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Bombyx mori nucleopolyhedrovirus Bm96 suppresses viral virulence in Bombyx mori larvae
Hiroyuki Hikida1, Ryuhei Kokusho2, Noriko Matsuda-Imai1
1Department of Agricultural and Environmental Biology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1, Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Abstract:
Bombyx mori nucleopolyhedrovirus (BmNPV) is a severe pathogen for the domestic silkworm, Bombyx mori. BmNPV harbors over 140 protein-coding genes in its 128.4 kilobase pair-long double-stranded genome. However, many BmNPV genes are still uncharacterized. Here we investigated the role of BmNPV Bm96 in both B. mori cultured cells and larvae. We found that Bm96 is mainly expressed at the late stage of infection and accumulation of Bm96 protein peaks at 24 h post infection (hpi) and declines gradually at 48 hpi in B. mori cultured cells. Compared with the wild-type viruses, Bm96-deletion viruses exhibited higher viral propagation and fast-killing phenotype in B. mori larvae. These results strongly suggest that Bm96 negatively regulates the propagation of BmNPV in B. mori larvae. Furthermore, we observed that larvae infected with Bm96-deletion viruses showed lower locomotory activity at the late stage of infection compared with those infected with the wild-type viruses.
Insights
The Bombyx mori nucleopolyhedrovirus (BmNPV) Bm96 protein negatively regulates viral propagation in silkworms. Deleting Bm96 accelerates BmNPV infection and causes a fast-killing phenotype in Bombyx mori.
Area of Science:
- Virology
- Insect Pathology
- Molecular Biology
Background:
- Bombyx mori nucleopolyhedrovirus (BmNPV) is a significant pathogen affecting the domestic silkworm, Bombyx mori.
- The BmNPV genome contains over 140 protein-coding genes, but many remain uncharacterized.
- Understanding gene function is crucial for controlling BmNPV outbreaks.
Purpose of the Study:
- To investigate the function of the uncharacterized BmNPV gene, Bm96.
- To determine the role of Bm96 in viral replication and pathogenesis in Bombyx mori cells and larvae.
Main Methods:
- Expression analysis of Bm96 protein in Bombyx mori cultured cells post-infection.
- Generation and analysis of Bm96-deletion BmNPV mutants.
- Comparison of viral propagation and lethality between wild-type and Bm96-deletion viruses in Bombyx mori larvae.
- Assessment of larval locomotory activity.
Main Results:
- Bm96 protein expression is highest at 24 hours post-infection and declines by 48 hours post-infection in cultured cells.
- Bm96-deletion viruses showed increased viral propagation in Bombyx mori larvae.
- Larvae infected with Bm96-deletion viruses exhibited a fast-killing phenotype.
- A reduction in locomotory activity was observed in larvae infected with Bm96-deletion viruses.
Conclusions:
- Bm96 negatively regulates the propagation of BmNPV in Bombyx mori larvae.
- The Bm96 gene plays a critical role in the BmNPV life cycle and pathogenesis.
- Further research into Bm96 could lead to novel strategies for managing BmNPV infections in silkworms.
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