JC virus intranuclear inclusions associated with PML-NBs: analysis by electron microscopy and structured illumination microscopy
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Updated: May 25, 2026

Temporal Analysis of the Nuclear-to-cytoplasmic Translocation of a Herpes Simplex Virus 1 Protein by Immunofluorescent Confocal Microscopy
Published on: November 4, 2018
Yukiko Shishido-Hara1, Shizuko Ichinose2, Toshiki Uchihara3
1Department of Pathology, Kyorin University School of Medicine, Tokyo, Japan.
Abstract:
Progressive multifocal leukoencephalopathy is a fatal demyelinating disorder caused by JC virus infection. JC virus was recently found to target promyelocytic leukemia nuclear bodies (PML-NBs), punctuate domains in the nuclei. Thus, the virus progenies cluster in dots as intranuclear inclusions (ie, as dot-shaped inclusions). In the present study, both the viral major and minor capsid proteins were expressed from polycistronic expression vectors with a powerful promoter, and formation into virus-like particles (VLPs) was examined by electron microscopy. When the upstream regulatory sequence including the agnogene (nt 275 to 490) was present, capsid protein expression was suppressed, but numerous VLPs were efficiently formed with restricted accumulation to PML-NBs. VLPs were uniform, and the cells were severely degraded. In contrast, when the 5' terminus of the agnogene (nt 275 to 409; 135 bp) was deleted, capsid protein expression was markedly enhanced, but VLPs were more randomly produced in the nucleus outside of PML-NBs. VLPs were pleomorphic, and cell degradation was minimal. JC virus association with PML-NBs was confirmed in human brain tissues by structured illumination microscopy. PML-NBs were shaped in spherical shells, with viral capsid proteins circumscribing the surface. These findings indicate that PML-NBs are intranuclear locations for pathogenic JC virus proliferation. Either the agnogene or its product likely supports efficient progeny production at PML-NBs, leading to subsequent degeneration of host glial cells.
Insights
JC virus, the cause of progressive multifocal leukoencephalopathy, proliferates within promyelocytic leukemia nuclear bodies (PML-NBs). The agnogene regulates efficient viral progeny production at these sites, leading to host cell destruction.
Area of Science:
- Virology
- Cell Biology
- Neuroscience
Background:
- Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease caused by JC virus (JCV) infection.
- JCV has been observed to target promyelocytic leukemia nuclear bodies (PML-NBs), which are nuclear domains, leading to dot-shaped intranuclear inclusions of viral progeny.
Purpose of the Study:
- To investigate the role of the agnogene and PML-NBs in JC virus replication and pathogenesis.
- To characterize the formation and localization of virus-like particles (VLPs) in relation to PML-NBs.
Main Methods:
- Expression of JCV major and minor capsid proteins using polycistronic vectors.
- Electron microscopy to examine VLP formation.
- Structured illumination microscopy to confirm JCV association with PML-NBs in human brain tissues.
Main Results:
- Presence of the agnogene (nt 275-490) suppressed capsid expression but led to efficient VLP formation localized to PML-NBs, resulting in severe cell degradation.
- Deletion of the 5' terminus of the agnogene (nt 275-409) enhanced capsid expression but resulted in random VLP production outside PML-NBs, with minimal cell degradation.
- JCV capsid proteins were observed circumscribing spherical shells of PML-NBs in human brain tissues.
Conclusions:
- PML-NBs serve as intranuclear sites for pathogenic JC virus proliferation.
- The agnogene and its product are likely crucial for efficient viral progeny production at PML-NBs, driving host glial cell degeneration.
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