Generation and characterization of a new mammalian cell line continuously expressing virus-like particles of Japanese encephalitis virus for a subunit vaccine candidate

• Published in: BMC biotechnology Vol. 14; no. 1; p. 62
• Main Authors: Hua, Rong-Hong, Li, Ye-Nan, Chen, Zhen-Shi, Liu, Li-Ke, Huo, Hong, Wang, Xiao-Lei, Guo, Li-Ping, Shen, Nan, Wang, Jing-Fei, Bu, Zhi-Gao
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 10.07.2014; BioMed Central
• Subjects: Animals; Antibodies, Neutralizing - immunology; Antibodies, Neutralizing - metabolism; Antigens; Cell Line; Cloning; Cricetinae; Encephalitis Virus, Japanese - metabolism; Female; Flow cytometry; Genetic aspects; Genetic engineering; Hogs; Immunization; Infections; Japanese Encephalitis Vaccines - biosynthesis; Japanese Encephalitis Vaccines - genetics; Japanese Encephalitis Vaccines - immunology; Japanese encephalitis virus; Membrane Glycoproteins - genetics; Membrane Glycoproteins - metabolism; Mice; Mice, Inbred BALB C; Microscopy; Protein expression; Proteins; Recombinant Proteins - biosynthesis; Recombinant Proteins - genetics; Rodents; Vaccines; Vaccines, Virus-Like Particle - biosynthesis; Vaccines, Virus-Like Particle - genetics; Vaccines, Virus-Like Particle - immunology; Viral Envelope Proteins - genetics; Viral Envelope Proteins - metabolism; Viral Matrix Proteins - genetics; Viral Matrix Proteins - metabolism
• ISSN: 1472-6750; 1472-6750
• DOI: 10.1186/1472-6750-14-62

Japanese encephalitis virus (JEV) is the most important cause of epidemic encephalitis in most Asian regions. There is no specific treatment available for Japanese encephalitis, and vaccination is the only effective way to prevent JEV infection in humans and domestic animals. The purpose of this study is to establish a new mammalian cell line stably and efficiently expressing virus-like particle of JEV for potential use of JEV subunit vaccine. We generated a new cell clone (BJ-ME cells) that stably produces a secreted form of Japanese encephalitis virus (JEV) virus-like particle (VLP). The BJ-ME cells were engineered by transfecting BHK-21 cells with a code-optimized cDNA encoding JEV prM and E protein expression plasmid. Cell line BJ-ME can stably produces a secreted form of Japanese encephalitis virus virus-like particle (JEV-VLP) which contains the JEV envelope glycoprotein (E) and membrane protein (M). The amount of JEV-VLP antigen released into the culture fluid of BJ-ME cells was as high as 15-20 μg/ml. JEV-VLP production was stable after multiple cell passages and 100% cell expression was maintained without detectable cell fusion or apoptosis. Cell culture fluid containing the JEV-VLP antigen could be harvested five to seven times continuously at intervals of 4-6 days while maintaining the culture. Mice immunized with the JEV-VLP antigen with or without adjuvant developed high titers of neutralizing antibodies and 100% protection against lethal JEV challenge. These results suggest that the recombinant JEV-VLP antigen produced by the BJ-ME cell line is an effective, safe and affordable subunit Japanese encephalitis vaccine candidate, especially for domestic animals such as pig and horse.