Li Shuang, Gao Mingchun, Zhang Runxiang, Song Ge, Song Jun, Liu Dandan, Cao Yongsheng, Li Tingting, Ma Bo, Liu Xiangtao, Wang Junwei
College of Veterinary Medicine, Northeast Agriculture University, Harbin, People's Republic of China.
Virus Genes. 2010 Dec;41(3):406-13. doi: 10.1007/s11262-010-0529-9. Epub 2010 Sep 16.
Foot-and-mouth disease virus (FMDV) serotype Asia 1 is one of the most predominant endemic serotypes in China. Our previous study has generated a full-length cDNA clone (pBSAs) of an Asia 1 serotype FMDV (As1/CHA/05) isolated from bovine. To further study the properties of this virus, a mutant in the 3A region of the cDNA clone (pBSAs-3A10D), containing the deletion at position 93-102 of the 3A protein of As1/CHA/05, was generated by PCR and cloning. After synthesis of RNA in vitro and transfection, the recombinant rvAs-3A10D virus was recovered from BHK-21 cells. Characterization of the rvAs-3A10D revealed that the infectivity, immunoreactivity, and replication kinetics in BHK-21 and PK-15 cells and virulence in mice of the rvAs-3A10D were similar to that of its parent virus. Notably, while wild-type and recombinant viruses containing full-length sequence of the 3A replicated well in primary calf kidney cells, the mutant rvAs-3A10D failed to replicate in primary calf kidney cells in vitro. Apparently, the full-length sequence of 3A in As1/CHA/05 is a necessary component for its replication in calf kidney cells. The availability of this 3A deletion infectious cDNA clone may help in further investigating the virulent determinants of FMDV and potentially developing FMDV vaccines.
口蹄疫病毒(FMDV)亚洲1型是中国最主要的地方性血清型之一。我们之前的研究已构建了一个从牛分离得到的亚洲1型口蹄疫病毒(As1/CHA/05)的全长cDNA克隆(pBSAs)。为了进一步研究该病毒的特性,通过PCR和克隆构建了一个cDNA克隆(pBSAs-3A10D)的3A区域突变体,其在As1/CHA/05的3A蛋白第93 - 102位存在缺失。在体外合成RNA并转染后,从BHK - 21细胞中获得了重组rvAs - 3A10D病毒。对rvAs - 3A10D的特性分析表明,其在BHK - 21和PK - 15细胞中的感染性、免疫反应性、复制动力学以及在小鼠中的毒力与其亲本病毒相似。值得注意的是,虽然含有3A全长序列的野生型和重组病毒在原代牛肾细胞中能良好复制,但突变体rvAs - 3A10D在体外原代牛肾细胞中无法复制。显然,As1/CHA/05中3A的全长序列是其在牛肾细胞中复制的必要组成部分。这种3A缺失感染性cDNA克隆的可用性可能有助于进一步研究口蹄疫病毒的毒力决定因素,并有可能开发口蹄疫病毒疫苗。