Categorias: Todos - epidemiology - characteristics - structure

por R G 15 anos atrás

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B3: Enteroviruses

Enteroviruses are a subgroup of picornaviruses, sharing the family with rhinoviruses, cardioviruses, apthoviruses, and hepatoviruses. They consist of several types including Coxsackie A and B, Echo, and Polio viruses.

B3:  Enteroviruses

Enteroviruses

Enteroviruses are picornaviruses.

Other picornaviruses include:


  • rhinoviruses (115 serotypes)
  • cardioviruses
  • apthoviruses (foot and mouth disease of cattle, sheep)
  • hepatoviruses
  • General

    Pleconaril

    Blocks uncoating step

    Not FDA-approved

    Coxsackievirus infection
    Time

    Seasonality?

    Tropical

    Year-round

    Temperate

    Summer, autumn

    Due to water exposure

    Person

    Common in children

    Place

    DCC

    DCC = Day care centers

    Widespread

    Transmission

  • What route?
  • What is the reservoir?
  • Human host needed

    No known animal reservoirs

    Fecal-oral

    Contaminated water

    Poliovirus

    Eradicated in U.S.

    Echovirus, Coxsackie A21 or A24

    Rhinovirus-like "colds"

    Enterovirus 72

    Hepatitis A disease

    Cocksackievirus A

    Herpangina

    Herpangina: an infectious disease, esp. of children, characterized by a sudden occurrence of fever, loss of appetite, and throat ulcerations, caused by a Coxsackie virus.

    Hand-foot-and-mouth disease

    Self-limiting

    Blister-like rash on hands, feet

    Cold-like symptoms

    Cocksacievirus B

    Pancreatic (diabetes) and resp. infections

    Polio-like paralysis

    Pleurodynia

  • Bornholm disease
  • "Devil's Grip"
  • Cardio

    Pericarditis

    Myocarditis

    CNS

    Encephalitis

    Viral meningitis

    General properties

    Sensitive

    Formaldehyde

    Hypochlorite

    Resistant

    Common disinfectants

    Low pH

    67 serotypes

    Cultured in primates

    Shed in feces

    Grow at 37 degrees

    GI tract

    Structure

    Infection time course

    Infection time course

  • 1-2 h: host shutoff
  • 2.5-3 h: viral protein synthesis, vacuolation of cytoplasm\
  • 3-4 h: permeabilization of host plasma membrane
  • 4-6 h: virus assembly
  • 6-10 h: virus release
  • Icosahedral

    Small

  • Picornaviridae

  • Pico for small
  • Molecular

    Infectious mRNA to polyprotein P1

    Untranslated regions at both termini

    1st third of polyprotein is P1 (capsid)

    No easy way to summarize:

    Multiplication mechanism:





  • Attachment via VP1 to specific host cell surface receptors
  • Genome immediately translated to yield polyprotein
  • First 1/3 of polyprotein is P1 (capsid), remainder (P2, P3) for replication
  • P1 cleaved into VP0, VP1, VP3 with viral protease
  • VP0 cleaved to VP2 and VP4 =>maturation and infectivity
  • RNA-directed RNA polymerase makes (-) strand intermediate, template for genome copies
  • Capsid assembly, genome insertion
  • Protease (protein 2A) cleaves host cap binding protein complex => host shutoff
  • Exits host cells by lysis
  • Viral encoded RNA polymerase

    VPg protein

    5' end

    VP1-4 capsid proteins

    Treatment
    Post-polio

    No specific AV

    Prevention

    Complete Eradication?

  • Virulent poliovirus "replaced" with attenuated strain; risk of VAPP (vaccine-associated paralytic polio)
  • Still endemic in developing countries
  • Goal to eradicate worldwide within decade
  • Hard to justify cost ($250 million per year) when few children get it
  • Must be cooperative effort worldwide
  • Delays will lessen urgency
  • Total eradication needed before vaccination can safely be stopped, otherwise further epidemics possible
  • Vaccines

    Live Sabin

    Poliomyelitis

  • Some risk of contracting mutated virus
  • CDC panel now advises return to Salk vaccine
  • Spread to other house members

    Can be good or bad

    Economical, stable, administered in field

    Confers intestinal immunity (IgM)

    Killed Salk

    Preferred

    Induces humoral immunity

    Safe for immunodeficient

    No viral replication

    Epidemiology
    1% paralysis, death from resp. failure
    99% asymptomatic
    Incubation period

    2-10 days

    Paradox

    Exposure postponed to older children, adults

    Disease more severe

    Improved sanitation correlated with increased epidemics

    Children w/ poor hygiene & sanitation

    Diagnosis
    Kits
    PCR
    Serology

    4-fold Ab increase

    Tissue culture
    Clinical
    Infantile paralysis (possible)
    Paralytic polio

    Meningitis-like symptoms

    Stiff neck

    Head ache

    Malaise

    Fever

    Post-polio syndrome

    Symptoms

    Non life-threatening

    Unlike ALS

    ALS-like

  • Joint pain
  • Fatigue
  • Difficulty swallowing
  • Weakness in certain muscle groups
  • Decreased endurance
  • 30-40 years after acute

    Characteristics
    Pathophysiology

  • Polioviral replication in tonsil and intestinal epithelial cells, lymphoid tissue
  • Infection of draining lymph nodes
  • Primary viremia
  • Seeding of reticuloendothelial organs and target organ (CNS in polio)
  • Viral infection of cells =>lytic death
  • Some symptoms may be caused by host immune response to tissue injury
  • Molecular mimicry: virus-induced autoimmune response
  • Types

    Other
    Polio
    S.T.A.R.
    Echo
    Cocksackie

    B

    A