Clostridium tetani

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Description and Significance

Clostridium tetani is a rod-shaped, anaerobic, and endospore-forming bacterium that is responsible for the tetanus disease, a condition of the central nervous system affecting an estimated 350,000 people a year, worldwide [1]. Single rods, or bacillica, have terminal spherical endospores creating a "clubbed appearence" [2]. This bacterium is gram-positive, a characteristic shared by the other related species belonging to the Clostridium genus. Bacteria classified as Clostridium are important pathogens, such as C. botulinum, an organism producing a toxin in food/wound that causes botulism and C. perfringens, that causes a wide range of symptoms, from food poisoning to gas gangrene [3] .The peptoidoglycan structure of the C. tetani's cell wall allows it to retain the violet crystals in a gram stain. The resulting appearance under a microscope is often described as resembling a tennis racket or a collection of drumsticks. The organism is an obligate anaerobe found in soil and most often in animal feces.

Genome Structure

According to a study published by Yale University in 2003 entitled "The Genome Sequence of Clostridium tetani, the Causative Agent of Tetanus Disease", the genome of Clostridium tetani consists of a 2,799,250-bp chromosome encoding 2,372 open reading frames, or ORFs. An ORF is a portion of an organsims genome that potentially codes for the structure of a protein. It was found that a plasmid of Clostridium tetani, named pE88 in sequencing, harbors the genes for the tetanus toxin (tetX) and its direct transcriptional regulator TetR. The tetanus toxin and a collagenase are encoded on this 74,082-bp plasmid that contains 61 ORFs. The results of the study showed 28 of the 61 ORFs code for proteins that show similarities to those with known structures and functions including collagenase. Collegenase is an exotoxin that aids in the pathogenesis and spread of tetanus by targeting muscle and connective tissues; the sequence of which was identified alongside that of the tetanus toxin [4].


According to the Yale University 2003 study, the origin of the bacterial plasmid pE88, coding for the tetanus toxin, remains unclear. The study concluded over 50% of all ORFs on pE88 are unique to C. tetani. However, homologous ORFs were found when compared with the genomes of both Clostridium perfringens (15), and Clostridium acetobutylicum, coding for proteins involved in lipid degredation and amino acid decomposition. Many of these comprise the Clostridial "backbone" ORFs.

Cell Structure and Metabolism

Clostridium tetani is a rod-shaped, obligate anaerobe that are saprophytic in nature. The bacteria form endospores through sporulation when survival becomes difficult in the presence of oxygen. In its vegetative state, the bacteria are sensitive to external elements such as temperature and have evenly distributed flagella around its surface for motility. As they mature, C. tetani form spherical terminal endospores that are enclosed in multiple layers of protective coats, allowing for resistant dormant survival. Endospores can survive extremely long periods of time until environmental stimuli trigger germination [5].

Ecology

Pathology

For more information, see: Tetanus.

Clostridium tetani spores enter body tissue through wounds, lacerations, and burns, settling in dead cells that lack oxygen. Initially unnoticed, the spores are then able to germinate and spread, long before diagnosis and pursuit of treatment. All identified strains have been found to produce a common toxin called tetanospasmin. The potent neurotoxin blocks the release of necessary neurotransmitters in the central nervous system's transmission of inhibitory nerve impulses [6]. It is the inhibitory neuron messages that allow the muscles of the body to relax by halting the release of acetylcholine from exitatory neurons, which stimulate muscle contraction. The resulting effect in humans begins with muscle spasms at the sight of infection. As the infection spreads along neurons of the spinal chord and brain, it could lead to spastic paralysis and may be fatal. The most recognized associated manifistation of the disease is trismus, or lockjaw. The muscles and nerves of the neck and jaw are commonly the first to be affected before spreading to other parts of the body. Death is usually the result of breathing difficulties that arise due to the spasms and lead to respiratory arrest.

Symtoms

Tetanus has been known to take up to 10 years before manifestations may be observed. Aside from lockjaw, difficulty in swallowing, drooling, and persistent back spasms are among early signs. Later symtoms include perfuse sweating, hyperthermia, cardiac arrythmias and fluctuations in blood pressure. These manifestations indicate the toxic affects of both the somatic and autonomic nervous systems that involve voluntary and involuntary muscle contractions, respectively. The disease can also be transferred to a fetus by a mother with no immunity through the placenta, where nutrients are absorbed into the blood of the developing baby via the umbilical chord. This is a neonatal infection and the baby is born with the disease [7].

Treatment and Prevention

Therapy for suspected cases and diagnoses include antibiotics, such as penicillin and tetracyclines in addition to antitoxin treatment and prompt surgical treatment of the infected wounds and tissues. Vaccination is available for proactive prevention. Individuals are actively immunized with DPT (diphtheria, pertussis, tetanus) toxoid as infants, and should continue vaccination in ten year intervals. The toxoid prompts human cells to make neuralizing antibodies against the binding component of the tetanus toxin. Individuals are passively immunized with tetanus immuno globulin [8].

The tetanus disease is relatively uncommon in North America and industrialized countries. The condition is more common in underdeveloped countries where immunizations are not widely available and agricultural regions where contact with animal fecal matter is likely.

Application to Biotechnology

Current Research

  1. http://microbes.historique.net
  2. http://ncbi.nlm.nih.gov
  3. Wells, CL and Wilkins TD Botulism and Clostridium botulinum and Antibiotic-Associated Diarrhea, Pseudomembranous Colitis. Baron's Medical Microbiology. Baron S et al, eds. 4th ed. Univ of Texas Medical Branch: 1996
  4. Brüggemann, Holger and Sebastian Bäumer, Wolfgang Florian Fricke Arnim Wiezer, Heiko Liesegang, Iwona Decker, Christina Herzberg, Rosa Martínez-Arias, Rainer Merkl, Anke Henne and Gerhard Gottschalk. The Genome Sequence of Clostridium Tetani, the Causative Agent of Tetanus Disease. Proceedings of National Academy of Sciences of the United States of America (PNAS). Yale University: 27 Jan 2003
  5. Bacterial Endospores. Cornell University Department of Microbiology. College of Agriculture and Life Sciences: Teaching, Research and Extension. 2007 <http://www.micro.cornell.edu/cals/micro/research/labs/angert-lab/bacterialendo.cfm>
  6. http://bioweb.uwlax.edu
  7. Todar, Ken. Pathogenic Clostridia. Ken Todar's Microbial World. University of Wisconsin: Madison. 2005 <http://bioinfo.bact.wisc.edu/themicrobialworld/clostridia.html>
  8. Kaiser, Dr. Gary E."Tetanus." 7 Jan 2005<http://student.ccbcmd.edu>