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[基于犬2型腺病毒构建转移载体]

[Construction of a transfer vector based on canine adenovirus type-2].

作者信息

Li Zhong, Zhang Shou-Feng, Cui Yan, Wang Xiao-Hu, Liu Ye, Hu Rong-Liang

机构信息

Military Veterinary Institute, Academy of Military Medical Sciences, PIA, Changchun 130062, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2007 Mar;23(2):319-22.

Abstract

Canine adenovirus type 2 (CAV-2) has been proposed as a vector for recombinant vaccine. Alternatively, it may be an attractive tool for gene transfer due to lack of pre-existing immunity in humans. In this study, a transfer vector based on CAV-2, in which the 1381bp fragment of the E3 region was deleted, and a linker containing the Not I, Cla I, Fse I restriction enzyme sites were cloned into the deleted region. The recombinant CAV-2 genome was released from the plasmids enzyme digestion and transfected into MDCK cells by lipofectamine to obtain the recombinant virus. No significant difference in morphology, hemagglutination and replication between the recombinant and the wide type CAV-2 was found. These results indicated that this recombinant virus CAV-2-deltaE3 (NF) may be an efficient vector for gene transfer and the capacity of the vector for inserted foreign gene was up to 3.3kb.

摘要

犬2型腺病毒(CAV-2)已被提议作为重组疫苗的载体。另外,由于人类不存在预先存在的免疫力,它可能是一种有吸引力的基因转移工具。在本研究中,构建了一种基于CAV-2的转移载体,其中E3区域的1381bp片段被删除,并将含有Not I、Cla I、Fse I限制性酶切位点的接头克隆到删除区域。通过酶切从质粒中释放重组CAV-2基因组,并通过脂质体转染到MDCK细胞中以获得重组病毒。重组CAV-2与野生型CAV-2在形态、血凝和复制方面未发现显著差异。这些结果表明,这种重组病毒CAV-2-deltaE3(NF)可能是一种有效的基因转移载体,该载体插入外源基因的能力高达3.3kb。

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