Related Experiment Video
Updated: Feb 5, 2026

In Vitro Selection of Aptamers to Differentiate Infectious from Non-Infectious Viruses
Published on: September 7, 2022
Infectious Bronchitis Virus Nonstructural Protein 4 Alone Induces Membrane Pairing
Nicole Doyle1, Benjamin W Neuman2, Jennifer Simpson3
1The Pirbright Institute, Pirbright, Surrey GU24 0NF, UK. nicole.doyle@pirbright.ac.uk.
Abstract:
Positive-strand RNA viruses, such as coronaviruses, induce cellular membrane rearrangements during replication to form replication organelles allowing for efficient viral RNA synthesis. Infectious bronchitis virus (IBV), a pathogenic avian Gammacoronavirus of significant importance to the global poultry industry, has been shown to induce the formation of double membrane vesicles (DMVs), zippered endoplasmic reticulum (zER) and tethered vesicles, known as spherules. These membrane rearrangements are virally induced; however, it remains unclear which viral proteins are responsible. In this study, membrane rearrangements induced when expressing viral non-structural proteins (nsps) from two different strains of IBV were compared. Three non-structural transmembrane proteins, nsp3, nsp4, and nsp6, were expressed in cells singularly or in combination and the effects on cellular membranes investigated using electron microscopy and electron tomography. In contrast to previously studied coronaviruses, IBV nsp4 alone is necessary and sufficient to induce membrane pairing; however, expression of the transmembrane proteins together was not sufficient to fully recapitulate DMVs. This indicates that although nsp4 is able to singularly induce membrane pairing, further viral or host factors are required in order to fully assemble IBV replicative structures. This study highlights further differences in the mechanism of membrane rearrangements between members of the coronavirus family.
Insights
Infectious bronchitis virus (IBV) non-structural protein 4 (nsp4) alone induces membrane pairing, a key step in coronavirus replication. However, other viral or host factors are needed for full replication organelle formation.
Area of Science:
- Virology
- Cell Biology
- Molecular Biology
Background:
- Positive-strand RNA viruses, including coronaviruses, remodel host cell membranes to create replication organelles for efficient RNA synthesis.
- Infectious bronchitis virus (IBV), an avian gammacoronavirus, induces double membrane vesicles (DMVs), zippered endoplasmic reticulum (zER), and spherules.
Purpose of the Study:
- To identify the specific viral non-structural proteins (nsps) responsible for inducing membrane rearrangements during IBV replication.
- To compare membrane rearrangement induction by nsps from different IBV strains.
Main Methods:
- Expression of IBV non-structural transmembrane proteins (nsp3, nsp4, nsp6) individually and in combination in cells.
- Investigation of cellular membrane effects using electron microscopy and electron tomography.
Main Results:
- IBV nsp4 alone was found to be necessary and sufficient for inducing membrane pairing, a distinct finding compared to other coronaviruses.
- Co-expression of nsp3, nsp4, and nsp6 did not fully recapitulate the formation of double membrane vesicles (DMVs).
Conclusions:
- IBV nsp4 plays a crucial role in initiating membrane rearrangements by inducing membrane pairing.
- Full assembly of IBV replication structures requires additional viral or host factors beyond nsp3, nsp4, and nsp6.
More Related Videos
Related Concept Videos
Introduction to Membrane Proteins
Membrane Proteins
What are Viruses?
Protein Diffusion in the Membrane
DNA Base Pairing
Tail-anchoring of Proteins in the ER Membrane

