Bombyx mori Nucleopolyhedrovirus (BmNPV) Induces G2/M Arrest to Promote Viral Multiplication by Depleting BmCDK1.
Bombyx mori Nucleopolyhedrovirus (BmNPV) Induces G2/M Arrest to Promote Viral Multiplication by Depleting BmCDK1.
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家蚕核多角体病毒 (BmNPV) 通过消耗 BmCDK1 诱导 G2/M 阻滞以促进病毒增殖
DOI:
10.3390/insects12121098
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发表时间:
2021-12-08
期刊:
影响因子:
3
通讯作者:
Pan MH
中科院分区:
文献类型:
--
作者:
Xiao Q;Dong ZQ;Zhu Y;Zhang Q;Yang X;Xiao M;Chen P;Lu C;Pan MH
Simple Summary Baculoviruses arrest the cell cycle in the S or G2/M phase in insect cells, but the exact mechanism of this process still remains obscure. Bombyx mori nucleopolyhedrovirus (BmNPV), one of the best characterized baculoviruses, is an important pathogen in silkworms. In the present study, we determined that downregulation of BmCDK1 and BmCyclin B expression was required for BmNPV-mediated G2/M phase arrest, which plays an essential role in facilitating BmNPV replication. Further investigations showed that BmNPV IAP1 interacted with BmCDK1. The overexpression of the BmNPV iap1 gene led to the accumulation of cells in the G2/M phase, and BmNPV iap1 gene knockdown attenuated the effect of BmNPV-mediated G2/M phase arrest. These findings enhance the understanding of BmNPV pathogenesis, and indicate a novel mechanism through which baculoviruses impact the cell cycle progression. Abstract Understanding virus–host interaction is very important for delineating the mechanism involved in viral replication and host resistance. Baculovirus, an insect virus, can cause S or G2/M phase arrest in insect cells. However, the roles and mechanism of Baculovirus-mediated S or G2/M phase arrest are not fully understood. Our results, obtained using flow cytometry (FCM), tubulin-labeling, BrdU-labeling, and CellTiter 96® AQueous One Solution Cell Proliferation Assay (MTS), showed that Bombyx mori nucleopolyhedrovirus (BmNPV) induced G2/M phase arrest and inhibited cellular DNA replication as well as cell proliferation in BmN-SWU1 cells. We found that BmNPV induced G2/M arrest to support its replication and proliferation by reducing the expression of BmCDK1 and BmCyclin B. Co-immunoprecipitation assays confirmed that BmNPV IAP1 interacted with BmCDK1. BmNPV iap1 was involved in the process of BmNPV-induced G2/M arrest by reducing the content of BmCDK1. Taken together, our results improve the understanding of the virus–host interaction network, and provide a potential target gene that connects apoptosis and the cell cycle.
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DOI:
10.1074/jbc.m117.776112
发表时间:
2017-03-24
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Fan Y;Mok CK;Chan MC;Zhang Y;Nal B;Kien F;Bruzzone R;Sanyal S
通讯作者:
Sanyal S
影响因子:
5.4
作者:
Chen, CJ;Makino, S
通讯作者:
Makino, S
影响因子:
2.8
作者:
Li, Gang;Zhou, Kaiyue;Xu, Anying
通讯作者:
Xu, Anying
影响因子:
5.4
作者:
Dove, B;Brooks, G;Hiscox, JA
通讯作者:
Hiscox, JA
影响因子:
64.8
作者:
LEE, MG;NORBURY, CJ;NURSE, P
通讯作者:
NURSE, P