Immunogenicity and safety of virus-like particle of the porcine encephalomyocarditis virus in pig
- Hye-Young Jeoung†1, 2,
- Won-Ha Lee†2,
- WooSeog Jeong1,
- Bo-Hye Shin1,
- Hwan-Won Choi3,
- Hee Soo Lee1 and
- Dong-Jun An1Email author
© Jeoung et al; licensee BioMed Central Ltd. 2011
Received: 13 December 2010
Accepted: 15 April 2011
Published: 15 April 2011
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.
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
Recombinant EMCV VLPs could represent a new vaccine candidate to protect against EMCV infection in pig farms.
KeywordsEMCV virus-like particles vaccine candidate
The porcine encephalomyocarditis virus (EMCV) is a member of the genus Cardiovirus of the family Picornaviridae, the genome is a single-stranded positive sense RNA of approximately 7.8 kb with a unique large open reading frame (ORF) . Porcine EMCV infection, which is characterized by acute myocarditis and sudden death in preweaned piglets and severe reproductive failure in sows, results in severe economic losses for swine production [2–4].
An inactivated EMCV vaccine is considered as one of the effective strategies for preventing EMCV infection in domestic and wild animals [5, 6]. Recently, vaccination with porcine EMCV virus-like particles (VLPs) has also been examined as a novel candidate for protection against porcine EMCV . However, VLP-based vaccines against porcine EMCV produced using a baculovirus system have not yet been developed.
One of the most important technological developments to emerge from the baculovirus expression system was the observation that the expression of viral capsid proteins could lead to the assembly of VLPs that mimic the overall structure of authentic viral particles but are devoid of viral nucleic acids . VLPs represent a highly effective alternative vaccine strategy. They have been shown to stimulate B-cell-mediated immune responses, and are also highly effective at stimulating CD4 proliferative responses and cytotoxic T-lymphocyte (CTL) responses [9–11]. VLPs have thus been developed as novel vaccine candidate for many kinds of viruses including bluetongue virus , rabbit hemorrhagic disease virus , severe acute respiratory syndrome (SARS) virus , Norwalk-like viruses , and parvovirus . Moreover, hepatitis B virus (Recombivax HB, Merck) and human papillomavirus (Gardasil®, Merck) VLPs have been approved for use as vaccines.
In this study, we generated a recombinant baculovirus Bac-P12A3C, which contains the structural protein P1, the nonstructural protein 2A and the protease 3C of porcine EMCV K3 (wild strain) to induce formation of VLPs that mimic the antigenic structure of authentic porcine EMCV particles. We then evaluated the protective immune response induced by the recombinant VLPs in mice and their immunogenicity in swine.
2. Materials and methods
2.1. Viruses, cells and antibodies
The Korean porcine EMCV K3 strain (pEMCV-K3) isolated in 1990 and the monoclonal antibody (MAb) 3F10 against the VP1 protein of pEMCV-K3 were used as described previously . The Spodoptera frugiperda (Sf9) insect cells were maintained in Grace medium (Invitrogen, USA) containing 5% fetal bovine serum (Gibco, USA), lactalbumin hydrolysate (Gibco, USA), and an antibiotics-antimycotic solution (Gibco, USA) at 27°C, and infected Sf9 cells were maintained in Sf 900 II SFM (Gibco, USA) without fetal bovine serum.
2.2. Construction of recombinant baculovirus transfer vectors and generation of recombinant baculovirus
Genes of the capsid protein P1, the nonstructural protein 2A and the protease 3C of pEMCV-K3 were amplified and cloned into a pFastBac™ HTB (Invitrogen, USA) as described previously . The P12A3C gene was then inserted down stream of the polyhedron promoter (PPH). Recombinant baculovirus was generated by site-specific transposition of pFastBac/P12A3C into a baculovirus shuttle vector (bacmid) propagated in DH10Bac cells (Invitrogen, USA) by using the Bac to Bac baculovirus expression system (Invitrogen, USA) according to the manufacturer's instructions. Recombinant baculovirus (Bac-P12A3C) was plaque purified, and then the presence of the P12A and 3C genes of pEMCV-K3 was confirmed by PCR using previously described primer sets .
2.3. Expression of recombinant proteins
Sf9 cells in 6-well culture plates were infected with recombinant baculovirus at a multiplicity of infection (MOI) of 10 for 72 h. Vero cells were infected with pEMCV-K3 grown in 6-well culture plates (as a positive control). The expressed recombinant proteins were analyzed by immunofluorescence assay (IFA) and Western blotting analysis as previously described .
2.4. Morphology of VLPs
Sf9 cells in 25 cm2 flasks were infected with recombinant baculovirus at an MOI of 10 and harvested at 4 day post-infection (dpi). The harvested cells were clarified by centrifugation, concentrated using polyethylene glycol precipitation and then, loaded onto a 20-60% (w/v) discontinuous sucrose step density gradient as described previously . The peak fraction from the sucrose gradient was allowed to settle on glow-discharged carbon-coated grids for morphological examination by transmission electron microscopy (TEM, Tecnai G2) at the Korea Basic Science Institute. The grid was blotted dry, and stained with 1% uranyl acetate. The sample was visualized using a transmission electron microscope at 60,000 × magnification.
2.5. Animal experiments
2.5.1 Efficacy of EMCV VLPs in mice
Female BALB/c mice (aged 6-8 weeks) were used for the immunization and challenge trials. The mice were randomly divided into four groups, with fifteen mice in each group. All groups were intramuscularly (I.M) inoculated with 0.1 ml antigen two times at an interval of 2 weeks. Group 1 was inoculated with PBS as a negative control, and Group 2 was inoculated with a commercial killed vaccine (Choongang Vaccine Laboratory, Korea) as a positive control. Group 3 and Group 4 were inoculated with 0.5 μg and 0.1 μg respectively, of crude protein extract from Bac-P12A3C infected cells containing VLPs. On 14 day post-vaccination, ten mice in each group were challenged intramuscularly with 0.1 ml of the pEMCV-K3 strain containing 106 TCID50/ml (1000MLD50/ml) per mouse. The remainder in each group was analyzed for humoral immune response as described previous .
2.5.2 Safety and Immunization in swine
Twelve pigs, weighing approximately 30-40 kg each, that were antibody - negative against EMCV were separated into six groups of two pigs each. Antigen was mixed with an equal volume of an Montandide IMS 1313™ N VG (Seppic, France), and all groups were inoculated intramuscularly with 1.0 ml antigen-adjuvant mixture. Group 1 was inoculated with PBS as a negative control, and Group 2 was inoculated with commercial vaccine as a positive control. Group 3 and Group 5 were inoculated once each with 2.0 μg and 0.2 μg of crude protein, respectively, which was extracted from Bac-P12A3C infected cells containing VLPs. Group 4 and Group 6 were inoculated twice in a 2 week interval with 2.0 μg and 0.2 μg respectively, of crude protein extracted from Bac-P12A3C infected cells containing VLPs. After each immunization, all swine were observed for 30 min and monitored for clinical signs during the immunization period at 2 day intervals. Sera were collected every week for 50 days from immunized swine to analyze seroconversion. Neutralizing EMCV antibodies were detected in collected sera using an in vitro neutralization assay as described previous .
2.6. Statistics analysis
Results of neutralizing antibodies levels were presented as the means ± SEM. The significance of the variability among the experimental groups was determined by two-way ANOVA. A probability value (P) of < 0.05 was considered significant.
3.1. Expression and identification of VLPs in vitro
Sf9 cells were transfected with a bacmid contained the P12A and 3C genes, and recombinant baculoviruses (Bac-P12A3C) were identified by plaque assay and confirmed by PCR (data not shown). Cells were infected with Bac-P12A3C at an MOI of 10, and cells and supernatants were harvested and analyzed at 3 dpi, at which point most of the cells showed cytopathic effects (CPE).
3.2. Analysis of VLP morphology
3.3. Seroconversion and protection of immunized mice
3.4. Safety and immunity in swine
Virus-like particles are promising vaccine candidates for triggering neutralizing antibody response since they can authentically mimic the viral surface and are antigenicity similar to the parental virus. In addition, they are safely devoid of infectious genetic material [8, 18]. VLPs have been produced extensively as human and veterinary vaccine candidates due to their strong immunogenicity. The baculovirus expression system has been widely used for generation of these VLPs due to the high productivity of the system and the ability to achieve rapid production scale implementation . VLPs have been successfully generated from many other Picornaviridae family members, including enterovirus , poliovirus  and foot-and mouth disease virus (FMDV) .
In a previous study, we engineered a DNA vaccine that produced pEMCV-K3 VLPs and confirmed that the VLP antigen exhibited good antigenicity and protective immunity in mice . In the present study, we used a baculovirus expression system to generate EMCV VLPs, verified that Bac-P12A3C is capable of expressing a fusion protein, and confirmed P1 protein is correctly processed by the 3C protease into the VP1 protein (approximately 30 kDa) as previously demonstrated [7, 23]. These data also showed that Bac-P12A3C has the ability to self-assemble into 30 nm to 40 nm VLPs with a similar morphology to authentic virus particles of porcine EMCV showed by TEM [7, 20, 22, 24].
Mice immunized with 0.1 μg of crude protein containing VLPs (60%), 0.5 μg crude protein containing VLPs (90%), or the commercial vaccine (100%) displayed different levels of protection in viral challenge experiments. Correspondingly, a linear relationship between the levels of neutralizing antibody and the protective efficacy of EMCV vaccines against lethal EMCV challenge has been demonstrated [7, 23]. VLP-based vaccines have been shown to confer protection in animal models against many viral challenges (i.e., enterovirus , foot and mouth disease virus , influenza virus  parvovirus , human immunodeficiency  and rotavirus . Together, these findings indicate that VLPs can be dramatically effective immunogens .
To assess the safety of the VLP, two doses of crude protein including VLPs were tested, with the higher dose (2.0 μg) 10-fold higher than the lower dose (0.2 μg). No immunization related clinical signs were observed in any group. After the second immunization, the levels of neutralizing antibodies were similar to those obtained with the commercial vaccine and were more effective than single-dose immunization in inducing the production and maintenance of neutralizing antibodies in swine. The twice immunization were more effective in inducing the production and maintenance of neutralizing antibodies in swine than primary immunization. Correspondingly, the conventional inactivated vaccine is also administered twice, as the second boost is needed to effectively induce neutralizing antibody . The production of neutralizing antibodies has been correlated with protection against viral infection and is an important feature of an effective vaccine. In addition, some data suggest that the induction of high level of EMCV specific neutralizing antibodies may be essential for protection against EMCV infection [5, 30, 31]. This study demonstrates that twice immunizations with a VLP vaccine can effectively induce neutralizing antibodies. Thus, this approach may have significant application as a novel vaccine strategy to control EMCV. In future studies, we plan to investigate this VLP vaccine for efficiency, safety, and effects on litter size in pregnant swine.
Based on the results presented on this study, we conclude that porcine EMCV VLPs generated using a baculovirus expression system are safe and demonstrate good antigenicity and immunogenicity. The antigenicity from vaccination against EMCV with these VLP indicate such systems have as promising vaccines for this disease.
We are grateful to Ms. Hyun-Jeong Kim and Mr. Sung Yub Kim for technical assistance; and the Korea Basic Science Institute for use of equipment for electron microscopy.
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