Genomic characterization of equine coronavirus

被引:71
作者
Zhang, Jianqiang
Guy, James S.
Snijder, Eric J.
Denniston, Doug A.
Timoney, Peter J.
Balasuriya, Udem B. R.
机构
[1] Univ Kentucky, Dept Vet Sci, Lexington, KY 40546 USA
[2] N Carolina State Univ, Coll Vet Med, Dept Populat Hlth & Pathobiol, Raleigh, NC 27606 USA
[3] Leiden Univ, Med Ctr, Dept Med Microbiol, Mol Virol Lab, Leiden, Netherlands
关键词
equine coronavirus; entire genome; subgenomic RNA; transcription regulatory sequence; non-structural protein 3;
D O I
10.1016/j.virol.2007.06.035
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The complete genome sequence of the first equine coronavirus (ECoV) isolate, NC99 strain was accomplished by directly sequencing 11 overlapping fragments which were RT-PCR amplified from viral RNA. The ECoV genome is 30,992 nucleotides in length, excluding the poly A tail. Analysis of the sequence identified 11 open reading frames which encode two replicase polyproteins, five structural proteins (hemagglutinin esterase, spike, envelope, membrane, and nucleocapsid) and four accessory proteins (NS2, p4.7, p 12.7, and I). The two replicase polyproteins are predicted to be proteolytically processed by three virus-encoded proteases into 16 non-structural proteins (nsp1-16). The ECoV nsp3 protein had considerable amino acid deletions and insertions compared to the nsp3 proteins of bovine coronavirus, human coronavirus OC43, and porcine hemagglutinating encephalomyelitis virus, three group 2 coronaviruses pbylogenetically most closely related to ECoV. The structure of subgenomic mRNAs was analyzed by Northern blot analysis and sequencing of the leader-body junction in each sg mRNA. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:92 / 104
页数:13
相关论文
共 91 条
[1]   The nucleoprotein is required for efficient coronavirus genome replication [J].
Almazán, F ;
Galán, C ;
Enjuanes, L .
JOURNAL OF VIROLOGY, 2004, 78 (22) :12683-12688
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]  
[Anonymous], 1993, Biol. Chem. Hoppe Seyler, DOI DOI 10.1515/BCHM3.1993.374.1-6.143
[4]   Genetic characterization of equine arteritis virus during persistent infection of stallions [J].
Balasuriya, UBR ;
Hedges, JF ;
Smalley, VL ;
Navarrette, A ;
McCollum, WH ;
Timoney, PJ ;
Snijder, EJ ;
MacLachlan, NJ .
JOURNAL OF GENERAL VIROLOGY, 2004, 85 :379-390
[5]   Two amino acid changes at the N-terminus of transmissible gastroenteritis coronavirus spike protein result in the loss of enteric tropism [J].
Ballesteros, ML ;
Sanchez, CM ;
Enjuanes, L .
VIROLOGY, 1997, 227 (02) :378-388
[6]   The papain-like protease of severe acute respiratory syndrome coronavirus has deubiquitinating activity [J].
Barretto, N ;
Jukneliene, D ;
Ratia, K ;
Chen, ZB ;
Mesecar, AD ;
Baker, SC .
JOURNAL OF VIROLOGY, 2005, 79 (24) :15189-15198
[7]   SITE-SPECIFIC ALTERATION OF TRANSMISSIBLE GASTROENTERITIS VIRUS SPIKE PROTEIN RESULTS IN MARKEDLY REDUCED PATHOGENICITY [J].
BERNARD, S ;
LAUDE, H .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :2235-2241
[8]   Sequence and structure-based prediction of eukaryotic protein phosphorylation sites [J].
Blom, N ;
Gammeltoft, S ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (05) :1351-1362
[9]   Spike protein assembly into the coronavirion: Exploring the limits of its sequence requirements [J].
Bosch, BJ ;
de Haan, CAM ;
Smits, SL ;
Rottler, PJM .
VIROLOGY, 2005, 334 (02) :306-318
[10]   Coronavirus genome structure and replication [J].
Brian, DA ;
Baric, RS .
CORONAVIRUS REPLICATION AND REVERSE GENETICS, 2005, 287 :1-30