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Middle East respiratory syndrome coronavirus (MERS-CoV) causes severe respiratory disease in humans with a case fatality rate of over 39%, and poses a considerable threat to public health. A lack of approved vaccine or drugs currently constitutes a roadblock in controlling disease outbreak and spread. In this study, we generated MERS-CoV VLPs using the baculovirus expression system. Electron microscopy and immunoelectron microscopy results demonstrate that MERS-CoV VLPs are structurally similar to the native virus. Rhesus macaques inoculated with MERS-CoV VLPs and Alum adjuvant induced virus-neutralizing antibodies titers up to 1:40 and induced specific IgG antibodies against the receptor binding domain (RBD), with endpoint titers reaching 1:1,280. MERS-CoV VLPs also elicited T-helper 1 cell (Th1)-mediated immunity, as measured by ELISpot. These data demonstrate that MERS-CoV VLPs have excellent immunogenicity in rhesus macaques, and represent a promising vaccine candidate.
Middle East respiratory syndrome coronavirus (MERS-CoV) is a betacoronavirus infecting humans, but MERS-CoV disease is markedly different from other human coronaviruses including HCoV-HKU1, HCoV-NL63, HCoV-OC43 and HCoV-229E, which are known to cause mild respiratory infections. Rather, MERS-CoV infection is similar to Severe Acute Respiratory Syndrome coronavirus (SARS-CoV), as disease is associated with acute respiratory distress syndrome. In addition, MERS-CoV infection can result in kidney failure, ultimately leading to death [1–3]. As of 29 October 2015, 628 deaths from 1635 cases of MERS-CoV had been identified worldwide, a case fatality rate of 39.02% . Human infections with MERS-CoV typically occur in countries located in the Middle East, but in May 2015 an outbreak was reported in South Korea, in which three super-spreaders were found to be responsible for the majority of infections, as well as evidence of tertiary human-to-human transmission . As such, there is an urgent need for the development of an efficacious vaccine against MERS-CoV.
Past vaccine strategies against viral pathogens comprise of live-attenuated viruses that were passaged in animal hosts or cell lines before immunization, however these vaccines are not always sufficiently immunogenic, and there are safety concerns associated with the use of live-attenuated vaccines in some populations, particularly the young, old, pregnant or immunocompromised. Inactivated vaccines are safe for use, but typically only induce humoural immunity and very low levels of cell-mediated responses. There are no reports of inactivated MERS-CoV being tested as a vaccine, but an inactivated SARS-CoV vaccine appears to have little effect in mice and domestic ferrets [6–8]. Recently, candidate vaccines are genetically engineered to be replication-deficient or avirulent before use, therefore eliminating the concern that live-attenuated vaccines could revert to virulence. A recombinant MERS-CoV lacking the E structural protein was previously developed as a candidate vaccine; however, its protective efficacy has not yet been demonstrated .
Other MERS-CoV candidate vaccines currently being developed include spike (S) protein nanoparticles , modified vaccinia virus vectors  and immunogens based on the full-length S DNA and subunit protein S1 , all of which have been shown to be able to induce neutralizing antibodies against MERS-CoV. Virus-like particles (VLPs) are protein-only subunit vaccines that emulate the morphology of the native virus. Compared with inactivated or live-attenuated virus vaccines, VLPs are able to induce robust humoural and cellular immune responses without the risk of reversion to virulence [13, 14]. Furthermore, VLPs for any pathogen can be generated under BSL-2 conditions.
In this study, we constructed recombinant baculovirus co-expressing the S, envelope (E) and membrane (M) genes. Infection of Sf9 cells with this recombinant baculovirus resulted in the successful assembly of MERS-CoV VLPs. We then confirmed the structural integrity of VLPs and evaluated the immunogenicity of MERS-CoV VLPs as a vaccine candidate in rhesus macaques.
The MERS-CoV S, E, M genes were cloned into the modified pFastBacDual vector in the locations shown (Figure (Figure1)1) and the recombinant plasmid was confirmed by enzyme digestion analysis as well as DNA sequencing and the recombinant plasmid was tranfected into Sf9 cells to obtain recombinant baculovirus. The titer of recombinant baculovirus stocks at the third passage was determined to be 3.7×107 infectious units (IFU)/ml. Infection of Sf9 cells with recombinant baculovirus yielded MERS-CoV VLPs, which were purified with a discontinuous sucrose gradient for further studies.
Immunofluorescence assay confirmed the recombinant baculovirus was expressed in Sf9 cells. The results of immunofluorescence studies demonstrated the expression of three structural proteins (Figure (Figure2).2). The morphology of MERS-CoV VLPs was investigated by electron microscopy. Under TEM, the diameters of MERS-CoV VLPs were approximately 100 nm, and spikes were readily observable around the spherical particles (Figure (Figure3A).3A). To ensure that S was incorporated into the VLPs, immunoelectron microscopy was performed with a gold-tagged antibody against the RBD of S. Results show that the gold particles appear on the MERS-CoV VLPs (Figure (Figure3B),3B), demonstrating that the particle contain S. Each composition of the MERS-CoV VLPs was confirmed by Western blot, and bands corresponding to S, M and E in MERS-CoV VLPs were observed (Figure (Figure4).4). These results demonstrate that MERS-CoV VLPs autonomously assemble in insect cells that have been infected by our recombinant baculovirus, and are structurally similar to the native virus .
Our next objective was to answer whether expression from insect or mammalian cells have any difference on glycosylation levels on the S protein. To investigate this, the pcDNA3.1-MERS-S transfected BSR cell lysates were compared with purified MERS-CoV VLPs by Western blot. S expressed in insect cells was slightly larger than those produced in mammalian cells (Figure (Figure55).
To evaluate the humoral immune response in immunized nonhuman primates (NHPs), we measured serum neutralizing antibody against MERS-CoV live virus. The titers were determined as the highest serum dilutions that completely prevent CPE in at least 50% of the wells, and the virus-neutralizing antibodies titers up to 1:40 after fourth immunization (Figure (Figure6A6A and and6C).6C). We also measured serum IgG antibody concentrations against the RBD protein using ELISA. Results showed that NHPs immunized with the VLPs and Alum adjuvant were able to induce considerable amounts of IgG antibody, with endpoint titers up to 1:1,280 when measured at 8 weeks after vaccination (Figure (Figure6B).6B). In contrast, MERS-CoV virus-neutralizing antibodies or RBD-specific IgG was not detected in mock-vaccinated NHPs.
To assess T-cell responses in NHPs following vaccination, the extent of IFN-γ and IL-4 secretion from the PBMCs of NHPs were determined using ELISpot assays. Results show that the PBMCs of VLP-vaccinated NHPs had significantly higher release of IFN-γ upon stimulation with purified RBD antigen, compared to PBMCs from mock-vaccinated animals (Figure (Figure7A).7A). In contrast, IL-4 secretion was not substantially different between the two groups (Figure (Figure7B7B).
VLP production via the baculovirus expression system platform in insect cells is a tried and tested strategy for vaccine development. Several VLP-based prophylactics have been successfully produced, tested, and commercialized. These include Cervarix™ (GlaxoSmithKline), which is a vaccine against human papillomavirus (HPV) and thus cervical cancer ; FluBlok®, which is a trivalent hemagglutinin vaccine approved by the FDA . Ingelvac, CircoFLEX® and Circumvent® PCV are two approved animal vaccines against porcine circovirus (PCV) type 2 . Furthermore, a variety of influenza VLPs also demonstrate excellent immunogenicity. Novavax (MD, USA) has produced a VLP-based vaccine targeting H1N1 influenza virus, which has recently shown encouraging results in a Phase II trial .
Past findings showed that SARS-CoV VLPs could be readily assembled by the co-infection of insect cells with baculoviruses expressing M and E. The co-expression of S, E and M by a single recombinant virus allowed for the efficient assembly and release of VLPs not only closely resembled SARS-CoV in size and particle morphology, but also virus morphogenesis . However, in our study co-infection of the MERS-CoV S and M recombinant baculoviruses in insect cells did not result in VLPs formation, as assessed by TEM (data not shown). Rather, we demonstrated that VLPs consisting three structural envelope proteins (S, E, M) can be generated in insect cells with similar morphology to MERS-CoV virions. The expression of S protein from insect cells was slightly larger than that from mammalian cells, suggesting that the glycosylation of our VLPs is complete. To our knowledge, this is the first report which showed the successful generation of MERS-CoV VLPs consisting of immunogenic proteins.
We currently lack an animal model in which challenge with MERS-CoV will cause uniform lethality [21, 22]. The NHPs develop transient infection but do not die from infection, whereas transgenic mice overexpressing DPP4 die from MERS-CoV infection [23, 24]. As such, the protective efficacy of candidate vaccines against MERS-CoV cannot be evaluated in animals under the most stringent conditions. Due to the immunological similarity of rhesus macaques to humans [21, 25], the next best choice is to determine whether our MERS-CoV VLPs are able to elicit robust levels of immunogenicity in NHPs, in hope that humans will react to the vaccine in a similar manner. This rationale is supported by a past study that also used rhesus macaques for the evaluation of a candidate countermeasure against MERS-CoV infection .
Our results showed that MERS-CoV VLPs are immunogenic, able eliciting robust levels of specific humoural and cell-mediated immunity in vaccinated NHPs. After immunization with Alum adjuvant, rhesus macaques develop virus-neutralizing antibodies and high levels of MERS-CoV specific IgG antibodies against the RBD. Vaccination with MERS-CoV VLPs also resulted in T-cell responses to RBD, as assessed by ELIspot assay of peptide-stimulated PBMCs. IFN-γ, but not IL-4 secretion was detected from PBMCs, suggesting that VLPs elicited a Th1-mediated response. Since both specific humoral immunity and cell immunity is indispensable for effective vaccination , this suggests that our VLP-based vaccine has potential to be protective in humans against MERS-CoV challenge. Future experiments should involve efficacy testing in rhesus macaques, transgenic mice overexpressing DPP4, and the safety testing of this VLP-based vaccine candidate in phase I clinical trials.
In order to acquire a ternary promoter transfer plasmid, a gene segment contains a terminator and a p10 promoter sequence flanking with several restriction enzyme sequences was synthesized. The modified sequences were cloned into the BamHI and HindIII sites of the pFastBacDual vector (Invitrogen, Carlsbad, CA), under the control of the polyhedron promoter. The S, E and M gene sequences of MERS-CoV isolate Al-Hasa_15_2013 were obtained from NCBI (GenBank accession No. KF600645). The genes were codon-optimized for the best possible expression levels in insect cells and biochemically synthesized (Sangon Biotech, China). The full-length gene encoding the S protein was inserted into XhoI and KpnI sites, under the control of the p10 promoter, the E gene was cloned into the BamHI and EcoRI sites, under the control of the polyhedron promoter, and the M gene was inserted into the SalI and NotI sites, under the control of the additional p10 promoter, generating the recombinant plasmid pFastBacDual-SEM. The plasmid was examined by restriction enzyme analysis to confirm the correct orientation of the insertions. Bacmid transfer plasmids expressing site-specific transpositions of the S, E and M genes were then transformed into E.coli DH10Bac competent cells to generate recombinant bacmids. The recombinant bacmids were authenticated by PCR using pUC/M13 Forward and Reverse primers, and then transfected into Sf9 insect cells using Liposome 2000, following the Bac-to-Bac Expression Systems manual (Invitrogen, USA). Supernatant containing recombinant baculovirus was harvested 5 days after transfection as the viral stock.
Titers of baculovirus stocks were determined using a rapid titration kit (BacPakBaculovirus Rapid Titer Kit; Clontech, USA). Sf9 insect cells were maintained as suspension cultures in serum-free SF900II medium (Life technologies, USA) at 27°C, with agitation at a speed of 120 rpm. MERS-CoV VLPs were produced by infecting Sf9 cells with recombinant baculovirus at a multiplicity of infection (MOI) of 0.5, and harvested at 96 h post infection (hpi). Suspensions were first centrifuged to remove cell debris, and the supernatants were then ultracentrifuged at 100,000 g for 1 h to obtain the VLPs pellet, before purification by a 30–40–50% discontinuous sucrose gradient. Bands between 30-40% sucrose, which represent MERS-CoV VLPs, were collected.
Immunofluorescence assay was performed as previously described . Briefly, Sf9 cells were infected with the recombinant baculovirus for 48 h, and then fixed with 4% paraformaldehyde for 20 minutes at room temperature. Subsequently, cells were incubated with the primary antibodies (mouse polyclonal antibodies against MERS-CoV S, E and M protein, respectively) that contained 1% bovine serum albumin for 1 h. After three washes with PBS containing 0.05%Tween 20 (PBST), secondary antibodies (FITC-labeled goat against mouse IgG) and 0.3% Evans blue were added for 50 minutes at room temperature. The cells were observed using a fluorescence microscope after washing.
MERS-CoV VLPs were loaded onto grids, kept at room temperature for 5 min, stained with 1% sodium phosphotungstate, and then examined with transmission electron microscope (TEM). For immunoelectron microscopy (IEM), the MERS-CoV VLPs were loaded onto formvar-coated grids after removal of excess sample solution, incubated with mouse anti-S antibodies, labeled with gold-tagged goat anti-mouse IgG antibody (Sigma-Aldrich, SaintLouis, MO, USA), and then observed with the TEM.
Purified MERS-CoV VLPs were transferred onto a Polyvinylidene fluoride (PVDF) membrane (Immobilin-P, Millipore, USA) after SDS-PAGE under denaturing conditions for Western blotting with anti-S, E, M mouse polyclonal antibodies.
Briefly, BSR cells were transfected with pcDNA3.1-MERS-S and cells were lysed 3 days later. The lysates from BSR cells and MERS-CoV VLPs from Sf9 cells were compared by using anti-S polyclonal sera by Western blotting.
Six rhesus macaques were randomized into two groups. One group was vaccinated intramuscularly (IM) in the gastrocnemius muscle with 250 μg of MERS-CoV VLPs and mixed with 250 μg Alum adjuvant (Thermo, USA) per animal, and the other group was given an equivalent volume of PBS as a control. Identical vaccinations were then repeated at 14-day intervals three more times for both groups. Blood samples were obtained from the femoral vein of animals prior to each vaccination.
RBD-specific antibodies from the sera of immunized and control monkeys were measured by indirect ELISA. Genes encoding RBD protein (spike residues 358-662) [28, 29] of MERS-CoV were amplified by PCR using synthesized MERS-CoV S sequences (GenBank accession no. KF600645) as the template and cloned into the pET-30a expression vector. The proteins were purified by Ni-NTA affinity chromatograph column (Thermo, USA), according to manufacturer instructions. Briefly, 96-well microtiter plates (Corning Costar, USA) were pre-coated with 100 μL of purified RBD antigen at a concentration of 1 μg/mL diluted in 0.05 mol/L carbonate-bicarbonate buffer (pH 9.6) and incubated at 4°C overnight. After the plates were blocked for 2 h at 37°C, 100 μL of serum samples 2-fold serially diluted were added to the wells, and incubated at 37°C for 1 h. After three washes with PBST, 100 μL of HRP-labeled goat polyclonal antibody against monkey IgG (Abcam, UK) was added (diluted 1:20,000), and incubated at 37°C for 1 h. After washing with PBST three times, 100 μL of the substrate 3, 3′, 3, 5′-tetramethylvenzidine (TMB) (Sigma, USA) was added to each well, incubated for 30 min, and then stopped with 50 μL of 2 M H2SO4. Optical density values were measured using an ELISA plate reader at a wavelength of 450 nm (Bio-Rad, USA).
Neutralizing antibody titers of NHPs sera detected as previously described . Briefly, the 2-fold serially diluted serum samples of NHPs were incubated with 100 TCID50 of virus for 1 h at 37°C before added to the monolayer of Vero E6 cells in triplicate. Virus supernatant was removed after 1 h of culture at 37°C then replaced with fresh medium. Cells were observed daily for cytopathic effect (CPE) and recorded on day 3 post-infection. The highest dilution of the monkey sera that completely prevented CPE in 50% of the wells (NT50) were defined as the virus neutralization antibody.
Lymphocytes isolated from the peripheral blood mononuclear cells (PBMCs) from inoculated monkeys at 2 weeks after the second immunization were plated at a density of 2×105 cells per well in a 96-well ELISpot plate (Mabtech AB, Sweden), which had been pre-coated with IFN-γ or IL-4. Purified RBD antigen was added at a final concentration of 10 μg/ml to stimulate cytokine production, and the rest of the assay was carried out according to manufacturer instructions. Spot forming cells (SFCs) were counted using an automated ELISpot reader (AID ELISPOT reader-iSpot, AID GmbH, GER).
The environment and housing facilities for rhesus macaques is in accordance with the National Standards of Laboratory Animal Requirements of China (GB 14925-2001). Animal studies were strictly conducted with the recommendations of the Veterinary Institute at the Academy of Military Medical Sciences and approved by the Animal Welfare and Ethics Committee (permit number SCXK-2012-017).
We are grateful to Professor Gary Wong (Public Health Agency of Canada) and Professor Xuejie Yu (Shandong University) for editing the manuscript.
CONFLICTS OF INTEREST
The authors declare no competing interests.
This work was supported by the open project of The State Key Laboratory of Respiratory Disease in China (Grant No.2014SKRD-001), and supported by grants from the National Science and Technology Pillar Program during the Twelfth Five-year Plan Period (2013BAD12B04).