Polyomaviruses BK And JC-DNA quantitation in kidney allograft biopsies

被引:26
作者
Costa, Cristina [1 ]
Bergallo, Massimiliano [1 ]
Sidoti, Francesca [1 ]
Astegiano, Sara [1 ]
Terlizzi, Maria Elena [1 ]
Mazzucco, Gianna
Segoloni, Giuseppe P. [2 ]
Cavallo, Rossana [1 ]
机构
[1] Univ Turin, Dept Microbiol & Publ Hlth, Virol Unit, I-10126 Turin, Italy
[2] Univ Turin, Dept Internal Med, Renal Transplant Unit, Osped Molinette, I-10126 Turin, Italy
关键词
Kidney transplantation; BKV; JCV; Renal biopsy; Polyomavirus-associated nephropathy; Ureteral stenosis; RENAL-TRANSPLANTATION; VIRAL-DNA; NEPHROPATHY; VIRUS; RECIPIENT; SV40;
D O I
10.1016/j.jcv.2008.08.006
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Background: Polyomavirus-associated nephropathy(PVAN) is one of the most common viral disease affecting renal allograft, with BK being the most frequent causal agent and JCV being considered responsible in < 3% of the cases. Objectives: To quantify polyomaviruses BK and JC load by real-time TaqMan PCR in tissue specimens (renal and ureteral) from kidney transplant recipients. Study design and methods: One-hundred-thirty-eight specimens (125 kidneys, 13 ureters) obtained from 109 patients were evaluated by quantitative real-time PCR for the detection of BKV- and JCV-DNA. Demographic, virological, and histopathological data were collected. Results: BKV-DNA was positive in 32 of 109 patients (29.6%) and JCV-DNA in 20 of 109 patients (18.3%). The highest BK viral loads (> 10(4) genome equivalents/cell) were found in two renal samples with histopathologically confirmed PVAN; while JC viral load was > 10(4) genome equivalents/cell in one ureteral sample. Conclusions: Although quantitation of viral DNA on renal allograft biopsies could be complementary to histopathological evaluation and the highest viral load are detectable in renal specimens with PVAN, the identification of a diagnostic cut-off should require further studies. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:20 / 23
页数:4
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