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Ultrastructural degenerative changes of age-dependent ECHO 9 virus-induced polymyositis in infant mice

Virchows Archiv. B, Cell Pathology Including Molecular Pathology
|January 1, 1981
PubMed

Insights

Echo 9 virus infection in newborn mice causes polymyositis and muscle fiber necrosis. Early ultrastructural changes include sarcoplasmic reticulum dilation, myofibril disruption, and ultimately, muscle cell death.

Area of Science:

  • Virology
  • Pathology
  • Cell Biology

Background:

  • Echo 9 virus (ECHO 9 virus) is known to cause various human illnesses.
  • The pathogenesis of ECHO 9 virus-induced muscle damage at the cellular level requires further elucidation.

Purpose of the Study:

  • To investigate the ultrastructural changes in muscle tissue following experimental inoculation with ECHO 9 virus in newborn mice.
  • To characterize the temporal progression of viral myopathy and identify cellular events associated with virus propagation.

Main Methods:

  • Newborn NMRI mice were experimentally inoculated with ECHO 9 virus.
  • Muscle tissues were examined using electron microscopy to observe ultrastructural changes at various time points post-infection.
  • Histopathological analysis was performed to assess the extent of muscle damage.

Main Results:

  • Infection led to diffuse polymyositis within 4 days, progressing to paresis and death between 7-11 days.
  • Early ultrastructural changes (24-48 h post-inoculation) included sarcoplasmic reticulum dilation and myofibril disruption.
  • Muscle fiber necrosis occurred due to virus-mediated nuclear and organellar injury, with formation of contraction bands.
  • Pronounced proliferation of sarcoplasmic reticulum membranes was observed in muscle fibers, myoblasts, and myotubes of mice infected within 18 hours of birth.

Conclusions:

  • ECHO 9 virus infection in newborn mice induces significant muscle pathology, characterized by polymyositis and necrosis.
  • The study reveals specific ultrastructural alterations in muscle cells, highlighting the role of sarcoplasmic reticulum and myofibrils in viral myopathy.
  • Age at inoculation is a critical factor, as cytological alterations were specific to mice infected very early in life.

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