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病原生物学教研室 Department of pathogenic Biology of Gannan Medical University

医学微生物学 Medical Microbiology. 病原生物学教研室 Department of pathogenic Biology of Gannan Medical University. 张文平. Anaerobic bacteria. Clostridium Tetani. Structure. anaerobic gram-positive rod that forms terminal spores motile with peritrichous flagella colonies often swarm on agar plates

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病原生物学教研室 Department of pathogenic Biology of Gannan Medical University

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  1. 医学微生物学 Medical Microbiology 病原生物学教研室 Department of pathogenic Biology of Gannan Medical University 张文平

  2. Anaerobic bacteria

  3. Clostridium Tetani

  4. Structure • anaerobic gram-positive rod that forms terminal spores • motile with peritrichous flagella • colonies often swarm on agar plates • does not produce acid from glucose • contains a plasmid that produces a toxin called tetanospasmin

  5. Pathogenesis Tetanospasmin is responsible for the infamous toxemia called tetanus.

  6. tetanolysin, a hemolysin that is inactivated by cholesterol and has no role in pathogenesis. tetanospasmin, a spasmogenic toxin responsible for the classical symptoms of the disease. two toxins

  7. Tetanus Toxin (tetanospasmin) (LONG) single polypeptide chain (called the progenitor toxin) cleaved into a heavy chain (fragment B) and light chain (fragment A) Fragment B binds to the receptor of nerve (ganglioside) The A fragment has toxic (enzymatic) activity. It is transported within the axon and across synaptic junctions until it reaches the central nervous system. There it becomes rapidly fixed to gangliosides at the presynaptic inhibitory motor nerve endings, and is taken up into the axon by endocytosis. The effect of the toxin is to block the release of inhibitory neurotransmitters (glycine and gamma-amino butyric acid) across the synaptic cleft, which is required to check the nervous impulse.

  8. sardonic smile (risus sardonicus) lockjaw Rigid paralysis

  9. Diagnosis • Diagnosis of tetanus is obvious in advanced cases. • The patient should be treated on a clinical basis without waiting for laboratory data.

  10. Treatment depends on early diagnosis and the use of Human tetanus immunoglobulin (HTIG)before a lethal amount of toxin becomes fixed to neural tissue. . Control: Injections of tetanus toxoid are prophylactic Treatment and Control

  11. Clostridium perfringens

  12. Pathogenesis • Produces several tissue degradingenzymes (including lecithinase [α-toxin], proteolytic and saccharolytic enzymes). • Necrosis and destruction of blood vessels and the surrounding tissue result. • This creates an anaerobic environment in adjacent tissue and the organism spreads systemically.

  13. Diseases • Gas gangrene, once initiated, may spread and cause death within hours.

  14. Diseases • A significant cause of food poisoning by enterotoxin producing strains.

  15. Diagnosis • Nagler reaction: exploits the action of its lecithinase. • On the egg yolk medium, colonies are surrounded by zones of turbidity, and the effect is specifically inhibited if C. perfringens antiserum containing αantitoxin is present on the medium.

  16. stormy fermentation Nagler reaction

  17. Clostridium Botulinum

  18. Morphology • a large anaerobic bacillus that forms subterminal endospores

  19. Pathogenesis Botulinum Toxin(neurotoxin) • heat-labile(boiling) • the most potent toxin • The botulinum toxin is specific for peripheral nerve endings. • The toxin binds to the motor neuron and preventsthe release of acetylcholine which is required for a nerve to simulate the muscle. • flaccid paralysis

  20. Food-borne Botulism : blurred vision, inability to swallow, difficulty in speech, descending weakness of skeletal muscles and respiratory paralysis Infant Botulism : constipation and weak sucking ability and generalized weakness Diagnosis flaccid paralysis

  21. A multivalent toxoidevokes good protective antibiody response. Treat: intravenous injection of antitoxin Once the botulinum toxin has bound to nerve endings, its activity is unaffected by antitoxin. Control and Treatment

  22. endogenous versusexogenous infection • Most anaerobes in the normal flora are non-spore formers and anaerobic infections often occur from this source. • Non-spore-formers rarely produceexotoxins in contrast to spore-formers. • Contamination of wounds can also occur with anaerobic spore-formers (e.g. clostridia) which are common in the environment (e.g. soil).

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