Bacterial artificial chromosome clones of viruses comprising the towne cytomegalovirus vaccine.

Journal of Biomedicine and Biotechnology Pub Date : 2012-01-01 Epub Date: 2011-11-30 DOI:10.1155/2012/428498
Xiaohong Cui, Stuart P Adler, Andrew J Davison, Larry Smith, El-Sayed E Habib, Michael A McVoy
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Abstract

Bacterial artificial chromosome (BAC) clones have proven invaluable for genetic manipulation of herpesvirus genomes. BAC cloning can also be useful for capturing representative genomes that comprise a viral stock or mixture. The Towne live attenuated cytomegalovirus vaccine was developed in the 1970s by serial passage in cultured fibroblasts. Although its safety, immunogenicity, and efficacy have been evaluated in nearly a thousand human subjects, the vaccine itself has been little studied. Instead, genetic composition and in vitro growth properties have been inferred from studies of laboratory stocks that may not always accurately represent the viruses that comprise the vaccine. Here we describe the use of BAC cloning to define the genotypic and phenotypic properties of viruses from the Towne vaccine. Given the extensive safety history of the Towne vaccine, these BACs provide a logical starting point for the development of next-generation rationally engineered cytomegalovirus vaccines.

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含有巨细胞病毒疫苗的细菌人工染色体克隆病毒。
细菌人工染色体(BAC)克隆已被证明对疱疹病毒基因组的遗传操作是无价的。BAC克隆也可用于捕获包含病毒库存或混合物的代表性基因组。汤恩巨细胞病毒减毒活疫苗是在20世纪70年代通过培养成纤维细胞的连续传代而开发出来的。虽然它的安全性、免疫原性和有效性已经在近千名人类受试者中进行了评估,但疫苗本身的研究却很少。相反,基因组成和体外生长特性是从对实验室库存的研究中推断出来的,这些库存可能并不总是准确地代表构成疫苗的病毒。在这里,我们描述了使用BAC克隆来定义来自Towne疫苗的病毒的基因型和表型特性。鉴于Towne疫苗广泛的安全性历史,这些BACs为开发下一代合理工程巨细胞病毒疫苗提供了一个合乎逻辑的起点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Biomedicine and Biotechnology
Journal of Biomedicine and Biotechnology 生物-生物工程与应用微生物
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