Protective immunity against Toxoplasma gondiiinduced by DNA immunization with the gene encoding a novel vaccine candidate: calcium-dependent protein kinase 3
© Zhang et al.; licensee BioMed Central Ltd. 2013
Received: 5 August 2013
Accepted: 29 October 2013
Published: 31 October 2013
Toxoplasma gondii can infect almost all warm-blood animals including human beings. The plant-like calcium-dependent protein kinases (CDPKs) harbored by T. gondii are involved in gliding motility, cell invasion, egress and some other developmental processes, and so have been implicated as important virulence factors.
In the present study, we constructed a DNA vaccine expressing T. gondii CDPK3 (TgCDPK3) and evaluated its protective efficacy against T. gondii infection in Kunming mice. The gene sequence encoding TgCDPK3 was inserted into the eukaryotic expression vector pVAX I, and mice were immunized with pVAX-CDPK3 intramuscularly.
The results showed that mice immunized with pVAX-CDPK3 developed a high level of specific antibodies and a strong lymphoproliferative response. The significantly increased levels of IFN-γ, IL-2, IL-12 (p70) and IL-23 and high ratio of IgG2a to IgG1 antibody titers indicated that a Th1 type response was elicited after immunization with pVAX-CDPK3. Furthermore, the percentage of CD4+ T cells in mice vaccinated with pVAX-CDPK3 was significantly increased. After lethal challenge with the tachyzoites of the virulent T. gondii RH strain, the mice immunized with pVAX-CDPK3 prolonged the survival time from 10 days to 24 days (13.5 ± 4.89) compared to untreated mice or those received PBS or pVAX I which died within 7 days (P < 0.05). In chronic infection model (10 cysts of the T. gondii PRU strain), the numbers of brain cysts of the mice immunized with pVAX-CDPK3 reduced significantly when compared with those in control groups (P < 0.05), and the rate of reduction could reach to about 50%.
TgCDPK3 can generate protective immunity against acute and chronic T. gondii infection in Kunming mice and is a promising vaccine candidate for further development of an effective vaccine against T. gondii.
KeywordsToxoplasma gondii Toxoplasmosis TgCDPK3 DNA vaccine Protective immunity
Toxoplasma gondii, an obligate intracellular protozoan parasite, is responsible for toxoplasmosis in a wide range of hosts including humans, mammals, birds and marine mammals [1–5]. T. gondii infection in immune-competent individuals is rarely symptomatic, but toxoplasmosis occurred in fetus and immunocompromised hosts may result in severe disease or even lethal damage [5–7]. Meanwhile, the infection can cause serious economic losses to the livestock industry, especially in sheep and goats, as the course of abortion, stillbirth and neonatal loss , and also the infected animals are major sources of T. gondii transmission to humans [4, 6].
No available chemical treatments could completely eliminate T. gondii in infected animals, so immunoprophylaxis is considered to be high priority for prevention and control of the parasite [9, 10]. Although the only licensed vaccine based on the attenuated-live T. gondii S48 strain (Toxovax®) can be used to prevent the incidence of abortion in sheep , it is limited to be further explored in food-producing animals or humans in view of the safety concerns on its reverting to a virulence wild type. The current efforts have been made on the development of DNA vaccines due to the superiority of much safer than live-type vaccines, as well as their ability to induce primarily Th1 cell-mediated immune and CD8+ cytotoxic T cells (CTL) responses [12, 13].
A family of calcium-dependent protein kinases (CDPK) is known as key effectors in regulating calcium related signaling pathways in apicomplexan, which control a diverse array of functions in the life cycle including gliding motility, cell invasion, egress and some other developmental processes that occur at distinct stages in their complex life . TgCDPK3, a characteristic member of CDPKs, is localized to the parasite periphery in intracellular and extracellular parasites and partially to the apical end of the intracellular parasite . The TgCDPK3 knockout strain showed fewer parasites per vacuole than parental strains, which implied that the gene can partially influence the division of T. gondii. However, no studies have evaluated the immunogenicity of TgCDPK3 and its potential as a vaccine candidate against T. gondii infection.
In this context, the objectives of the present study were to examine the various immune responses in mice induced by DNA immunization with a eukaryotic plasmid expressing TgCDPK3, and to evaluate the potential of TgCDPK3 as a vaccine candidate against infection with two different genotypes of T. gondii in Kunming mice.
Specific-pathogen-free (SPF) female inbred Kunming mice of 6–8 weeks old were purchased from Center of Laboratory Animals, Lanzhou Institute of Biological Products, Lanzhou, China. All mice were handled in strict accordance with the Good Animal Practice requirements of the Animal Ethics Procedures and Guidelines of the People’s Republic of China. This study was approved by the Animal Ethics Committee of Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences (Approval No. LVRIAEC2012-011).
T. gondii RH and PRU strains were used in this study. Tachyzoites of the highly virulent T. gondii RH strain (Type I) were propagated by serial intraperitoneal passage in Kunming mice. The peritoneal fluid of mice was centrifuged for 10 min at 1 000 × g at 4°C to remove the cellular debris and then re-suspended in sterile phosphate-buffered saline (PBS). The obtained tachyzoites were also used for Toxoplasma lysate antigen (TLA) preparation according to our previous studies  and total RNA extraction was followed by the instruction of the RNAprep Pure Tissue Kit (TIANGEN, China) manual. Cysts of the PRU strain (Type II) were maintained in the laboratory by oral passage of infective brain homogenate in Kunming mice.
Construction of the eukaryotic expression plasmid
The complete open reading frame (ORF) of TgCDPK3 was amplified by reverse transcription-polymerase chain reaction (RT-PCR) using primers K3F (5′-GCGGGTACCATGGCGGATCCGCTCTCGTTCTTCAAC-3′) and K3R (5′-GGGCGGCCGCTCACTCATGTTGCGACTCAC-3′), in which the Kpn I and Not I restriction sites were introduced and shown in italic, respectively. After purification using the TIANquick Midi Purification Kit (TIANGEN, China), the PCR products were inserted into pVAX I (Invitrogen) through Kpn I and Not I sites. The resulting plasmid was named pVAX-CDPK3. The concentration of extracted pVAX-CDPK3 was determined by spectrophotometry at OD260 and OD280. The plasmids were diluted with sterile phosphate buffered saline (PBS) to a final concentration of 1 μg/μl and stored at -20°C.
Expression of pVAX-CDPK3 in vitro
Recombinant plasmid pVAX-CDPK3 was transfected into HEK293 cells grown in 6-well plates using lipofectamine 2000 reagent (Invitrogen) according to the manufacturer’s instructions. The expression of pVAX-CDPK3 in vitro was assayed by indirect immunofluorescence assay (IFA) at 48 after transfection. The protocol of IFA followed previous report . Briefly, the transfected cells were firstly fixed with 100% acetone and washed with PBS-0.1% Triton-X-100 (PBST). Then goat anti-T. gondii tachyzoites polyclonal antibody (1: 50 dilution in PBST) and fluorescein isothiocyanate (FITC) labeled rabbit anti-goat mouse IgG antibody (1:2 000, Sigma, USA) were added into each well in proper order. As a negative control, the HEK293 cells were transfected with pVAX I.
Immunization and challenge
A total of 100 female Kunming mice were randomly divided into four groups (25 per group). For the experimental group, mice were immunized with 100 μl (100 μg) pVAX-CDPK3 by intramuscular injections and boosted with a two-week interval. Mice were injected with empty pVAX I vector or PBS as negative control groups, and the blank control group received nothing. The sera of all groups were collected from the mouse tail vein prior to each immunization and stored at -20°C for ELISA. Pre-immune serum samples were used as negative controls.
Two weeks after the third inoculation, ten mice in all groups were challenged intraperitoneally with 1 × 103 tachyzoites of the virulent T. gondii RH strain and the survival time were recorded daily until all mice were dead. Three mice of each group were inoculated orally with 10 tissue cysts of the PRU strain and the brain cysts were determined at four weeks after the challenge.
Expression and purification of TgCDPK3 protein in bacteria
The obtained whole coding region was inserted into the prokaryotic expression vector pET-30a, formed pET-CDPK3, and then transformed into E. coli BL21 (DE3) strain and grown in Luria Bertani (LB) with 25 μg/ml kanamycin (Sangon, China). The expression of recombinant TgCDPK3 (rTgCDPK3) was under the condition of 0.6 mM IPTG (Sangon, China) and shaking for 8 hour at 35°C. The rTgCDPK3 protein was purified using Ni-NTA His bind resin (Novagen) according to the manufacturer’s instructions. The products were visualized by the sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).
Immunoblotting analysis of the recombinant protein
The reactogenicity of rTgCDPK3 protein was then detected by immunoblotting. Following SDS-PAGE, rTgCDPK3 protein was electrotransferred onto nitrocellulose (NC) membranes (Pall, USA). Nonspecific binding sites were blocked with 5% bovine serum albumin (BSA) in PBS for 1 h at room temperature (RT). The NC membranes were then incubated with the sera of immunized mice on week 6 (diluted in 1:1 000) for 1 h at RT. After being washed 3 times with PBST (0.5% Tween 20 in PBS), the membranes were incubated with diluted secondary antibody (goat anti-mouse IgG-HRP, Sigma, USA; 1:5 000) for 1 h at RT. Proteins were visualized with 4-chloro-1-naphthol (4-CN, Sangon, China) according to the manufacture’ instruction. Sera collected before vaccinations were used as negative control.
rTgCDPK3-specific humoral immune response was evaluated by ELISA using SBA Clonotyping System-HRP Kit (Southern Biotech CO., LTD, Birmingham, USA) according to the manufacture’s instruction. A total of 100 μl rTgCDPK3 (10 μg/ml) was coated on 96-well microtiter plates at 4°C overnight. Mouse serum samples were added to the wells and incubated at room temperature for 1 h with gentle shaking. Then each well was incubated with 100 μl of HRP conjugated anti-mouse IgG diluted in 1:250, anti-mouse IgG1 or IgG2a (1:500) for 1 h. After added substrate solution (pH 4.0) (1.05% citrate substrate buffer; 1.5% ABTS; 0.03% H2O2) for 20 min, the absorbance was measured at 405 nm. All measurements were performed in triplicate.
Lymphocyte proliferation assay by MTS
Two weeks after the last immunization, three mice per group were euthanized, and their splenocytes were aseptically harvested through a wire mesh and then purified by removing the red blood cells using RBC lysis solution (Sigma, USA). The lymphocytes from each group were then cultured in triplicate at a density of 2 × 105 cells per well in complete medium (DMEM medium + 10% FCS + 100 U/ml penicillin/streptomycin). The cells were stimulated with TLA (10 μg/ml), concanavalin A (ConA; 5 μg/ml; Sigma) or medium alone served as positive and negative controls respectively, at 37°C in a 5% CO2 incubator. The proliferative activity was measured using MTS method (Promega, USA) after four days. The stimulation index (SI) was calculated by using the formula (OD570TLA/OD570M): (OD570ConA/OD570M).
The T cell subclasses, CD4+ and CD8+ in spleen were determined to the percentage using flow cytometry with staining by phycoerythrin (PE)-labeled anti-mouse CD3 (eBioscience), Allophycocyanin (APC)-labeled anti-mouse CD4 (eBioscience) and fluorescein isothiocyanate (FITC)-labeled anti-mouse CD8 (eBioscience) antibodies. After washing by PBS, the cells were fixed with FACScan buffer (PBS containing 1% BSA and 0.1% Sodium azide) and% paraformaldehyde. All the samples were analyzed of fluorescence profiles on a FACScan flow cytometer (BD Biosciences) using SYSTEM II software (Coulter).
The splenocytes without RBC from each group were co-cultured with TLA for positive control and medium alone for negative control in 96-well flat-bottom microtiter plates as described in the section of lymphocyte proliferation assay. Culture supernatants were harvested at 24 h for determination of IL-2 and IL-4, 72 h for IL-10, and 96 h for IL-23, IFN-γ and IL-12(p70) using commercial ELISA kits according to the manufacturer’s instructions (Biolegend, USA). The analysis was performed with the data from three independent experiments.
All statistical analyses were performed following the procedure of SAS (Statistical Analysis System, Version 8.0). The differences of each variable including antibody responses, lymphoproliferation assays, cytokine production, and percentages of CD4+ and CD8+ T cells among all the groups were compared by one-way ANOVA. The level of significant difference in comparisons between groups was defined as P < 0.05.
Detection of the eukaryotic and prokaryotic expression of TgCDPK3
Western blotting and antibody responses
To determine the reactogenicity of rTgCDPK3 protein, western blotting showed that the anti-CDPK3 antibody could recognize the protein at the position of approximately 70 kDa. No band was found when the protein reacted with the negative sera (Figure 2).
Evaluation of splenocyte proliferation
Splenocyte proliferative responses and the percentages of T cell subsets in immunized mice 2 weeks after the last immunization
SI (Mean ± SD)
CD3 + CD4 + CD8- (%)
CD3 + CD8 + CD4- (%)
1.30 ± 0.18**
20.33 ± 3.06**
8.90 ± 2.95
0.89 ± 0.07
14.17 ± 1.88
6.47 ± 1.20
0.91 ± 0.01
13.70 ± 2.41
6.37 ± 1.25
0.97 ± 0.01
15.27 ± 1.89
5.03 ± 0.40
Percentages of CD4+ and CD8+ T lymphocyte
As shown in Table 1, the percentages of CD3+ CD4+ T lymphocytes in pVAX-CDPK3 group (CD4+ with 20.33 ± 3.06) were higher than those in PBS group (CD4+ with 13.70 ± 2.41), in pVAX I group (CD4+ with 14.17 ± 1.88), or in blank control (CD4+ with 15.27 ± 1.89) (P < 0.05). The ratio of CD3+ CD8+ T cells in the spleen of vaccinated mice was slightly higher than that in all the controls, but the difference was not statistically significant (P > 0.05). There was no difference in terms of the percentages of CD3+ CD4+ and CD3+ CD8+ T lymphocytes among the three control groups.
Cytokine production by spleen cells
Cytokine production by splenocytes of immunized Kunming mice after stimulation by toxoplasma lysate antigen a
Cytokine production (pg/ml)
612.11 ± 128.56**
263.79 ± 35.43**
32.42 ± 2.74**
870.12 ± 226.50**
129.63 ± 77.42**
87.59 ± 7.14**
34.91 ± 11.23
322.50 ± 179.17
15.14 ± 7.63
19.93 ± 22.65
36.34 ± 4.83
356.13 ± 175.27
22.31 ± 4.40
27.12 ± 18.46
47.28 ± 16.60
477.25 ± 87.53
22.65 ± 21.90
23.68 ± 14.13
Protective activity induced by vaccination with pVAX-CDPK3
Mean tissue cyst load in the brain of immunized mice after challenge with 10 cysts of T. gondii PRU strain
Number of brain cysts (Means ± SD)
3377.78 ± 226.08
3166.67 ± 258.77
3232.78 ± 196.64
1566.67 ± 167.10**
T. gondii can infect all types of nucleated cells and evolves several pathways to assure entry-exit from the cells . Plant-like CDPKs are considered to play important signaling roles in the signal transduction cascades. Among them, TgCDPK3 activity, which is likely determined by calcium and potassium concentration, can control the calcium-dependent permeabilization of the parasitophorous vacuole membrane (PVM) and regulate microneme secretion and thus plays a vital role in the rapid induction of parasite egress [15, 18]. Considering the crucial biological characteristics of TgCDPK3, we firstly studied the various immune responses elicited by immunization with the DNA vaccine coding TgCDPK3 protein and evaluated its vaccinal potentiality.
In recent years, many studies have evaluated the protective immune responses elicited by different single antigens including ADF, NTPase, IMP, ROM1, ROP18 and elF4A [16, 19–23], which showed partial protection against T. gondii in mice model. In the present study, vaccination of Kunming mice with pVAX-CDPK3 can induce high levels of specific humoral and cellular immune responses, resulting in effective protective immunity, showing increased survival time (RH strain: 13.5 ± 4.89 days, P < 0.05) and reduced brain cysts (PRU strain: 50%, P < 0.05) contrasted with the control mice, which demonstrated that TgCDPK3 is a promising DNA vaccine candidate against toxoplasmosis.
Specific antibody response has been considered to be important in immunity against T. gondii. In the present study, the mice immunized intramuscularly with pVAX-CDPK3 produced specific antibodies against T. gondii CDPK3, which may have the ability to kill the parasite by the attachment of the parasite to the host cell receptors, or the complement protein [24, 25].
Due to the obligate intracellular lifestyle, T cell-mediated adaptive immune responses involving in CD4+ and CD8+ T cells are known to be important in resistance against primary T. gondii infection and reactivation of chronic toxoplasmosis [26–28]. In the present study, a significantly proliferative response of splenocytes from pVAX-CDPK3 vaccinated mice indicated that vigorous cellular immune responses were induced by the DNA vaccine. Furthermore, similar to the results from DNA vaccination with ROP2, actin depolymerizing factor protein (ADP) and rhomboid protein (ROM1) of T. gondii[29–31], the percentages of both CD4+ T cells were also increased in pVAX-CDPK3 immunized mice, which again stated an activated CD4+ T cells immune response.
It is well established that the development of Th1-type lymphocytes are considered to play a critical role in the protective immunity against T. gondii[32–34]. So, the present study further analyzed the CD4+ T cells with a helper T cell type 1 (Th1) cytokine secretion profile and antibodies subclass. Under our experimental conditions, a mixed humoral response (IgG1/ IgG2a) with high ratio of IgG2a to IgG1 antibody titers was observed in the pVAX-CDPK3 vaccinated mice, and Th1 type response correlative cytokines (IFN-γ, IL-2 and IL-12) released from spleen cells of vaccinated mice were observed. The low level increase of Th2 cytokines (IL-4 and IL-10) induced by pVAX-CDPK3, which is also detected in the mice immunized with eIF4A, MIC6 and PLP [19, 35, 36], is likely because the antigen in the cytosol of antigen presenting cells (APCs) was not only processed and presented by MHC Class I molecules but was also present by MHC Class II molecules. These finding revealed that a predominant Th1 type cell immune response has been driven by immunization with pVAX-CDPK3.
Cytokines play an important role in immunity against T. gondii infection by both stimulating macrophages and CTL protective immunity during the innate and adaptive immune response [37, 38]. IL-4 and IL-10 can promote the proliferation and differentiation of activated B cells, mast cells and peripheral lymphocytes and were showed to play an important role during the early phase of acute T. gondii infection [39, 40], which partially contributed to protection against the acute stage of T. gondii infection in the present study. IL-23 secreted by activated macrophages and dendritic cells has been shown to enhance the production of the most critical cytokine, IFN-γ, in mediating host protection against T. gondii infection. IFN-γ, which was produced by T cells and NK cells, can restrict the growth of T. gondii in the acute phase of the infection and the reactivation of parasites from dormant cysts through triggering lysosomal activity, inducing nitric oxide production and modulating metabolic activity of some antigen presenting cells [38, 41, 42]. Furthermore, IFN-γ in combined with IL-2 and IL-12 is involved in the protection against parasitic invasions . Therefore, our results of the high level of IFN-γ, IL-2, IL-12 (p70) and IL-23 in the mice immunized with pVAX-CDPK3 suggested that these Th1-type cytokines confer host resistance against T. gondii infection.
The present study evaluated, for the first time, the immunogenicity and protective potency of a DNA vaccine encoding TgCDPK3, and demonstrated that TgCDPK3 is a potential vaccine candidate against acute and chronic toxoplasmosis in the mice model, and warrant further studies in other apicomplexan parasites.
Project support was provided by the National Natural Science Foundation of China (Grant Nos. 31101812, 31230073 and 31172316), and the Science Fund for Creative Research Groups of Gansu Province (Grant No. 1210RJIA006).
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