Skip to main content
Log in

Ac154 carried out anti-apoptotic role during AcMNPV infection process in the host insect cells

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

AcMNPV is the first baculovirus to be sequenced and is considered a model of baculovirus. ac154 is a later expression gene in AcMNPV genome and its function is unknown. In this study, we explored the function of Ac154 in AcMNPV infection process in host Sf9 cells. The results showed that Ac154 was distributed in both nucleus and cytoplasm. Knockout of ac154 did not affect the production of BV, but the yield of progeny virus was reduced, indicating the auxiliary function of Ac154 in virus production. MTT assay showed that Ac154 promoted the proliferation and inhibited apoptosis of Sf9 cells. Overexpression of ac154 gene significantly increased the transcription level of anti-apoptotic gene p35, and delayed the expression of the pro-apoptotic protein SfP53 and reduced its expression level, which indicated its anti-apoptotic role in the host cells. In conclusion, our results demonstrated Ac154 could delay apoptosis process in host cells by regulating the transcription of p35 gene and the expression of SfP53 protein, which provided a more favorable environment for progeny virus replication and packaging, thereby promoting the proliferation of progeny virus. So we provided a potentially improved bac-to-bac eukaryotic protein expression system and biopesticide in this work.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

References

  1. Lai Q, Zhu L, Xu L, Yuan M, Wu W, Yang K (2019) AcMNPV PKIP is associated with nucleocapsid of budded virions and involved in nucleocapsid assembly. Virus Res 268:27–37

    Article  CAS  Google Scholar 

  2. Li Y, Shen S, Hu L, Deng F, Vlak JM, Hu Z, Wang H, Wang M (2018) The functional oligomeric state of tegument protein GP41 is essential for baculovirus budded virion and occlusion-derived virion assembly. J Virol 92:e02083

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Fang Z, Que Y, Li J, Zhang Z (2019) The deletion of the AcMNPV ac124 gene resulted in a decrease in chitinase transcription. Virus Res 263:151–158

    Article  CAS  Google Scholar 

  4. Wu CP, Huang YJ, Wang JY, Wu YL, Lo HR, Wang JC, Chao YC (2010) Autographa californica multiple nucleopolyhedrovirus LEF-2 is a capsid protein required for amplification but not initiation of viral DNA replication. J Virol 84:5015–5024

    Article  CAS  Google Scholar 

  5. Wang H, Xu W, Kong X, Fan Y, Wu X (2019) Bombyx mori nucleopolyhedrovirus protein Bm11 is involved in occlusion body production and occlusion-derived virus embedding. Virology 527:12–20

    Article  CAS  Google Scholar 

  6. Ono C, Kamagata T, Taka H, Sahara K, Asano S, Bando H (2012) Phenotypic grouping of 141 BmNPVs lacking viral gene sequences. Virus Res 165:197–206

    Article  CAS  Google Scholar 

  7. Mohammad M, Mazhar H, Leila M, Sassan A (2015) The baculovirus anti-apoptotic p35 protein functions as an inhibitor of the host RNA interference antiviral response. J Virol 89:8182–8192

    Article  Google Scholar 

  8. Zhang Y, Hu X, Mu J, Hu Y, Zhou Y, Zhao H, Wu C, Pei R, Chen J, Chen X, Wang Y (2018) Ac102 participates in nuclear actin polymerization by modulating BV/ODV-C42 ubiquitination during Autographa californica multiple nucleopolyhedrovirus infection. J Virol 92:e00005–e00018

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Fu Y, Wang R, Liang A (2018) Function analysis of Ac-PCNA and Sf-PCNA during the Autographa californica multiple nucleopolyhedrovirus infection process. Mol Cell Biochem 443:57–68

    Article  CAS  Google Scholar 

  10. Wu C, Wang S (2012) A pH-sensitive heparin-binding sequence from Baculovirus gp64 protein is important for binding to mammalian cells but not to Sf9 insect cells. J Virol 86:484–491

    Article  CAS  Google Scholar 

  11. Bossert M, Carstens EB (2018) Sequential deletion of AcMNPV homologous regions leads to reductions in budded virus production and late protein expression. Virus Res 256:125–133

    Article  CAS  Google Scholar 

  12. Cao L, Li X, Zheng S, Liang A, Fu Y (2016) SfP53 and filamentous actin (F-actin) are the targets of viral pesticide AcMNPV-BmK IT (P10/PH) in host Spodoptera frugiperda 9 cells. Biotechnol Lett 38:2059–2069

    Article  CAS  Google Scholar 

  13. Chen G, Yan Q, Fang Y, Wu L, Krell PJ, Feng G (2018) The N terminus of Autographa californica multiple nucleopolyhedrovirus DNA polymerase is required for efficient viral DNA replication and virus and occlusion body production. J Virol 92:e00398

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Miao Y, Liang A, Fu Y (2016) Baculovirus antiapoptotic protein P35 regulated the host apoptosis to enhance virus multiplication. Mol Cell Biochem 423:67–73

    Article  CAS  Google Scholar 

  15. Chen YR, Zhong S, Fei Z, Hashimoto Y, Xiang JZ, Zhang S, Blissard GW (2013) The transcriptome of the baculovirus Autographa californica multiple nucleopolyhedrovirus in Trichoplusia ni cells. J Virol 87:6391–6405

    Article  CAS  Google Scholar 

  16. Xing K, Deng R, Wang J, Feng J, Huang M, Wang X (2005) Analysis and prediction of baculovirus promoter sequences. Virus Res 113:64–71

    Article  CAS  Google Scholar 

  17. Mitchell JK, Byers NM, Friesen PD (2013) Baculovirus F-box protein LEF-7 modifies the host DNA damage response to enhance virus multiplication. J Virol 87:12592–12599

    Article  CAS  Google Scholar 

  18. Huang N, Wu W, Yang K, Passarelli AL, Rohrmann GF, Clem RJ (2011) Baculovirus infection induces a DNA damage response that is required for efficient viral replication. J Virol 85:12547–12556

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The present work was supported by grants from National Natural Science Foundation of China (No. 31272100) and Natural Science Foundation of Shanxi Province (No. 201801D121193) to YJ Fu. It was also supported by grants from Shanxi ‘1331 project’ Collaborative Innovation Center (1331 CIC) to Y. Fu.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yuejun Fu.

Ethics declarations

Conflict of interest

The authors have no potential conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bai, H., Liang, A. & Fu, Y. Ac154 carried out anti-apoptotic role during AcMNPV infection process in the host insect cells. Mol Cell Biochem 463, 79–90 (2020). https://doi.org/10.1007/s11010-019-03631-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11010-019-03631-7

Keywords

Navigation