Rearrangement patterns of JC virus noncoding control region from different biological samples

被引:38
作者
Pietropaolo, V
Videtta, M
Fioriti, D
Mischitelli, M
Arancio, A
Orsi, N
Degener, AM
机构
[1] Univ Roma La Sapienza, Fac Med, Dept Publ Hlth Sci, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, Dept Expt Med & Pathol, I-00185 Rome, Italy
关键词
JCV; NCCR; nucleotide sequence; rearrangement patterns;
D O I
10.1080/714044482
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The JC virus (JCV) is generally considered the etiological agent of progressive multifocal leukoencephalopathy (PML), a demyelinating brain illness, often associated with immunosuppression and significantly frequent in acquired immunodeficiency syndrome (AIDS) patients. The primary infection by JCV is usually asymptomatic and the virus can remain in a latent status in the kidney. As a consequence of immunological alterations of the host, the virus can show a genetic variability in the noncoding control region (NCCR) due to deletions, duplications, and insertions as compared with the archetype. The NCCR of the archetype strain can be divided into six regions, named boxes A to F. In this study, the authors evaluated the presence of the JCV genome in different biological samples, such as urine, peripheral blood mononuclear cells (PBMCs) and cerebral spinal fluid (CSF) by means of polymerase chain reaction (PCR). After sequencing of the PCR fragments, the NCCR structure of isolated JCV strains was analyzed in order to verify the presence of different viral variants. An analysis of the homology and of the multiple alignment of the obtained sequences in comparison with the archetype strain has been carried out. The results indicated the presence of different rearrangements among the analyzed samples. Whereas in the urine, the NCCR structure always appeared very similar to that of the archetype, in the PBMCs and CSF, the NCCR sequences showed specific and characteristic rearrangements as compared to the archetype. These different rearrangements could be correlated with the emerging of an NCCR organization more suitable for the development of PML.
引用
收藏
页码:603 / 611
页数:9
相关论文
共 44 条
[1]   Genotype profile of human polyomavirus JC excreted in urine of immunocompetent individuals [J].
Agostini, HT ;
Ryschkewitsch, CF ;
Stoner, GL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (01) :159-164
[2]   HUMAN POLYOMAVIRUS JC PROMOTER ENHANCER REARRANGEMENT PATTERNS FROM PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY BRAIN ARE UNIQUE DERIVATIVES OF A SINGLE ARCHETYPAL STRUCTURE [J].
AULT, GS ;
STONER, GL .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :1499-1507
[3]   Chronic lymphocytic leukemia complicated by progressive multifocal leukoencephalopathy withouth apparent immunodepression [J].
Bagnato, F ;
Pietropoaolo, V ;
Di Taranto, C ;
Lorenzano, S ;
Toni, D .
EUROPEAN JOURNAL OF NEUROLOGY, 2001, 8 (04) :367-368
[4]   Progressive multifocal leukoencephalopathy [J].
Berger J.R. .
Current Treatment Options in Neurology, 2000, 2 (4) :361-368
[5]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[6]   Archetypal and rearranged sequences of human polyomavirus JC transcription control region in peripheral blood leukocytes and in cerebrospinal fluid [J].
Ciappi, S ;
Azzi, A ;
De Santis, R ;
Leoncini, F ;
Sterrantino, G ;
Mazzotta, F ;
Mecocci, L .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :1017-1023
[7]   Coordinate effects of human immunodeficiency virus type 1 protein Tat and cellular protein Purα on DNA replication initiated at the JC virus origin [J].
Daniel, DC ;
Wortman, MJ ;
Schiller, RJ ;
Liu, H ;
Gan, L ;
Mellen, JS ;
Chang, CF ;
Gallia, GL ;
Rappaport, J ;
Khalili, K ;
Johnson, EM .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :1543-1553
[8]  
Degener AM, 1999, J MED VIROL, V58, P413, DOI 10.1002/(SICI)1096-9071(199908)58:4&lt
[9]  
413::AID-JMV15&gt
[10]  
3.0.CO