4.2 Article

Toxoplasma gondii: Protective immunity against experimental toxoplasmosis induced by a DNA vaccine encoding the perforin-like protein 1

Journal

EXPERIMENTAL PARASITOLOGY
Volume 128, Issue 1, Pages 38-43

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.exppara.2011.02.005

Keywords

Toxoplasma gondii; Toxoplasmosis; Perforin-like protein 1 (PLP1); Immunity; DNA vaccine; Mice

Categories

Funding

  1. National Natural Science Foundation of China [30901067]
  2. Natural Science Foundation of Guangdong Province [9451064201003715]
  3. State Key Laboratory of Veterinary Etiological Biology
  4. Lanzhou Veterinary Research Institute
  5. Chinese Academy of Agricultural Sciences [SKLVEB2009KFKT014, SKLVEB2010KFKT010]
  6. Program for Changjiang Scholars and Innovative Research Team in University [IRT0723]
  7. Specialized Research Fund for the Doctoral Program of Higher Education [20094404120016]
  8. South China Agricultural University [2009K034, 5500-209073, 4100-K09320]

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Toxoplasma gondii is an important zoonotic parasite infecting about one third of the world population, causing congenital infections and eye disease. T. gondii perforin-like protein 1 (TgPLP1) is believed to be involved in the acute virulence of T. gondii in mice, and is therefore of interest as a vaccine candidate. In this study, we constructed a DNA vaccine expressing TgPLP1, and evaluated the immune response in Kunming mice. The gene sequence encoding TgPLP1 was inserted into the eukaryotic expression vector pVAX I, and Kunming mice were immunized intramuscularly with the plasmid. After immunization, we evaluated the immune response using lymphoproliferative assay, cytokine and antibody measurements, and the survival times of mice challenged lethally with 1 x 10(3) tachyzoites of the virulent T. gondii RH strain. The results showed that pVAX/TgPLP1 alone or with pVAX/IL-18 developed specific anti-TLA (T. gondii lysate antigen) antibodies and specific lymphocyte proliferative responses. Co-injection of pVAX/IL-18 significantly increased the production of IFN-gamma and IL-2. Further, challenge experiments showed that co-immunization of pVAX/TgPLP1 with pVAX/IL-18 significantly (P < 0.05) increased survival time (12.7 +/- 1.2 days) of immunized mice, compared with pVAX/TgPLP1 alone (11.3 +/- 0.9 days). These results demonstrate that TgPLP1 is a potential vaccine candidate against toxoplasmosis, worth further evaluation in other animal hosts. IL-18 could enhance the immune effect of TgPLP1, prolonging the survival time of immunized mice. (C) 2011 Elsevier Inc. All rights reserved.

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