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Journal of Virology, May 1999, p. 4110-4119, Vol. 73, No. 5
Marie Curie Research Institute, The Chart,
Oxted, Surrey RH1 0TL, United Kingdom
Received 28 December 1998/Accepted 9 February 1999
Many stages of the herpes simplex virus maturation pathway have not
yet been defined. In particular, little is known about the assembly of
the virion tegument compartment and its subsequent incorporation into
maturing virus particles. Here we describe the construction of a herpes
simplex virus type 1 (HSV-1) recombinant in which we have replaced the
gene encoding a major tegument protein, VP22, with a gene expressing a
green fluorescent protein (GFP)-VP22 fusion protein (GFP-22). We show
that this virus has growth properties identical to those of the
parental virus and that newly synthesized GFP-22 is detectable in live
cells as early as 3 h postinfection. Moreover, we show that GFP-22
is incorporated into the HSV-1 virion as efficiently as VP22, resulting
in particles which are visible by fluorescence microscopy.
Consequently, we have used time lapse confocal microscopy to monitor
GFP-22 in live-cell infection, and we present time lapse animations of
GFP-22 localization throughout the virus life cycle. These animations
demonstrate that GFP-22 is present in a diffuse cytoplasmic location
when it is initially expressed but evolves into particulate material
which travels through an exclusively cytoplasmic pathway to the cell
periphery. In this way, we have for the first time visualized the
trafficking of a herpesvirus structural component within live, infected cells.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Live-Cell Analysis of a Green Fluorescent
Protein-Tagged Herpes Simplex Virus Infection
*
Corresponding author. Mailing address: Marie Curie
Research Institute, The Chart, Oxted, Surrey RH1 0TL, United Kingdom.
Phone: 01883 722306. Fax: 01883 714375. E-mail:
g.elliott{at}mcri.ac.uk.
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