Department of Bioinformatics, Faculty of Engineering, Soka University, Hachioji, Tokyo 192-8577, Japan.
Microbiol Immunol. 2011 Oct;55(10):694-703. doi: 10.1111/j.1348-0421.2011.00374.x.
Friend murine leukemia virus clone A8 causes spongiform neurodegeneration in the rat brain, and the env gene of A8 is a primary determinant of neuropathogenicity. In order to narrow down the critical region within the env gene that determines neuropathogenicity, we constructed chimeric viruses having chimeric env between A8 and non-neuropathogenic 57 on the background of A8 virus. After replacement of the BamHI (at nucleotide 5715)-AgeI (at nucleotide 6322) fragment of A8 virus with the corresponding fragment of 57, neuropathogenicity was lost. In contrast, the chimeric viruses that have the BamHI (5715)-AgeI (6322) fragment of A8 induced spongiosis in 100% of infected rats at the same or slightly lower intensity than A8 virus. These results indicate that the BamHI (5715)-AgeI (6322) fragment of A8, which contains the signal sequence and the N-terminal half of RBD, is crucial for the induction of spongiform neurodegeneration. In the BamHI (5715)-AgeI (6322) fragment, seven amino acids differed between A8 and 57, one in the signal sequence and six in RBD, which suggests that these amino acids significantly contribute to the neuropathogenicity of A8.
友鼠白血病病毒克隆 A8 可引起大鼠脑的海绵状神经退行性变,而 A8 的 env 基因是神经致病性的主要决定因素。为了缩小决定神经致病性的 env 基因内的关键区域,我们构建了在 A8 病毒背景下具有 A8 与非神经致病性 57 之间嵌合 env 的嵌合病毒。在用 A8 病毒的 BamHI(核苷酸 5715)-AgeI(核苷酸 6322)片段替换相应的 57 片段后,神经致病性丧失。相比之下,具有 A8 的 BamHI(5715)-AgeI(6322)片段的嵌合病毒在相同或稍低的强度下感染大鼠时可引起海绵状变性,感染率为 100%。这些结果表明,包含信号序列和 RBD N 端一半的 A8 的 BamHI(5715)-AgeI(6322)片段对于诱导海绵状神经退行性变至关重要。在 BamHI(5715)-AgeI(6322)片段中,A8 和 57 之间有七个氨基酸不同,一个在信号序列中,六个在 RBD 中,这表明这些氨基酸对 A8 的神经致病性有显著贡献。