Isolation and characterization of a novel strain (YH01) of Micropterus salmoides rhabdovirus and expression of its glycoprotein by the baculovirus expression system
Autor: | Xiaoying Hang, Weida Shi, Yinglei Wu, Li Liu, Haiqi Zhang, Yuan Xuemei, Lyu Sunjian |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Carps Insecta viruses Sf9 Genome Viral Biology Recombinant virus Article General Biochemistry Genetics and Molecular Biology Virus Cell Line law.invention 03 medical and health sciences 0302 clinical medicine Plasmid law Animals General Pharmacology Toxicology and Pharmaceutics Gene Phylogeny Polymerase chain reaction Glycoproteins chemistry.chemical_classification General Veterinary Ovary General Medicine Virology Recombinant Proteins 030104 developmental biology Genetic Techniques chemistry 030220 oncology & carcinogenesis Recombinant DNA Bass Female Rhabdoviridae Glycoprotein Baculoviridae Plasmids |
Zdroj: | Journal of Zhejiang University-SCIENCE B. 20:728-739 |
ISSN: | 1862-1783 1673-1581 |
DOI: | 10.1631/jzus.b1900027 |
Popis: | As one of the most important aquatic fish, Micropterus salmoides suffers lethal and epidemic disease caused by rhabdovirus at the juvenile stage. In this study, a new strain of M. salmoides rhabdovirus (MSRV) was isolated from Yuhang, Zhejiang Province, China, and named MSRV-YH01. The virus infected the grass carp ovary (GCO) cell line and displayed virion particles with atypical bullet shape, 300-500 nm in length and 100-200 nm in diameter under transmission electron microscopy. The complete genome sequence of this isolate was determined to include 11 526 nucleotides and to encode five classical structural proteins. The construction of the phylogenetic tree indicated that this new isolate is clustered into the Vesiculovirus genus and most closely related to the Siniperca chuatsi rhabdovirus. To explore the potential for a vaccine against MSRV, a glycoprotein (1-458 amino acid residues) of MSRV-YH01 was successfully amplified and cloned into the plasmid pFastBac1. The high-purity recombinant bacmid-glycoprotein was obtained from DH10Bac through screening and identification. Based on polymerase chain reaction (PCR), western blot, and immunofluorescence assay, recombinant virus, including the MSRV-YH01 glycoprotein gene, was produced by transfection of SF9 cells using the pFastBac1-gE2, and then repeatedly amplified to express the glycoprotein protein. We anticipate that this recombinant bacmid system could be used to challenge the silkworm and develop a corresponding oral vaccine for fish. |
Databáze: | OpenAIRE |
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