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Updated: Aug 11, 2026

Methodology for the Efficient Generation of Fluorescently Tagged Vaccinia Virus Proteins
Published on: January 17, 2014
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.
Abstract:
The assembly of the intracellular mature virus (IMV) of vaccinia virus (VV), the prototype member of the poxviridae, is poorly understood and controversial. We have previously proposed that the IMV is composed of a continuous double-membraned cisterna derived from the smooth ER, whereby the genome-containing core is enwrapped by a part of this cisterna. In the present study we characterize a mutant virus in which the synthesis of the major core protein A10L can be conditionally expressed. Without A10L, IMVs are not made; immature viruses (IVs) and regularly stacked membrane structures that contain viral DNA, accumulate instead. By immunolabelling of thawed cryo-sections these stacks contain most of the viral core proteins and low levels of viral membrane proteins. Importantly, the stacked membranes could be labelled with antibodies to an ER marker protein, implying that they are derived from this cellular compartment. By electron tomography (ET) on semi-thin cryo-sections we show that the membranes of the stacks are continuous with the membranes of the IVs. Direct continuities with ER cisternae, to which the stacks are tightly apposed, were, however, not unequivocally seen. Finally, ET revealed how the IV membranes separated to become two-membrane profiles. Taken together, this study shows that VV core proteins and the viral DNA can coassemble onto ER-derived membranes that are continuous with the membranes of the IVs.
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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