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Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model

Toxoplasma gondii infection evokes a strong Th1-type response with interleukin (IL)-12 and interferon (IFN)-γ secretion. Recent studies suggest that the infection of pregnant mice with T. gondii may lead to adverse pregnancy results caused by subversion of physiological immune tolerance at maternofe...

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Autores principales: Wang, Cong, Cheng, Weisheng, Yu, Qian, Xing, Tian, Chen, Shoubin, Liu, Lei, Yu, Li, Du, Jian, Luo, Qingli, Shen, Jilong, Xu, Yuanhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992278/
https://www.ncbi.nlm.nih.gov/pubmed/29910815
http://dx.doi.org/10.3389/fimmu.2018.01222
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author Wang, Cong
Cheng, Weisheng
Yu, Qian
Xing, Tian
Chen, Shoubin
Liu, Lei
Yu, Li
Du, Jian
Luo, Qingli
Shen, Jilong
Xu, Yuanhong
author_facet Wang, Cong
Cheng, Weisheng
Yu, Qian
Xing, Tian
Chen, Shoubin
Liu, Lei
Yu, Li
Du, Jian
Luo, Qingli
Shen, Jilong
Xu, Yuanhong
author_sort Wang, Cong
collection PubMed
description Toxoplasma gondii infection evokes a strong Th1-type response with interleukin (IL)-12 and interferon (IFN)-γ secretion. Recent studies suggest that the infection of pregnant mice with T. gondii may lead to adverse pregnancy results caused by subversion of physiological immune tolerance at maternofetal interface rather than direct invasion of the parasite. Genotype-associated dense granule protein GRA15(II) tends to induce classically activated macrophage (M1) differentiation and subsequently activating NK, Th1, and Th17 cells whereas rhoptry protein ROP16(I/III) drives macrophages to alternatively activated macrophage (M2) polarization and elicits Th2 immune response. Unlike the archetypal strains of types I, II, and III, type Chinese 1 strains possess both GRA15(II) and ROP16(I/III), suggesting a distinct pathogenesis of Toxoplasma-involved adverse pregnancies. We constructed T. gondii type Chinese 1 strain of WH3Δrop16 based on CRISPR/Cas9 technology to explore the ROP16(I/III)-deficient/GRA15(II)-dominant parasites in induction of trophoblast apoptosis in vitro and abnormal pregnant outcomes of mice in vivo. Our study showed that Toxoplasma WH3Δrop16 remarkably induced apoptosis of trophoblasts. C57BL/6 pregnant mice injected with the tachyzoites of WH3Δrop16 presented increased absorptivity of fetuses in comparison with the mice infected with WH3 wild type (WH3 WT) parasites although no remarkable difference of virulence to mice was seen between the two strains. Additionally, the mice inoculated with WH3Δrop16 tachyzoites exhibited a notable expression of both IL-17A and IFN-γ, while the percentage of CD4(+)CD25(+)FoxP3 [T regulatory cells (Tregs)] were diminished in splenocytes and placenta tissues compared to those infected with WH3 WT parasites. Accordingly, expressions of IL-4, IL-10, and transforming growth factor beta 1, the pivotal cytokines of Th2 and Tregs response, were significantly dampened whereas IFN-γ and IL-12 expressions were upregulated in WH3Δrop16-infected mice, which gave rise to more prominent outcomes of abnormal pregnancies. Our results indicated that the WH3Δrop16 parasites with gra15(II) background of T. gondii type Chinese 1 strains may cause miscarriage and stillbirth due to subversion of the maternal immune tolerance and system immunity of the animals and the GRA15(II) effector contributes to the process of adverse pregnant consequences.
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spelling pubmed-59922782018-06-15 Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model Wang, Cong Cheng, Weisheng Yu, Qian Xing, Tian Chen, Shoubin Liu, Lei Yu, Li Du, Jian Luo, Qingli Shen, Jilong Xu, Yuanhong Front Immunol Immunology Toxoplasma gondii infection evokes a strong Th1-type response with interleukin (IL)-12 and interferon (IFN)-γ secretion. Recent studies suggest that the infection of pregnant mice with T. gondii may lead to adverse pregnancy results caused by subversion of physiological immune tolerance at maternofetal interface rather than direct invasion of the parasite. Genotype-associated dense granule protein GRA15(II) tends to induce classically activated macrophage (M1) differentiation and subsequently activating NK, Th1, and Th17 cells whereas rhoptry protein ROP16(I/III) drives macrophages to alternatively activated macrophage (M2) polarization and elicits Th2 immune response. Unlike the archetypal strains of types I, II, and III, type Chinese 1 strains possess both GRA15(II) and ROP16(I/III), suggesting a distinct pathogenesis of Toxoplasma-involved adverse pregnancies. We constructed T. gondii type Chinese 1 strain of WH3Δrop16 based on CRISPR/Cas9 technology to explore the ROP16(I/III)-deficient/GRA15(II)-dominant parasites in induction of trophoblast apoptosis in vitro and abnormal pregnant outcomes of mice in vivo. Our study showed that Toxoplasma WH3Δrop16 remarkably induced apoptosis of trophoblasts. C57BL/6 pregnant mice injected with the tachyzoites of WH3Δrop16 presented increased absorptivity of fetuses in comparison with the mice infected with WH3 wild type (WH3 WT) parasites although no remarkable difference of virulence to mice was seen between the two strains. Additionally, the mice inoculated with WH3Δrop16 tachyzoites exhibited a notable expression of both IL-17A and IFN-γ, while the percentage of CD4(+)CD25(+)FoxP3 [T regulatory cells (Tregs)] were diminished in splenocytes and placenta tissues compared to those infected with WH3 WT parasites. Accordingly, expressions of IL-4, IL-10, and transforming growth factor beta 1, the pivotal cytokines of Th2 and Tregs response, were significantly dampened whereas IFN-γ and IL-12 expressions were upregulated in WH3Δrop16-infected mice, which gave rise to more prominent outcomes of abnormal pregnancies. Our results indicated that the WH3Δrop16 parasites with gra15(II) background of T. gondii type Chinese 1 strains may cause miscarriage and stillbirth due to subversion of the maternal immune tolerance and system immunity of the animals and the GRA15(II) effector contributes to the process of adverse pregnant consequences. Frontiers Media S.A. 2018-06-01 /pmc/articles/PMC5992278/ /pubmed/29910815 http://dx.doi.org/10.3389/fimmu.2018.01222 Text en Copyright © 2018 Wang, Cheng, Yu, Xing, Chen, Liu, Yu, Du, Luo, Shen and Xu. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Wang, Cong
Cheng, Weisheng
Yu, Qian
Xing, Tian
Chen, Shoubin
Liu, Lei
Yu, Li
Du, Jian
Luo, Qingli
Shen, Jilong
Xu, Yuanhong
Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model
title Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model
title_full Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model
title_fullStr Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model
title_full_unstemmed Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model
title_short Toxoplasma Chinese 1 Strain of WH3Δrop16(I/III)/gra15(II) Genetic Background Contributes to Abnormal Pregnant Outcomes in Murine Model
title_sort toxoplasma chinese 1 strain of wh3δrop16(i/iii)/gra15(ii) genetic background contributes to abnormal pregnant outcomes in murine model
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992278/
https://www.ncbi.nlm.nih.gov/pubmed/29910815
http://dx.doi.org/10.3389/fimmu.2018.01222
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