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Mouse Elberfeld (ME) virus determines the cell surface alterations when mixedly infecting poliovirus-infected cells

Insights

Mixed picornavirus infections show ME virus dominates cell surface changes, causing distinct alterations like large vacuoles. Poliovirus induces different changes, but ME virus effects prevail in mixed infections.

Area of Science:

  • Virology
  • Cell Biology
  • Microscopy

Background:

  • Picornaviruses are small RNA viruses known to cause various cytopathic effects in host cells.
  • Understanding viral interactions during mixed infections is crucial for deciphering disease pathogenesis.
  • HEp-2 cells are a commonly used human epithelial cell line for studying viral infections.

Purpose of the Study:

  • To compare the distinct surface alterations induced by poliovirus and ME virus in HEp-2 cells.
  • To investigate the outcome of mixed infections on cellular surface morphology and integrity.
  • To determine the dominant virus in dictating cytopathic effects during co-infection.

Main Methods:

  • Scanning and transmission electron microscopy to visualize cellular surface changes.
  • 51Cr-release assay to quantify cytolytic membrane damage.
  • Chronological analysis of cytopathic alterations in singly and dually infected cells.

Main Results:

  • ME virus infection caused large membranous structures (vacuoles, sheets, blebs) not observed with poliovirus.
  • Polio virus induced cell pycnosis, filopodia elongation, and microvilli condensation.
  • Mixed infections predominantly displayed ME virus-specific surface alterations, irrespective of poliovirus replication.
  • ME virus-specific cytolytic damage and 51Cr-release were more pronounced than poliovirus-induced damage.

Conclusions:

  • ME virus dictates the characteristic surface alterations during mixed infections with poliovirus in HEp-2 cells.
  • ME virus-induced cytopathic effects, particularly membrane damage, are dominant even when poliovirus replicates.
  • Cellular internal structure alterations are primarily influenced by ME virus when poliovirus replication is suppressed.

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