Related Experiment Video
Updated: Apr 9, 2026

Highly Sensitive Assay for Measurement of Arenavirus-cell Attachment
Published on: March 2, 2016
African swine fever virus assembles a single membrane derived from rupture of the endoplasmic reticulum
Cristina Suarez1, German Andres2, Androniki Kolovou1
1Electron Microscopy (EM) Core Facility and Department of Infectious Diseases, Heidelberg University Hospital, Heidelberg, Germany.
Abstract:
Collective evidence argues that two members of the nucleocytoplasmic large DNA viruses (NCLDVs) acquire their membrane from open membrane intermediates, postulated to be derived from membrane rupture. We now study membrane acquisition of the NCLDV African swine fever virus. By electron tomography (ET), the virion assembles a single bilayer, derived from open membrane precursors that collect as ribbons in the cytoplasm. Biochemically, lumenal endoplasmic reticulum (ER) proteins are released into the cytosol, arguing that the open intermediates are ruptured ER membranes. ET shows that viral capsid assembles on the convex side of the open viral membrane to shape it into an icosahedron. The viral capsid is composed of tiny spikes with a diameter of ∼5 nm, connected to the membrane by a 6 nm wide structure displaying thin striations, as observed by several complementary electron microscopy imaging methods. Immature particles display an opening that closes after uptake of the viral genome and core proteins, followed by the formation of the mature virion. Together with our previous data, this study shows a common principle of NCLDVs to build a single internal envelope from open membrane intermediates. Our data now provide biochemical evidence that these open intermediates result from rupture of a cellular membrane, the ER.
Insights
African swine fever virus, a large DNA virus, acquires its membrane from ruptured endoplasmic reticulum (ER) intermediates. This study reveals a common viral assembly mechanism for nucleocytoplasmic large DNA viruses (NCLDVs).
Area of Science:
- Virology
- Cell Biology
- Structural Biology
Background:
- Nucleocytoplasmic large DNA viruses (NCLDVs) are known to acquire membranes from open intermediates.
- The exact origin and mechanism of membrane acquisition by NCLDVs remain under investigation.
Purpose of the Study:
- To investigate the membrane acquisition mechanism of the African swine fever virus (ASFV), a prominent NCLDV.
- To provide biochemical and structural evidence for the origin of ASFV's viral envelope.
Main Methods:
- Electron tomography (ET) to visualize viral assembly and membrane structure.
- Complementary electron microscopy techniques for high-resolution imaging.
- Biochemical assays to detect cellular protein release.
Main Results:
- ASFV assembles a single bilayer envelope from open membrane precursors resembling cytoplasmic ribbons.
- Biochemical data indicate these precursors are ruptured endoplasmic reticulum (ER) membranes.
- Viral capsid formation involves assembly on the membrane precursor, shaping it into an icosahedron.
Conclusions:
- ASFV utilizes a common NCLDV strategy of forming a single internal envelope from open membrane intermediates.
- This study provides the first biochemical evidence that these intermediates originate from ER membrane rupture.
More Related Videos
11:40Simplified Reverse Genetics Method to Recover Recombinant Rotaviruses Expressing Reporter Proteins
Published on: April 17, 2020
09:13Using Reverse Genetics to Manipulate the NSs Gene of the Rift Valley Fever Virus MP-12 Strain to Improve Vaccine Safety and Efficacy
Published on: November 1, 2011
Related Concept Videos
SNAREs and Membrane Fusion
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
Vesicular Tubular Clusters
With the help of motor proteins such...
Intralumenal Vesicles and Multivesicular Bodies
Insertion of Single-pass Transmembrane Proteins in the RER
Integral transmembrane proteins possess transmembrane and extra membrane domains. The transmembrane domains are primarily made of 20-25 hydrophobic amino acids arranged in a helical secondary confirmation. These...
Coat Assembly and GTPases
Coat assembly depends on the local availability of phosphatidylinositol phosphates or PIPs and GTP-binding proteins. Adaptor proteins, which link the coat proteins to the membrane, bind to these PIPs and play a crucial role in controlling...
Directing Proteins to the Rough Endoplasmic Reticulum