Abstract
DNA polymerase (DNApol) is present in all baculoviruses and plays a crucial role in viral DNA replication. Previously we showed that the DNApol of the alphabaculovirus group II Spodoptera litura nucleopolyhedrovirus (SpltNPV) could partially substitute for the DNApol of a group I alphabaculovirus, Autographa californica multiple nucleopolyhedrovirus (AcMNPV). However, it is not known if a betabaculovirus DNApol could subsititute for the alphabaculovirus DNApol in AcMNPV. In this report, DNApol of the betabaculovirus Pieris rapae granulovirus (PiraGV) was inserted into a dnapol-null AcMNPV bacmid, creating Bac-AcΔpol:PrPol. The repair virus did not spread to neighboring cells; virus growth curve and real-time PCR revealed that the PiraGV dnapol substitution abrogated AcMNPV DNA replication and virus production. Immunofluorescence microscopy showed that PiraGV DNApol could be expressed and localized to the nucleus. Collectively, our results suggested that the alphabaculovirus AcMNPV DNApol could not be replaced by a DNApol from the betabaculovirus, PiraGV.
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Acknowledgements
We thank Professor Baoshan Chen (College of Life Science and Technology, Guangxi University) for his generous gift of the PiraGV genome DNA used in this study.
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This research was supported by a National Natural Science Foundation of China (No. 31572006), incremental project of Chinese Academy of Agricultural Sciences (No. 2015ZL058), innovation project of Chinese Academy of Agricultural Sciences, and the Central Level Public Interest Research Institute for Basic R & D Special Fund Business (Nos. 2013RG001-2, 2014RG002-3).
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Chen, G., Fang, Y., Wu, L. et al. A betabaculovirus DNA polymerase cannot substitute for the DNA polymerase of the alphabaculovirus Autographa californica nucleopolyhedrovirus. Arch Virol 162, 3487–3492 (2017). https://doi.org/10.1007/s00705-017-3468-0
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DOI: https://doi.org/10.1007/s00705-017-3468-0