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Clostridium tetani

Clostridium tetani

For medical students3 min readUpdated 2026-10-10

Clostridium tetani is a Gram-positive, spore-forming bacterium that causes tetanus, a severe acute wound infection affecting the nervous system. The primary danger of this microorganism lies in its production of a potent neurotoxin that triggers generalized muscle spasms.

AppearanceGram-positive bacilli shaped like characteristic "drumsticks"
ToxicityLethal dose of the exotoxin is only 1 ng/kg (second only to botulinum toxin)
Infection TypeSapronosis; the pathogen persists in soil as spores for decades
TargetProteins of the neuroexocytosis apparatus, blocking CNS inhibitory neurons

Morphological and Tinctorial Characteristics

Clostridium tetani is a large, straight bacillus with rounded ends. The microorganism is motile due to flagella distributed over the entire perimeter of the cell (peritrichous). In smears, the bacteria lie haphazardly or form chains. They stain Gram-positive (G+).

The hallmark of Clostridium tetani is its ability to form terminal spores whose diameter significantly exceeds the width of the vegetative cell, giving the bacterium its characteristic "drumstick" appearance. The spores are extremely resistant to environmental factors: they withstand low temperatures down to -60 °C, survive boiling for up to 6 hours, and are resistant to phenol and formalin. They can only be reliably eradicated by autoclaving at 130 °C for 20 minutes, whereas vegetative forms are killed by boiling within just 5 minutes.

Cultural and Biochemical Properties

The bacterium is an obligate anaerobe, meaning it grows and multiplies exclusively in oxygen-free conditions at a temperature of 37 °C.

On solid nutrient media (nutrient agar, gelatin), the pathogen can form two types of colonies:

When inoculated on blood agar, growth is accompanied by a zone of hemolysis. In liquid Kitt-Tarozzi medium, the microorganism grows slowly, causing uniform turbidity and releasing a specific unpleasant odor.

The biochemical activity of C. tetani is extremely low. The bacterium is inert to most carbohydrates, and its proteolytic properties are limited to the slow breakdown of proteins with the formation of ammonia, indole, and volatile fatty acids. The pathogen produces gelatinase and a renin-like enzyme.

Pathogenicity Factors

The primary weapon of the pathogen is tetanus exotoxin. It is identical across all 10 serovars of the bacterium and is released upon lysis of the microbial cell. The toxin consists of two fractions:

  1. Tetanospasmin (neurotoxin): The main factor of pathogenesis. It binds to the neuromuscular junction and reaches the motor neurons of the spinal cord and brainstem via retrograde axonal transport. There, it blocks the release of inhibitory neurotransmitters, leading to uncontrolled clonic and tonic muscle contractions.
  2. Tetanolysin: Destroys erythrocytes and exerts a membrane-toxic effect on the tissues of the heart, lungs, liver, and kidneys, significantly worsening the patient's general condition.

Epidemiology and Clinical Presentation

Tetanus is a universally distributed sapronosis. The natural reservoir of infection is soil, where spores enter with human and animal feces (the pathogen is a normal inhabitant of the intestine). Transmission occurs via contact (wound route) when infected soil enters damaged tissues, creating anaerobic conditions. An infected person is not contagious to others.

The incubation period lasts from 1 day to several weeks (averaging 6–14 days). An important prognostic rule: the shorter the incubation period, the more severe the infection. The disease begins acutely with the classic triad:

Diagnosis and Prophylaxis

Post-infection immunity is not established after tetanus because the lethal dose of the toxin is significantly below the threshold required to activate an immune response.

Diagnosis includes bacterioscopy (searching for "drumsticks") and bacteriological culture on Kitt-Tarozzi medium. The gold standard for detecting the exotoxin is the biological assay in white mice using the neutralization test (NT).

The foundation of protection against infection is routine immunization. It begins at 3 months of age with vaccines containing tetanus toxoid (DTaP, DT), followed by revaccination every 10 years. In case of injuries, emergency specific prophylaxis is administered: injection of toxoid combined with specific human immunoglobulin or heterologous horse serum (administered using Besredka's desensitization method).

Mnemonic

The classic clinical triad of tetanus can be remembered by the descending direction of spasm development: J-F-B (Jaw — Face — Back), representing trismus, "risus sardonicus", and opisthotonos.

Frequently asked questions

Which antibiotics are used for etiotropic therapy of tetanus?

For etiotropic therapy of tetanus, sources indicate:

  • Metronidazole and tinidazole.
  • Benzylpenicillin as the drug of choice for infection caused by Clostridium tetani.

Lincomycin and clindamycin belong to lincosamides, whose activity spectrum includes the tetanus pathogen.

Which specific inhibitory neurotransmitters are blocked by tetanospasmin?

Tetanospasmin blocks the secretion of glycine and $\gamma$-aminobutyric acid (GABA). This neurotoxin cleaves synaptobrevin and vesicle-associated membrane protein, halting the release of these inhibitory neurotransmitters from spinal cord interneurons. As a result, a deficit of inhibitory influences occurs, leading to disinhibition of motor neurons and their hyperexcitation, clinically manifested by sustained muscle contractions and spasms.

What is the antigenic structure of Clostridium tetani?

The antigenic structure of Clostridium tetani is represented by two main antigens:

  • O-antigen — a somatic, thermostable antigen common to all variants of the pathogen.
  • H-antigen — a flagellar, thermolabile antigen. Based on differences in its structure, 10 serological variants (serovars) of the bacterium are distinguished.

Regardless of the serovar, all strains of the microorganism produce an exotoxin that is absolutely identical in its antigenic properties.

How exactly is the biological assay in white mice performed to detect tetanus exotoxin?

The biological assay in white mice is performed in the format of a neutralization test using anti-tetanus serum.

  • Part of the test material filtrate is mixed with anti-tetanus serum, incubated for 40 minutes, and administered to the first group of animals.
  • Filtrate without serum is administered to the second group of animals.
  • If Clostridium tetani is present, the animals in the second group develop symptoms of tetanus.
Is immunity formed after recovering from tetanus?

No, it is not formed. The lethal dose of tetanus exotoxin is negligibly small, and its quantity is insufficient to trigger a full-scale immune response.

Why is the bacterium called a "drumstick"?

The microorganism acquires this appearance due to the presence of a terminally (at the end) located spore. Its diameter is larger than the width of the vegetative cell itself.

How does the incubation period affect the prognosis of the disease?

There is a direct prognostic rule: the shorter the incubation period, the more severe and aggressive the infection courses.

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