Session 4 Bact (G+ve Rods Non Spore) PDF
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Faculty of Pharmacy, Cairo University
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This document details Microbiology session notes about Gram-positive bacteria. It covers important details about Gram positive rods, including Corynebacterium diphtheriae, and Listeria monocytogenes, and their properties, transmission, virulence factors, and clinical presentation. The document also includes important details about diphtheria, testing, and treatments.
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Bact: G+ve rods. (Non spore) Micro 3: 4th Year Gram positive rods Non-spore forming Spore forming...
Bact: G+ve rods. (Non spore) Micro 3: 4th Year Gram positive rods Non-spore forming Spore forming Aerobic Aerobic Anaerobic Corynebacterium diphtheriae Bacillus anthracis “Clostridium” Listeria monocytogenes Bacillus cereus C. tetani C. perfringens Anaerobic C. botulinum C. difficile Propionibacterium species Aerobic-non-spore forming: Corynebacterium diphtheriae: Gram-positive rod, non-motile Properties (Chinese letters): Club shaped rods with beaded appearance consist of highly polymerized rich polyphosphateStained bluish with methylene blue (metachromatic). [IMP] Transmission by Respiratory droplets Epidemiology: disease of childhood Toxigenic strains family of Corynebacteriophages carry gene for diphtheria exotoxin. Diphteria exotoxin: Consists of 2 fragments Fragment A: catalytic inhibits elongation factor 2inhibit protein synthesis in eukaryotic cells Virulence Fragment B: binds to cell surface R facilitates the delivery of fragment A to the cytosol Factors: Based on two primary determinants: [IMP] 1- ability to colonize in the nasopharyngeal (encoded by the bacteria) 2- ability to produce diphteria exotoxin (encoded by the corynebacteriophage) Non-toxigenic strains rarely associated with clinical disease. Infection starts in the nose a purulent nasal discharge. Spreads to involve the pharynx covered by pseudo-membranemade up of bacteria, epithelial cells, leucocytes, fibrin and bloodDifficulty in respiration Pathogenesis Life-threatening systemic complications: Distant effects on the heart and the nervous system. [IMP] The action of diphtheria toxin on peripheral motor neurons and the myocardium cause: loss of motor function (e.g. difficulty in swallowing) Congestive heart failure session 4 1 Micro 3: 4th Year ❖ “Diphtheria”: a highly contagious diseaseaffect Upper RT ❖ The incubation period is 2-6 days. ❖ Asymptomatic carriersimportant source of infection ❖ Two types of diphteria: nasopharyngeal and cutaneous: due to local inflammation effect in the upper respiratory tract and skin Clinical symptoms: 1-in nasopharyngeal diphteria: Low-grade fever Cervical lymph nodes: Enlargement is common and the surrounding edema of the Disease subcutaneous tissues may cause a “Bull neck” appearance. Rarely, in cases of pharyngeal diphtheria, necrosis cause perforation. 2-in cutaneous diphteria: The skin lesions covered by gray brown pseudomembrane. Throat swab: Stain: Gram-positive rods Culture: on Loffler’s serum or McLeod’s medium (tellurite blood agar medium) Lab Diagnosis Test for toxigenicity: [IMP] 1- Elek’s test (in vitro): differentiate between toxigenic & non-toxigenic diphteria. 2- Guinea pig inoculation (in vivo): The M.O. is injected into both guinea pigs. The nonprotected one dies while the protected one remains alive. Must proceed rapidly. 1- Antitoxin (20,000-100,000 units) intravenously 2- Penicillin or erythromycin 3- Tracheotomy may be required In laryngeal diphtheria. Treatment session 4 2 Micro 3: 4th Year a) Active immunization: Vaccine is mixed with pertussis and tetanus (DPT) b) Passive immunization with diphtheria antitoxin : [IMP]Schick’s test: Method for determining susceptibility to diphtheria. 0.1 ml diphtheria Positive reaction False Positive reaction toxin is injected into Redness at the site of injection after 3 days the skin of the (Absence of circulating antibody) (Hypersensitivity to the toxin). forearm: use of a control injection of the same Positive reaction False Positive reaction amount of heated No Redness Redness toxin (toxoid) into the other forearm Interpretation of test: 1. Positive: when the test results in a wheal (raised mark on skin) of 5-10 mm diameter. reaching its peak in 4-7 days. Prevention The control arm shows no reaction. lacks antibodies against the toxin susceptible to the disease. 2. Pseudo-positive: - only a red colored inflammation (erythema)and it disappears within 4 days. - happens on both the arms hypersensitive to the toxin. 3. Negative reaction: Indicates that the person is immune. 4. Combined reaction: the erythema fades off after 4 days only in the control arm. - It progresses on the test arm to a typical positive. - The subject is interpreted to be both susceptible and hypersensitive. session 4 3 Micro 3: 4th Year Listeria monocytogenes facultative intracellular: Can move from cell to cell without exposed to antibodies. General characters catalase positive - beta-hemolytic Epidemiology - Immunocompromised adults & pregnancy transmission: via the fecal-oral route Important food borne pathogen: can grow at refrigerator temperatures. produce Biofilms ability to survive harsh environments. binds host cells via host protein cadherin (epithelial attachment Surface proteins protein that is found in the BBB & placenta & GIT) allowing entry "internalins" into the cell. (A and B) (the bacteria can infect neonates and cause meningitis) pore-forming cytotoxic protein Cytotoxic Phagocytized L. monocytogenes can lyse the internalized protein: vacuole "Listeriolysin O” LLO: responsible for the beta-hemolysis on blood agar. - L. monocytogenes replicates rapidly in the host cytosol and Virulence the bacterial densely covers its surface with the bacterial protein ActA factors[IMP] protein ActA. - induces host actin polymerization allows L. monocytogenes to move rapidly between cellsavoid antibody detection. Two types of Listeria monocytogenes movement[IMP] session 4 4 Micro 3: 4th Year Adult listeriosis Pregnant women[IMP] in immunocompromised adults especially Infected mothers are asymptomatic or has with renal transplantation an influenza-like illness, in fetus severe. a) Early onset syndrome: include: meningitis, septicemia, pyogenic granulomas in multiple organs endocarditis. b) Late onset syndrome: meningitis in the young (neonates), meningitis 1-4 weeks after delivery & suffer Pathogenesis: elderly, and immunocompromised from physical retardation (neurological Healthy individuals infected with L. damage) monocytogenes typically have a self- limiting gastrointestinal infection with fever and diarrhea. Febrile gastroenteritis: characterized by watery diarrhea, fever, and no vomiting. 1. Specimen: blood sample, cerebrospinal fluid (CSF). 2. Gram stain: small gram +ve rods Diagnosis 3. Test for motility: Tumbling movement ( at 30 C or less) 4. Cultivation on blood agar: grey, ß-hemolytic colonies. Treatment: by a combined therapy of ampicillin and gentamicin. Anaerobic non-spore forming: Gram positive bacilli Propionibacterium species - Members of the normal flora of skin. - Propionibacterium acnes (opportunistic pathogen) causes Acne vulgaris - Produce lipases that split free fatty acids off from skin lipidstissue inflammation acne formation. session 4 5