State Key Laboratory of Pathogens and Bio-security, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China.
Virol J. 2011 Mar 4;8:93. doi: 10.1186/1743-422X-8-93.
The virulence of A/Vietnam/1194/2004 (VN1194) in mice attenuated after serial passages in MDCK cells and chicken embryos, because the enriched large-plaque variants of the virus had significantly reduced virulence. In contrast, the small-plaque variants of the virus and the variants isolated from the brain of mice that were infected with the parental virus VN1194 had much higher virulence in mice. The virulence attenuation of serially propagated virus may be caused by the reduced neurotropism in mice. Our whole genome sequence analysis revealed substitutions of a total of two amino acids in PB1, three in PB2, two in PA common for virulence attenuated variants, all or part of which may be correlated with the virulence attenuation and reduced neurotropism of the serially propagated VN1194 in mice. Our study indicates that serial passages of VN1194 in vitro lead to adaptation and selection of variants that have markedly decreased virulence and neurotropism, which emphasizes the importance of direct analysis of original or less propagated virus samples.
在 MDCK 细胞和鸡胚中连续传代后,A/Vietnam/1194/2004(VN1194)在小鼠中的毒力减弱,因为病毒的丰富大斑块变异体毒力显著降低。相比之下,病毒的小斑块变异体和从感染亲本病毒 VN1194 的小鼠脑中分离出的变异体在小鼠中具有更高的毒力。连续传代病毒的毒力减弱可能是由于其在小鼠中的神经嗜性降低所致。我们的全基因组序列分析显示,在毒力减弱的变异体中,总共在 PB1 中有两个氨基酸取代,在 PB2 中有三个氨基酸取代,PA 中有两个氨基酸取代,它们全部或部分可能与连续传代的 VN1194 在小鼠中的毒力减弱和神经嗜性降低有关。我们的研究表明,VN1194 在体外的连续传代导致了毒力和神经嗜性明显降低的变异体的适应和选择,这强调了直接分析原始或较少传代的病毒样本的重要性。