Protective efficacy of recombinant Toxoplasma gondii dense granule protein 15 against toxoplasmosis in C57BL/6 mice

• Published in: Vaccine 2024-04, Vol.42 (9), p.2299-2309
• Main Authors: Hasan, Tanjila, Shimoda, Naomi, Nakamura, Shu, Fox, Barbara A., Bzik, David J., Ushio-Watanabe, Nanako, Nishikawa, Yoshifumi
• Format: Article
• Language: English
• Subjects: Antibodies; Antigens; Cell culture; Cell proliferation; Cloning; Congenital diseases; Effectiveness; GRA15; Granular materials; Immune response (cell-mediated); Immune response (humoral); Immunity; Immunization; Immunoglobulin G; Immunomodulation; Immunostimulation; Immunostimulatory activity; Infections; Laboratory animals; Life sciences; Macrophages; Medical research; Molecular weight; NF-κB protein; Parasites; Parasitic diseases; Proteins; Protozoa; Public health; Recombinant vaccine; Sheep; Spleen; Survival; Toxoplasma; Toxoplasma gondii; Toxoplasmosis; Vaccines; Veterinary medicine; Virulence; Zoonoses; γ-Interferon
• ISSN: 0264-410X; 1873-2518
• DOI: 10.1016/j.vaccine.2024.02.062

Toxoplasma gondii is a pervasive protozoan parasite that is responsible for significant zoonoses. A wide array of vaccines using different effector molecules of T. gondii have been studied worldwide to control toxoplasmosis. None of the existing vaccines are sufficiently effective to confer protective immunity. Among the different Toxoplasma-derived effector molecules, T. gondii dense granule protein 15 from the type II strain (GRA15 (II)) was recently characterized as an immunomodulatory molecule that induced host immunity via NF-κB. Therefore, we assessed the immunostimulatory and protective efficacy of recombinant GRA15 (II) (rGRA15) against T. gondii infection in a C57BL/6 mouse model. We observed that rGRA15 treatment increased the production of IL-12p40 from mouse peritoneal macrophages in vitro. Immunization of mice with rGRA15 induced the production of anti-TgGRA15-specific IgG, IgG1 and IgG2c antibodies. The rGRA15-sensitized spleen cells from mice inoculated with the same antigen strongly promoted spleen cell proliferation and IFN-γ production. Immunization with rGRA15 significantly enhanced the survival rate of mice and dramatically decreased parasite burden in mice challenged with the Pru (type II) strain. These results suggested that rGRA15 triggered humoral and cellular immune responses to control infection. However, all of the immunized mice died when challenged with the GRA15-deficient Pru strain or the RH (type I) strain. These results suggest that GRA15 (II)-dependent immunity plays a crucial role in protection against challenge infection with the type II strain of T. gondii. This study is the first report to show GRA15 (II) as a recombinant vaccine antigen against Toxoplasma infection.