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Polydnavirus integration in lepidopteran host cells in vitro.

D E Gundersen-Rindal1, D E Lynn

  • 1US Department of Agriculture, Agricultural Research Service, Insect Biocontrol Laboratory, Beltsville, MD 20705, USA. gundersd@ba.ars.usda.gov

Journal of Insect Physiology
|May 29, 2003
PubMed
Summary

Polydnavirus (PDV) DNA integrates into gypsy moth cell genomes, evidenced by junction clones. This viral DNA integration in vitro suggests a host-derived mechanism, not viral proteins.

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Area of Science:

  • Virology
  • Genetics
  • Insect molecular biology

Background:

  • Polydnavirus (PDV) DNA exhibits long-term persistence in infected lepidopteran cell cultures.
  • This persistence suggests potential permanent integration into the host cell genome.

Purpose of the Study:

  • To provide supportive evidence for the in vitro integration of polydnavirus DNA into lepidopteran cell genomes.
  • To identify precise integration sites and characterize the mechanism of polydnavirus integration.

Main Methods:

  • Preparation of cloned libraries from Lymantria dispar cell lines infected with Glyptapanteles indiensis PDV (GiPDV).
  • Isolation of junction clones containing both insect chromosomal and viral sequences.
  • Sequence comparison of linear and circular forms of GiPDV genome segment F to identify integration junctions.

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Main Results:

  • Identified junction clones with both insect and GiPDV sequences in L. dispar cell lines.
  • Determined identical virus sequence junctions with a CATG palindromic repeat, despite variable host chromosomal sequences.
  • Observed a novel L. dispar retrotransposon near the integration site, suggesting a host-derived integration mechanism.

Conclusions:

  • Polydnavirus DNA integrates into the L. dispar cell genome in vitro.
  • Integration appears to be mediated by a host-derived mechanism, potentially involving retrotransposon activity.
  • Further research is needed to determine if this integration occurs in vivo within the lepidopteran host.