Characterization of Prototype Foamy Virus Infectivity in Transportin 3 Knockdown Human 293t Cell Line

J Microbiol Biotechnol. 2017 Feb 28;27(2):380-387. doi: 10.4014/jmb.1606.06011.

Abstract

The foamy viruses are currently considered essential for development as vectors for gene delivery. Previous studies demonstrated that prototype foamy virus (PFV) can infect and replicate prevalently in a variety of cell types for its exclusive replication strategy. However, the virus-host interaction, especially PFV-transportin3 (TNPO3), is still poorly understood. In our investigation of the role of TNPO3 in PFV infection, we found lower virus production in TNPO3 knockdown (KD) cells compared with wild-type 293T cells. PCR analysis revealed that viral DNAs were mostly altered to circular forms: both 1-long terminal repeat (1-LTR) and 2-LTR in TNPO3 KD cells. We therefore suggest that TNPO3 is required for successful PFV replication, at least at/after the nuclear entry step of viral DNA. These findings highlight the obscure mysteries of PFV-host interaction and the requirement of TNPO3 for productive infection of PFV in 293T cells.

Keywords: 1-long terminal repeat; 293 T cell; Transportin-3; prototype foamy virus.

MeSH terms

  • DNA, Viral
  • Gene Knockdown Techniques
  • HEK293 Cells
  • Host-Pathogen Interactions
  • Humans
  • Spumavirus / genetics
  • Spumavirus / physiology*
  • Terminal Repeat Sequences
  • Transfection
  • Virus Replication*
  • beta Karyopherins / genetics
  • beta Karyopherins / physiology*

Substances

  • DNA, Viral
  • TNPO3 protein, human
  • beta Karyopherins