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用于快速恢复重组痘苗病毒的Cas9介导的痘病毒重组体恢复技术(CASPRR)

Cas9-Mediated Poxvirus Recombinant Recovery (CASPRR) for Fast Recovery of Recombinant Vaccinia Viruses.

作者信息

Gowripalan Anjali, Smith Stewart A, Tscharke David C

机构信息

John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.

出版信息

Methods Mol Biol. 2025;2860:115-130. doi: 10.1007/978-1-0716-4160-6_8.

Abstract

Generation of recombinant vaccinia viruses opens many avenues for poxvirus research; however current methods for virus production can be laborious. Traditional methods rely on recombination strategies that produce engineered viruses at a low frequency, which then need to be identified and isolated from a large background of parent virus. For this reason, marker and reporter genes are often included, but in many cases these require removal in subsequent steps and the entire process is relatively inefficient. Cas9-mediated selection is a technique that repurposes Cas9/guide RNA complexes to amplify chosen subsets of vaccinia viruses. We refer to this approach as Cas9-mediated poxvirus recombinant recovery (CASPRR). Transient introduction of appropriately guided Cas9 allows for recovery of marker-free recombinant viruses in just 5 days, and requires no additional virus modification. Following three rounds of purification, pure virus stocks are obtained. A newer method, stable expression of Cas9 and guide RNAs in a permissive cell line, allows for additional process streamlining, removing cell type-specific concerns related to transient transfection of Cas9. Within this chapter, the protocol for CASPRR is described in both a transient and stable expression model. These methods can be utilized to accelerate recovery of recombinant vaccinia viruses and be applied to generation of vaccinia libraries or novel therapeutic agents.

摘要

重组痘苗病毒的产生为痘病毒研究开辟了许多途径;然而,目前的病毒生产方法可能很繁琐。传统方法依赖于重组策略,这种策略产生工程病毒的频率较低,然后需要从大量亲本病毒背景中识别和分离出来。因此,通常会包含标记基因和报告基因,但在许多情况下,这些基因需要在后续步骤中去除,并且整个过程效率相对较低。Cas9介导的选择是一种将Cas9/引导RNA复合物重新用于扩增选定的痘苗病毒亚群的技术。我们将这种方法称为Cas9介导的痘病毒重组体回收(CASPRR)。短暂引入适当引导的Cas9可在短短5天内回收无标记的重组病毒,并且无需额外的病毒修饰。经过三轮纯化后,可获得纯病毒株。一种更新的方法,即在允许的细胞系中稳定表达Cas9和引导RNA,可进一步简化流程,消除与Cas9短暂转染相关的细胞类型特异性问题。在本章中,将在短暂和稳定表达模型中描述CASPRR的方案。这些方法可用于加速重组痘苗病毒的回收,并应用于痘苗文库或新型治疗剂的产生。

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