Unit

UNIT 4.13 Generation of High-Titer Defective HSV-1 Vectors

  1. Filip Lim1,
  2. Rachael L. Neve2

Published Online: 1 MAY 2001

DOI: 10.1002/0471142301.ns0413s06

Current Protocols in Neuroscience

Current Protocols in Neuroscience

How to Cite

Lim, F. and Neve, R. L. 2001. Generation of High-Titer Defective HSV-1 Vectors. Current Protocols in Neuroscience. 6:4.13:4.13.1–4.13.17.

Author Information

  1. 1

    Universidad Autonoma de Madrid, Madrid, Spain

  2. 2

    Harvard Medical School & McLean Hospital, Belmont, Massachusetts

Publication History

  1. Published Online: 1 MAY 2001
  2. Published Print: FEB 1999

This is not the most recent version of the article. View current version (1 JAN 2013)

Abstract

There are two types of replication-deficient herpes simplex virus type 1 (HSV-1) vectors: those in which the foreign DNA of interest is cloned into the viral genome itself, and those that are comprised of a plasmid (amplicon) carrying minimal HSV-1 sequences that allow it to be packaged into virus particles with the aid of a helper virus. This unit describes the generation of helper virus stocks. Preparation of recombinant amplicon vector particles by transfection of amplicon and superinfection of helper virus into cells, and harvesting of packaged particles, is also delineated. Thorough characterization of the viral vector stock involves measuring (1) the helper virus plaque-forming units per ml (pfu/ml) on 2-2 cells, (2) the wild-type HSV-1 pfu/ml on Vero cells, and (3) the amplicon stock infectious vector units per ml (ivu/ml) on PC12 cells. Support protocols detail methods for determining titers of helper virus and wild-type virus by plaque assay, and of amplicon stocks by vector assay.