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Rescue of avian adeno-associated virus from a recombinant plasmid containing deletions in the viral inverted terminal repeats

机译:从重组质粒拯救禽腺相关病毒,该重组质粒在病毒反向末端重复序列中含有缺失

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We have previously reported the complete genome sequence of avian adeno-associated virus (AAAV) strain YZ-1, isolated from healthy chickens in China. In this study, we describe the successful rescue of infectious virions from a recombinant plasmid containing the genome of YZ-1 with deletions in the viral inverted terminal repeats (ITRs). The complete genome of YZ-1 was cloned into a bacterial plasmid by a modified "A-T" cloning method. Six recombinant plasmids were selected for further experiments. Sequence analysis indicated that the six clones shared identical internal sequences except for the various deletions within ITRs at either end of the cloned genome. The recombinant plasmid pYZ525, harboring a YZ-1 genome with a 96-nt deletion at the 5' end, was used to transfect CEL or HEK293 cells in the presence of the CELO virus or a helper plasmid, and rescued virions were obtained by both of the methods despite the presence of the deletions. Here, for the first time, we provide evidence that a certain number of nt deletions in the ITRs are not lethal for the rescue of viable AAAV from recombinant plasmids. This study provides insight into the unique biology of AAAV and the mechanism of viral replication.
机译:我们以前曾报道过从中国健康鸡中分离得到的禽腺相关病毒(AAAV)株YZ-1的完整基因组序列。在这项研究中,我们描述了从包含YZ-1基因组的重组质粒中成功挽救感染性病毒体的方法,该基因组在病毒反向末端重复序列(ITRs)中缺失。通过改良的“ A-T”克隆方法将YZ-1的完整基因组克隆到细菌质粒中。选择了六个重组质粒用于进一步的实验。序列分析表明,除了克隆基因组任一端ITR内的各种缺失外,这六个克隆共有相同的内部序列。重组质粒pYZ525在5'末端带有一个96-nt缺失的YZ-1基因组,用于在CELO病毒或辅助质粒存在的情况下转染CEL或HEK293细胞,并通过两种方法获得了拯救的病毒体尽管存在删除方法,在这里,我们首次提供证据表明,ITR中一定数量的nt缺失对从重组质粒中拯救出活的AAAV并不致命。这项研究为AAAV的独特生物学和病毒复制机制提供了见识。

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