Enterovirus receptors and virus replication in human leukocytes

被引:27
作者
Vuorinen, T [1 ]
Vainionpää, R
Heino, J
Hyypiä, T
机构
[1] Univ Turku, Dept Virol, FIN-20520 Turku, Finland
[2] Univ Turku, MediCity Res Lab, FIN-20520 Turku, Finland
[3] Univ Helsinki, Dept Virol, Haartman Inst, FIN-00014 Helsinki, Finland
关键词
D O I
10.1099/0022-1317-80-4-921
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Although enteroviruses cause a great variety of diseases including meningitis, paralysis and myocarditis, the life-cycle of these viruses in man is still quite poorly understood. The role of human leukocytes as a target for enterovirus infections was studied in this report. Despite great similarity in the structure and replication of coxsackievirus B3 (CBV3), echovirus 1 (EV1), and poliovirus 1 (PV1), the ability of these viruses to infect human peripheral blood mononuclear cells (PBMC), and B (Raji), T (Molt-4) and monocytic (U-937) cell lines differed markedly. CBV3 attached both to PBMC and the three haematopoietic cell lines studied, whereas EV1 bound only to PBMC, Generally, the attachment of PV1 was very poor, The binding assays mostly correlated with the expression of CD55 (decay accelerating factor, DAF) and alpha(2)beta(1)-integrin (VLA-2), which are known to act as receptors for CBV3 and EV1, respectively, as well as with the expression of the PV receptor on the cell surface, To analyse virus replication in the cells, viral protein and nucleic acid syntheses were studied by immunoprecipitation and RT-PCR, CBV3 was able to replicate in Raji and Molt-4 cells, even though no expression of DAF was detected, whereas in the monocytic cell line, viral protein synthesis was detected only after transfection of virus RNA. Neither CBV3 nor EV1 replicated in PBMC and all haematopoietic cells studied seemed to be poorly permissive for PV1 replication.
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页码:921 / 927
页数:7
相关论文
共 29 条
[1]   MANY RHINOVIRUS SEROTYPES SHARE THE SAME CELLULAR RECEPTOR [J].
ABRAHAM, G ;
COLONNO, RJ .
JOURNAL OF VIROLOGY, 1984, 51 (02) :340-345
[2]   Identification of enteroviruses in clinical specimens by competitive PCR followed by genetic typing using sequence analysis [J].
Arola, A ;
Santti, J ;
Ruuskanen, O ;
Halonen, P ;
Hyypia, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (02) :313-318
[3]   Isolation of a common receptor for coxsackie B viruses and adenoviruses 2 and 5 [J].
Bergelson, JM ;
Cunningham, JA ;
Droguett, G ;
KurtJones, EA ;
Krithivas, A ;
Hong, JS ;
Horwitz, MS ;
Crowell, RL ;
Finberg, RW .
SCIENCE, 1997, 275 (5304) :1320-1323
[4]   IDENTIFICATION OF THE INTEGRIN VLA-2 AS A RECEPTOR FOR ECHOVIRUS-1 [J].
BERGELSON, JM ;
SHEPLEY, MP ;
CHAN, BMC ;
HEMLER, ME ;
FINBERG, RW .
SCIENCE, 1992, 255 (5052) :1718-1720
[5]   COXSACKIEVIRUS B3 ADAPTED TO GROWTH IN RD CELLS BINDS TO DECAY-ACCELERATING FACTOR (CD55) [J].
BERGELSON, JM ;
MOHANTY, JG ;
CROWELL, RL ;
JOHN, NFS ;
LUBLIN, DM ;
FINBERG, RW .
JOURNAL OF VIROLOGY, 1995, 69 (03) :1903-1906
[6]   THE INTEGRIN VLA-2 BINDS ECHOVIRUS 1 AND EXTRACELLULAR-MATRIX LIGANDS BY DIFFERENT MECHANISMS [J].
BERGELSON, JM ;
CHAN, BMC ;
FINBERG, RW ;
HEMLER, ME .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :232-239
[7]  
BERGSTEN J, 1994, CONTROL ENG, V41, P41
[8]  
COLONNO RJ, 1987, BIOESSAYS, V5, P270
[9]  
DAGAN R, 1992, ISRAEL J MED SCI, V28, P369
[10]   CHARACTERIZATION OF A 100-KILODALTON BINDING-PROTEIN FOR THE 6 SEROTYPES OF COXSACKIE-B VIRUSES [J].
DEVERDUGO, UR ;
SELINKA, HC ;
HUBER, M ;
KRAMER, B ;
KELLERMANN, J ;
HOFSCHNEIDER, PH ;
KANDOLF, R .
JOURNAL OF VIROLOGY, 1995, 69 (11) :6751-6757