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Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains

Toxoplasma gondii is a protozoan parasite, occurring worldwide, endangers human health and causes enormous economic losses to the Ministry of Agriculture. A safe and effective vaccination is needed to handle these problems. In addition, ideal vaccine production is a challenge in the future. In this...

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Autores principales: Wang, Luyao, Tang, Ding, Yang, Chenghang, Yang, Jing, Fang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157538/
https://www.ncbi.nlm.nih.gov/pubmed/31935935
http://dx.doi.org/10.3390/vaccines8010016
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author Wang, Luyao
Tang, Ding
Yang, Chenghang
Yang, Jing
Fang, Rui
author_facet Wang, Luyao
Tang, Ding
Yang, Chenghang
Yang, Jing
Fang, Rui
author_sort Wang, Luyao
collection PubMed
description Toxoplasma gondii is a protozoan parasite, occurring worldwide, endangers human health and causes enormous economic losses to the Ministry of Agriculture. A safe and effective vaccination is needed to handle these problems. In addition, ideal vaccine production is a challenge in the future. In this study, we knocked out the adenylosuccinate lyase (ADSL) gene and found that the gene reduces the growth rate of T. gondii tachyzoites in vitro under standard growth conditions by plaque or replication experiments. Furthermore, mice that were immunized with tachyzoites of the ME49ΔADSL strain induced 100% protection efficacy against challenge with the type 1 strain RH, type 2 strain ME49 and type 3 strain VEG. All mice that were immunized with ME49ΔADSL had a survival rate of 100% when they were reinfected with wild-type strains, either 30 days or 70 days after immunization, and immunization was also protective against homologous infection with 50 T. gondii ME49 tissue cysts. In addition, the level of Toxoplasma-specific IgG was significantly elevated at 30 and 70 days after immunization. ME49ΔADSL induced high levels of Th1 cytokines (interferon gamma (IFN-γ), interleukin (IL)-12) at 4 weeks after immunization and spleen cell cultures from mice vaccinated for 150 days were able to produce robust INF-γ and IL-12 levels in the supernatant. The results of the present study showed that ΔADSL vaccination induced a T. gondii-specific cellular immune response against further infections. These results suggest that the ADSL-deficient vaccine can induce anti-Toxoplasma gondii humoral and cellular immune responses and has 100% immune protection against post-challenge by the type 1 strain RH, type 2 strain ME49 and type 3 strain VEG. It will be used as an excellent candidate for live vaccines and may contribute in a positive meaning to control human toxoplasmosis.
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spelling pubmed-71575382020-05-01 Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains Wang, Luyao Tang, Ding Yang, Chenghang Yang, Jing Fang, Rui Vaccines (Basel) Article Toxoplasma gondii is a protozoan parasite, occurring worldwide, endangers human health and causes enormous economic losses to the Ministry of Agriculture. A safe and effective vaccination is needed to handle these problems. In addition, ideal vaccine production is a challenge in the future. In this study, we knocked out the adenylosuccinate lyase (ADSL) gene and found that the gene reduces the growth rate of T. gondii tachyzoites in vitro under standard growth conditions by plaque or replication experiments. Furthermore, mice that were immunized with tachyzoites of the ME49ΔADSL strain induced 100% protection efficacy against challenge with the type 1 strain RH, type 2 strain ME49 and type 3 strain VEG. All mice that were immunized with ME49ΔADSL had a survival rate of 100% when they were reinfected with wild-type strains, either 30 days or 70 days after immunization, and immunization was also protective against homologous infection with 50 T. gondii ME49 tissue cysts. In addition, the level of Toxoplasma-specific IgG was significantly elevated at 30 and 70 days after immunization. ME49ΔADSL induced high levels of Th1 cytokines (interferon gamma (IFN-γ), interleukin (IL)-12) at 4 weeks after immunization and spleen cell cultures from mice vaccinated for 150 days were able to produce robust INF-γ and IL-12 levels in the supernatant. The results of the present study showed that ΔADSL vaccination induced a T. gondii-specific cellular immune response against further infections. These results suggest that the ADSL-deficient vaccine can induce anti-Toxoplasma gondii humoral and cellular immune responses and has 100% immune protection against post-challenge by the type 1 strain RH, type 2 strain ME49 and type 3 strain VEG. It will be used as an excellent candidate for live vaccines and may contribute in a positive meaning to control human toxoplasmosis. MDPI 2020-01-06 /pmc/articles/PMC7157538/ /pubmed/31935935 http://dx.doi.org/10.3390/vaccines8010016 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Luyao
Tang, Ding
Yang, Chenghang
Yang, Jing
Fang, Rui
Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains
title Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains
title_full Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains
title_fullStr Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains
title_full_unstemmed Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains
title_short Toxoplasma gondiiADSL Knockout Provides Excellent Immune Protection against a Variety of Strains
title_sort toxoplasma gondiiadsl knockout provides excellent immune protection against a variety of strains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157538/
https://www.ncbi.nlm.nih.gov/pubmed/31935935
http://dx.doi.org/10.3390/vaccines8010016
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