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Updated: Dec 20, 2025

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Measurement of BK-polyomavirus Non-Coding Control Region Driven Transcriptional Activity Via Flow Cytometry
Published on: July 13, 2019
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Archetype JC polyomavirus DNA associated with extracellular vesicles circulates in human plasma samples
Stefano Scribano1, Mirko Guerrini1, Rosaria Arvia1
1Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Summary
JC polyomavirus (JCPyV) DNA was detected in extracellular vesicles (EV) from HIV patients at risk for progressive multifocal leukoencephalopathy (PML). This finding suggests EVs may play a role in JCPyV persistence and spread to the central nervous system.
Area of Science:
- Virology
- Neuroscience
- Immunology
Background:
- JC polyomavirus (JCPyV) causes progressive multifocal leukoencephalopathy (PML) in immunocompromised individuals.
- Viruses, including JCPyV, may utilize extracellular vesicles (EVs) for propagation.
Purpose of the Study:
- To determine if JCPyV-DNA is present in circulating plasma EVs from patients at risk for PML.
- To investigate the potential role of EVs in JCPyV infection and pathogenesis.
Main Methods:
- Plasma samples from 120 HIV-positive patients and 50 healthy donors were analyzed.
- Extracellular vesicles (EVs) were isolated and characterized.
- JCPyV-DNA presence and quantity were measured using Multiplex real-time TaqMan PCR.
- Immunoelectron microscopy (IEM) was used to detect JCPyV Vp1 antigen in EVs.
Main Results:
- JCPyV-DNA was detected in 28% of HIV-positive patients and 4% of healthy donors.
- JCPyV-DNA was found in 42% of characterized plasma EVs from viremic samples.
- IEM confirmed the presence of JCPyV Vp1 antigen within plasma-derived EVs.
Conclusions:
- Extracellular vesicles harbor JCPyV-DNA and JCPyV Vp1 antigen.
- EV-associated JCPyV-DNA may offer insights into viral persistence and neuroinvasion mechanisms.
- This study highlights a potential novel pathway for JCPyV dissemination.
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