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The Bombyx mori nucleopolyhedrovirus (BmNPV) ODV-E56 envelope protein is also a per os infectivity factor
Xingwei Xiang1, Lin Chen, Aiqin Guo
1College of Animal Sciences, Zhejiang University, Huajiachi Campus, Hangzhou 310029, PR China.
Abstract:
The Bombyx mori nucleopolyhedrovirus (BmNPV) odv-e56 gene is a late gene and encodes an occlusion-derived virus (ODV)-specific envelope protein, ODV-E56. To determine its role in the BmNPV life cycle, an odv-e56 null virus, BmE56D, was constructed through homologous recombination. A repaired virus was also constructed, named BmE56DR. The production of budded virion (BV) and polyhedra, the replication of viral DNA, and the morphological of infected BmN cells were analyzed, revealing no significant difference among the BmE56D, the wild-type (WT), and the BmE56DR virus. Larval bioassays demonstrated that injection of BmE56D BV into the hemocoel could kill B. mori larvae as efficiently as repaired and WT viruses, however BmE56D was unable to infect the B. mori larvae when inoculated per os. Thus, these results indicated that ODV-E56 envelope protein of BmNPV is also a per os infectivity factor (PIF), but is not essential for virus replication.
Insights
The Bombyx mori nucleopolyhedrovirus ODV-E56 envelope protein is crucial for per os infection in silkworm larvae. While essential for oral infection, it is not required for viral replication within the insect.
Area of Science:
- Virology
- Insect Pathology
- Molecular Biology
Background:
- Bombyx mori nucleopolyhedrovirus (BmNPV) is a significant pathogen of silkworms.
- The odv-e56 gene encodes the ODV-E56 envelope protein, a late viral gene product.
Purpose of the Study:
- To elucidate the role of the ODV-E56 envelope protein in the BmNPV life cycle.
- To investigate the necessity of ODV-E56 for viral replication and infectivity.
Main Methods:
- Construction of an odv-e56 null virus (BmE56D) and a repaired virus (BmE56DR) via homologous recombination.
- Analysis of budded virion (BV) and polyhedra production, viral DNA replication, and cell morphology.
- Larval bioassays using per os inoculation and hemocoel injection.
Main Results:
- No significant differences in BV/polyhedra production, viral DNA replication, or cell morphology between BmE56D, WT, and BmE56DR viruses.
- BmE56D BV efficiently killed larvae upon injection into the hemocoel.
- BmE56D failed to infect larvae when administered per os.
Conclusions:
- The ODV-E56 envelope protein is a per os infectivity factor (PIF) for BmNPV.
- ODV-E56 is not essential for viral replication within Bombyx mori cells.
- This protein plays a critical role in the oral route of BmNPV infection.
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