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从含有病毒反向末端重复序列缺失的重组质粒中拯救禽腺相关病毒。

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

机构信息

Ministry of Education Key Lab for Avian Preventive Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.

出版信息

Arch Virol. 2012 Jan;157(1):129-34. doi: 10.1007/s00705-011-1121-x. Epub 2011 Sep 27.

Abstract

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.

摘要

我们之前曾报道过一株从中国健康鸡中分离的禽腺相关病毒(AAAV)YZ-1 株的全基因组序列。在本研究中,我们描述了利用含有 YZ-1 基因组的重组质粒,通过缺失病毒反向末端重复序列(ITR)成功拯救出传染性病毒粒子的方法。通过改良的“A-T”克隆方法,将 YZ-1 的全基因组克隆到细菌质粒中。选择了六个重组质粒进行进一步实验。序列分析表明,除克隆基因组两端的 ITR 内存在各种缺失外,这六个克隆体共享相同的内部序列。携带 5'端 96nt 缺失的重组质粒 pYZ525,在 CELO 病毒或辅助质粒的存在下转染 CEL 或 HEK293 细胞,两种方法均获得了拯救的病毒粒子。在这里,我们首次提供证据表明,ITR 中一定数量的 nt 缺失对于从重组质粒中拯救有活力的 AAAV 并不致命。本研究为了解 AAAV 的独特生物学和病毒复制机制提供了线索。

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