Progressive multifocal leucoencephalopathy: detection of papovavirus JC in kidney tissue
Abstract:
Cellular DNA of the kidney from a patient with PML was analyzed by reassociation kinetics for the presence of JC virus DNA. Various amounts of viral DNA sequences were detected in different areas of the kidney. The highest concentration (175 genome equivalents/cell) was found in the renal medulla and there were almost none in the renal cortex. Differentiation from the closely related BK virus was carried out by reassociation kinetics and restriction enzyme cleavage with subsequent Southern blot analysis. The enzyme Hind II, which does not cleave within the BK virus genome, generated four restriction enzyme fragments in the cellular DNA from the kidney, thus documenting the presence of JC virus DNA. By examination of the renal DNA with the "no-cut" restriction enzyme XHO I and the "one-cut" enzymes Eco RI and BAM HI it was possible to show that free and not integrated viral DNA was present in these cells. Nonhomogeneous defective DNA bands were not detectable. By in situ hybridization the epithelial cells lining the collecting tubules were found as predominant site of the viral infection in the kidney.
Insights
JC virus DNA was detected in kidney cells of a patient with progressive multifocal leukoencephalopathy (PML). The virus primarily infected epithelial cells in the collecting tubules, with higher concentrations in the renal medulla.
Area of Science:
- Nephrology
- Virology
- Molecular Biology
Background:
- Progressive multifocal leukoencephalopathy (PML) is a rare, demyelinating disease of the central nervous system.
- JC virus (JCV) is the causative agent of PML, and its presence in other organs, such as the kidney, is of clinical interest.
Purpose of the Study:
- To investigate the presence and localization of JC virus DNA in the kidney of a patient with PML.
- To differentiate JCV from the related BK virus (BKV) and determine the state of viral DNA (integrated vs. free).
Main Methods:
- Reassociation kinetics to detect viral DNA sequences.
- Restriction enzyme cleavage (Hind II, XHO I, Eco RI, BAM HI) and Southern blot analysis for viral DNA characterization.
- In situ hybridization to identify infected cell types.
Main Results:
- JC virus DNA was detected in various kidney areas, with the highest concentration in the renal medulla (175 genome equivalents/cell) and minimal presence in the renal cortex.
- Restriction enzyme analysis confirmed the presence of JCV and differentiated it from BKV.
- Analysis indicated that the viral DNA was free and not integrated into the host genome.
- In situ hybridization identified epithelial cells lining the collecting tubules as the predominant site of JCV infection in the kidney.
Conclusions:
- The kidney, particularly the renal medulla and collecting tubules, harbors JC virus DNA in patients with PML.
- The findings suggest that the kidney could be a reservoir for JCV, with free viral DNA present in infected epithelial cells.
Related Concept Videos
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
Cytomegalovirus Disease


