Genomic Mutations of Viral Protein 1 and BK Virus Nephropathy in Kidney Transplant Recipients

被引:27
|
作者
Boldorini, Renzo [1 ]
Allegrini, Sara [1 ]
Miglio, Umberto [1 ]
Paganotti, Alessia [2 ]
Veggiani, Claudia [2 ]
Mischitelli, Monica [3 ]
Monga, Guido [1 ]
Pietropaolo, Valeria [3 ]
机构
[1] Univ Amedeo Avogadro E Piedmont, Dept Med Sci, Fac Med, I-28100 Novara, Italy
[2] Osped Maggiore La Carita, Dept Pathol, Novara, Italy
[3] Univ Roma La Sapienza, Dept Publ Hlth Sci, Rome, Italy
关键词
polyomavirus; BK virus nephropathy; viral capsid protein; transcriptional control region; polymerase chain reaction; sequence analysis; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; POLYOMAVIRUS-ASSOCIATED NEPHROPATHY; REPLICATION; NEPHRITIS; STRAINS; DNA;
D O I
10.1002/jmv.21520
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Genomic variabilityin the viral protein 1 region of BK polyomavirus (BKV) may change the ability of the virus to replicate. The significance of such changes was studied in clinical samples taken from kidney transplant patients with and without BKV nephropathy. A 94 base-pair fragment of viral protein 1 was amplified from 68 urine, 28 blood, and 12 renal biopsy samples from eight patients with BKV nephropathy, and from 100 urine samples, 17 blood and three renal biopsy samples from 41 of 218 controls. The DNA was sequenced and the amino acid changes were predicted by the Expert Protein Analysis System program (ExPASy, Swiss Institute of Bioinformatics, Geneva, Switzerland). Single base-pair mutations were detected more frequently in the samples from the BKV nephropathy patients than in the controls, and this was the only statistically significant finding of the study (P < 0.05), thus suggesting a greater genetic instability in BKV nephropathy associated strains. The amino acid changes were distributed at random in both BKV nephropathy patients and controls. However, one aspartic acid-to-asparagine substitution at residue 75 was detected in all samples of the one patient with BKV-associated nephropathy, who developed disease progression confirmed by histology, and not in any of the other patient or control samples. Whether this specific amino acid change plays a role in disease deserves further study. J. Med. Virol. 81:1385-1393, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1385 / 1393
页数:9
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