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Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
Bombyx mori nucleopolyhedrovirus BM5 protein regulates progeny virus production and viral gene expression
Ryuhei Kokusho1, Yoshikazu Koh1, Masaru Fujimoto1
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) orf5 (Bm5) is a core gene of lepidopteran baculoviruses and encodes the protein with the conserved amino acid residues (DUF3627) in its C-terminus. Here, we found that Bm5 disruption resulted in lower titers of budded viruses and fewer numbers of occlusion bodies (OBs) in B. mori cultured cells and larvae, although viral genome replication was not affected. Bm5 disruption also caused aberrant expression of various viral genes at the very late stage of infection. Immunocytochemical analysis revealed that BM5 localized to the nuclear membrane. We also found that DUF3627 is important for OB production, transcriptional regulation of viral genes, and subcellular localization of BM5. Compared with wild-type BmNPV infection, larval death was delayed when B. mori larvae were infected with Bm5 mutants. These results suggest that BM5 is involved in progeny virus production and regulation of viral gene expression at the very late stage of infection.
Insights
The Bombyx mori nucleopolyhedrovirus (BmNPV) orf5 (Bm5) protein is crucial for producing progeny viruses and occlusion bodies. Its disruption affects viral gene expression and delays host larval death.
Area of Science:
- Virology
- Molecular Biology
- Insect Pathology
Background:
- Bombyx mori nucleopolyhedrovirus (BmNPV) is a significant pathogen affecting silkworms.
- orf5 (Bm5) is a core gene in lepidopteran baculoviruses, encoding a protein with a conserved DUF3627 domain.
- The function of Bm5 in the viral life cycle remains largely uncharacterized.
Purpose of the Study:
- To investigate the role of the Bm5 protein in BmNPV replication and pathogenesis.
- To elucidate the function of the DUF3627 domain within the BM5 protein.
Main Methods:
- Generation and characterization of Bm5 deletion mutants in B. mori.
- Quantification of viral titers and occlusion bodies (OBs) in infected cells and larvae.
- Analysis of viral gene expression using transcriptomic approaches.
- Immunocytochemical localization of the BM5 protein.
Main Results:
- Bm5 disruption significantly reduced budded virus titers and occlusion body formation.
- Viral genome replication was unaffected, but late-stage viral gene expression was aberrant.
- BM5 protein was localized to the nuclear membrane.
- The DUF3627 domain is essential for OB production, viral gene regulation, and BM5 localization.
- Bm5 mutants delayed larval mortality compared to wild-type BmNPV.
Conclusions:
- BM5 plays a critical role in progeny virus production, particularly OB assembly.
- BM5 is involved in regulating viral gene expression during the late stages of infection.
- The BM5 protein, via its DUF3627 domain, influences baculovirus pathogenesis and host-pathogen interactions.
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