Lang Yifei, Gao Shandian, Du Junzheng, Shao Junjun, Cong Guozheng, Lin Tong, Zhao Furong, Liu Lihong, Chang Huiyun
State Key Laboratory of Veterinary Etiological Biology, National Foot and Mouth Disease Reference Laboratory, Key Laboratory of Epizootic Diseases of Grazing Animals of Ministry of Agriculture, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China.
State Key Laboratory of Veterinary Etiological Biology, National Foot and Mouth Disease Reference Laboratory, Key Laboratory of Epizootic Diseases of Grazing Animals of Ministry of Agriculture, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China.
Vet Microbiol. 2014 Dec 5;174(3-4):554-559. doi: 10.1016/j.vetmic.2014.10.018. Epub 2014 Oct 27.
Bovine viral diarrhea virus (BVDV) is one of the wide distributed pathogenic viruses of livestock and wild animals worldwide. E2 glycoprotein is a major structural component of the BVDV virion and plays a key role in viral attachment to host cells and inducing immune responses against viral infection. In order to gain detailed information of the E2 coding region of BVDV circulating in China, 46 positive samples were tested by RT-PCR for the E2 coding region. The 1122 nt nucleotide sequences of full-length E2 were harvested and analyzed. The results suggested that full-length E2 was an ideal target for BVDV genotyping and divided the domestic BVDV isolates into 9 subgenotypes, namely BVDV-1a, -1b1, -1c, -1d, -1o, -1m, -1p, -1q and BVDV-2a, showing great diversity. The difference of nonsynonymous and synonymous substitution rates (dN-dS) inferred both positive and purifying selection of the E2. However, combination of positive and purifying selection at different points indicated purifying selection within the complete E2. Protein properties analysis based on glycosylation sites and epitope prediction demonstrated that the biological character of E2 among individual BVDV subgenotype was similar, but may alter due to amino acid changes. For the first time, the comprehensive collection of E2 sequences of Chinese BVDV isolates was elucidated, which would provide information for future vaccine design and BVD control in China.
牛病毒性腹泻病毒(BVDV)是一种在全球范围内广泛传播的家畜和野生动物致病病毒。E2糖蛋白是BVDV病毒粒子的主要结构成分,在病毒附着于宿主细胞以及诱导针对病毒感染的免疫反应中起关键作用。为了详细了解在中国流行的BVDV的E2编码区信息,对46份阳性样本进行了E2编码区的RT-PCR检测。收集并分析了全长1122 nt的E2核苷酸序列。结果表明,全长E2是BVDV基因分型的理想靶点,可将国内BVDV分离株分为9个亚基因型,即BVDV-1a、-1b1、-1c、-1d、-1o、-1m、-1p、-1q和BVDV-2a,显示出高度的多样性。非同义替换率和同义替换率(dN-dS)的差异表明E2存在正向选择和纯化选择。然而,不同位点的正向选择和纯化选择相结合表明在完整的E2内存在纯化选择。基于糖基化位点的蛋白质特性分析和表位预测表明,单个BVDV亚基因型中E2的生物学特性相似,但可能因氨基酸变化而改变。首次阐明了中国BVDV分离株E2序列的综合收集情况,这将为中国未来的疫苗设计和BVD防控提供信息。