Virus-like Particle Vaccine Containing Toxoplasma gondii Rhoptry Protein 13 Induces Protection against T. gondii ME49 Infection in Mice

Abstract

Toxoplasma gondii can infect humans worldwide, causing serious diseases in pregnant women and immunocompromised individuals. T. gondii rhoptry protein 13 (ROP13) is known as one of the key proteins involved in host cell invasion. In this study, we generated virus-like particles (VLPs) vaccine expressing T. gondii rhoptry ROP13 and investigated VLPs vaccine efficacy in mice. Mice immunized with ROP13 VLPs vaccine elicited significantly higher levels of T. gondii-specific IgG, IgG1, IgG2a, and IgA antibody responses following boost immunization and challenge infection, whereas antibody inductions were insignificant upon prime immunization. Differing immunization routes resulted in differing antibody induction, as intranasal immunization (IN) induced greater antibody responses than intramuscular immunization (IM) after boost and challenge infection. IN immunization induced significantly higher levels of IgG and IgA antibody responses from feces, antibody-secreting cells (ASCs), CD4⁺ T, CD8⁺ T cells and germinal center B cell responses in the spleen compared to IM immunization. Compared to IM immunization, IN immunization resulted in significantly reduced cyst counts in the brain as well as lesser body weight loss, which contributed to better protection. All of the mice immunized through either route survived, whereas all naïve control mice perished. These results indicate that the ROP13 VLPs vaccine could be a potential vaccine candidate against T. gondii infection.

Toxoplasma gondii can infect almost all warm-blooded animals such as humans, animals, and birds [1]. Although T. gondii transmission occurs through feline feces, ingestion of raw, undercooked meat contaminated with T. gondii tachyzoites and bradyzoites leads to human infection. Symptoms can be severe in the immunocompromised or in patients receiving organ transplantation, as its infection can affect various organs including the brain and the eyes. Vertical transmission of T. gondii through the placenta can occur, and its fetal infection induces abortion and stillbirth in pregnant women [2]. An effective human vaccine against T. gondii infection is currently unavailable. DNA, subunit or protein vaccines against T. gondii have been studied but were unsuccessful [3,4]. As such, finding novel vaccines that are highly effective against T. gondii infection remains a great challenge for researchers. Recently, we reported that influenza virus-like particles (VLPs) vaccines containing T. gondii antigenic proteins (IMC, MIC8, ROP18, ROP13, ROP4) provide protection against T. gondii (RH) and/or T. gondii (ME49) infections [5–8]. T. gondii ROP13 secreted by T. gondii rhoptry organ has been recognized as an important antigen. Since there is no comparative study on immunization route on ROP13 VLPs, in this study, the vaccine efficacies induced by ROP13 VLPs immunization by intramuscular (IM) and intranasal (IN) routes were evaluated and compared.

Recombinant baculoviruses expressing ROP13 protein and related influenza VLPs vaccine were generated and characterized as indicated previously [8]. Female BALB/c mice (n=6 per group) were used for ROP13 VLPs immunization by intranasal or intramuscular routes as described previously [8]. Blood from mice was collected by retro-orbital plexus puncture 30 days after prime and boost immunization and challenge infection. Isolated sera from blood were used to determine IgG, IgG1, IgG2a, and IgA by enzyme-linked immunosorbent assay (ELISA). Mice fecal samples were collected 30 days after challenge infection. Feces homogenized in PBS were centrifuged at 13,500 RPM, 10 min for supernatant acquisition. The obtained supernatants were used to measure IgG and IgA antibody responses [5]. To measure antibody-secreting cell (ASC) from the spleen of sacrificed mice, isolated splenocytes (1×10⁶ cells/well) were cultured for 3 days at 37°C with 5% CO₂ in plates coated with 4 μg/ml of T. gondii RH antigen. After 3 days, plates were incubated with IgG and IgA (1:2,000 dilution in PBST) for 1 hr at 37°C to measure the level of antibodies being secreted. Additionally, to determine the splenic CD4⁺, CD8⁺ T cell, and germinal center B cell populations, splenocytes (1×10⁶ cells) were added to each tube. Surface markers were stained with fluorophore-conjugated antibodies specific to cell phenotypes (CD3e-PE-Cy7, CD4-FITC, CD8-PE, CD45-FITC, GL7-PE) (BD Biosciences, San Jose, California, USA). Cells were acquired and data were analyzed using BD Accuri C6 Flow Cytometer and C6 Analysis software, respectively (BD Biosciences). To determine the cysts count after infection, brain tissues were harvested from mice at 1 month post-infection, and homogenized in 400 μl of PBS. Homogenized solutions were resuspended in 45% Percoll and centrifuged for 20 min at 4°C, 12,100 RPM. Afterward, cyst layers were carefully collected and washed with PBS at 6,000 RPM for 20 min. All data were presented as mean±SD and statistical significances between groups were analyzed by 1-way ANOVA and Student’s t-test using GraphPad Prism version 5.0. P-values (*P<0.05, **P<0.01, ***P<0.001) were considered statistically significant.

Mice serum samples collected after prime, boost immunization and challenge infection were used to measure T. gondii-specific antibody responses. ROP13 VLPs immunization through the intranasal route (IN) induced higher levels of T. gondii-specific IgG (Fig. 1A), IgG1 (Fig. 1B), IgG2a (Fig. 1C) and IgA (Fig. 1D) antibody responses after boost and challenge infection compared to IM. At 4 weeks following challenge infection with T. gondii ME49, CD4⁺ T cell, CD8⁺ T cell, and germinal center B cell responses in immunized mice were observed. As shown in Fig. 2, significantly higher population of CD4⁺ T cell (17.8%, Fig. 2A), CD8⁺ T cells (8.7%, Fig. 2B) and germinal center B cells (5.2%, Fig. 2C) were shown from IN immunization compared to IM immunization. The antibody secretions were measured from splenocytes isolated after challenge infection. Compared to IN immunization, the levels of IgG (Fig. 2D) and IgA (Fig. 2E) in ASC of IM immunization was lower. These results indicated that IN immunization induced higher levels of ASC responses compared to IM immunization. Based on these results, ROP13 VLPs significantly reduced the cysts count in both IN and IM, with better protection being demonstrated by the former (Fig. 2F). T. gondii-specific IgG and IgA antibody responses in the feces were examined by obtaining feces after challenge infection. As shown in Fig. 3A, B, IN immunization elicited significantly higher levels of T. gondii-specific IgG and IgA antibodies in the feces compared to IM immunization. The body weight changes and survival rates were measured for 60 days as illustrated in Fig. 4A, B. IN immunization showed less body weight loss (9%) compared to IM immunization (13%). All mice from IN and IM immunization groups survived (Fig. 4B).

Fig. 1.

T. gondii-specific antibody response in sera. (A) T. gondii-specific IgG, (B) IgG1, (C) IgG2a, and (D) IgA in sera were determined. *P<0.05, **P<0.01, ***P<0.001. Data are expressed as mean±SD.

Fig. 2.

Protective immune responses induced by ROP13 VLPs vaccination. Four weeks after challenge infection, splenocytes were isolated from mice. (A) CD4⁺ and (B) CD8⁺ T cells in spleen (C) B cell in germinal center. The splenocyte obtained from mice challenge-infected with T. gondii at 1 month after boost. (D) IgG and (E) IgA antibody-secreting responses. (F) Cyst counts in the brain, one month after challenge infection. (*P<0.05, **P<0.01). Naïve+Cha, Naïve mice were challenge-infected.

Fig. 3.

IgG (A) and IgA (B) antibody responses in fecal samples. Feces were collected at 1 month after challenge infection with T. gondii. *P<0.05, **P<0.01.

Fig. 4.

Body weight (A) and survival (B) of mice immunized with ROP13 VLPs and challenge with T. gondii ME49 (450 cyst). *P<0.05, **P<0.01. Data are expressed as mean±SD.

In this study, we investigated the protective efficacy of T. gondii ROP13 vaccine generated in a virus-like particle form using ROP13, a protein secreted from the rhoptries which assists host cell invasion [4]. In this study, influenza VLPs expressing ROP13 were generated and protective immunity induced by IN or IM ROP13 VLPs immunizations were evaluated. In comparison to IM immunization, IN immunization induced higher levels of T. gondii-specific IgG, IgG1, IgG2a, and IgA antibody responses in sera, ASC and T cell responses, along with a significant reduction of cyst counts in the brain.

In general, memory B cells and plasma cells for specific antigens after immunization gradually decrease and are present at low levels. However, upon additional immunization or specific pathogen invasion, rapid proliferation of memory B cells and plasma cells occur [9,10]. In the present study, ROP13 VLPs immunization elicited high levels of IgG and IgA secretions from splenocytes after 3 days of in vitro cultures, in which IN immunization showed higher ASC response than IM immunization. We observed significantly higher levels of CD4⁺, CD8⁺ T cell, and B cell responses in VLPs immunization compared to naïve control. CD4⁺ T cells activated by ROP13 VLPs differentiated into Th1 and Th2 cells. Subsequent B cell activation by Th1 and Th2 cells leads to IgG2a and IgG1 antibody production in large quantities [11,12]. We found significantly higher levels of IgG, IgG1, IgG2a, and IgA antibody responses in sera from IN than IM immunization after immunization and challenge infection with T. gondii ME49. Mucosal immunity seems to play a critical role in enhancing immunity induced through IN immunization than by IM immunization. In the current study, IN immunization induced higher levels of mucosal IgG and IgA antibody responses in feces compared to IM immunization. Immunized mice were infected with T. gondii ME49 through the oral route, which is its natural route of infection. Thus, in the present study, IN immunization induced higher levels of T. gondii-specific IgG and IgA antibody responses in feces which might contribute to better protection against T. gondii ME49 infection than IM immunization. Bradyzoite (cyst) formation in the brains can occur upon infection with T. gondii ME49. ROP13 VLPs immunization by IN route showed significantly decreased brain cyst count. Mice immunized with ROP13 VLPs showed 100% survival, but all naïve mice died by day 35 after lethal challenge infection.

In summary, this study demonstrates that ROP13 VLPs is an effective vaccine against T. gondii ME49 infection in which IN immunization showed higher vaccine efficacy than IM immunization. T. gondii-specific IgG, IgG1, IgG2a, and IgA antibody responses in sera, mucosal IgG and IgA antibodies from feces, CD4⁺ T cells, and CD8⁺ T cells responses were higher in IN immunization than IM immunization, which may have contributed to significant cyst count reductions in the brain.