Identification of gangliosides GD1b and GT1b as receptors for BK virus

被引:142
作者
Low, JA
Magnuson, B
Tsai, B
Imperiale, MJ
机构
[1] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Canc Ctr 6304, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1128/JVI.80.3.1361-1366.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Gangliosides have been shown to be plasma membrane receptors for both murine polyomavirus and SV40, while JC virus uses serotonin receptors. In contrast, little is known of the membrane receptor and entry pathway for BK virus (BKV), which can cause severe disease in immunosuppressed bone marrow and renal transplant patients. Using sucrose flotation assays, we investigated BKV binding to and interaction with human erythrocyte membranes and determined that this interaction was dependent on a neuraminidase-sensitive, proteinase K-resistant molecule. BKV was found to interact with the gangliosides GT1b and GD1b. The terminal alpha 2-8-linked disialic acid motif, present in both of these gangliosides, is likely to be important for this interaction. We also determined that the addition of GD1b and GT1b to LNCaP cells, which are normally resistant to BKV infection, made them susceptible to the virus. In addition, BKV interacted with membranes extracted from the endoplasmic reticulum (ER) and infection was blocked by the addition of brefeldin A, which interferes with transport from the ER to the Golgi apparatus. These data demonstrate that BKV uses the gangliosides GT1b and GD1b as receptors and passes through the ER on the way to the nucleus.
引用
收藏
页码:1361 / 1366
页数:6
相关论文
共 52 条
[1]   A SEROLOGICAL INVESTIGATION OF BK-VIRUS AND JC-VIRUS INFECTIONS IN RECIPIENTS OF RENAL-ALLOGRAFTS [J].
ANDREWS, CA ;
SHAH, KV ;
DANIEL, RW ;
HIRSCH, MS ;
RUBIN, RH .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (01) :176-181
[2]   ASSOCIATION OF BK VIRUS WITH FAILURE OF PROPHYLAXIS AGAINST HEMORRHAGIC CYSTITIS FOLLOWING BONE-MARROW TRANSPLANTATION [J].
BEDI, A ;
MILLER, CB ;
HANSON, JL ;
GOODMAN, S ;
AMBINDER, RF ;
CHARACHE, P ;
ARTHUR, RR ;
JONES, RJ .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (05) :1103-1109
[3]   CLASS-I MAJOR HISTOCOMPATIBILITY PROTEINS ARE AN ESSENTIAL COMPONENT OF THE SIMIAN VIRUS-40 RECEPTOR [J].
BREAU, WC ;
ATWOOD, WJ ;
NORKIN, LC .
JOURNAL OF VIROLOGY, 1992, 66 (04) :2037-2045
[4]   EVOLUTION OF NEW SPECIES OF VIRAL DNA DURING SERIAL PASSAGE OF SIMIAN VIRUS-40 AT HIGH MULTIPLICITY [J].
BROCKMAN, WW ;
LEE, TNH ;
NATHANS, D .
VIROLOGY, 1973, 54 (02) :384-397
[5]   SEROEPIDEMIOLOGY OF HUMAN PAPOVAVIRUSES - DISCOVERY OF VIRGIN POPULATIONS AND SOME UNUSUAL PATTERNS OF ANTIBODY PREVALENCE AMONG REMOTE PEOPLES OF WORLD [J].
BROWN, P ;
TSAI, T ;
GAJDUSEK, DC .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1975, 102 (04) :331-340
[6]   SIALYLOLIGOSACCHARIDE RECEPTORS OF BINDING VARIANTS OF POLYOMA-VIRUS [J].
CAHAN, LD ;
SINGH, R ;
PAULSON, JC .
VIROLOGY, 1983, 130 (02) :281-289
[7]  
COLE CN, 2001, FIELDS VIROLOGY, V2, P2141
[8]  
COLEMAN DV, 1983, CLIN EXP IMMUNOL, V53, P289
[9]   A PROSPECTIVE-STUDY OF HUMAN POLYOMAVIRUS INFECTION IN PREGNANCY [J].
COLEMAN, DV ;
WOLFENDALE, MR ;
DANIEL, RA ;
DHANJAL, NK ;
GARDNER, SD ;
GIBSON, PE ;
FIELD, AM .
JOURNAL OF INFECTIOUS DISEASES, 1980, 142 (01) :1-8
[10]   HUMAN POLYOMAVIRUS INFECTION IN RENAL-ALLOGRAFT RECIPIENTS [J].
COLEMAN, DV ;
GARDNER, SD ;
FIELD, AM .
BRITISH MEDICAL JOURNAL, 1973, 3 (5876) :371-375