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Volume 54, Issue 1, Pages 122-126 (July 2009)


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BK Virus Nephropathy Due to KOM-3 Strain

Gavin S.W. Chan, FRCPA1Corresponding Author Informationemail address, Hoi Wah Tsoi, MPhil2, Samson S.Y. Wong, MRCPath, DTMH2, Chiu Leong Li3, Herman Tse, MBBS2, Kuok Un I3, Kwok Yung Yuen, MD, FRCS, FRCPath2, Kwok Wah Chan, FRCPath1

Received 11 July 2008; accepted 17 September 2008. published online 20 November 2008.

Interstitial nephritis caused by BK polyomavirus is an important complication of kidney transplantation. A diagnosis of BK virus nephropathy is established by a combination of characteristic histological, immunostaining, and ultrastructural findings. We report the first documented case of BK virus nephropathy caused by the KOM-3 strain in a patient after kidney transplantation. The biopsy specimen showed the characteristic histological and ultrastructural findings of BK virus, but was negative on immunostaining with a monoclonal antibody directed against BK virus large T antigen (LTag). Kidney tissue was subjected to polymerase chain reaction amplification using BK virus LTag-specific primers followed by DNA sequencing. Sequence results showed 100% homology to the KOM-3 strain, which has a 4–amino acid deletion in the C terminus of LTag compared with the reference sequence DUN strain. This deletion can explain the negative immunostaining results because the monoclonal antibody is directed against an epitope in this region. The patient lost his graft 2 months after diagnosis. Pathologists should be aware of this potential pitfall in interpreting immunostaining for BK virus. The incidence and prognostic implications of KOM-3 strain require additional studies.

1 Department of Pathology, Queen Mary Hospital, LKS Faculty of Medicine, The University of Hong Kong, Hong King

2 Department of Microbiology, Queen Mary Hospital, LKS Faculty of Medicine, The University of Hong Kong, Hong King

3 Department of Nephrology, Centro Hospitalar Conde De S Januario, Macau

Corresponding Author InformationAddress correspondence to Gavin S.W. Chan, FRCPA, Department of Pathology, Queen Mary Hospital, Hong Kong

 Originally published online as doi: 10.1053/j.ajkd.2008.09.014 on November 20, 2008.

PII: S0272-6386(08)01407-8

doi:10.1053/j.ajkd.2008.09.014


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