Recombinant Toxoplasma gondii phosphoglycerate mutase 2 confers protective immunity against toxoplasmosis in BALB/c mice

被引:13
作者
Wang, Hai-Long [1 ,2 ]
Wen, Li-Min [1 ,2 ]
Pei, Yan-Jiang [3 ]
Wang, Fen [4 ]
Yin, Li-Tian [1 ,2 ]
Bai, Ji-Zhong [5 ]
Guo, Rui [1 ,2 ]
Wang, Chun-Fang [6 ]
Yin, Guo-Rong [1 ,2 ]
机构
[1] Shanxi Med Univ, Acad Basic Med, Taiyuan 030001, Shanxi, Peoples R China
[2] Shanxi Med Univ, Dept Biochem & Mol Biol, Taiyuan 030001, Shanxi, Peoples R China
[3] Xian Red Cross Hosp, Dept Gen Surg, Xian 710000, Shanxi, Peoples R China
[4] Cent Hosp Enshi Prefecture, Dept Infect Control, Enshi 445000, Hubei, Peoples R China
[5] Univ Auckland, Dept Physiol, Fac Med & Hlth Sci, Private Bag 92-019, Auckland 1142, New Zealand
[6] Shanxi Med Univ, Lab Anim Ctr, Shanxi Key Lab Lab Anim & Anim Models Human Dis, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Toxoplasma gondii; Phosphoglycerate mutase 2; Recombinant protein; Mucosal immunity; Nasal vaccine; VETERINARY VACCINES; MICROARRAY ANALYSIS; HOST-RESISTANCE; CHOLERA-TOXIN; IFN-GAMMA; PROTEINS; IMMUNIZATION; TACHYZOITES; INDUCTION; INFECTION;
D O I
10.1051/parasite/2016012
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Toxoplasmosis is one of the most widespread zoonoses worldwide. It has a high incidence and can result in severe disease in humans and livestock. Effective vaccines are needed to limit and prevent infection with Toxoplasma gondii. In this study, we evaluated the immuno-protective efficacy of a recombinant Toxoplasma gondii phosphoglycerate mutase 2 (rTgPGAM 2) against T. gondii infection in BALB/c mice. We report that the mice nasally immunised with rTgPGAM 2 displayed significantly higher levels of special IgG antibodies against rTgPGAM 2 (including IgG1, IgG2a and IgAs) and cytokines (including IFN-gamma, IL-2 and IL-4) in their blood sera and supernatant of cultured spleen cells compared to those of control animals. In addition, an increased number of spleen lymphocytes and enhanced lymphocyte proliferative responses were observed in the rTgPGAM 2-immunised mice. After chronic infection and lethal challenge with the highly virulent T. gondii RH strain by oral gavage, the survival time of the rTgPGAM 2-immunised mice was longer (P < 0.01) and the survival rate (70%) was higher compared with the control mice (P < 0.01). The reduction rate of brain and liver tachyzoites in rTgPGAM 2-vaccinated mice reached approximately 57% and 69% compared with those of the control mice (P < 0.01). These results suggest that rTgPGAM 2 can generate protective immunity against T. gondii infection in BALB/c mice and may be a promising antigen in the further development of an effective vaccine against T. gondii infection.
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页数:10
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