SEQUENCE OF THE SPIKE PROTEIN OF THE PORCINE EPIDEMIC DIARRHEA VIRUS

被引:91
作者
DUARTE, M [1 ]
LAUDE, H [1 ]
机构
[1] INRA, UNITE ENDOCRINOL MOLEC, CR JOUY EN JOSAS, F-78350 JOUY EN JOSAS, FRANCE
关键词
D O I
10.1099/0022-1317-75-5-1195
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
The complete sequence of the spike (S) gene of the Br1/87 isolate of porcine epidemic diarrhoea virus (PEDV) was determined from cDNA clones. The predicted polypeptide was 1383 amino acids long, contained 29 potential N-linked glycosylation sites and showed structural features similar to those of the coronavirus spike protein. The PEDV S protein, like that of the members of the transmissible gastroenteritis virus (TGEV)-related subset, lacks a proteolytic site to yield cleaved amino and carboxy subunits S1 and S2. Viral polypeptide species of the expected M(r), i.e. 170K/190K, were observed in PEDV-infected cells. Sequence comparison confirmed that, within the subset, PEDV was most closely related to the human respiratory coronavirus HCV 229E. However, PEDV S protein has an additional 250 residue N-terminal domain which is absent from HCV 229E and porcine respiratory coronavirus, the respiratory variant of TGEV. Alignment of the S1 regions revealed a second domain of about 90 residues with increased sequence divergence which might possibly express virus-specific determinants.
引用
收藏
页码:1195 / 1200
页数:6
相关论文
共 29 条
[1]   DEDUCED SEQUENCE OF THE BOVINE CORONAVIRUS SPIKE PROTEIN AND IDENTIFICATION OF THE INTERNAL PROTEOLYTIC CLEAVAGE SITE [J].
ABRAHAM, S ;
KIENZLE, TE ;
LAPPS, W ;
BRIAN, DA .
VIROLOGY, 1990, 176 (01) :296-301
[2]   CLONING AND SEQUENCING OF THE GENE ENCODING THE SPIKE PROTEIN OF THE CORONAVIRUS-IBV [J].
BINNS, MM ;
BOURSNELL, MEG ;
CAVANAGH, D ;
PAPPIN, DJC ;
BROWN, TDK .
JOURNAL OF GENERAL VIROLOGY, 1985, 66 (APR) :719-726
[3]   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
[4]  
BRITTON P, 1991, NATURE, V353, P394, DOI 10.1038/353394a0
[6]  
DEBOUCK P, 1980, AM J VET RES, V41, P219
[7]   CDNA CLONING AND SEQUENCE-ANALYSIS OF THE GENE ENCODING THE PEPLOMER PROTEIN OF FELINE INFECTIOUS PERITONITIS VIRUS [J].
DEGROOT, RJ ;
MADURO, J ;
LENSTRA, JA ;
HORZINEK, MC ;
VANDERZEIJST, BAM ;
SPAAN, WJM .
JOURNAL OF GENERAL VIROLOGY, 1987, 68 :2639-2646
[8]   4 MAJOR ANTIGENIC SITES OF THE CORONAVIRUS TRANSMISSIBLE GASTROENTERITIS VIRUS ARE LOCATED ON THE AMINO-TERMINAL HALF OF SPIKE GLYCOPROTEIN-S [J].
DELMAS, B ;
RASSCHAERT, D ;
GODET, M ;
GELFI, J ;
LAUDE, H .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :1313-1323
[9]   CARBOHYDRATE-INDUCED CONFORMATIONAL-CHANGES STRONGLY MODULATE THE ANTIGENICITY OF CORONAVIRUS TGEV GLYCOPROTEIN-S AND GLYCOPROTEIN-M [J].
DELMAS, B ;
LAUDE, H .
VIRUS RESEARCH, 1991, 20 (02) :107-120
[10]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395