UMR "Émergence des Pathologies Virales" (EPV: Aix-Marseille Univ-IRD 190 -Inserm 1207 -EHESP-IHU Méditerranée Infection), Marseille, France.
PLoS One. 2018 Feb 13;13(2):e0193069. doi: 10.1371/journal.pone.0193069. eCollection 2018.
Reverse genetics is key technology for producing wild-type and genetically modified viruses. The ISA (Infectious Subgenomic Amplicons) method is a recent versatile and user-friendly reverse genetics method to rescue RNA viruses. The main constraint of its canonic protocol was the requirement to produce (e.g., by DNA synthesis or fusion PCR) 5' and 3' modified genomic fragments encompassing the human cytomegalovirus promoter (pCMV) and the hepatitis delta virus ribozyme/simian virus 40 polyadenylation signal (HDR/SV40pA), respectively. Here, we propose the ultimately simplified "Haiku" designs in which terminal pCMV and HDR/SV40pA sequences are provided as additional separate DNA amplicons. This improved procedure was successfully applied to the rescue of a wide range of viruses belonging to genera Flavivirus, Alphavirus and Enterovirus in mosquito or mammalian cells using only standard PCR amplification techniques and starting from a variety of original materials including viral RNAs extracted from cell supernatant media or animal samples. We also demonstrate that, in specific experimental conditions, the presence of the HDR/SV40pA is not necessary to rescue the targeted viruses. These ultimately simplified "Haiku" designs provide an even more simple, rapid, versatile and cost-effective tool to rescue RNA viruses since only generation of overlapping amplicons encompassing the entire viral genome is now required to generate infectious virus. This new approach may completely modify our capacity to obtain infectious RNA viruses.
反向遗传学是生产野生型和基因修饰病毒的关键技术。ISA(感染亚基因组扩增子)方法是一种最近出现的多功能、用户友好的反向遗传学方法,可用于拯救 RNA 病毒。其规范方案的主要限制是需要分别产生(例如,通过 DNA 合成或融合 PCR)包含人巨细胞病毒启动子(pCMV)和肝炎 delta 病毒核酶/猿猴病毒 40 多聚腺苷酸化信号(HDR/SV40pA)的 5'和 3'修饰基因组片段。在这里,我们提出了最终简化的“俳句”设计,其中末端 pCMV 和 HDR/SV40pA 序列作为额外的单独 DNA 扩增子提供。该改进的程序成功应用于从各种原始材料(包括从细胞上清液或动物样本中提取的病毒 RNA)在蚊子或哺乳动物细胞中拯救属于黄病毒属、甲病毒属和肠道病毒属的多种病毒。我们还证明,在特定实验条件下,HDR/SV40pA 的存在对于拯救目标病毒并非必需。这些最终简化的“俳句”设计提供了一种更简单、快速、多功能且具有成本效益的工具来拯救 RNA 病毒,因为现在仅需要生成包含整个病毒基因组的重叠扩增子即可生成感染性病毒。这种新方法可能会彻底改变我们获得感染性 RNA 病毒的能力。