Identification of SV40 in brain, kidney and urine of healthy and SIV-infected rhesus monkeys

被引:34
作者
Newman, JS
Baskin, GB
Frisque, RJ
机构
[1] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[2] Tulane Univ, Tulane Reg Primate Res Ctr, Dept Pathol, Covington, LA 70433 USA
关键词
SV40; variants; archetype; strain typing; SIV; JC virus; PML;
D O I
10.3109/13550289809114538
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent reports of simian virus 40 (SV40) sequences in human tumors have prompted investigations into the poorly understood association of this polyomavirus with its primate host, the rhesus monkey (Macaca mulatta), In the present study we have used PCR to analyze tissues from 20 monkeys for the presence of SV40. Five of the animals, which were infected with simian immunodeficiency virus (SIV), were found to exhibit SV40-induced lesions and to have SV40 sequences present in their kidney and brain. Lesions associated with SV40 were not observed in 15 SIV- monkeys, and SV40 DNA was detected in kidney and urine of only one of these animals. Three regions of SV40 DNA were examined in each tissue: the non coding transcriptional control region (TCR), the sequences encoding the host range domain (HRD) within the carboxy-terminus of T antigen (TAg), and a portion of the VP1 gene. Each region contained nucleotide alterations compared to the SV40 reference strain 776. In all six animals, the TCR had an archetype structure containing a single 72 bp enhancer element. In addition, the TCR amplified from two animals lacked one of three copies of a GC-rich 21 bp repeat which is part of the promoter in strain 776. Multiple clones of unique HRD sequences were derived from different animals, and in some instances from the same animal. No correlation was found between a particular HRD sequence and its presence in a specific tissue type, Nucleotide changes identified within the VP1 gene indicate that this region, as with the closely-related human polyomavirus JCV, may permit the typing of the virus into individual strains. This study is the first to characterize SV40 sequences present in both healthy and SN-infected animals and supports the suggestion that strain 776 is not the predominant type of SV40 circulating in its natural host.
引用
收藏
页码:394 / 406
页数:13
相关论文
共 64 条
[1]   JC virus regulatory region rearrangements and genotypes in progressive multifocal leukoencephalopathy: Two independent aspects of virus variation [J].
Agostini, HT ;
Ryschkewitsch, CF ;
Singer, EJ ;
Stoner, GL .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :659-664
[2]   Co-infection with two JC virus genotypes in brain, cerebrospinal fluid or urinary tract detected by direct cycle sequencing of PCR products [J].
Agostini, HT ;
Ryschkewitsch, CF ;
Singer, EJ ;
Stoner, GL .
JOURNAL OF NEUROVIROLOGY, 1996, 2 (04) :259-267
[3]   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
[4]   2 MAJOR TYPES OF JC VIRUS DEFINED IN PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY BRAIN BY EARLY AND LATE CODING REGION DNA-SEQUENCES [J].
AULT, GS ;
STONER, GL .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :2669-2678
[5]   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
[6]  
BUCHMAN AR, 1981, DNA TUMOR VIRUSES 2, P799
[7]  
CARBONE M, 1994, ONCOGENE, V9, P1781
[8]  
Carbone M, 1996, ONCOGENE, V13, P527
[9]   Simian virus 40, poliovaccines and human tumors: a review of recent developments [J].
Carbone, M ;
Rizzo, P ;
Pass, HI .
ONCOGENE, 1997, 15 (16) :1877-1888
[10]   T-ANTIGEN KINASE INHIBITS SIMIAN-VIRUS 40 DNA-REPLICATION BY PHOSPHORYLATION OF INTACT T-ANTIGEN ON SERINE-120 AND SERINE-123 [J].
CEGIELSKA, A ;
MOAREFI, I ;
FANNING, E ;
VIRSHUP, DM .
JOURNAL OF VIROLOGY, 1994, 68 (01) :269-275