Ko Chin-Koo, Kang Mun-Il, Lim Geum-Ki, Kim Gye-Yeop, Yoon Soon-Seek, Park Jong-Tae, Jeong Cheol, Park Sung-Hee, Park Su-Jin, Kim You-Jung, Jeong Jae-Ho, Kim Sang-Ki, Park Sang-Ilk, Kim Ha-Hyun, Kim Kyoung-Yoon, Cho Kyoung-Oh
Veterinary Medical Research Center, College of Veterinary Medicine, Chonnam National University, Gwangju, South Korea.
Virus Genes. 2006 Apr;32(2):129-36. doi: 10.1007/s11262-005-6867-3.
The different bovine coronavirus (BCoV) strains or isolates exhibited various degrees of substitutions, resulting in altered antigenicity and pathogenicity of the virus. In the previous our study, we demonstrated that the spike glycoprotein gene of Korean winter dysentery (WD) BCoV had a genetic property of both enteric (EBCV) and respiratory BCoV (RBCV) and were significantly distinct from the ancestral enteric strains. In the present study, therefore, we analyzed the other structure genes, the hemagglutinin/esterase (HE) protein, the transmembrane (M) protein and the small membrane (E) protein to characterize 10 WD BCoV circulated in Korea during 2002-2003 and compared the nucleotide and deduced amino acid sequences with the other known BCoV. Phylogenetic analysis indicated that the HE gene among BCoV could be divided into three groups. The first group included only RBCV, while the second group contained calf diarrhea BCoV, RBCV, WD and EBCV, respectively. The third group possessed only all Korean WD strains which were more homologous to each other and were sharply distinct from the other known BCoV, suggesting Korean WD strains had evolutionary distinct pathway. In contrast, the relative conservation of the M and E proteins of BCoV including Korean WD strains and the other coronaviruses suggested that structural constraints on these proteins are rigid, resulting in more limited evolution of these proteins. In addition, BCoV and human coronavirus HCV-OC43 contained four potential O-glycosylation sites in the M gene. However, the M gene sequence of both BCoV and HCV-OC43 might not contain a signal peptide, suggesting the M protein might be unlikely to be exposed to the O-glycosylation machinery in vivo.
不同的牛冠状病毒(BCoV)毒株或分离株表现出不同程度的替换,导致病毒的抗原性和致病性发生改变。在我们之前的研究中,我们证明韩国冬季痢疾(WD)BCoV的刺突糖蛋白基因具有肠道型(EBCV)和呼吸道型BCoV(RBCV)的遗传特性,并且与祖先肠道毒株明显不同。因此,在本研究中,我们分析了其他结构基因,即血凝素/酯酶(HE)蛋白、跨膜(M)蛋白和小膜(E)蛋白,以鉴定2002 - 2003年在韩国流行的10株WD BCoV,并将核苷酸和推导的氨基酸序列与其他已知的BCoV进行比较。系统发育分析表明,BCoV中的HE基因可分为三组。第一组仅包括RBCV,而第二组分别包含犊牛腹泻BCoV、RBCV、WD和EBCV。第三组仅包含所有韩国WD毒株,它们彼此之间同源性更高,并且与其他已知的BCoV明显不同,这表明韩国WD毒株具有独特的进化途径。相比之下,包括韩国WD毒株和其他冠状病毒在内的BCoV的M和E蛋白相对保守,这表明这些蛋白的结构限制较为严格,导致这些蛋白的进化更为有限。此外,BCoV和人冠状病毒HCV - OC43在M基因中含有四个潜在的O - 糖基化位点。然而,BCoV和HCV - OC43的M基因序列可能都不包含信号肽,这表明M蛋白在体内可能不太可能暴露于O - 糖基化机制。