Efficient Expression and Processing of Ebola Virus Glycoprotein Induces Morphological Changes in BmN Cells but Cannot Rescue Deficiency of Bombyx Mori Nucleopolyhedrovirus GP64
Autor: | Xingjia Shen, Sun Luping, Ellen Ayepa, Na Liu, Miao Yang, Yaqin Shen, Charles Amanze, Bifang Hao, Shuwen Yang, Jinshan Huang, Fanbo Xu |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Signal peptide glycoprotein viruses 030106 microbiology Cell lcsh:QR1-502 Gene Expression Biology medicine.disease_cause Virus Replication Article lcsh:Microbiology law.invention Cell Line Cell membrane 03 medical and health sciences Viral Proteins Ebola virus baculovirus law Virology medicine Animals signal peptide Cells Cultured Glycoproteins chemistry.chemical_classification Infectivity fungi Transfection Ebolavirus Nucleopolyhedroviruses Recombinant Proteins 030104 developmental biology Infectious Diseases medicine.anatomical_structure chemistry Gene Knockdown Techniques Recombinant DNA Microbial Interactions Glycoprotein Protein Processing Post-Translational |
Zdroj: | Viruses Volume 11 Issue 11 Viruses, Vol 11, Iss 11, p 1067 (2019) |
ISSN: | 1999-4915 |
DOI: | 10.3390/v11111067 |
Popis: | Ebola virus (EBOV) disease outbreaks have resulted in many fatalities, yet no licensed vaccines are available to prevent infection. Recombinant glycoprotein (GP) production may contribute to finding a cure for Ebola virus disease, which is the key candidate protein for vaccine preparation. To explore GP1,2 expression in BmN cells, EBOV-GP1,2 with its native signal peptide or the GP64 signal peptide was cloned and transferred into a normal or gp64 null Bombyx mori nucleopolyhedrovirus (BmNPV) bacmid via transposition. The infectivity of the recombinant bacmids was investigated after transfection, expression and localization of EBOV-GP were investigated, and cell morphological changes were analyzed by TEM. The GP64 signal peptide, but not the GP1,2 native signal peptide, caused GP1,2 localization to the cell membrane, and the differentially localized GP1,2 proteins were cleaved into GP1 and GP2 fragments in BmN cells. GP1,2 expression resulted in dramatic morphological changes in BmN cells in the early stage of infection. However, GP1,2 expression did not rescue GP64 deficiency in BmNPV infection. This study provides a better understanding of GP expression and processing in BmN cells, which may lay a foundation for EBOV-GP expression using the BmNPV baculovirus expression system. |
Databáze: | OpenAIRE |
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