Amplification of a full-length Borna disease virus (BDV) cDNA from total RNA of cells persistently infected with BDV

Microbiol Immunol. 1997;41(6):481-6. doi: 10.1111/j.1348-0421.1997.tb01881.x.

Abstract

We have developed a novel reverse transcriptase-polymerase chain reaction (RT-PCR) to amplify the full-length 8.9 kilobase (kbp) cDNA of the Borna disease virus (BDV) RNA genome from the total cellular RNA of MDCK cells persistently infected with BDV (MDCK/BDV). Antigenomic BDV cDNA was reverse transcribed using a 53-mer oligonucleotide primer, corresponding to the 5'-terminus of a putative 3'-leader sequence of the BDV RNA genome, for 2 hr at 42 C followed by 30 min at 55 C. PCR was performed in the presence of this 53-mer antigenomic primer and a 25-mer primer, corresponding to the 3'-terminus of the BDV antigenomic cDNA, by use of an rTth DNA polymerase with proof-reading activity. The amplified full-length BDV cDNA was detected in as little as 20 ng of total cellular RNA of MDCK/BDV. This RT-PCR method should be a useful technique to study the molecular quasispecies of BDV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Borna disease virus / genetics*
  • Cells, Cultured
  • DNA, Complementary / genetics*
  • DNA, Viral / genetics*
  • Dogs
  • Molecular Sequence Data
  • Polymerase Chain Reaction / methods*
  • RNA, Viral / genetics*
  • Sequence Analysis, DNA

Substances

  • DNA, Complementary
  • DNA, Viral
  • RNA, Viral

Associated data

  • GENBANK/U04608