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Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis
Toxoplasma gondii is a ubiquitous apicomplexan protozoan parasite that can infect all warm-blooded animals, causing toxoplasmosis. Thus, efficient diagnosis methods for acute T. gondii infection are essential for its management. Circulating antigens (CAgs) are reliable diagnostic indicators of acute...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848078/ https://www.ncbi.nlm.nih.gov/pubmed/33537014 http://dx.doi.org/10.3389/fmicb.2020.612252 |
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author | Liu, Qi Jiang, Wei Chen, Yun Zhang, Manyu Geng, Xiaoling Wang, Quan |
author_facet | Liu, Qi Jiang, Wei Chen, Yun Zhang, Manyu Geng, Xiaoling Wang, Quan |
author_sort | Liu, Qi |
collection | PubMed |
description | Toxoplasma gondii is a ubiquitous apicomplexan protozoan parasite that can infect all warm-blooded animals, causing toxoplasmosis. Thus, efficient diagnosis methods for acute T. gondii infection are essential for its management. Circulating antigens (CAgs) are reliable diagnostic indicators of acute infection. In this study, we established a mouse model of acute T. gondii infection and explored new potential diagnostic factors. CAgs levels peaked 60 h after T. gondii inoculation and 31 CAgs were identified by immunoprecipitation-liquid chromatography-tandem mass spectrometry, among which RuvB-like helicase (TgRuvBL1), ribonuclease (TgRNaseH1), and ribosomal protein RPS2 (TgRPS2) were selected for prokaryotic expression. Polyclonal antibodies against these three proteins were prepared. Results from indirect enzyme-linked immunosorbent assay indicated that anti-rTgRuvBL1, anti-rTgRNase H1, and anti-rTgRPS2 mouse sera were recognized by natural excretory-secretory antigens from T. gondii tachyzoites. Moreover, immunofluorescence assays revealed that TgRuvBL1 was localized in the nucleus, while TgRNase H1 and TgRPS2 were in the apical end. Western blotting data confirmed the presence of the three proteins in the sera of the infected mice. Moreover, mice immunized with rTgRuvBL1 (10.0 ± 0.30 days), TgRNaseH1 (9.67 ± 0.14 days), or rTgRPS2 (11.5 ± 0.34 days) had slightly longer lifespan when challenged with a virulent T. gondii RH strain. Altogether, these findings indicate that these three proteins can potentially be diagnostic candidates for acute toxoplasmosis. However, they hold poor protective potential against highly virulent T. gondii infection. |
format | Online Article Text |
id | pubmed-7848078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78480782021-02-02 Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis Liu, Qi Jiang, Wei Chen, Yun Zhang, Manyu Geng, Xiaoling Wang, Quan Front Microbiol Microbiology Toxoplasma gondii is a ubiquitous apicomplexan protozoan parasite that can infect all warm-blooded animals, causing toxoplasmosis. Thus, efficient diagnosis methods for acute T. gondii infection are essential for its management. Circulating antigens (CAgs) are reliable diagnostic indicators of acute infection. In this study, we established a mouse model of acute T. gondii infection and explored new potential diagnostic factors. CAgs levels peaked 60 h after T. gondii inoculation and 31 CAgs were identified by immunoprecipitation-liquid chromatography-tandem mass spectrometry, among which RuvB-like helicase (TgRuvBL1), ribonuclease (TgRNaseH1), and ribosomal protein RPS2 (TgRPS2) were selected for prokaryotic expression. Polyclonal antibodies against these three proteins were prepared. Results from indirect enzyme-linked immunosorbent assay indicated that anti-rTgRuvBL1, anti-rTgRNase H1, and anti-rTgRPS2 mouse sera were recognized by natural excretory-secretory antigens from T. gondii tachyzoites. Moreover, immunofluorescence assays revealed that TgRuvBL1 was localized in the nucleus, while TgRNase H1 and TgRPS2 were in the apical end. Western blotting data confirmed the presence of the three proteins in the sera of the infected mice. Moreover, mice immunized with rTgRuvBL1 (10.0 ± 0.30 days), TgRNaseH1 (9.67 ± 0.14 days), or rTgRPS2 (11.5 ± 0.34 days) had slightly longer lifespan when challenged with a virulent T. gondii RH strain. Altogether, these findings indicate that these three proteins can potentially be diagnostic candidates for acute toxoplasmosis. However, they hold poor protective potential against highly virulent T. gondii infection. Frontiers Media S.A. 2021-01-18 /pmc/articles/PMC7848078/ /pubmed/33537014 http://dx.doi.org/10.3389/fmicb.2020.612252 Text en Copyright © 2021 Liu, Jiang, Chen, Zhang, Geng and Wang. http://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(s) 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 | Microbiology Liu, Qi Jiang, Wei Chen, Yun Zhang, Manyu Geng, Xiaoling Wang, Quan Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis |
title | Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis |
title_full | Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis |
title_fullStr | Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis |
title_full_unstemmed | Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis |
title_short | Study on Circulating Antigens in Serum of Mice With Experimental Acute Toxoplasmosis |
title_sort | study on circulating antigens in serum of mice with experimental acute toxoplasmosis |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848078/ https://www.ncbi.nlm.nih.gov/pubmed/33537014 http://dx.doi.org/10.3389/fmicb.2020.612252 |
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