Insertion of cellular sequence and RNA recombination in the structural protein coding region of cytopathogenic bovine viral diarrhoea virus

J Gen Virol. 2003 Feb;84(Pt 2):447-452. doi: 10.1099/vir.0.18773-0.

Abstract

The cytopathogenic bovine viral diarrhoea virus (cp BVDV) strain KS86-1cp was isolated from a calf persistently infected with the noncytopathogenic (ncp) strain KS86-1ncp after it was exposed to cp BVDV strain Nose and developed mucosal disease (MD). Molecular analysis revealed that an insertion of a cellular gene and a duplication of the viral RNA encoding the nucleocapsid protein C and part of N(pro) had occurred in the C coding region of the Nose and KS86-1cp genomes. The inserted cellular gene was closely related to the cINS sequence. Remarkably, the 5' upstream region from the insertion of KS86-1cp had high sequence identity to that of Nose, but differed from that of KS86-1ncp. In contrast, the region downstream from the insertion of KS86-1cp showed high identity to KS86-1ncp, but not to Nose. These data reveal that KS86-1cp is a chimeric virus generated by homologous RNA recombination in a calf with MD.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Bovine Virus Diarrhea-Mucosal Disease / virology
  • Cattle
  • Cell Line
  • Cells, Cultured
  • Cytopathogenic Effect, Viral
  • Diarrhea Viruses, Bovine Viral / genetics*
  • Diarrhea Viruses, Bovine Viral / pathogenicity
  • Molecular Sequence Data
  • Nucleocapsid Proteins / genetics
  • RNA, Viral / genetics*
  • Recombination, Genetic*
  • Sequence Analysis, DNA
  • Viral Structural Proteins / chemistry
  • Viral Structural Proteins / genetics*

Substances

  • Nucleocapsid Proteins
  • RNA, Viral
  • Viral Structural Proteins