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Journal of Virology, August 2005, p. 10077-10082, Vol. 79, No. 15
0022-538X/05/$08.00+0 doi:10.1128/JVI.79.15.10077-10082.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Hadassah Rivkin, and
Nor Chejanovsky*
Entomology Department, Institute of Plant Protection, ARO, The Volcani Center, POB 6 Bet Dagan 50250, Israel
Received 2 July 2004/ Accepted 25 April 2005
The role of the Autographa californica multiple nucleopolyhedrovirus (AcMNPV) immediate-early protein IE0 in the baculoviral infection is not clear. In this study, we constructed the recombinant virus vAc
ie0 null for ie0 expression by targeted mutagenesis replacing exon0 with the cat gene. We found that vAc
ie0 replicated efficiently in Spodoptera littoralis SL2 cells, which are poorly permissive for AcMNPV. In contrast, in Spodoptera frugiperda SF9 cells, which are fully permissive for AcMNPV, vAc
ie0 DNA replication and budded virus production were delayed. These results and recently published data (X. Dai et al., J. Virol. 78:9633-9644, 2004) indicate that ie0 is not essential for AcMNPV replication but enhances it in permissive SF9 cells.
Contribution 507/04 from the Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel.
Present address: Animal Health Biotechnology Unit, Temasek Life Sciences Laboratory, National University of Singapore, 1 Research Link, Singapore 117604.
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