JC virus regulatory region tandem repeats in plasma and central nervous system isolates correlate with poor clinical outcome in patients with progressive multifocal leukoencephalopathy

被引:58
作者
Pfister, LA
Letvin, NL
Koralnik, IJ
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Neurol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Med, Div Viral Pathogenesis, Boston, MA 02215 USA
关键词
D O I
10.1128/JVI.75.12.5672-5676.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
JC virus (JCV), the causative agent of progressive multifocal leukoencephalopathy (PML), has a hypervariable regulatory region (JCV RR), A conserved archetype form is found in the urines of healthy and immunocompromised individuals, whereas forms with tandem repeats and deletions are found in the brains of PML patients, Type I JCV RR, seen in MAD-1, the first sequenced strain of JCV, contains two 98-bp tandem repeats each containing a TATA box. Type II JCV RR has additional 23-bp and 66-bp inserts or fragments thereof and only one TATA box, We cloned and sequenced JCV RR from different anatomic compartments of PML patients and controls and correlated our findings with the patients' clinical outcome. Twenty-three different sequences were defined in 198 clones obtained from 16 patients, All 104 clones with tandem repeats were type II JCV RR, Patients with poor clinical outcome had high proportions of JCV RR clones with both tandem repeats in plasma (54%) and brain or cerebrospinal fluid (85%), In those who became survivors of PML, archetype sequences predominated in these anatomic compartments (75 and 100%, respectively). In patients with advanced human immunodeficiency virus infection without PML, only 8% of JCV RR clones obtained in the plasma contained tandem repeats. These data suggest that the presence of tandem repeats in plasma and CNS JCV RR clones is associated with poor clinical outcome in patients with PML.
引用
收藏
页码:5672 / 5676
页数:5
相关论文
共 36 条
  • [1] Genotype profile of human polyomavirus JC excreted in urine of immunocompetent individuals
    Agostini, HT
    Ryschkewitsch, CF
    Stoner, GL
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (01) : 159 - 164
  • [2] Archetypal and rearranged sequences of human polyomavirus JC transcription control region in peripheral blood leukocytes and in cerebrospinal fluid
    Ciappi, S
    Azzi, A
    De Santis, R
    Leoncini, F
    Sterrantino, G
    Mazzotta, F
    Mecocci, L
    [J]. JOURNAL OF GENERAL VIROLOGY, 1999, 80 : 1017 - 1023
  • [3] REPLICATIVE CIS-ADVANTAGE OF POLYOMAVIRUS REGULATORY REGION MUTANTS IN DIFFERENT MURINE CELL-LINES
    DESIMONE, V
    AMATI, P
    [J]. JOURNAL OF VIROLOGY, 1987, 61 (05) : 1615 - 1620
  • [4] POLYOMAVIRUS MUTATION THAT CONFERS A CELL-SPECIFIC CIS ADVANTAGE FOR VIRAL-DNA REPLICATION
    DESIMONE, V
    LAMANTIA, G
    LANIA, L
    AMATI, P
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (08) : 2142 - 2146
  • [5] INFECTION OF HUMAN POLYOMAVIRUSES JC AND BK IN PERIPHERAL-BLOOD LEUKOCYTES FROM IMMUNOCOMPETENT INDIVIDUALS
    DORRIES, K
    VOGEL, E
    GUNTHER, S
    CZUB, S
    [J]. VIROLOGY, 1994, 198 (01) : 59 - 70
  • [6] Latency and reactivation of JC virus in peripheral blood of human immunodeficiency virus type 1-infected patients
    Dubois, V
    Dutronc, H
    Lafon, ME
    Poinsot, V
    Pellegrin, JL
    Ragnaud, JM
    Ferrer, AM
    Fleury, HJA
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (09) : 2288 - 2292
  • [7] Prevalence of JC Virus viraemia in HIV-infected patients with or without neurological disorders: a prospective study
    Dubois, V
    Moret, H
    Lafon, ME
    Janvresse, CB
    Dussaix, E
    Icart, J
    Karaterki, A
    Ruffault, A
    Taoufik, Y
    Vignoli, C
    Ingrand, D
    [J]. JOURNAL OF NEUROVIROLOGY, 1998, 4 (05) : 539 - 544
  • [8] FERRANTE P, IN PRESS J NEUROVIRO
  • [9] FRISQE RJ, 1992, MOL NEUROVIROLOGY, P69
  • [10] HUMAN POLYOMAVIRUS JC-VIRUS GENOME
    FRISQUE, RJ
    BREAM, GL
    CANNELLA, MT
    [J]. JOURNAL OF VIROLOGY, 1984, 51 (02) : 458 - 469