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J Vet Sci. 2005 Jun;6(2):125-133 |
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Immunogenicity of baculovirus expressed recombinant proteins of Japanese encephalitis virus in mice
Dong-Kun Yang1,*, Chang-Hee Kweon1, Byoung-Han Kim1, Seong-In Lim1, Jun-Hun Kwon1, Seong-Hee Kim1, Jae-Young Song1, Hong-Ryul Han2 |
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1National Veterinary Research and Quarantine Service, Ministry of Agriculture and Forestry, Anyang 430-824, Korea. 2Department of Veterinary Internal Medicine, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea. |
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Genes encoding for the premembrane and envelope
(prME), envelope (E) and nonstructural protein (NS1) of
Japanese encephalitis virus (JEV) were cloned. Each
protein was expressed in baculovirus expression system. Of
the three proteins expressed in baculovirus system, only
prME had hemagglutination activity. The prME (72 and
54 kDa), E (54 kDa) and NS1 (46 kDa) proteins could be
detected by Western blotting in the recombinant virus
infected cells. Immunogenicity of the recombinant proteins
obtained from infected Spodoptera frugiperda (Sf-9) cells
was examined in mice. The 3 week-old ICR mice
immunized intraperitoneally with three recombinant
proteins three times were challenged with a lethal JEV. A
survival rate was increased from about 7.7% in unimmunized
mice to 92.3% in E + prME and only E groups. The
complete protection was shown in prME and live vaccine
inoculated groups, respectively. We also measured
neutralizing antibody and three immunoglobulin subtypes
of IgG1, IgG2a and IgG2b in the sera of mice before and
after challenge. Titers of IgG1 antibodies were approximately
two to three times higher than that of IgG2b antibodies in
all the immunized groups as compared to the control
group. However, IgG2a antibody level somewhat increased
after challenge, indicating T-helper type 1 (Th1) cell
response. The results of this study can provide useful
information for developing efficacious subunit vaccine
against JEV. |
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