Department of Radiation Oncology and Molecular Radiation Sciences, The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
PLoS One. 2018 Jun 27;13(6):e0199563. doi: 10.1371/journal.pone.0199563. eCollection 2018.
The adenoviruses are essential tools for basic research and therapeutic development. Robust methods for the generation of mutant and recombinant viruses are crucial for these diverse applications. Here we describe a simple plasmid-based method that permits highly efficient modification of the adenoviral genome and rapid production of high-titer virus stocks. The 36-kilobase genome of adenovirus serotype 5 was divided into seven tractable blocks that could be individually modified in a single step and reassembled in vitro. Because the system is composed of compact modules, modifications at different loci can be readily recombined. Viral assemblies were delivered to packaging cells by electroporation, a strategy that consistently resulted in the de novo production of 108 infectious units in 3-5 days. In principle, a similar strategy could be applied to any other adenovirus serotype or to other double-strand DNA viruses.
腺病毒是基础研究和治疗开发的重要工具。对于这些多样化的应用,生成突变体和重组病毒的稳健方法至关重要。在这里,我们描述了一种简单的基于质粒的方法,该方法允许对腺病毒基因组进行高效修饰,并快速生产高滴度病毒株。腺病毒血清型 5 的 36 千碱基基因组被分成七个易于处理的块,可以在单个步骤中单独修饰,并在体外重新组装。由于该系统由紧凑的模块组成,因此不同部位的修饰可以很容易地重组。通过电穿孔将病毒组装体递送至包装细胞,该策略一致导致在 3-5 天内从头产生 108 个感染单位。原则上,类似的策略可以应用于任何其他腺病毒血清型或其他双链 DNA 病毒。