Clostridium tetani From Wikipedia, the free encyclopedia Jump to: navigation, search Clostridium tetani| | Clostridium tetani with characteristic ‘tennis racket’ appearance. | Scientific classification| Kingdom:| Bacteria| Phylum:| Firmicutes| Class:| Clostridia| Order:| Clostridiales| Family:| Clostridiaceae| Genus:| Clostridium| Species:| C. tetani| Binomial name| Clostridium tetani Flugge, 1881| Clostridium tetani is a rod-shaped, anaerobic bacterium of the genus Clostridium. Like other Clostridium species, it is Gram-positive, and its appearance on a gram stain resembles tennis rackets or drumsticks.  C. etani is found as spores in soil or as parasites in the gastrointestinal tract of animals. C. tetani produces a potent biological toxin, tetanospasmin, and is the causative agent of tetanus, a disease characterized by painful muscular spasms that can lead to respiratory failure and, in up to 40% of cases, death. Contents[hide] * 1 History * 2 Characteristics * 3 Vaccination * 4 Toxicity * 4. 1 Toxin Action * 5 Treatment * 6 References * 6. 1 Further reading * 7 External links |  History Tetanus was well known to ancient people, who recognized the relationship between wounds and fatal muscle spasms.
In 1884, Arthur Nicolaier isolated the strychnine-like toxin of tetanus from free-living, anaerobic soil bacteria. The etiology of the disease was further elucidated in 1884 by Antonio Carle and Giorgio Rattone, who demonstrated the transmissibility of tetanus for the first time. They produced tetanus in rabbits by injecting their sciatic nerve with pus from a fatal human tetanus case in that same year. In 1889, C. tetani was isolated from a human victim, by Kitasato Shibasaburo, who later showed that the organism could produce disease when injected into animals, and that the toxin could be neutralized by specific antibodies.
In 1897, Edmond Nocard showed that tetanus antitoxin induced passive immunity in humans, and could be used for prophylaxis and treatment. Tetanus toxoid vaccine was developed by P. Descombey in 1924, and was widely used to prevent tetanus induced by battle wounds during World War II.   Characteristics C. tetani is a rod-shaped, obligate anaerobe which stains Gram positive in fresh cultures; established cultures may stain Gram negative.  During vegetative growth, the organism cannot survive in the presence of oxygen, is heat-sensitive and exhibits flagellar motility.
As the bacterium matures, it develops a terminal spore, which gives the organism its characteristic appearance. C. tetani spores are extremely hardy as they are resistant to heat and most antiseptics.  The spores are distributed widely in manure-treated soils and can also be found on human skin and in contaminated heroin.   Vaccination Tetanus can be prevented through the use of an effective vaccine, simple or adsorbed Tetanus vaccine, combined Tetanus and Killed Polio vaccine, or the older DTP (diphtheria, tetanus, pertussis) vaccine. Side effects are rare, but if they do occur, include: * Fever * Pain at the injection site Unexplained crying in infants, irritability in older children or adults. Severe reactions are extremely rare and include anaphylaxis, seizures and encephalopathy. These events are thought to occur less if only the tetanus-diphtheria component of the vaccine is given. It is recommended that all infants receive the vaccine at 2, 4, 6, and 15 months of age. A fifth booster dose should be given at 4-6 years of age. After that, it should be given every 10 years. However, if a bite, scratch, or puncture occurs more than five years after the last dose of vaccine, the patients should receive another dose of vaccine. edit] Toxicity C. tetani usually enters a host through a wound to the skin and then it replicates. Once an infection is established, C. tetani produces two exotoxins, tetanolysin and tetanospasmin. Eleven strains of C. tetani have been identified, which differ primarily in flagellar antigens and in their ability to produce tetanospasmin. The genes that produce toxin are encoded on a plasmid which is present in all toxigenic strains, and all strains that are capable of producing toxin produce identical toxins.  Tetanolysin serves no known benefit to C. etani. Tetanospasmin is a neurotoxin that causes the clinical manifestations of tetanus. Tetanus toxin is generated in living bacteria, and is released when the bacteria lyse, such as during spore germination or during vegetative growth. A minimal amount of spore germination and vegetative cell growth are required for toxin production.  On the basis of weight, tetanospasmin is one of the most potent toxins known. The estimated minimum human lethal dose is 2. 5 nanograms per kilogram of body weight, or 175 nanograms in a 70 kg (154 lb) human. 2] The only toxins more lethal to humans are botulinum toxin, produced by close relative Clostridium botulinum and the exotoxin produced by Corynebacterium diphtheriae, the causative agent of diphtheria. Tetanospasmin is a zinc-dependent metalloproteinase that is structurally similar to botulinum toxin but with different effects. C. tetani synthesizes tetanospasmin as a single 150kDa polypeptide progenitor toxin that is then cleaved by a protease into two fragments; fragment A (a 50kDa “light chain”) and fragment B (a 100 kDa “heavy chain”) which remain connected via a disulfide bridge.
Cleavage of the progenitor toxin into A and B fragments can be induced artificially by trypsin.   Toxin Action Tetanospasmin is distributed in the blood and lymphatic system of the host. The toxin acts at several sites within the central nervous system, including peripheral nerve terminals, the spinal cord, and brain, and within the sympathetic nervous system. The toxin is taken up into the nerve axon and transported across synaptic junctions, until it reaches the central nervous system, where it is rapidly fixed to gangliosides at the presynaptic junctions of inhibitory motor nerve endings. 2] The clinical manifestations of tetanus are caused when tetanus toxin blocks inhibitory impulses, by interfering with the release of neurotransmitters, including glycine and gamma-aminobutyric acid. This leads to unopposed muscle contraction and spasm. Characteristic features are risus sardonicus (a rigid smile), trismus (commonly known as “lock-jaw”), and opisthotonus (rigid, arched back). Seizures may occur, and the autonomic nervous system may also be affected. Tetanospasmin appears to prevent the release of neurotransmitters by selectively cleaving a component of synaptic vesicles called synaptobrevin II. 4]  Treatment Main article: Tetanus When a tetanus infection becomes established, treatment usually focuses on controlling muscle spasms, stopping toxin production, and neutralizing the effects of the toxin. Treatment includes administration of tetanus immune globulin (TIG), which comprises antibodies that inhibit tetanus toxin (also known as tetanus antitoxins), by binding to and removing unbound tetanus toxin from the body. Binding of the toxin to the nerve endings appears to be an irreversible event, and TIG is ineffective at removing bound toxin. Recovery of affected nerves requires the sprouting of a new axon terminal. 4] Large doses of antibiotics (such as metronidazole or intramuscular doxycycline) are also given once tetanus infection is suspected in order to halt toxin production. Prevention of tetanus includes vaccination and cleaning the primary wound. Prophylaxis is effective in the form of a tetanus toxoid vaccine, which is given with or without passive immunization with tetanus immune globulin. Very few cases of tetanus have occurred in individuals with up-to-date tetanus vaccinations. DPT vaccine (diphtheria-pertussis-tetanus) is administered in most of the world.
It is given at 2, 4, 6, and 15–18 months of age, followed by a booster before entry to school (4-6 years). This regimen provides protection from tetanus for about 10 years, and every 10 years thereafter, a booster shot of tetanus vaccine is recommended.  Tetanus is not contagious from person to person, and is the only vaccine-preventable disease that is infectious but not contagious. A C. tetani infection does not result in tetanus immunity, and tetanus vaccination should be given as soon as the patient has stabilized.   References 1. ^ a b Ryan KJ; Ray CG (editors) (2004). Sherris Medical Microbiology (4th ed. ed. ). McGraw Hill.
ISBN 0838585299. 2. ^ a b c d e f Atkinson W, Hamborsky J, McIntyre L, Wolfe S (eds). (2006). Epidemiology and Prevention of Vaccine-Preventable Diseases (The Pink Book) (9th ed. ed. ). Public Health Foundation. http://www. cdc. gov/vaccines/pubs/pinkbook/downloads/tetanus. pdf. 3. ^ Madigan M; Martinko J (editors). (2005). Brock Biology of Microorganisms (11th ed. ed. ). Prentice Hall. ISBN 0131443291. 4. ^ a b c d e Todar, Ken (2005) Pathogenic Clostridia, Ken Todar’s Microbial World, University of Wisconsin – Madison.  Further reading * Clinical Microbiology, ISBN 0-940780-49-6  External links * Pathema-Clostridium Resource
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