Fusion of a fluorescent protein to the pUL25 minor capsid protein of pseudorabies virus allows live-cell capsid imaging with negligible impact on infection

Kevin P. Bohannon, Patricia J Sollars, Gary E Pickard, Gregory A. Smith

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

In order to resolve the location and activity of submicroscopic viruses in living cells, viral proteins are often fused to fluorescent proteins (FPs) and visualized by microscopy. In this study, we describe the fusion of FPs to three proteins of pseudorabies virus (PRV) that allowed imaging of capsids in living cells. Included in this study are the first recombinant PRV strains expressing FP-pUL25 fusions based on a design applied to herpes simplex virus type 1 by Homa and colleagues. The properties of each reporter virus were compared in both in vitro and in vivo infection models. PRV strains expressing FP-pUL25 and FP-pUL36 preserved wild-type properties better than traditional FP-pUL35 isolates in assays of plaque size and virulence in mice. The utility of these strains in studies of axon transport, nuclear dynamics and viral particle composition are documented. G 2012 SGM.

Original languageEnglish (US)
Pages (from-to)124-129
Number of pages6
JournalJournal of General Virology
Volume93
Issue number1
DOIs
StatePublished - Jan 1 2012

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Suid Herpesvirus 1
Capsid
Capsid Proteins
Infection
Proteins
Viruses
Cell Nucleus Active Transport
Human Herpesvirus 1
Viral Proteins
Virion
Axons
Virulence
Microscopy

ASJC Scopus subject areas

  • Virology

Cite this

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