Characterization of vpr vector constructed from chimeric simian and human immunodeficiency virus

J Vet Med Sci. 2003 May;65(5):633-6. doi: 10.1292/jvms.65.633.

Abstract

Chimeric simian and human immunodeficiency viruses (SHIVs) are useful tool for investigating AIDS pathogenesis and for development of vaccine. We constructed a SHIV-vpr vector (designated as SHIV-3sj) by replacing vpr region with restriction enzyme sites. SHIV-3sj was designed to express inserted gene along with its viral replication. Five cytokine genes were inserted into SHIV-3sj, and ability of viral replication and expression of the inserted genes were examined. The short insert including RANTES and IL-5 resulted in the successful expression from SHIV-3sj, while the construct having longer genes including IL-2, IL-6 and IL-12p35 failed to become replication competent. These results suggest that the length of the insert is an important factor for the replication ability of SHIV-3sj vector.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Chemokine CCL5 / genetics
  • DNA, Recombinant / genetics*
  • Gene Expression
  • Genes, vpr / genetics*
  • Genetic Vectors / genetics*
  • Genetic Vectors / physiology*
  • HIV-1 / genetics*
  • HIV-1 / physiology
  • Humans
  • Interleukin-12 / genetics
  • Interleukin-2 / genetics
  • Interleukin-5 / genetics
  • Interleukin-6 / genetics
  • Kinetics
  • Molecular Sequence Data
  • Open Reading Frames / genetics
  • Simian Immunodeficiency Virus / genetics*
  • Simian Immunodeficiency Virus / physiology
  • T-Lymphocytes / virology
  • Virus Replication / genetics*

Substances

  • Chemokine CCL5
  • DNA, Recombinant
  • Interleukin-2
  • Interleukin-5
  • Interleukin-6
  • Interleukin-12

Associated data

  • GENBANK/M19921