Journal
JOURNAL OF CLINICAL VIROLOGY
Volume 59, Issue 2, Pages 120-125Publisher
ELSEVIER
DOI: 10.1016/j.jcv.2013.11.009
Keywords
BK virus; Donor-to-host transmission; Kidney transplantation
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Funding
- local faculty grant (Forschungskommission Heinrich-Heine-Universitat Dusseldorf)
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Background: BK virus associated nephropathy (BKVN) leads to renal allograft dysfunction and loss. However, it is still unclear whether BKV replication in the transplant recipient is a result of reactivation in the recipient's native kidneys or whether BKV originates from the donor kidney. Study design: Urine of 249 donor/recipient pairs was investigated for the presence of BKV-DNA by qPCR before living transplantation (Tx) and consecutively after Tx. In BKV positive samples, the VP1 typing region (TR) and, in case of the presence of sufficient amount of DNA, the complete VP1 gene, the NCCR and a fragment of the Large T-antigen were sequenced and compared between donors and corresponding recipients before and after Tx. Results: In 20 pairs, sequencing of the BKV TR succeeded in donors and corresponding recipients after Tx. The derived sequences were completely identical in donor and post-Tx recipient samples. For comparison, identical TR sequences were detected in only 24% of 1068 randomly assembled pairs. This difference was statistically highly significant (p< 0.0001, Fisher's exact test). Furthermore, all VP1, Large T-antigen and NCCR BKV sequences were also identical between donors and corresponding post-Tx recipients. In two of the 20 donor/recipient pairs, VP1 TR sequencing was also successful from the recipient before Tx. In both cases the sequence differed from the sequence detected in donor and recipient after Tx giving further evidence that recipient BKV was replaced by donor BKV after Tx. Conclusions: Our study for the first time provides evidence of BKV donor origin in renal transplant recipients. (C) 2013 Elsevier B.V. All rights reserved.
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