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Journal of Virology, December 1999, p. 10272-10280, Vol. 73, No. 12
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Efficient trans-Complementation of the Flavivirus
Kunjin NS5 Protein but Not of the NS1 Protein Requires Its Coexpression
with Other Components of the Viral Replicase
Alexander A.
Khromykh,1,*
Petra L.
Sedlak,1
Kimberley J.
Guyatt,1
Roy A.
Hall,2 and
Edwin G.
Westaway1
Sir Albert Sakzewski Virus Research Centre,
Royal Children's Hospital, Brisbane, Queensland
4029,1 and Department of
Microbiology, University of Queensland, St. Lucia, Brisbane,
Queensland 4072,2 Australia
Received 6 July 1999/Accepted 8 September 1999
Successful trans-complementation of the defective
Kunjin virus (KUN) RNA FLdGDD with a deletion of the RNA
polymerase motif GDD in the NS5 gene by using a BHK cell
line, repBHK, that continuously produced a functionally active KUN
replication complex (RC) from replicon RNA was recently reported
(A. A. Khromykh, M. T. Kenney, and E. G. Westaway,
J. Virol. 72:7270-7279, 1998). In order to identify whether this
complementation of FLdGDD RNA was provided by the wild-type
NS5 protein alone or with the help of other nonstructural (NS) proteins
also expressed in repBHK cells, we generated BHK cell lines stably
producing the individual NS5 protein (SRns5BHK) or the NS1-NS5
polyprotein (SRns1-5BHK) by using a heterologous expression
vector based on a modified noncytopathic Sindbis replicon. Western blot
analysis with anti-NS5 antibodies showed that the level of production
of NS5 was significantly higher in SRns5BHK cells than in SRns1-5BHK
cells. Despite the higher level of expressed NS5,
trans-complementation of FLdGDD RNA was much
less efficient in SRns5BHK cells than in SRns1-5BHK cells and produced
at least 100-fold less of the secreted complemented virus. In contrast, efficient complementation of KUN RNA with lethal cysteine-to-alanine mutations in the NS1 gene was achieved both in BHK cells producing the
individual KUN NS1 protein from the Sindbis replicon vector and in
repBHK cells, with both cell lines expressing similar amounts of NS1
protein. These results clearly demonstrate that flavivirus NS5
coexpressed with other components of the viral replicase possesses much
higher functional (trans-complementing) activity than
individually expressed NS5 and that efficient
trans-complementation of mutated flavivirus NS1 and NS5
proteins occurs by different mechanisms. The results are interpreted
and discussed in relation to our proposed model of formation of the
flavivirus RC largely based on previous ultrastructural and biochemical
analyses of KUN replication.
*
Corresponding author. Mailing address: Sir Albert
Sakzewski Virus Research Centre, Royal Children's Hospital, Herston
Rd., Brisbane, Queensland 4029, Australia. Phone: (617) 3253-1568. Fax:
(617) 3253-1401. E-mail:
a.khromykh{at}mailbox.uq.edu.au.
This is publication no. 96 from the Sir Albert Sakzewski Virus
Research Centre.
Journal of Virology, December 1999, p. 10272-10280, Vol. 73, No. 12
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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