bmnpv-miR-3 facilitates BmNPV infection by modulating the expression of viral P6.9 and other late genes in Bombyx mori

被引:52
作者
Singh, C. P. [1 ]
Singh, J. [2 ]
Nagaraju, J. [1 ]
机构
[1] Ctr DNA Fingerprinting & Diagnost, Mol Genet Lab, Ctr Excellence Genet & Genom Silkmoths, Hyderabad 500001, Andhra Pradesh, India
[2] Univ Pune Campus, Natl Ctr Cell Sci, Pune 411007, Maharashtra, India
关键词
miRNA; Bombyx mori; Baculovirus; BmNPV; P6.9; NUCLEAR POLYHEDROSIS-VIRUS; DNA-BINDING PROTEIN; RNA-INTERFERENCE; IMMUNE-SYSTEM; C-ELEGANS; NUCLEOPOLYHEDROVIRUS INFECTION; MICRORNA FUNCTIONS; ENCODED MICRORNAS; CELLS; IDENTIFICATION;
D O I
10.1016/j.ibmb.2014.03.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During the last decade, microRNAs (miRNAs) have emerged as fine tuners of gene expression in various biological processes including host pathogen interactions. Apart from the role of host encoded miRNAs in host virus interactions, recent studies have also indicated the key role of virus-encoded miRNAs in the regulation of host defense responses. In the present study, we show that bmnpv-miR-3, a Bombyx mod nucleopolyhedrovirus (BmNPV) encoded miRNA, regulates the expression of DNA binding protein (P6.9) and other late genes, vital for the late stage of viral infection in the host, Bombyx mori. We have performed both cell culture and in vivo experiments to establish the role of bmnpv-miR-3 in the infection cycle of BmNPV. Our findings showed that bmnpv-miR-3 expresses during early stage of infection, and negatively regulates the expression of P6.9. There was an upregulation in P6.9 expression upon blocking of bmnpv-miR-3 by Locked Nucleic Acid (LNA), whereas overexpression of bmnpv-miR-3 resulted in a decreased expression of P6.9. Besides, a remarkable enhancement and reduction in the viral loads were observed upon blocking and overexpression of bmnpv-miR-3, respectively. Furthermore, we have also assessed the host immune response using one of the Lepidoptera-specific antimicrobial proteins, Gloverin-1 upon blocking and overexpression of bmnpv-miR-3, which correlated viral load with the host immune response. All these results together; clearly imply that bmnpv-miR-3-mediated controlled regulation of BmNPV late genes in the early stage of infection helps BmNPV to escape the early immune response from the host. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:59 / 69
页数:11
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