Evaluation of Toxoplasma gondii as a live vaccine vector in susceptible and resistant hosts
© Zou et al; licensee BioMed Central Ltd. 2011
Received: 6 April 2011
Accepted: 28 August 2011
Published: 28 August 2011
Toxoplasma gondii has been shown to trigger strong cellular immune responses to heterologous antigens expressed by the parasite in the inbred mouse model . We studied the immune response induced by T. gondii as an effective vaccine vector in chickens and rabbits.
T. gondii RH strain was engineered to express the yellow fluorescent protein (YFP) in the cytoplasm. A subcutaneous injection of the transgenic T. gondii YFP in chickens afforded partial protection against the infection of transgenic E. tenella YFP. T. gondii YFP induced low levels of antibodies to YFP in chickens, suggesting that YFP specific cellular immune response was probably responsible for the protective immunity against E. tenella YFP infection. The measurement of T-cell response and IFN-γ production further confirmed that YFP specific Th1 mediated immune response was induced by T. gondii YFP in immunized chickens. The transgenic T. gondii stimulated significantly higher YFP specific IgG titers in rabbits than in chickens, suggesting greater immunogenicity in a T. gondii susceptible species than in a resistant species. Priming with T. gondii YFP and boosting with the recombinant YFP can induce a strong anti-YFP antibody response in both animal species.
Our findings suggest that T. gondii can be used as an effective vaccine vector and future research should focus on exploring avirulent no cyst-forming strains of T. gondii as a live vaccine vector in animals.
A variety of viruses and bacteria have been used successfully as live vaccine vectors [2–6]. The antigen delivering efficiency and the type of immune response of live vaccine vectors depends on their replication at infected sites and in target cells . An effective live vaccine vector should have the capacity to infect a wide range of target cells with high efficiency and present effectively heterologous antigens to T cells. In addition, a live vaccine vector should also satisfy the requirement of safety and the ease of transfection of foreign DNA into the vector .
Toxoplasma gondii is an obligate intracellular parasite. It can infect any nucleated cells of warm-blood vertebrates [9–12] and induce strong humoral, mucosal and cellular immune responses, making it an attractive system for delivering heterologous antigens . Avirulent strains of T. gondii have been tested to immunize livestock and studied in experimental animals to prevent congenital toxoplasmosis . A commercial live S48 strain vaccine (Ovilis. Toxovax®) for veterinary use has already been approved in some countries [14–16]. Because of the strong immunogenicity, availability of avirulent strains and the ease of genetically engineering stable parasite lines, T. gondii has the potential to be explored as a live vaccine vector for bacterial, viral and parasite pathogens .
Studies on the immune response to T. gondii infection have been conducted extensively in the mouse [1, 18, 19]. Green fluorescent protein (GFP) has been extensively utilized as the reporter protein in genetic manipulation [20–22], and it was also used as a model antigen to study the antigen delivery to target the specific immune response pathway . We posed the following questions: (-) Could foreign antigens expressed by T. gondii stimulate antigen-specific protective immune responses in chickens; (-) whether there is any difference in antigen specific immune responses induced by transgenic T. gondii in chickens, which are naturally resistant to T. gondii infection, and rabbits, which are susceptible to T. gondii infection.
In this study, we developed a transgenic T. gondii that expressed the yellow fluorescent protein (YFP), a yellow version of GFP , as a model antigen. We firstly demonstrated that the transgenic T. gondii YFP elicited YFP-specific immune responses that conferred partial protection against a challenge with YFP-expressing E. tenella. We also showed that immunization with transgenic T. gondii YFP induced greater YFP-specific humoral immune responses in rabbits than in chickens. Our data have obvious implications on the utilization of T. gondii or other apicomplexa protozoa as a live vaccine vector. A commercial live vaccine strain S48 or avirulent no cyst-forming strains of T. gondii need to be used to explore T. gondii as a live vaccine vector in animals in the future study.
Materials and methods
The wild type RH strain of T. gondii and its stably transfected line were maintained by serial passages in African green monkey kidney (VERO) (Shanghai Institutes For Biological sciences, CAS) cells in DMEM supplemented with FBS (10% v/v), penicillin (200 U ml-1) and streptomycin (20 mg ml-1) in a humidified atmosphere of 5% CO2 at 37°C. Stable YFP-transfected Eimeria tenella (E. tenella YFP) was constructed, maintained and propagated in coccidia-free 4-day-old AA broilers , briefly YFP expression vector was transfected into the wild type E. tenella sporozoites, and the transfected sporozoites were inoculated into chickens. At 6-9 days post-infection, oocysts were collected from feces of chickens according to procedures described previously . The YFP positive oocysts were sorted by a MoFloTM cell sorter (Dako Cytomation, Denmark) four times until the percentage of fluorescent oocysts reached 90%.
Transgenic T. gondii
The RH strain T. gondii tachyzoites were propagated, harvested and purified according to established protocols . Freshly purified tachyzoites were suspended in the complete cytomix buffer to a final concentration of 5 × 107 ml-1. The pTgmicYFP plasmid was linearized with the restriction endonuclease BglII and transfected to the parasites by electroporation . Fifty-150 μl linearized pTgmicYFP, 100 U BglII and 1 × 107 tachyzoites in a 4 mm cuvette were subjected to electroporation (Gene Pulser II™, Bio-Rad, USA) at a peak voltage of 2 kV and a capacitance of 25 μF. After electroporation, the parasites were left undisturbed at room temperature for 20 min and then inoculated onto confluent MDBK or VERO cells (Shanghai Institutes For Biological sciences, CAS) in the modified DMEM medium.
The transfected tachyzoites were released and sorted by a MoFlo™cell sorter (Dako Cytomation, Denmark), and the sorted tachyzoites were cultured again in MDBK or VERO cells. After about five passage-sorting cycles, the transgenic line, named as T. gondii YFP was cloned by limiting dilution in 96-well plates .
YFP expression in the transfected tachyzoites was verified by Western blotting. The transgenic and wild parasites were harvested from VERO cells, lysed in SDS sample buffer, and boiled for 10 min. The YFP protein was identified by Western blotting using rabbit anti-GFP antisera (Proteintech, China), goat anti-rabbit IgG conjugated to alkaline phosphatase (Proteintech, China) and chemiluminescent detection (CWBIO, China).
YFP expression by the transgenic line in vivo was studied in mice. The transgenic T. gondii YFP was propogated in Balb/c mice by i.p. inoculation with 1 × 104 tachyzoites per animal. Replicating T. gondii YFP tachyzoites in murine macrophages were harvested from the peritoneal cavity with 4 ml of sterile saline 3 days after inoculation. Parasites in intact macrophages were examined by fluorescence microscopy with 488 nm excitation and 508 nm emission filters.
To determine the fitness of T. gondii YFP, the transgenic and wild type T. gondii at a ratio of 7:3 were inoculated i.p. to mice at 104/animal. The proportion of T. gondii YFP, which were harvested from the peritoneal cavity 3-5 days after inoculation, was measured by FACS after each passage in mice.
Tachyzoite antigens preparation and expression of YFP proteins in bacteria
A crude extract of proteins was obtained by repeated freezing and thawing of 2 × 108 RH tachyzoites in liquid nitrogen. The lysates were centrifuged at 5000 × g for 20 min at 4°C and the supernatants were collected. The YFP gene was cloned from the pTgtubNP-YFP/sagCAT vector . The cloned gene was inserted into the pET-21a vector (Novatech, France). The resulting plasmid was transformed to E. coli BL21 (DE3) cells (Transgen Company, China) with ampicillin selection. The recombinants were harvested after 6 h of induction with IPTG (Isopropyl β-D-1-Thiogalactopyranoside). The YFP protein was purified using a His bind buffer kit (Novatech, France).
Animals and immunization
AA broiler chickens were separately caged in an air-conditioned room. The 15-day-old chickens (n = 10) were immunized s.c. or i.m. with the transgenic or wild type T. gondii (5 × 106/chicken) in complete cytomix buffer (CCB), 160 μg recombinant YFP emulsified in Freund complete adjuvant (FCA) or CCB. Female New Zealand white rabbits (90 days of age) were inoculated with 1 × 107 parasites. The immunized or non-immunized chickens and rabbits were boosted i.m. with 160 μg (chicken) or 500 μg (rabbit) YFP emulsified with FCA. The booster dose was administered 20 (chicken) or 35 (rabbit) days after the primary immunization. Serum anti-YFP antibodies were determined by ELISA 10 days after the primary immunization or the booster immunization.
Additional groups of 10 day old white Leghorn chickens (n = 10) were immunized s.c. twice with the transgenic or wild type T. gondii tachyzoites or160 μg recombinant YFP emulsified in Freund complete adjuvant (FCA) or complete cytomix buffer (un-immunized control) at a dose interval of 15 days. The primary immunization tachyzoites was 5 × 106, and the booster dose was 1 × 107. All chickens were challenged orally with transgenic E. tenella YFP oocysts (1 × 103) 15 days after the booster immunization dose. The immune protection of T. gondii YFP against E. tenella YFP, which carry the same model antigen, was assessed by fecal oocyst excretion and cecum lesions 9 days after the challenge.
Determination of antibody titers
Serum antigen specific IgG of the immunized chickens or rabbits was measured by ELISA. A 96-well microtiter plates were coated with the recombinant YFP harvested from E. coli BL21 bacteria (described above) at 2 μg/ml or tachyzoite antigens at 5 μg/ml in 0.05 M bicarbonate buffer (pH 9.6) overnight at 4°C, and blocked for 2 h at 37°C with 5% milk powder (Difco™skim milk, BD) in PBST(PBS containing 0.05% Tween 20)before washing with PBST. Serially diluted serum samples were added and incubated for 1 h at 37°C. Antigen-specific antibodies were detected with HRP-labeled anti-chicken IgG with 1:1000 dilution or anti-rabbit IgG with 1:5000 dilution in 2% milk-PBST for 1 h at 37°C. The ELISA was developed with 100 μl/well of 10 mg/ml TMB solution in 0.025 M phosphate-citrate buffer (Sigma). The reaction was stopped by 0.2 M H2SO4 and the optical density (OD) at 450 and 630 nm was measured by a plate reader (Bio-Rad, CA, USA). The serum antibody titer was defined as the highest dilution that gave a test/naïve serum OD ratio of 2.1 or higher.
Primer sequences used in Real-time RT-PCR
The cecum of the challenged chickens was collected and fixed in 2.5% (v/v) glutaraldehyde-polyoxymethylene solution immediately after euthanization. The tissue samples were dehydrated and embedded in paraffin wax. Serial paraffin sections (4 um) were obtained and incubated at 37°C for at least 12 h. Paraffin was removed by three consecutive washings in xylol for 5 min each, and then hydrated with in 100, 95, 80, 70 and 50% alcohol and then deionized water. The histological paraffin sections were stained with Hematoxylin & Eosin (HE) and examined under a light microscope.
The data were analyzed using the one-sided student's t-test. A P value less than 0.05 or 0.01 was considered significant.
Transgenic T. gondii expressing the heterologous protein YFP
We engineered transgenic T. gondii expressing YFP as a model antigen by transfection of T. gondii RH with the plasmid pTgmicYFP containing a strong MIC2 promoter (Figure 1A). A stable transgenic line was cloned after several passages in mice and FACS sorting and limiting dilution. The exotic YFP protein expression was confirmed by western blotting. The transgenic T. gondii produced an expected band of 54.6 kDa protein recognized by anti-GFP antibodies, while no positive band was detected for the wild type T. gondii (Figure 1B). Fluorescence microscopy showed that T. gondii YFP expressed abundant YFP protein which was located in the cytoplasm of the parasites (Figure 1C). The transgenic T. gondii was co-passaged with the wild type T. gondii in mice and the proportion of the two lines remained constant after 4 passages (Figure 1D); this indicated that the fitness of the transgenic parasites was not altered after the integration of the exotic DNA into the parasite genome.
Immunization with transgenic T. gondii YFP conferred partial protection against challenge with E. tenella YFP
Histological examination of the cecum showed shedding of mucosal cells and inflammatory cell infiltration of the lamina propria in all groups, but the lesions in the transgenic T gondii group were less severe than the wild type and naïve groups and comparable to the rYFP immunized group (Figure 2C). These data suggest that the transgenic T. gondii YFP can elicit YFP specific immune responses in chickens. Previous studies showed that poultry are protected from coccidiosis mainly by cellular immunity [31, 32]. The protection against E. tenella YFP infection in chickens observed in this study indicated that T. gondii YFP induced YFP specific cellular immunity.
Humoral immune responses of chickens and rabbits to the transgenic T. gondii
Transgenic T. gondii elicited YFP-specific cytokines expression
Transgenic organisms expressing model antigens (e.g. ovalbumin, β-galactosidase) have been conveniently used to search for effective vaccine vectors. Protective effects of the model antigen specific immune response are evaluated by challenging the host with a different virus or bacteria strain or species expressing the same antigen . Although some studies have already begun to explore the apicomplexan parasites as live vaccine vectors [34–38], there had been no studies to use transgenic parasites to express model antigen and induced immunity against infection by other transgenic Apicomplexa parasites, which have more complex life cycles and express more proteins than viruses and bacteria. Although both Eimeria tenella and Toxoplasma gondii are intracellular Apicomplexa parasites, there are significant differences in genome, proteome and life cycle [39, 40]. Our study showed that the transgenic T. gondii expressing YFP induced immunity that partially protected chickens from the challenge with the transgenic E. tenella also expressing YFP. Therefore this study paved the way for the application of a heterologous challenge system to apicomplexa parasites.
Variations in susceptibility of different animal species to T. gondii infection are well known. The resistance is probably attributable to innate immunity or a rapid and strong immune response before the parasite can even disseminate. Chickens inoculated with T. gondii do not show any clinical symptoms , while rabbits are highly susceptible to T. gondii infection . Both chickens and rabbits were chosen to evaluate the humoral immunity induced by the transgenic T. gondii. We observed that the YFP specific humoral immune response in the rabbit was significantly higher than that in the chicken. This implied that the susceptibility was one important determinant of the strength of immune responses. It was reported that six of seven T. gondii isolates from chickens were avirulent in mice, suggesting that the chicken was possibly more susceptible to avirulent T. gondii infection. Therefore, the avirulent T. gondii strain may be an effective vaccine vector for chickens.
It was reported that subunit vaccines predominantly induced high level neutralizing antibodies. To enhance the humoral immune response induced by the transgenic T. gondii in resistant animals, chickens immunized with T. gondii YFP were boosted with the YFP protein. The combined immunization regimen induced a high level humoral response in chickens compared to the weak humoral immunity induced by the transgenic parasite alone. Chicken whether or not they are vaccinated with T. gondii YFP prior to injection with rYFP produce the equivalent titers of anti-YFP antibody, this may be due to the superior ability of rYFP emulsified in FCA to induce high antibody titer which makes the effect of a boost is not visible. For the elicitation of strong cellular and humoral immune responses by transgenic T. gondii, the immunization with a combination of trangesnic parasites-based vaccine and a subunit vaccine should be considered.
Some intracellular pathogens have the coding capacity to produce distinct proteins that are sorted into different intracellular compartments [43, 44]. Studies have shown that only a few proteins of T. gondii can stimulate CD8 T cell-dependent immunity in mice model [44, 45]. Secreted, not cytoplasmic, antigens of T. gondii primed IFN-γ expressing CD8 T cells in mice which was susceptible to T. gondii infection . Chicks, which were resistant to T. gondii infection, have many immunological mechanisms in common with mammals but have evolved distinct immunity to pathogens . Here we showed that cytoplasm-localized YFP expressed by T. gondii can produce protective immune response in chicks that conferred partial protection against challenge with E. tenella YFP. To investigate whether this partial protection was related to the cytoplasm localization of YFP, a transgenic T. gondii line which secreted YFP need to be constructed in the future study to investigate the influences of antigen compartmentalization on the immune response in chickens.
In conclusion, our study demonstrated the feasibility of using T. gondii as a delivery system to induce antigens specific protective immunity against the heterologous pathogen. The recombinant T. gondii-based vaccine priming and subunit vaccine boosting approach would be more effective than immunization with the transfected parasites alone in some animal species. The optimizations of T. gondii as a live vaccine vector to enhance the immune response need to be conducted in the future study.
National Animal Protozoa Laboratorya, and Department of Veterinary Pathologyb, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China. c Department of Etiology, Molecular Parasitology Laboratory, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, China.
d Institute of Pathogen Biology, Chinese Academy of Medical Sciences, Dong Dan San Tiao 9, Beijing 100730, China.
This study was supported by Graduate Research and Innovation Program (Project numbers: 15059206) and the National S & T Major Program (Grant No. 2008ZX10004-011). We declare that the experiments complied with the current laws of China where they were performed.
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