| Literature DB >> 22948418 |
Yu-Ching Liaw1, Cheng-Hsu Chen, Kuo-Hsiung Shu, Chiung-Yao Fang, Wei-Chih Ou, Pei-Lain Chen, Cheng-Huang Shen, Mien-Chun Lin, Deching Chang, Meilin Wang.
Abstract
Kidney cells are the common host for JC virus (JCV) and BK virus (BKV). Reactivation of JCV and/or BKV in patients after organ transplantation, such as renal transplantation, may cause hemorrhagic cystitis and polyomavirus-associated nephropathy. Furthermore, JCV and BKV may be shed in the urine after reactivation in the kidney. Rearranged as well as archetypal non-coding control regions (NCCRs) of JCV and BKV have been frequently identified in human samples. In this study, three JC/BK recombined NCCR sequences were identified in the urine of a patient who had undergone renal transplantation. They were designated as JC-BK hybrids 1, 2, and 3. The three JC/BK recombinant NCCRs contain up-stream JCV as well as down-stream BKV sequences. Deletions of both JCV and BKV sequences were found in these recombined NCCRs. Recombination of DNA sequences between JCV and BKV may occur during co-infection due to the relatively high homology of the two viral genomes.Entities:
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Year: 2012 PMID: 22948418 DOI: 10.1007/s11262-012-0815-9
Source DB: PubMed Journal: Virus Genes ISSN: 0920-8569 Impact factor: 2.332