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Coxsackieviruses and ECHO Viruses

Coxsackievirus, Echovirus

For medical students2 min readUpdated 2026-10-10

Coxsackieviruses and ECHO viruses are RNA pathogens belonging to the family Picornaviridae (genus Enterovirus). They cause a wide spectrum of pathologies ranging from mild respiratory and enteric infections to severe involvements of the nervous system, skeletal muscles, and myocardium.

FamilyPicornaviridae, genus Enterovirus (RNA-containing)
CoxsackiePathogenic to suckling mice (basis of classical isolation methods)
ECHONon-pathogenic to laboratory animals (cultivated in vitro)
Coxsackie ATropism for muscles, causes diffuse myositis and necrosis
Coxsackie BTropism for CNS, muscle necrosis, and visceral organ involvement

General Characteristics and Taxonomy

Both groups of pathogens belong to the family Picornaviridae and the genus Enterovirus. They are compact RNA viruses, each comprising over 30 distinct serotypes.

The name Coxsackievirus is geographical, derived from the American town where the pathogen was first discovered and isolated.

The acronym ECHO stands for Enteric Cytopathogenic Human Orphan virus. The fundamental difference between ECHO viruses and Coxsackieviruses is that ECHO viruses are non-pathogenic to laboratory animals.

Coxsackieviruses: Groups A and B

Historically, the classification of Coxsackieviruses is based on their ability to cause specific pathological changes in newborn suckling mice. Based on these manifestations and clinical presentations, they are divided into two main groups.

Group A (Coxsackievirus A) Predominantly affects mucous membranes, skin, and skeletal muscles, causing focal necrosis and diffuse myositis. Characteristic clinical forms include:

Group B (Coxsackievirus B) Characterized by pronounced tropism for the central nervous system, visceral pathology (internal organ involvement), and skeletal muscle necrosis. Typical manifestations include:

ECHO Viruses

Since ECHO viruses do not infect laboratory animals, their study and cultivation are performed exclusively in cell cultures.

The clinical presentation of ECHO virus infections is highly variable and may include:

Microbiological Diagnostics

Specimens for enterovirus detection include feces and nasopharyngeal swabs. When central nervous system involvement is suspected, particularly in ECHO virus infections, cerebrospinal fluid (CSF) is additionally analyzed.

  1. Virological method (pathogen isolation):
  2. For Coxsackieviruses, the classical method involves inoculating suckling mice followed by analysis of pathological tissue changes.
  3. Coxsackieviruses B, certain Coxsackieviruses A serotypes, and all ECHO viruses are successfully isolated by inoculating cell cultures (e.g., HeLa cells or monkey kidney cells).
  4. Serological method:
  5. Based on detecting a rising titer of specific antibodies in paired acute and convalescent sera.
  6. Identification:
  7. Serotyping is performed using standardized assays: hemagglutination inhibition (HAI), complement fixation test (CFT), neutralization test (NT), and ELISA.

Mnemonic

To easily remember Coxsackievirus clinical features: Group "A" is for Angina (herpangina) and Alimentary/Aphthae (vesicles in hand, foot, and mouth disease), while Group "B" is for Body organs (myocarditis, pleurodynia) and Brain/nervous system involvement.

Frequently asked questions

Which cell cultures are used for the virological isolation of Coxsackie B and ECHO viruses?

Primary and continuous human and monkey tissue cell cultures are used.

  • Coxsackieviruses B are isolated by inoculating HeLa and monkey kidney cell cultures.
  • ECHO viruses are isolated using monkey kidney cell cultures.

Most enteroviruses replicate well in these cultures. Virus detection is indicated by a cytopathic effect (CPE), and they form plaques under agar overlay.

What are the mechanisms and routes of transmission for Coxsackieviruses and ECHO viruses in human populations?

Transmission occurs from an infected individual or asymptomatic carrier via several routes:

  • Aerosol mechanism (droplet route) — occurs predominantly during the first days of illness due to massive viral shedding from the upper respiratory tract during coughing and sneezing.
  • Fecal-oral mechanism — driven by prolonged persistence of the pathogen in the intestine (fecal shedding can last up to 5 months).
  • Vertical mechanism — transplacental transmission from mother to fetus is possible.
What is the primary microbiological difference between ECHO viruses and Coxsackieviruses?

ECHO viruses are completely non-pathogenic to laboratory animals. Coxsackieviruses, by contrast, are pathogenic to newborn suckling mice, a property historically used for their isolation.

What is Bornholm disease and which pathogen causes it?

It is epidemic pleurodynia—an illness characterized by severe paroxysmal chest pain, pleuritis, and fever. It is caused by Coxsackieviruses Group B.

What specimens are collected from a patient to diagnose ECHO virus infections?

Nasopharyngeal secretions, feces, and—in the presence of neurological symptoms such as meningitis—cerebrospinal fluid (CSF) are used for testing.

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