Abstract
Objectives
To analyze the mechanisms underlying the impact of recombinant Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV)-mediated BmK IT expression on the function of baculovirus GP64 envelope fusion protein and progeny virus production.
Results
Viral propagation assay indicated that overexpression GP64 could promote replication of AcMNPV. AcMNPV-mediated expression of BmK IT also promoted replication of AcMNPV. Immunofluorescence analysis showed BmK IT, which was regulated by very early promoter IE1 in AcMNPV, could make the GP64 protein move to the cytomembrane soon after transfection. BmK IT, which is regulated by P10 protein promoter (P10) and polyhedrosis promoter (PH), could promote the expression of GP64.
Conclusion
BmK IT, regulated by very early promoter IE1, P10 protein promoter (P10) and PH, accelerated the expression of GP64 protein, promoted its early cytomembrane localization and then triggered virus budding and progeny virus production.
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Acknowledgments
This project was supported by grants from ‘National Natural Science Foundation of China (No.31272100, 31372199 and 31400765)’, ‘Natural Science Foundation of Shanxi Province (No.2014011038-1)’, and ‘the Program for the Top Young Academic Leaders of Higher Learning Institutions of Shanxi’.
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Fu, Y., Miao, Y., Zheng, S. et al. AcMNPV-BmK IT improves the progeny virus production via baculovirus GP64 envelope fusion protein. Biotechnol Lett 38, 1673–1681 (2016). https://doi.org/10.1007/s10529-016-2146-8
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DOI: https://doi.org/10.1007/s10529-016-2146-8