Derivation of a JC virus-resistant human glial cell line: implications for the identification of host cell factors that determine viral tropism

被引:21
作者
Gee, GV
Manley, K
Atwood, WJ
机构
[1] Brown Univ, Dept Mol Microbiol & Immunol, Providence, RI 02912 USA
[2] Brown Univ, Grad Program Mol & Cell Biol & Biochem, Providence, RI 02912 USA
关键词
D O I
10.1016/S0042-6822(03)00389-1
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
JC virus (JCV) is a common human polyomavirus that infects 70-80% of the population worldwide. In immunosuppressed individuals, JCV infects oligodendrocytes and causes a fatal demyelinating disease known as progressive multifocal leukoencephalopathy (PML). The tropism of JCV is restricted to oligodendrocytes, astrocytes, and B lymphocytes. Several mechanisms may contribute to the restricted tropism of JCV, including the presence or absence of cell-type-specific transcription and replication factors and the presence or absence of cell-type-specific receptors. We have established a system to investigate cellular factors that influence viral tropism by selecting JCV-resistant cells from a susceptible glial cell line (SVG-A). SVG-A cells were subjected to several rounds of viral infection using JC virus (MI/SVEDelta,). A population of resistant cells emerged (SVGR2) that were refractory to infection with the Mad-4 strain of JCV, the hybrid virus MI/SVEDelta, as well as to the related polyomavirus SV40. SVGR2 cells were as susceptible as the SVG-A cells to infection with an unrelated amphotropic retrovirus. The stage at which these cells are resistant to infection was investigated and the block appears to be at early viral gene transcription. This system should ultimately allow us to identify glial specific factors that influence the tropism of JCV. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:101 / 109
页数:9
相关论文
共 48 条
[1]   INTERACTION OF THE HUMAN POLYOMAVIRUS, JCV, WITH HUMAN LYMPHOCYTES-B [J].
ATWOOD, WJ ;
AMEMIYA, K ;
TRAUB, R ;
HARMS, J ;
MAJOR, EO .
VIROLOGY, 1992, 190 (02) :716-723
[2]   EVALUATION OF THE ROLE OF CYTOKINE ACTIVATION IN THE MULTIPLICATION OF JC VIRUS (JCV) IN HUMAN FETAL GLIAL-CELLS [J].
ATWOOD, WJ ;
WANG, L ;
DURHAM, LC ;
AMEMIYA, K ;
TRAUB, RG ;
MAJOR, EO .
JOURNAL OF NEUROVIROLOGY, 1995, 1 (01) :40-49
[3]   CLASS-I MAJOR HISTOCOMPATIBILITY PROTEINS AS CELL-SURFACE RECEPTORS FOR SIMIAN VIRUS-40 [J].
ATWOOD, WJ ;
NORKIN, LC .
JOURNAL OF VIROLOGY, 1989, 63 (10) :4474-4477
[4]   MUTATIONS THAT ALTER AN ARG-GLY-ASP (RGD) SEQUENCE IN THE ADENOVIRUS TYPE-2 PENTON BASE PROTEIN ABOLISH ITS CELL-ROUNDING ACTIVITY AND DELAY VIRUS REPRODUCTION IN FLAT CELLS [J].
BAI, M ;
HARFE, B ;
FREIMUTH, P .
JOURNAL OF VIROLOGY, 1993, 67 (09) :5198-5205
[5]   STRATEGIES FOR THE IDENTIFICATION OF ICOSAHEDRAL VIRUS RECEPTORS [J].
BASS, DM ;
GREENBERG, HB .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (01) :3-9
[6]   VP1 DNA sequences of JC and BK viruses detected in urine of systemic lupus erythematosus patients reveal no differences from strains expressed in normal individuals [J].
Bendiksen, S ;
Rekvig, OP ;
Van Ghelue, M ;
Moens, U .
JOURNAL OF GENERAL VIROLOGY, 2000, 81 :2625-2633
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]   TRANSCRIPTIONAL REGULATION OF HUMAN JC POLYOMAVIRUS PROMOTERS BY CELLULAR PROTEINS YB-1 AND PUR-ALPHA IN GLIAL-CELLS [J].
CHEN, NN ;
KHALILI, K .
JOURNAL OF VIROLOGY, 1995, 69 (09) :5843-5848
[9]   THE CD4 (T4) ANTIGEN IS AN ESSENTIAL COMPONENT OF THE RECEPTOR FOR THE AIDS RETROVIRUS [J].
DALGLEISH, AG ;
BEVERLEY, PCL ;
CLAPHAM, PR ;
CRAWFORD, DH ;
GREAVES, MF ;
WEISS, RA .
NATURE, 1984, 312 (5996) :763-767
[10]   Sequences within the early and late promoters of archetype JC virus restrict viral DNA replication and infectivity [J].
Daniel, AM ;
Swenson, JJ ;
Mayreddy, RPR ;
Khalili, K ;
Frisque, RJ .
VIROLOGY, 1996, 216 (01) :90-101