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Egress of alphaherpesviruses: comparative ultrastructural study
H Granzow1, B G Klupp, W Fuchs
1Institutes of Infectology, Friedrich-Loeffler-Institutes, Federal Research Centre for Virus Diseases of Animals, D-17498 Insel Riems, Germany. Harald.Granzow@rie.bfav.de
Journal of Virology
|March 27, 2001
Summary
This study reveals how four alphaherpesviruses, including equine herpesvirus 1 (EHV-1) and herpes simplex virus 1 (HSV-1), exit cells. Viruses undergo deenvelopment and reenvelopment, with distinct membrane fusion processes during egress compared to entry.
Area of Science:
- Virology
- Cell Biology
- Microbiology
Background:
- Alphaherpesviruses, including equine herpesvirus 1 (EHV-1), herpes simplex virus 1 (HSV-1), infectious laryngotracheitis virus (ILTV), and pseudorabies virus (PrV), are significant pathogens.
- Understanding viral egress is crucial for developing antiviral strategies.
Purpose of the Study:
- To investigate and visualize the egress mechanisms of four alphaherpesviruses using electron microscopy.
- To compare the morphogenesis and egress pathways of EHV-1, HSV-1, ILTV, and PrV in infected cell lines.
Main Methods:
- Infected cell lines of various origins were analyzed using transmission electron microscopy.
- Immunogold labeling with a trans-Golgi network (TGN)-specific antiserum was employed.
- Studies utilized pseudorabies virus (PrV) mutants lacking glycoproteins gB and gH.
Main Results:
- Intranuclear assembly is followed by budding at the inner nuclear membrane, forming enveloped particles in the perinuclear space.
- Egress from the perinuclear cisterna involves fusion with the outer nuclear membrane, visualized for HSV-1 and EHV-1.
- Intracytoplasmic nucleocapsids are enveloped at the trans-Golgi network (TGN), forming mature virions distinct from those in the perinuclear space.
- Glycoproteins gB and gH are dispensable for the egress of PrV.
Conclusions:
- A deenvelopment-reenvelopment process similar to that observed in other herpesviruses occurs during the maturation of EHV-1, HSV-1, and ILTV.
- The membrane fusion events during viral egress differ significantly from those involved in virus entry and cell-to-cell spread.