Open AccessA vaccinia virus lacking A10L: viral core proteins accumulate on structures derived from the endoplasmic reticulum
Author(s) -
Rodriguez Dolores,
Bárcena Montserrat,
Möbius Wiebke,
Schleich Sibylle,
Esteban Mariano,
Geerts Willie J. C.,
Koster Abraham J.,
Griffiths Gareth,
Locker Jacomine Krijnse
Publication year - 2006
Publication title -
cellular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.542
H-Index - 138
eISSN - 1462-5822
pISSN - 1462-5814
DOI - 10.1111/j.1462-5822.2005.00632.x
Subject(s) - endoplasmic reticulum , biology , viral membrane , membrane , cisterna , virus , microbiology and biotechnology , membrane protein , viral protein , vaccinia , virology , viral envelope , biochemistry , golgi apparatus , gene , recombinant dna
Summary 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.