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Updated: Jun 22, 2026

Transsynaptic Tracing from Peripheral Targets with Pseudorabies Virus Followed by Cholera Toxin and Biotinylated Dextran Amines Double Labeling
Published on: September 14, 2015
Virion-incorporated glycoprotein B mediates transneuronal spread of pseudorabies virus
Dusica Curanovic1, Lynn W Enquist
1Department of Molecular Biology, Princeton University, NJ 08544, USA.
Abstract:
Transneuronal spread of pseudorabies virus (PRV) is a multistep process that requires several virally encoded proteins. Previous studies have shown that PRV glycoprotein B (gB), a component of the viral fusion machinery, is required for the transmission of infection to postsynaptic, second-order neurons. We sought to identify the gB-mediated step in viral transmission. We determined that gB is not required for the sorting of virions into axons of infected neurons, anterograde transport, or the release of virions from the axon. trans or cis expression of gB on the cell surface was not sufficient for transneuronal spread of the virus; instead, efficient incorporation of gB into virions was required. Additionally, neuron-to-cell spread of PRV most likely does not proceed through syncytial connections. We conclude that, upon gB-independent release of virions at the site of neuron-cell contacts, the virion-incorporated gB/gH/gL fusion complex mediates entry into the axonally contacted cell by fusion of the closely apposed membranes.
Insights
Pseudorabies virus (PRV) glycoprotein B (gB) is essential for transneuronal spread. Efficient incorporation of gB into virions, not cell surface expression, is required for viral transmission to postsynaptic neurons.
Area of Science:
- Virology
- Neuroscience
- Cell Biology
Background:
- Transneuronal spread of pseudorabies virus (PRV) involves multiple viral proteins.
- PRV glycoprotein B (gB) is crucial for transmitting infection to second-order neurons.
Purpose of the Study:
- To pinpoint the specific step mediated by gB in viral transneuronal transmission.
- To elucidate the mechanism of PRV spread between neurons.
Main Methods:
- Investigated the role of gB in virion sorting, axonal transport, and release.
- Assessed the necessity of gB incorporation into virions versus cell surface expression for spread.
- Examined PRV spread through syncytial connections.
Main Results:
- gB is not required for virion sorting into axons, anterograde transport, or axonal release.
- Cell surface expression of gB alone is insufficient for transneuronal spread; virion incorporation is necessary.
- PRV neuron-to-cell spread likely does not involve syncytial connections.
Conclusions:
- PRV virions are released independently of gB at neuron-cell contact sites.
- Virion-incorporated gB/gH/gL fusion complex mediates entry into contacted cells via membrane fusion.
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