| Virology Journal | |
| Immunogenicity and safety of virus-like particle of the porcine encephalomyocarditis virus in pig | |
| Dong-Jun An2  Hee Soo Lee2  Hwan-Won Choi3  Bo-Hye Shin2  WooSeog Jeong2  Won-Ha Lee1  Hye-Young Jeoung1  | |
| [1] Department of Genetic Engineering, School of Life Sciences and Biotechnology, Kyungpook National University, 1370 San-Kyuk-dong, Daegu 702-701, Republic of Korea;National Veterinary Research and Quarantine Service, Anyang, Gyeonggi-do, 430-824. Republic of Korea;Choongang Vaccine Laboratory, Daejeon, 305-348, Republic of Korea | |
| 关键词: vaccine candidate; virus-like particles; EMCV; | |
| Others : 1156830 DOI : 10.1186/1743-422X-8-170 |
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| received in 2010-12-13, accepted in 2011-04-15, 发布年份 2011 | |
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【 摘 要 】
Background
In this study, porcine encephalomyocarditis virus (EMCV) virus-like particles (VLPs) were generated using a baculovirus expression system and were tested for immunogenicity and protective efficacy in vivo.
Results
VLPs were successfully generated from Sf9 cells infected with recombinant baculovirus and were confirmed to be approximately 30-40 nm by transmission electron microscopy (TEM). Immunization of mice with 0.5 μg crude protein containing the VLPs resulted in significant protection from EMCV infection (90%). In swine, increased neutralizing antibody titers were observed following twice immunization with 2.0 μg crude protein containing VLPs. In addition, high levels of neutralizing antibodies (from 64 to 512 fold) were maintained during a test period following the second immunization. No severe injection site reactions were observed after immunization and all swine were healthy during the immunization period
Conclusion
Recombinant EMCV VLPs could represent a new vaccine candidate to protect against EMCV infection in pig farms.
【 授权许可】
2011 Jeoung et al; licensee BioMed Central Ltd.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 20150407140521996.pdf | 453KB | ||
| Figure 4. | 30KB | Image | |
| Figure 3. | 22KB | Image | |
| Figure 2. | 37KB | Image | |
| Figure 1. | 31KB | Image |
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【 参考文献 】
- [1]Palmenberg AC, Kirby EM, Janda MR, Drake NL, Duke GM, Potratz KF, Collett MS: The nucleotide and deduced amino acid sequences of the encephalomyocarditis viral polyprotein coding region. Nucleic Acids Res 1984, 12:2969-2985.
- [2]Koenen F, De Clercq K, Lefebvre J, Strobbe R: Reproductive failure in sows following experimental infection with a Belgian EMCV isolate. Vet Microbiol 1994, 39:111-116.
- [3]Billinis C, Paschaleri-Papadopoulou E, Psychas V, Vlemmas J, Leontides S, Koumbati M, Kyriakis SC, Papadopoulos O: Persistence of encephalomyocarditis virus (EMCV) infection in piglets. Vet Microbiol 1999, 70:171-177.
- [4]Gelmetti D, Meroni A, Brocchi E, Koenen F, Cammarata G: Pathogenesis of encephalomyocarditis experimental infection in young piglets: a potential animal model to study viral myocarditis. Vet Res 2006, 37:15-23.
- [5]Hunter P, Swanepoel SP, Esterhuysen JJ, Raath JP, Bengis RG, van der Lugt JJ: The efficacy of an experimental oil-adjuvanted encephalomyocarditis vaccine in elephants, mice and pigs. Vaccine 1998, 16:55-61.
- [6]Huneke RB, Michaels MG, Kaufman CL, Ildstad ST: Antibody response in baboons (Papio cynocephalus anubis) to a commercially available encephalomyocarditis virus vaccine. Lab Anim Sci 1998, 48:526-528.
- [7]Jeoung HY, Lee WH, Jeong W, Ko YJ, Choi CU, An DJ: Immune responses and expression of the virus-like particle antigen of the porcine encephalomyocarditis virus. Res Vet Sci 89:295-300.
- [8]Noad R, Roy P: Virus-like particles as immunogens. Trends Microbiol 2003, 11:438-444.
- [9]Schirmbeck R, Bohm W, Reimann J: Virus-like particles induce MHC class I-restricted T-cell responses. Lessons learned from the hepatitis B small surface antigen. Intervirology 1996, 39:111-119.
- [10]Rueda P, Martinez-Torrecuadrada JL, Sarraseca J, Sedlik C, del Barrio M, Hurtado A, Leclerc C, Casal JI: Engineering parvovirus-like particles for the induction of B-cell, CD4(+) and CTL responses. Vaccine 1999, 18:325-332.
- [11]Ball JM, Graham DY, Opekun AR, Gilger MA, Guerrero RA, Estes MK: Recombinant Norwalk virus-like particles given orally to volunteers: phase I study. Gastroenterology 1999, 117:40-48.
- [12]Roy P: Use of baculovirus expression vectors: development of diagnostic reagents, vaccines and morphological counterparts of bluetongue virus. FEMS Microbiol Immunol 1990, 2:223-234.
- [13]Laurent S, Vautherot JF, Madelaine MF, Le Gall G, Rasschaert D: Recombinant rabbit hemorrhagic disease virus capsid protein expressed in baculovirus self-assembles into viruslike particles and induces protection. J Virol 1994, 68:6794-6798.
- [14]Mortola E, Roy P: Efficient assembly and release of SARS coronavirus-like particles by a heterologous expression system. FEBS Lett 2004, 576:174-178.
- [15]Belliot G, Noel JS, Li JF, Seto Y, Humphrey CD, Ando T, Glass RI, Monroe SS: Characterization of capsid genes, expressed in the baculovirus system, of three new genetically distinct strains of "Norwalk-like viruses". J Clin Microbiol 2001, 39:4288-4295.
- [16]Antonis AF, Bruschke CJ, Rueda P, Maranga L, Casal JI, Vela C, Hilgers LA, Belt PB, Weerdmeester K, Carrondo MJ, Langeveld JP: A novel recombinant virus-like particle vaccine for prevention of porcine parvovirus-induced reproductive failure. Vaccine 2006, 24:5481-5490.
- [17]An DJ, Jeong W, Jeoung HY, Yoon SH, Kim HJ, Choi CU, Park BK: Encephalomyocarditis in Korea: serological survey in pigs and phylogenetic analysis of two historical isolates. Vet Microbiol 2009, 137:37-44.
- [18]Bellier B, Huret C, Miyalou M, Desjardins D, Frenkiel MP, Despres P, Tangy F, Dalba C, Klatzmann D: DNA vaccines expressing retrovirus-like particles are efficient immunogens to induce neutralizing antibodies. Vaccine 2009, 27:5772-5780.
- [19]Luckow VA, Summers MD: High level expression of nonfused foreign genes with Autographa californica nuclear polyhedrosis virus expression vectors. Virology 1989, 170:31-39.
- [20]Hu YC, Hsu JT, Huang JH, Ho MS, Ho YC: Formation of enterovirus-like particle aggregates by recombinant baculoviruses co-expressing P1 and 3CD in insect cells. Biotechnol Lett 2003, 25:919-925.
- [21]Ansardi DC, Porter DC, Morrow CD: Coinfection with recombinant vaccinia viruses expressing poliovirus P1 and P3 proteins results in polyprotein processing and formation of empty capsid structures. J Virol 1991, 65:2088-2092.
- [22]Cao Y, Lu Z, Sun J, Bai X, Sun P, Bao H, Chen Y, Guo J, Li D, Liu X, Liu Z: Synthesis of empty capsid-like particles of Asia I foot-and-mouth disease virus in insect cells and their immunogenicity in guinea pigs. Vet Microbiol 2009, 137:10-17.
- [23]Chen Z, Guo X, Ge X, Jia H, Yang H: Protective immune response in mice vaccinated with a recombinant adenovirus containing capsid precursor polypeptide P1, nonstructural protein 2A and 3C protease genes (P12A3C) of encephalomyocarditis virus. Vaccine 2008, 26:573-580.
- [24]Ko YJ, Choi KS, Nah JJ, Paton DJ, Oem JK, Wilsden G, Kang SY, Jo NI, Lee JH, Kim JH, et al.: Noninfectious virus-like particle antigen for detection of swine vesicular disease virus antibodies in pigs by enzyme-linked immunosorbent assay. Clin Diagn Lab Immunol 2005, 12:922-929.
- [25]Chung YC, Ho MS, Wu JC, Chen WJ, Huang JH, Chou ST, Hu YC: Immunization with virus-like particles of enterovirus 71 elicits potent immune responses and protects mice against lethal challenge. Vaccine 2008, 26:1855-1862.
- [26]Jin H, Xiao W, Xiao C, Yu Y, Kang Y, Du X, Wei X, Wang B: Protective immune responses against foot-and-mouth disease virus by vaccination with a DNA vaccine expressing virus-like particles. Viral Immunol 2007, 20:429-440.
- [27]Pushko P, Tumpey TM, Bu F, Knell J, Robinson R, Smith G: Influenza virus-like particles comprised of the HA, NA, and M1 proteins of H9N2 influenza virus induce protective immune responses in BALB/c mice. Vaccine 2005, 23:5751-5759.
- [28]Paliard X, Liu Y, Wagner R, Wolf H, Baenziger J, Walker CM: Priming of strong, broad, and long-lived HIV type 1 p55gag-specific CD8+ cytotoxic T cells after administration of a virus-like particle vaccine in rhesus macaques. AIDS Res Hum Retroviruses 2000, 16:273-282.
- [29]Fromantin C, Jamot B, Cohen J, Piroth L, Pothier P, Kohli E: Rotavirus 2/6 virus-like particles administered intranasally in mice, with or without the mucosal adjuvants cholera toxin and Escherichia coli heat-labile toxin, induce a Th1/Th2-like immune response. J Virol 2001, 75:11010-11016.
- [30]McLelland DJ, Kirkland PD, Rose KA, Dixon RJ, Smith N: Serologic responses of Barbary sheep (Ammotragus lervia), Indian antelope (Antilope cervicapra), wallaroos (Macropus robustus), and chimpanzees (Pan troglodytes) to an inactivated encephalomyocarditis virus vaccine. J Zoo Wildl Med 2005, 36:69-73.
- [31]Osorio JE, Hubbard GB, Soike KF, Girard M, van der Werf S, Moulin JC, Palmenberg AC: Protection of non-murine mammals against encephalomyocarditis virus using a genetically engineered Mengo virus. Vaccine 1996, 14:155-161.
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