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Poliovirus

Poliovirus

For medical students2 min readUpdated 2026-10-10

Poliomyelitis is an acute febrile infection caused by enteroviruses. The pathogen selectively targets the gray matter of the spinal cord and brainstem, which can lead to irreversible flaccid paralysis and paresis.

FamilyPicornaviridae (genus *Enterovirus*)
Primary targetMotor neurons of the anterior horns of the spinal cord
ImmunityLifelong, but type-specific (only to the acquired serotype)
Paralysis rateApproximately 1% of all infections

Properties of the Virus

The causative agent of poliomyelitis belongs to the species Enterovirus C, genus Enterovirus, family Picornaviridae. There are three known serotypes of the virus (1, 2, and 3). All of them are capable of causing human disease and are pathogenic to primates.

An important feature is the absence of cross-immunity: if a person has recovered from an infection caused by the first serotype, they are not protected against the second and third.

Pathogenesis of Infection

Human susceptibility to the virus is very high. Infection occurs through the mucous membranes of the respiratory and gastrointestinal tracts.

  1. Primary replication. The virus multiplies in the lymph nodes of the pharyngeal ring and the small intestine. At this stage, the pathogen is already actively excreted in feces and nasopharyngeal mucus, although symptoms are still absent.
  2. Dissemination. From the lymphatic system, the virus enters the bloodstream (viremia occurs) and then penetrates the central nervous system.
  3. CNS involvement. The virus destroys the cells of the anterior horns of the spinal cord, leading to the loss of motor functions—causing flaccid paralysis of the limbs and torso.

Clinical Course

On average, the incubation period lasts from 7 to 14 days. The disease can present in several forms:

The disease often begins with general infectious symptoms (fever, vomiting, sore throat). A biphasic course is characteristic: after the initial mild malaise, there is a temporary improvement, followed by a sharp deterioration with the development of paralysis.

Diagnosis

During the patient's life, stool and nasopharyngeal swabs are tested; post-mortem, brain tissue and lymph nodes are examined.

Specific Prophylaxis (Vaccines)

Two types of vaccines are used to prevent poliomyelitis:

  1. Inactivated Polio Vaccine (IPV): administered parenterally. It generates humoral immunity but does not create local gut immunity (the virus can still replicate there).
  2. Oral Polio Vaccine (OPV): contains attenuated (weakened) strains. In addition to systemic immunity, it establishes robust local mucosal immunity (secretory IgA), which blocks viral replication.

Thanks to OPV, the WHO launched a global polio eradication initiative in 1988, leading to the elimination of the infection in many countries.

Mnemonic

The Greek word "polios" means "gray." This is a clue to the virus's target: it specifically attacks the gray matter of the spinal cord.

Frequently asked questions

Why does poliovirus cause paralysis specifically?

The virus exhibits a tropism for motor neurons located in the anterior horns of the spinal cord. Destruction of these cells leads to the loss of motor functions and the development of flaccid paralysis.

What kind of immunity develops after recovering from poliomyelitis?

Lifelong immunity develops, with virus-neutralizing antibodies acting as the primary factor. However, it is type-specific—protecting only against the specific serotype that caused the disease.

What is VAPP and who gets it?

VAPP (Vaccine-Associated Paralytic Poliomyelitis) is a rare complication following the administration of the oral polio vaccine (OPV). It can occur in vaccinated individuals or their contacts, with the risk being particularly high in patients with primary immunodeficiencies (B-cell defects).

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