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Journal of Virology, March 2001, p. 2921-2928, Vol. 75, No. 6
Department of Gene Vectors, GSF-National Research Center
for Environment and Health, D-81377 Munich,
Germany,1 and Department of Pathology,
CRC Institute for Cancer Studies, University of Birmingham, B15 2TT
Birmingham, United Kingdom2
Received 31 May 2000/Accepted 11 December 2000
The genetic analysis of human herpesvirus 8 (HHV8), also termed
Kaposi's sarcoma-associated virus, has been hampered by severe difficulties in producing infectious viral particles and modifying the
viral genome. In this article, we report the successful cloning of the
HHV8 complete genome onto a prokaryotic F-plasmid replicon which allows
the propagation of the recombinant viral DNA in Escherichia coli. The insertion of the F-plasmid into the HHV8 genome
interrupts the ORF56 gene, whose expression product
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.6.2921-2928.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Spontaneous Activation of the Lytic Cycle in Cells
Infected with a Recombinant Kaposi's Sarcoma-Associated
Virus
by homology with
the Epstein-Barr virus BSLF1 gene
is supposed to be necessary for lytic DNA replication. After introduction of the recombinant HHV8 DNA
into 293 cells, early viral antigens are expressed, suggesting that
spontaneous lytic replication is initiated. However, completion of the
lytic program is prevented by the absence of the ORF56 protein, and a
quasi-latent state is established. Upon reintroduction of the ORF56
viral gene, the block is overcome and infectious HHV8 virions are
produced. As the recombinant HHV8 genome can be easily modified in
E. coli, this experimental system opens the way to an
extensive genetic analysis of other HHV8 functions.
*
Corresponding author. Mailing address: CRC Institute
for Cancer Studies, Department of Pathology, University of Birmingham, B15 2TT Birmingham, United Kingdom. Phone: 44/121/4144496. Fax: 44/121/4144486. E-mail: H.Delecluse{at}bham.ac.uk.
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