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Updated: Jan 7, 2026

Measurement of BK-polyomavirus Non-Coding Control Region Driven Transcriptional Activity Via Flow Cytometry
Published on: July 13, 2019
A study on the distribution of BK and JC polyomavirus in discarded donor kidneys
Wouter T Moest1,2, Aiko P J de Vries1,2, Reshma A Lalai1
1Division or Nephrology, Department of Internal Medicine, Leiden University Medical Center (LUMC), Leiden, Netherlands.
Introduction:
BK polyomavirus (BKPyV) and JC polyomavirus (JCPyV) are thought to establish persistent, low-grade infections in the kidney. However, their specific intrarenal reservoirs remain unclear. To explore their localization and potential presence prior to transplantation, we analyzed different kidney regions from deceased donors.
Method:
Donor kidneys discarded for donation and subsequently designated for research purposes between November 2023 and October 2024 were included. For each kidney, cortex, medulla, pelvis, and ureter were sampled. These samples were analyzed using qPCR for the presence of JCPyV and BKPyV.
Results:
In total, 10 kidneys were analyzed with a total 72 samples taken from the cortex: n = 22, medulla: n = 22, renal pelvis: n = 14, and ureter: n = 14. All samples tested negative for BKPyV. JCPyV DNA was detected in 4 out of 10 kidneys. When analyzed by tissue type, positive samples were found in 6/22(27.3%) cortex, 6/22(27.3%) medulla, 4/14(28.6%) renal pelvis, and 4/14(28.6%) ureter samples. The cycle threshold (Ct) values did not show significant differences among the various regions within the kidney. Notably, JCPyV distribution within individual kidneys was markedly heterogeneous, with substantial variation in Ct-values within the same kidney.
Conclusion:
JCPyV DNA was detected in 40% of kidneys from deceased donors, with comparable detection rates across cortex, medulla, pelvis, and ureter, suggesting no clear tissue preference. However, within individual kidneys, the distribution and Ct-values varied considerably. BKPyV DNA was not detected in any sample. These findings support the hypothesis that JCPyV may be present prior to transplantation and potentially donor-derived. The potential role of JCPyV in kidney transplant recipients and its relationship with BKPyV warrant further investigation.
Insights
JC polyomavirus (JCPyV) DNA was found in 40% of deceased donor kidneys, with varied distribution within organs. BK polyomavirus (BKPyV) was not detected, suggesting JCPyV may be donor-derived before transplantation.
Area of Science:
- Nephrology
- Virology
- Transplantation Immunology
Background:
- BK polyomavirus (BKPyV) and JC polyomavirus (JCPyV) establish persistent kidney infections.
- Intrarenal reservoirs and pre-transplant presence of these viruses remain unclear.
Purpose of the Study:
- To investigate the localization and potential pre-transplant presence of BKPyV and JCPyV in different kidney regions.
- To determine if JCPyV or BKPyV DNA is detectable in donor kidneys prior to transplantation.
Main Methods:
- Analysis of cortex, medulla, renal pelvis, and ureter samples from 10 deceased donor kidneys.
- Quantitative PCR (qPCR) used to detect JCPyV and BKPyV DNA.
Main Results:
- JCPyV DNA detected in 40% of kidneys (4/10).
- Comparable JCPyV detection rates across cortex, medulla, pelvis, and ureter.
- BKPyV DNA was not detected in any samples.
- Significant heterogeneity in JCPyV distribution and viral load (Ct values) within individual kidneys.
Conclusions:
- Findings support the hypothesis of pre-transplant, potentially donor-derived JCPyV.
- JCPyV shows no clear tissue preference within the kidney.
- Further research is needed on JCPyV's role in kidney transplant recipients and its relation to BKPyV.
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