A vaccinia virus lacking A10L: viral core proteins accumulate on structures derived from the endoplasmic reticulum

Dolores Rodriguez1, Montserrat Bárcena, Wiebke Möbius

  • 1Centro Nacional de Biotecnología, Campus Universidad Autónoma, 28049 Madrid, Spain.

Cellular Microbiology
|February 14, 2006
PubMed

Insights

Vaccinia virus (VV) assembly requires the core protein A10L for intracellular mature virus (IMV) formation. Viral DNA and core proteins coassemble on endoplasmic reticulum (ER)-derived membranes continuous with immature viruses (IVs).

Area of Science:

  • Virology
  • Cell Biology
  • Structural Biology

Background:

  • The assembly of intracellular mature virions (IMVs) of vaccinia virus (VV), a poxviridae member, remains poorly understood.
  • Previous hypotheses suggest IMV formation involves a double-membraned cisterna derived from the smooth endoplasmic reticulum (ER).

Purpose of the Study:

  • To investigate the role of the major core protein A10L in VV assembly.
  • To elucidate the origin and structure of membranes involved in VV morphogenesis.

Main Methods:

  • Characterization of a conditional A10L-expressing VV mutant.
  • Immunolabelling of cryo-sections to identify viral and cellular proteins.
  • Electron tomography (ET) of semi-thin cryo-sections to visualize membrane structures.

Main Results:

  • Conditional A10L expression is essential for IMV formation; its absence leads to accumulation of immature viruses (IVs) and stacked membrane structures containing viral DNA.
  • These stacked membranes are derived from the ER, as indicated by immunolabelling with ER marker proteins.
  • Electron tomography revealed continuity between the stacked membranes and IV membranes, with IV membranes separating into two-membrane profiles.

Conclusions:

  • VV core proteins and viral DNA can coassemble onto ER-derived membranes.
  • These membranes are continuous with those of IVs, providing insights into the mechanism of VV assembly.

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