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SfP53 and filamentous actin (F-actin) are the targets of viral pesticide AcMNPV-<Emphasis Type="Italic">Bm</Emphasis>K IT (P10/PH) in host <Emphasis Type="Italic">Spodoptera frugiperda</Emphasis> 9 cells
Authors:Leixi Cao  Xing Li  Shuhua Zheng  Aihua Liang  Yuejun Fu
Institution:1.Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Institute of Biotechnology,Shanxi University,Taiyuan,People’s Republic of China;2.University of Miami Miller School of Medicine,Miami,USA
Abstract:

Objectives

To analyze the anti-insect mechanism of viral pesticide AcMNPV-BmK IT(P10/PH) in the host Spodoptera frugiperda 9 (Sf9) cells.

Results

Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV)- mediated expression of BmK IT, regulated by P10 protein promoter (P10) and polyhedrosis promoter (PH), promoted the replication of progeny virus in host Sf9 cells. AcMNPV-BmK IT(P10) could accelerate the budding process (or speed) of budded virus (BV) in Sf9 cells. The impact of AcMNPV-BmK IT(P10) on the nuclear polymerization of filamentous actin (F-actin) participated in regulating the accelerated budding process. Unexpectedly, both AcMNPV-BmK IT(P10) and AcMNPV-BmK IT(PH) delayed the nuclear polymerization of F-actin and promoted the clearance of F-actin in the nucleus. SfP53, an important apoptosis factor, was involved in the regulation of AcMNPV-BmK IT(P10/PH) in Sf9 cells. AcMNPV-BmK IT(P10/PH) could also delay and promote the nuclear recruitment of SfP53 after 27 h post infection (h p.i.).

Conclusion

SfP53 and F-actin are the targets of viral pesticide AcMNPV-BmK IT (P10/PH) in host Sf9 cells, which provides the experimental basis for the development of recombinant baculovirus biopesticides.
Keywords:
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