| Literature DB >> 18336923 |
Thomas Bruun Rasmussen1, Ilona Reimann, Bernd Hoffmann, Klaus Depner, Ase Uttenthal, Martin Beer.
Abstract
This study describes the use of a novel and rapid long reverse transcription (RT)-PCR for the generation of infectious full-length cDNA of pestiviruses. To produce rescued viruses, full-length RT-PCR amplicons of 12.3 kb, including a T7-promotor, were transcribed directly in vitro, and the resulting RNA transcripts were electroporated into ovine cells. Infectious virus was obtained after one cell culture passage. The rescued viruses had a phenotype similar to the parental Border Disease virus strain. Therefore, direct generation of infectious pestiviruses from full-length RT-PCR cDNA products could be a valuable instrument for virus rescue, conservation and further characterization.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18336923 DOI: 10.1016/j.jviromet.2008.01.029
Source DB: PubMed Journal: J Virol Methods ISSN: 0166-0934 Impact factor: 2.014