH 3 CO 2 ammonia carbon dioxide
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Helicobacter pylori
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Blood test Detects antibodies to Helicobacter Antibodies can persist for years Useful for initial diagnosis only
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Breath test C O NH 2 urease urea NH 3 CO 2 ammonia carbon dioxide * *
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Stool Antigen test new cheap fast less accurate
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Treatment Helicobacter | treatment need an antibiotic! proton pump inhibitor too maybe some bismuth salts
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Why might Helicobacter be good?
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