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Functional analysis of a miRNA-like small RNA derived from Bombyx mori cytoplasmic polyhedrosis virus
Jian-Yong Guo1,2, Yong-Sheng Wang1,2, Tian Chen1
1School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang, China.
Abstract:
Bombyx mori cytoplasmic polyhedrosis virus (BmCPV) is a major pathogen of the economic insect silkworm, Bombyx mori. Virus-encoded microRNAs (miRNAs) have been proven to play important roles in host-pathogen interactions. In this study we identified a BmCPV-derived miRNA-like 21 nt small RNA, BmCPV-miR-1, from the small RNA deep sequencing of BmCPV-infected silkworm larvae by stem-loop quantitative real-time PCR (qPCR) and investigated its functions with qPCR and lentiviral expression systems. Bombyx mori inhibitor of apoptosis protein (BmIAP) gene was predicted by both target prediction software miRanda and Targetscan to be one of its target genes with a binding site for BmCPV-miR-1 at the 5' untranslated region. It was found that the expression of BmCPV-miR-1 and its target gene BmIAP were both up-regulated in BmCPV-infected larvae. At the same time, it was confirmed that BmCPV-miR-1 could up-regulate the expression of BmIAP gene in HEK293T cells with lentiviral expression systems and in BmN cells by transfecting mimics. Furthermore, BmCPV-miR-1 mimics could up-regulate the expression level of BmIAP gene in midgut and fat body in the silkworm. In the midgut of BmCPV-infected larvae, BmCPV-miR-1 mimics could be further up-regulated and inhibitors could lower the virus-mediated expression of BmIAP gene. With the viral genomic RNA segments S1 and S10 as indicators, BmCPV-miR-1 mimics could up-regulate and inhibitors down-regulate their replication in the infected silkworm. These results implied that BmCPV-miR-1 could inhibit cell apoptosis in the infected silkworm through up-regulating BmIAP expression, providing the virus with a better cell circumstance for its replication.
Insights
A novel virus-encoded microRNA, BmCPV-miR-1, from Bombyx mori cytoplasmic polyhedrosis virus (BmCPV) up-regulates the inhibitor of apoptosis protein (BmIAP) to promote viral replication. This mechanism helps the virus evade apoptosis and create a favorable environment for its proliferation in silkworms.
Area of Science:
- Virology
- Molecular Biology
- Insect Pathology
Background:
- Bombyx mori cytoplasmic polyhedrosis virus (BmCPV) is a significant silkworm pathogen.
- Virus-derived microRNAs (miRNAs) play crucial roles in host-pathogen interactions.
- Understanding viral small RNAs is key to controlling silkworm diseases.
Purpose of the Study:
- To identify and characterize a novel miRNA-like small RNA from BmCPV.
- To investigate the function of this viral small RNA in silkworm infection.
- To elucidate the molecular mechanism of BmCPV pathogenesis.
Main Methods:
- Small RNA deep sequencing and stem-loop quantitative real-time PCR (qPCR) for identification.
- Target prediction software (miRanda, Targetscan) for identifying target genes.
- Lentiviral expression systems, mimics, and inhibitors for functional studies in cell lines and silkworms.
Main Results:
- A 21 nt small RNA, BmCPV-miR-1, was identified from BmCPV-infected silkworms.
- The Bombyx mori inhibitor of apoptosis protein (BmIAP) was confirmed as a target of BmCPV-miR-1.
- BmCPV-miR-1 up-regulates BmIAP expression, inhibits apoptosis, and enhances viral replication in silkworms.
Conclusions:
- BmCPV-miR-1 promotes viral replication by up-regulating BmIAP and inhibiting host cell apoptosis.
- This viral miRNA provides a favorable cellular environment for BmCPV proliferation.
- BmCPV-miR-1 represents a novel target for managing silkworm diseases.
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