Comparison of genomic and predicted amino acid sequences of respiratory and enteric bovine coronaviruses isolated from the same animal with fatal shipping pneumonia

被引:64
作者
Chouljenko, VN
Lin, XQ
Storz, J
Kousoulas, KG [1 ]
Gorbalenya, AE
机构
[1] Louisiana State Univ, Sch Vet Med, Dept Pathobiol Sci, Baton Rouge, LA 70803 USA
[2] Sci Applicat Int Corp, Adv Biomed Comp Ctr, NCI, Frederick, MD 21702 USA
关键词
D O I
10.1099/0022-1317-82-12-2927
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 genome sequences are reported here of two field isolates of bovine coronavirus (BCoV), which were isolated from respiratory and intestinal samples of the same animal experiencing fatal pneumonia during a bovine shipping fever epizootic. Both genomes contained 31028 nucleotides and included 13 open reading frames (ORFs) flanked by 5'- and 3'-untranslated regions (UTRs). ORF1a and ORF1 b encode replicative polyproteins pp1a and pp1ab, respectively, that contain all of the putative functional domains documented previously for the closest relative, mouse hepatitis virus. The genomes of the BCoV isolates differed in 107 positions, scattered throughout the genome except the 5'-UTR. Differences in 25 positions were non-synonymous and were located in all proteins except pp 1 b. Six replicase mutations were identified within or immediately downstream of the predicted largest pp1a-derived protein, p195/p210. Single amino acid changes within p195/p210 as well as within the S glycoprotein might contribute to the different phenotypes of the BCoV isolates.
引用
收藏
页码:2927 / 2933
页数:7
相关论文
共 45 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]  
Ballesteros M L, 1995, Adv Exp Med Biol, V380, P557
[3]   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
[4]   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
[5]   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
[6]   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
[7]   RIBOSOMAL FRAMESHIFTING ON VIRAL RNAS [J].
BRIERLEY, I .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :1885-1892
[8]   HEPTAD REPEAT SEQUENCES ARE LOCATED ADJACENT TO HYDROPHOBIC REGIONS IN SEVERAL TYPES OF VIRUS FUSION GLYCOPROTEINS [J].
CHAMBERS, P ;
PRINGLE, CR ;
EASTON, AJ .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :3075-3080
[9]   Nucleotide and predicted amino acid sequences of all genes encoded by the 3′ genomic portion (9.5 kb) of respiratory bovine coronaviruses and comparisons among respiratory and enteric coronaviruses [J].
Chouljenko, VN ;
Kousoulas, KG ;
Lin, XQ ;
Storz, J .
VIRUS GENES, 1998, 17 (01) :33-42
[10]   IDENTIFICATION OF PUTATIVE POLYMERASE GENE-PRODUCT IN CELLS INFECTED WITH MURINE CORONAVIRUS A59 [J].
DENISON, M ;
PERLMAN, S .
VIROLOGY, 1987, 157 (02) :565-568