Replication and propagation of attenuated vesicular stomatitis virus vectors in vivo: vector spread correlates with induction of immune responses and persistence of genomic RNA

J Virol. 2007 Feb;81(4):2078-82. doi: 10.1128/JVI.02525-06. Epub 2006 Dec 6.

Abstract

Live-attenuated vesicular stomatitis virus (VSV) vectors expressing foreign antigens induce potent immune responses and protect against viral diseases in animal models. Highly attenuated (VSV-CT1) or single-cycle VSV (VSVDeltaG) vectors induce immune responses lower than those generated by attenuated wild-type VSV vectors when given intranasally. We show here that reduced spread of the more highly attenuated or single-cycle vectors to other organs, including lymph nodes, correlates with the reduction in the immune responses. A reverse transcription, real-time PCR assay for VSV genomic RNA (gRNA) sequences showed long-term persistence of gRNA from replicating vectors in lymph nodes, long after viral clearance. Such persistence may be important for induction of potent immune responses by VSV vectors.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antibodies, Viral / blood
  • Antibodies, Viral / immunology
  • Antibody Specificity
  • Genetic Vectors / administration & dosage*
  • Genetic Vectors / physiology
  • Immunization*
  • Injections, Intralymphatic
  • Lymph Nodes / virology
  • Mice
  • Mice, Inbred BALB C
  • Neutralization Tests
  • RNA, Viral / biosynthesis
  • Time Factors
  • Vesicular stomatitis Indiana virus / physiology*
  • Virus Replication

Substances

  • Antibodies, Viral
  • RNA, Viral