Zhang X M, Kousoulas K G, Storz J
Department of Veterinary Microbiology and Parasitology, School of Veterinary Medicine, Louisiana State University, Baton Rouge 70803.
Virology. 1991 Jul;183(1):397-404. doi: 10.1016/0042-6822(91)90154-4.
The entire nucleotide sequences of the spike glycoprotein (S) genes of the highly virulent bovine coronavirus (BCV) strain BCV-LY138, the avirulent BCV-L9 and related Norden Vaccine (BCV-Vaccine) strains were determined using the polymerase chain reaction (PCR) to amplify cDNAs obtained by reverse transcription of viral RNA, and to produce single strand cDNAs for DNA sequencing. The S gene sequences of these viral strains were compared with those of recently published strains BCV-Mebus, BCV-Quebec, and BCV-F15. An open reading frame of 4092 nucleotides, encoding a protein of 1363 amino acid residues, was found in all six strains. Frameshifts and insertions or deletions were not observed except for the BCV-F15. The S gene sequences were more than 98% conserved overall inspite of different origins of the six viruses. There were 45 to 56 nt differences between the virulent and avirulent groups while there were 6 to 14 nt differences among four avirulent strains. Comparison of the deduced amino acid sequences indicated that the S proteins had typical properties of membrane glycoproteins. Nineteen N-linked glycosylation sites were predicted in five strains, and 18 of them were conserved in the avirulent strain BCV-L9. The sequence KRRSRR at the predicted proteolytic cleavage site was identified in five strains while the sequence KRRSVR was found in BCV-F15. Substitutions of few amino acids in the putative fusogenic domains and two prolines at 507 and 567 in the antigenic domains may cause altered immunogenic and other functional properties of the S proteins specified by the virulent and avirulent BCV strains. Nine amino acid substitutions between the virulent and avirulent groups may correlate with BCV virulence.
利用聚合酶链反应(PCR)对高致病性牛冠状病毒(BCV)毒株BCV-LY138、无毒力的BCV-L9及相关诺登疫苗(BCV疫苗)毒株的刺突糖蛋白(S)基因的完整核苷酸序列进行了测定,以扩增通过病毒RNA逆转录获得的cDNA,并生成用于DNA测序的单链cDNA。将这些病毒毒株的S基因序列与最近发表的毒株BCV-Mebus、BCV-魁北克和BCV-F15的序列进行了比较。在所有六个毒株中均发现了一个4092个核苷酸的开放阅读框,编码一个由1363个氨基酸残基组成的蛋白质。除了BCV-F15外,未观察到移码和插入或缺失。尽管这六种病毒的起源不同,但S基因序列总体上保守性超过98%。有毒力组和无毒力组之间存在45至56个核苷酸差异,而四个无毒力毒株之间存在6至14个核苷酸差异。推导的氨基酸序列比较表明,S蛋白具有膜糖蛋白的典型特性。在五个毒株中预测有19个N-糖基化位点,其中18个在无毒力毒株BCV-L9中保守。在五个毒株中鉴定出预测的蛋白水解切割位点处的序列KRRSRR,而在BCV-F15中发现的序列为KRRSVR。推定的融合结构域中少数氨基酸的取代以及抗原结构域中507和567位的两个脯氨酸可能导致有毒力和无毒力BCV毒株所特有的S蛋白的免疫原性和其他功能特性发生改变。有毒力组和无毒力组之间的九个氨基酸取代可能与BCV毒力相关。