生物
放大器
鼠疫病毒
基因组
病毒学
病毒
遗传学
细菌人工染色体
互补DNA
聚合酶链反应
基因
黄病毒科
病毒性疾病
作者
Thomas Bruun Rasmussen,Ilona Reimann,Åse Uttenthal,Immanuel Leifer,Klaus Depner,Horst Schirrmeier,Martin Beer
标识
DOI:10.1016/j.vetmic.2009.09.037
摘要
Complete genome amplification of viral RNA provides a new tool for the generation of modified viruses. We have recently reported a full-genome amplification strategy for recovery of pestiviruses (Rasmussen et al., 2008). A full-length cDNA amplicon corresponding to the Border disease virus-Gifhorn genome was generated by long RT-PCR and then RNA transcripts derived from this amplicon were used to rescue infectious virus. Here, we have now used this full-genome amplification strategy for efficient and robust amplification of three additional pestivirus strains: the vaccine strain C and the virulent Paderborn strain of Classical swine fever virus plus the CP7 strain of Bovine viral diarrhoea virus. The amplicons were cloned directly into a stable single-copy bacterial artificial chromosome generating full-length pestivirus DNAs from which infectious RNA transcripts could be also derived.
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