Characterisation of extracellular vesicles in baculovirus infection of Spodoptera frugiperda cells

九氟化硫 夜蛾 苜蓿银纹夜蛾 生物 杆状病毒科 转染 病毒学 病毒 病毒包膜 重组DNA 细胞生物学 细胞培养 核型多角体病毒 分子生物学 基因 遗传学
作者
Lex J. C. Van Es,Robert D. Possee,Linda A. King
出处
期刊:Journal of extracellular biology [Wiley]
卷期号:3 (7)
标识
DOI:10.1002/jex2.163
摘要

Abstract Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is an enveloped DNA virus of the Baculoviridae family. This baculovirus is widely exploited for the biological control of insect pest species and as an expression platform to produce recombinant proteins in insect cells. Extracellular vesicles (EVs) are secreted by all cells and are involved in key roles in many biological processes through their cargo consisting of proteins, RNA or DNA. In viral infections, EVs have been found to transfer both viral and cellular cargo that can elicit either a pro‐ or antiviral response in recipient cells. Here, small EVs (sEVs) released by Spodoptera frugiperda (Sf) insect cells were characterised for the first time. Using S. frugiperda (SfC1B5) cells stably expressing the baculovirus gp64 , the viral envelope protein GP64 was shown to be incorporated into sEVs. Sf9 cells were also transfected with a bacmid AcMNPV genome lacking p6.9 (AcΔP6.9) to prevent budded virus production. The protein content of sEVs from both mock‐ and AcΔP6.9‐transfected cells were analysed by mass spectrometry. In addition to GP64, viral proteins Ac‐F, ME‐53 and viral ubiquitin were identified, as well as many host proteins including TSG101—which may be useful as a protein marker for sEVs.
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