Completion of the porcine epidemic diarrhoea coronavirus (PEDV) genome sequence

被引:439
作者
Kocherhans, R
Bridgen, A
Ackermann, M
Tobler, K
机构
[1] Univ Zurich, Fak Vet Med, Inst Virol, CH-8057 Zurich, Switzerland
[2] Univ Glasgow, Inst Biomed & Life Sci, Div Virol, Glasgow G11 5JR, Lanark, Scotland
关键词
porcine epidemic diarrhoea virus; coronavirus; ORF1; replicase gene;
D O I
10.1023/A:1011831902219
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The sequence of the replicase gene of porcine epidemic diarrhoea virus (PEDV) has been determined. This completes the sequence of the entire genome of strain CV777, which was found to be 28,033 nucleotides (nt) in length (excluding the poly A-tail). A cloning strategy, which involves primers based on conserved regions in the predicted ORF1 products from other coronaviruses whose genome sequence has been determined, was used to amplify the equivalent, but as yet unknown, sequence of PEDV. Primary sequences derived from these products were used to design additional primers resulting in the amplification and sequencing of the entire ORF1 of PEDV. Analysis of the nucleotide sequences revealed a small open reading frame (ORF) located near the 5' end (no 99-137), and two large, slightly overlapping ORFs, ORF1a (nt 297-12650) and ORF1b (nt 12605-20641). The ORF1a and ORF1b sequences overlapped at a potential ribosomal frame shift site. The amino acid sequence analysis suggested the presence of several functional motifs within the putative ORF1 protein. By analogy to other coronavirus replicase gene products, three protease and one growth factor-like motif were seen in ORF1a, and one polymerase domain, one metal ion-binding domain, and one helicase motif could be assigned within ORF1b. Comparative amino acid sequence alignments revealed that PEDV is most closely related to human coronavirus (HCoV)-229E and transmissible gastroenteritis virus (TGEV) and less related to murine hepatitis virus (MHV) and infectious bronchitis virus (IBV). These results thus confirm and extend the findings from sequence analysis of the structural genes of PEDV.
引用
收藏
页码:137 / 144
页数:8
相关论文
共 30 条
[1]   Engineering the largest RNA virus genome as an infectious bacterial artificial chromosome [J].
Almazán, F ;
González, JM ;
Pénzes, Z ;
Izeta, A ;
Calvo, E ;
Plana-Durán, J ;
Enjuanes, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) :5516-5521
[2]   MOUSE HEPATITIS-VIRUS STRAIN A59 RNA-POLYMERASE GENE ORF 1A - HETEROGENEITY AMONG MHV STRAINS [J].
BONILLA, PJ ;
GORBALENYA, AE ;
WEISS, SR .
VIROLOGY, 1994, 198 (02) :736-740
[3]   COMPLETION OF THE SEQUENCE OF THE GENOME OF THE CORONAVIRUS AVIAN INFECTIOUS-BRONCHITIS VIRUS [J].
BOURSNELL, MEG ;
BROWN, TDK ;
FOULDS, IJ ;
GREEN, PF ;
TOMLEY, FM ;
BINNS, MM .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :57-77
[4]   THE PRIMARY STRUCTURE AND EXPRESSION OF THE 2ND OPEN READING FRAME OF THE POLYMERASE GENE OF THE CORONAVIRUS MHV-A59 - A HIGHLY CONSERVED POLYMERASE IS EXPRESSED BY AN EFFICIENT RIBOSOMAL FRAMESHIFTING MECHANISM [J].
BREDENBEEK, PJ ;
PACHUK, CJ ;
NOTEN, AFH ;
CHARITE, J ;
LUYTJES, W ;
WEISS, SR ;
SPAAN, WJM .
NUCLEIC ACIDS RESEARCH, 1990, 18 (07) :1825-1832
[5]   SEQUENCE DETERMINATION OF THE NUCLEOCAPSID PROTEIN GENE OF THE PORCINE EPIDEMIC DIARRHEA VIRUS CONFIRMS THAT THIS VIRUS IS A CORONAVIRUS RELATED TO HUMAN CORONAVIRUS-229E AND PORCINE TRANSMISSIBLE GASTROENTERITIS VIRUS [J].
BRIDGEN, A ;
DUARTE, M ;
TOBLER, K ;
LAUDE, H ;
ACKERMANN, M .
JOURNAL OF GENERAL VIROLOGY, 1993, 74 :1795-1804
[6]  
Bridgen A, 1998, ADV EXP MED BIOL, V440, P781
[7]   AN EFFICIENT RIBOSOMAL FRAME-SHIFTING SIGNAL IN THE POLYMERASE-ENCODING REGION OF THE CORONAVIRUS IBV [J].
BRIERLEY, I ;
BOURSNELL, MEG ;
BINNS, MM ;
BILIMORIA, B ;
BLOK, VC ;
BROWN, TDK ;
INGLIS, SC .
EMBO JOURNAL, 1987, 6 (12) :3779-3785
[8]   CHARACTERIZATION OF AN EFFICIENT CORONAVIRUS RIBOSOMAL FRAMESHIFTING SIGNAL - REQUIREMENT FOR AN RNA PSEUDOKNOT [J].
BRIERLEY, I ;
DIGARD, P ;
INGLIS, SC .
CELL, 1989, 57 (04) :537-547
[9]  
Cavanagh D, 1997, ARCH VIROL, V142, P629
[10]   The genome organization of the nidovirales: Similarities and differences between arteri-, toro-, and coronaviruses [J].
de Vries, AAF ;
Horzinek, MC ;
Rottier, PJM ;
de Groot, RJ .
SEMINARS IN VIROLOGY, 1997, 8 (01) :33-47