Liu Shengwang, Xu Qianqian, Han Zongxi, Liu Xiaoli, Li Huixin, Guo Hongbo, Sun Nana, Shao Yuhao, Kong Xiangang
Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, The Chinese Academy of Agricultural Sciences, Harbin 150001, People's Republic of China.
Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, The Chinese Academy of Agricultural Sciences, Harbin 150001, People's Republic of China.
Infect Genet Evol. 2014 Apr;23:189-95. doi: 10.1016/j.meegid.2014.02.015. Epub 2014 Mar 5.
Recombination among infectious bronchitis viruses (IBVs), coupled with point mutations, insertions, and deletions that occur in the genome, is thought to contribute to the emergence of new IBV variants. In this study an IBV, ck/CH/LJL/111054, was isolated from a H120-vaccinated chicken, which presented with a suspected IBV infection. Phylogenetic analysis of the S1 subunit sequence confirmed that strain ck/CH/LJL/111054 is of the Connecticut-type; however, further extensive full-length genomic analysis identified the occurrence of recombination events. Therefore, strain ck/CH/LJL/111054 may have originated from recombination events between Conn- and Mass-like strains at three recombination breakpoints: two located within the nsp3 gene sequence and one in the nsp12 gene sequence. Further, the uptake of the 5' untranslated regions, nsp2, parts of nsp3, nsp4-11, and parts of nsp 12 from Mass-like virus by ck/CH/LJL/111054 might have resulted in changes in viral replication efficiency rather than antigenic changes, via cross-neutralization analysis with the H120 strain. Recombination events coupled with the accumulation of mutations in the ck/CH/LJL/111054 genome may account for its increased virulence in specific-pathogen free chickens.
传染性支气管炎病毒(IBV)之间的重组,再加上基因组中发生的点突变、插入和缺失,被认为促成了新的IBV变异株的出现。在本研究中,从一只接种过H120疫苗但疑似感染IBV的鸡中分离出一株IBV,即ck/CH/LJL/111054。对S1亚基序列的系统发育分析证实,ck/CH/LJL/111054毒株属于康涅狄格型;然而,进一步广泛的全长基因组分析确定了重组事件的发生。因此,ck/CH/LJL/111054毒株可能起源于Conn样毒株和Mass样毒株在三个重组断点处的重组事件:两个位于nsp3基因序列内,一个位于nsp12基因序列内。此外,通过与H120毒株的交叉中和分析,ck/CH/LJL/111054从Mass样病毒摄取5'非翻译区、nsp2、部分nsp3、nsp4 - 11和部分nsp12,可能导致病毒复制效率的改变而非抗原性改变。ck/CH/LJL/111054基因组中的重组事件与突变积累可能解释了其在无特定病原体鸡中的毒力增强。