Genome organization and reverse genetic analysis of a type 1 feline coronavirus

被引:50
作者
Tekes, Gergely [2 ]
Hofmann-Lehmann, Regina [3 ]
Stallkamp, Iris [2 ]
Thiel, Volker [1 ]
Thiel, Heinz-Juergen [2 ]
机构
[1] Kantonsspital, Res Dept, CH-9007 St Gallen, Switzerland
[2] Univ Giessen, Inst Virol, D-6300 Giessen, Germany
[3] Univ Zurich, Vetsuisse Fac, Clin Lab, Zurich, Switzerland
关键词
D O I
10.1128/JVI.02339-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this study we report the complete sequence and genome organization of the serotype I feline coronavirus (FCoV) strain Black. Furthermore, a reverse genetic system was established for this FCoV strain by cloning a full-length cDNA copy into vaccinia virus. This clone served as basis for the generation of recombinant FCoV (recFCoV) that was shown to bear the same features in vitro as the parental FCoV. Using this system, accessory 3abc genes in the FCoV genome were replaced by green fluorescent protein (recFCoV-GFP) and Renilla luciferase genes (recFCoV-RL). In addition, we showed that feline CD14(+) blood monocytes and dendritic cells can be easily detected after infection with recFCoV-GFP. Thus, our established reverse genetic system provides a suitable tool to study the molecular biology of serotype I FCoV.
引用
收藏
页码:1851 / 1859
页数:9
相关论文
共 60 条
[1]   Persistence and transmission of natural type I feline coronavirus infection [J].
Addie, DD ;
Schaap, IAT ;
Nicolson, L ;
Jarrett, O .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :2735-2744
[2]   Use of a reverse-transcriptase polymerase chain reaction for monitoring the shedding of feline coronavirus by healthy cats [J].
Addie, DD ;
Jarrett, O .
VETERINARY RECORD, 2001, 148 (21) :649-+
[3]   Cellular composition and interferon-γ expression of the local inflammatory response in feline infectious peritonitis (FIP) [J].
Berg, AL ;
Ekman, K ;
Belák, S ;
Berg, M .
VETERINARY MICROBIOLOGY, 2005, 111 (1-2) :15-23
[4]  
BLACK JW, 1980, VET MED SM ANIM CLIN, V75, P811
[5]   Gene 5 of the avian coronavirus infectious bronchitis virus is not essential for replication [J].
Casais, R ;
Davies, M ;
Cavanagh, D ;
Britton, P .
JOURNAL OF VIROLOGY, 2005, 79 (13) :8065-8078
[6]   Reverse genetics system for the avian coronavirus infectious bronchitis virus [J].
Casais, R ;
Thiel, V ;
Siddell, SG ;
Cavanagh, D ;
Britton, P .
JOURNAL OF VIROLOGY, 2001, 75 (24) :12359-12369
[7]   Control of coronavirus infection through plasmacytoid dendritic-cell-derived type I interferon [J].
Cervantes-Barragan, Luisa ;
Zuest, Roland ;
Weber, Friedernann ;
Spiegel, Martin ;
Lang, Karl S. ;
Akira, Shizuo ;
Thiel, Volker ;
Ludewig, Burkhard .
BLOOD, 2007, 109 (03) :1131-1137
[8]   Recombinant mouse hepatitis virus strain a59 from cloned, full-length cDNA replicates to high titers in vitro and is fully pathogenic in vivo [J].
Coley, SE ;
Lavi, E ;
Sawicki, SG ;
Fu, L ;
Schelle, B ;
Karl, N ;
Siddell, SG ;
Thiel, V .
JOURNAL OF VIROLOGY, 2005, 79 (05) :3097-3106
[9]   Heterologous gene expression from transmissible gastroenteritis virus replicon particles [J].
Curtis, KM ;
Yount, B ;
Baric, RS .
JOURNAL OF VIROLOGY, 2002, 76 (03) :1422-1434
[10]  
Das Sarma J, 2002, J NEUROVIROL, V8, P381, DOI [10.1080/13550280260422686, 10.1080/13550280290100815]