Characterization of the gene encoding the envelope fusion glycoprotein GP64 from Bombyx mori nucleopolyhedrovirus
Md Masmudur Rahman1, Karumathil P Gopinathan
1Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India.
Abstract:
We describe here the characterization of the gene gp64 encoding the envelope fusion protein GP64 (open reading frame) ORF 105 from Bombyx mori nucleopolyhedrovirus (BmNPV). gp64 was transcribed from the early to late stages of infection and the transcripts were seen from 6 to 72 h post infection (hpi). The early transcripts initiated from a consensus CAGT motif while the late transcripts arose from three conserved TAAG motifs, all of which were located in the near upstream region of the coding sequence. Both early and late transcripts terminated at a run of T residues following the second polyadenylation signal located 31 nt downstream of the translation termination codon. BmGP64 protein was detectable from 6 hpi and was present in larger quantities throughout the infection process from 12 hpi, in BmNPV-infected BmN cells. The persistent presence of GP64 in BmN cells differed from the protein expression pattern of GP64 in Autographa californica multinucleocapsid nucleopolyhedrovirus infection, where the protein levels decreased significantly by late times (48 hpi). BmGP64 was located in the membrane and cytoplasm of the infected host cells and as a component of the budded virions. The production of infectious budded virus and the fusion activity were reduced when glycosylation of GP64 was inhibited.
Insights
The Bombyx mori nucleopolyhedrovirus (BmNPV) envelope fusion protein GP64 is expressed throughout infection, unlike in other viruses. Its glycosylation is crucial for viral infectivity and fusion.
Area of Science:
- Virology
- Molecular Biology
- Insect Pathology
Background:
- The envelope fusion protein GP64 is essential for nucleopolyhedrovirus infection.
- Understanding GP64 expression and function in Bombyx mori nucleopolyhedrovirus (BmNPV) is key to viral pathogenesis.
Purpose of the Study:
- To characterize the gene encoding the BmNPV envelope fusion protein GP64.
- To investigate the transcription, translation, and localization of BmGP64.
- To determine the role of GP64 glycosylation in viral infectivity and cell fusion.
Main Methods:
- Gene characterization of gp64 in BmNPV.
- Analysis of gp64 transcription and transcript termination.
- Detection and localization of BmGP64 protein in infected cells.
- Assessment of viral infectivity and fusion activity upon glycosylation inhibition.
Main Results:
- gp64 gene transcription occurs from early to late infection stages (6–72 hpi).
- BmGP64 protein is detectable from 6 hpi and abundant from 12 hpi, persisting throughout infection.
- BmGP64 localizes to the membrane, cytoplasm, and budded virions.
- Inhibition of GP64 glycosylation reduces infectious budded virus production and fusion activity.
Conclusions:
- BmGP64 exhibits a distinct expression pattern compared to other baculoviruses.
- GP64 glycosylation is vital for BmNPV infectivity and cell-to-cell fusion.
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