| Literature DB >> 19836906 |
Thomas Bruun Rasmussen1, Ilona Reimann, Ase Uttenthal, Immanuel Leifer, Klaus Depner, Horst Schirrmeier, Martin Beer.
Abstract
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. Copyright 2009 Elsevier B.V. All rights reserved.Entities:
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Year: 2009 PMID: 19836906 DOI: 10.1016/j.vetmic.2009.09.037
Source DB: PubMed Journal: Vet Microbiol ISSN: 0378-1135 Impact factor: 3.293