期刊论文详细信息
PLoS One
Low Temperature-Dependent Salmonid Alphavirus Glycoprotein Processing and Recombinant Virus-Like Particle Formation
Marielle C. van Hulten1  Joseph Koumans1  Stephane Villoing2  Stefan W. Metz3  Just M. Vlak3  Femke Feenstra3  Gorben P. Pijlman3  Jan W. van Lent3 
[1]Intervet International BV, Boxmeer, The Netherlands
[2]Intervet Norbio, Bergen, Norway
[3]Laboratory of Virology, Wageningen University, Wageningen, The Netherlands
关键词: Insects;    Recombinant proteins;    Glycoproteins;    Baculoviruses;    Fish farming;    Protein expression;    Viral packaging;    Transmission electron microscopy;   
DOI  :  10.1371/journal.pone.0025816
学科分类:医学(综合)
来源: Public Library of Science
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【 摘 要 】
Pancreas disease (PD) and sleeping disease (SD) are important viral scourges in aquaculture of Atlantic salmon and rainbow trout. The etiological agent of PD and SD is salmonid alphavirus (SAV), an unusual member of the Togaviridae (genus Alphavirus). SAV replicates at lower temperatures in fish. Outbreaks of SAV are associated with large economic losses of ∼17 to 50 million $/year. Current control strategies rely on vaccination with inactivated virus formulations that are cumbersome to obtain and have intrinsic safety risks. In this research we were able to obtain non-infectious virus-like particles (VLPs) of SAV via expression of recombinant baculoviruses encoding SAV capsid protein and two major immunodominant viral glycoproteins, E1 and E2 in Spodoptera frugiperda Sf9 insect cells. However, this was only achieved when a temperature shift from 27°C to lower temperatures was applied. At 27°C, precursor E2 (PE2) was misfolded and not processed by host furin into mature E2. Hence, E2 was detected neither on the surface of infected cells nor as VLPs in the culture fluid. However, when temperatures during protein expression were lowered, PE2 was processed into mature E2 in a temperature-dependent manner and VLPs were abundantly produced. So, temperature shift-down during synthesis is a prerequisite for correct SAV glycoprotein processing and recombinant VLP production.
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