Growth behavior of bovine herpesvirus-1 in permissive and semi-permissive cells

被引:11
作者
Murata, T
Takashima, Y
Xuan, X
Otsuka, H
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Global Agr Sci, Bunkyo Ku, Tokyo 1138657, Japan
[2] Obihiro Univ Agr & Vet Med, Res Ctr Protozoan Mol Immunol, Obihiro, Hokkaido 0808555, Japan
[3] Nagoya Univ, Sch Med, Dis Mechanism & Control Res Inst, Lab Virol,Showa Ku, Nagoya, Aichi 4668550, Japan
关键词
bovine herpesvirus-1; immediate early protein; adsorption; penetration; quantitative competitive PCR;
D O I
10.1016/S0168-1702(99)00023-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bovine herpesvirus-1 (BHV-1) can replicate well in bovine-derived cell lines such as Madin Darby bovine kidney (MDBK) but grows poorly in hamster lung (HmLu-1). Virus replication, DNA synthesis, and immediate-early gene expression are severely restricted in HmLu-1. We compared adsorption and penetration of BHV-1 in permissive MDBK and semi-permissive HmLu-1 cells. At a low multiplicity of infection, BHV-1 attached to permissive MDBK cells twice as much as to HmLu-1. The presence of heparin inhibited the attachment of BHV-1 to MDBK cells by about 60%, but over 90% of the attachment was inhibited in HmLu-1. To investigate the penetration of BHV-1, we performed the quantitative measurement of viral DNA by quantitative competitive (QC)PCR in infected cells. In MDBK cells, virions attached to the cell surface, penetrated into the cells and were transported to the nucleus. However in HmLu-1, only a small fraction of the virions attached to the cell: surface were allowed to penetrate. Our results indicated that the replication of BHV-1 in semi-permissive HmLu-1 nias not dramatically restricted at one certain point but at some various stages including adsorption and penetration. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
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页码:29 / 41
页数:13
相关论文
共 42 条
[1]   OBSERVATIONS ON VIRUS OF INFECTIOUS BOVINE RHINOTRACHEITIS, AND ITS AFFINITY WITH HERPESVIRUS GROUP [J].
ARMSTRONG, J ;
ANDREWES, CH ;
PEREIRA, HG .
VIROLOGY, 1961, 14 (02) :276-&
[2]   ENTRY OF HERPES-SIMPLEX VIRUS-1 IN BJ CELLS THAT CONSTITUTIVELY EXPRESS VIRAL GLYCOPROTEIN D IS BY ENDOCYTOSIS AND RESULTS IN DEGRADATION OF THE VIRUS [J].
CAMPADELLIFIUME, G ;
ARSENAKIS, M ;
FARABEGOLI, F ;
ROIZMAN, B .
JOURNAL OF VIROLOGY, 1988, 62 (01) :159-167
[3]   BOVINE HERPESVIRUS-1 GIV-EXPRESSING CELLS RESIST VIRUS PENETRATION [J].
CHASE, CCL ;
LETCHWORTH, GJ .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :177-181
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]   NUCLEOTIDE-SEQUENCE OF BOVINE HERPESVIRUS TYPE-1 GLYCOPROTEIN GIII, A STRUCTURAL MODEL FOR GIII AS A NEW MEMBER OF THE IMMUNOGLOBULIN SUPERFAMILY, AND IMPLICATIONS FOR THE HOMOLOGOUS GLYCOPROTEINS OF OTHER HERPESVIRUSES [J].
FITZPATRICK, DR ;
BABIUK, LA ;
ZAMB, TJ .
VIROLOGY, 1989, 173 (01) :46-57
[6]  
Fukai K, 1998, INDIAN J MED RES, V108, P8
[7]   Suppression of high mobility group protein T160 expression impairs mouse cytomegalovirus replication [J].
Gariglio, M ;
Foresta, P ;
Sacchi, C ;
Lembo, M ;
Hertel, L ;
Landolfo, S .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :665-670
[8]   Entry of alphaherpesviruses mediated by poliovirus receptor-related protein 1 and poliovirus receptor [J].
Geraghty, RJ ;
Krummenacher, C ;
Cohen, GH ;
Eisenberg, RJ ;
Spear, PG .
SCIENCE, 1998, 280 (5369) :1618-1620
[9]  
HUANG AS, 1964, P SOC EXP BIOL MED, V116, P863, DOI 10.3181/00379727-116-29392
[10]  
Ianconescu M, 1996, IN VITRO CELL DEV-AN, V32, P249