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Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status
BACKGROUD: Enteromyxum leei is a myxozoan parasite that produces a slow-progressing intestinal disease. This parasite invades the paracellular space of the intestinal epithelium and progresses from the posterior to the anterior intestine. The aim of the present study was to gain insights into fish T...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069777/ https://www.ncbi.nlm.nih.gov/pubmed/30064468 http://dx.doi.org/10.1186/s13071-018-3007-1 |
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author | Piazzon, M. Carla Estensoro, Itziar Calduch-Giner, Josep A. del Pozo, Raquel Picard-Sánchez, Amparo Pérez-Sánchez, Jaume Sitjà-Bobadilla, Ariadna |
author_facet | Piazzon, M. Carla Estensoro, Itziar Calduch-Giner, Josep A. del Pozo, Raquel Picard-Sánchez, Amparo Pérez-Sánchez, Jaume Sitjà-Bobadilla, Ariadna |
author_sort | Piazzon, M. Carla |
collection | PubMed |
description | BACKGROUD: Enteromyxum leei is a myxozoan parasite that produces a slow-progressing intestinal disease. This parasite invades the paracellular space of the intestinal epithelium and progresses from the posterior to the anterior intestine. The aim of the present study was to gain insights into fish T cell responses in the gilthead sea bream-E. leei infection model using a PCR-array with 30 signature molecules for different leukocyte responses in head kidney, spleen, anterior and posterior intestine. RESULTS: The PCR-array results suggest that E. leei induced migration of T cells from head kidney to intestines where T(H1), CTL and T(H17) profiles were activated and kept in balance by the upregulation of regulatory cytokines. These results were partially validated by the use of cross-reacting antibodies and BrdU immunostaining to monitor proliferation. Zap70 immunostaining supported the increased number of T cells in the anterior intestine detected by gene expression, but double staining with BrdU did not show active proliferation of this cell type at a local level, supporting the migration from lymphohaematopoietic tissues to the site of infection. Global analyses of the expression profiles revealed a clear separation between infected and exposed, but non-infected fish, more evident in the target organ. Exposed, non-infected animals showed an intermediate phenotype closer to the control fish. CONCLUSIONS: These results evidence a clear modulation of the T cell response of gilthead sea bream upon E. leei infection. The effects occurred both at local and systemic levels, but the response was stronger and more specific at the site of infection, the intestine. Altogether, this research poses a promising basis to understand the response against this important parasite and establish effective preventive or palliative measures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3007-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6069777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60697772018-08-03 Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status Piazzon, M. Carla Estensoro, Itziar Calduch-Giner, Josep A. del Pozo, Raquel Picard-Sánchez, Amparo Pérez-Sánchez, Jaume Sitjà-Bobadilla, Ariadna Parasit Vectors Research BACKGROUD: Enteromyxum leei is a myxozoan parasite that produces a slow-progressing intestinal disease. This parasite invades the paracellular space of the intestinal epithelium and progresses from the posterior to the anterior intestine. The aim of the present study was to gain insights into fish T cell responses in the gilthead sea bream-E. leei infection model using a PCR-array with 30 signature molecules for different leukocyte responses in head kidney, spleen, anterior and posterior intestine. RESULTS: The PCR-array results suggest that E. leei induced migration of T cells from head kidney to intestines where T(H1), CTL and T(H17) profiles were activated and kept in balance by the upregulation of regulatory cytokines. These results were partially validated by the use of cross-reacting antibodies and BrdU immunostaining to monitor proliferation. Zap70 immunostaining supported the increased number of T cells in the anterior intestine detected by gene expression, but double staining with BrdU did not show active proliferation of this cell type at a local level, supporting the migration from lymphohaematopoietic tissues to the site of infection. Global analyses of the expression profiles revealed a clear separation between infected and exposed, but non-infected fish, more evident in the target organ. Exposed, non-infected animals showed an intermediate phenotype closer to the control fish. CONCLUSIONS: These results evidence a clear modulation of the T cell response of gilthead sea bream upon E. leei infection. The effects occurred both at local and systemic levels, but the response was stronger and more specific at the site of infection, the intestine. Altogether, this research poses a promising basis to understand the response against this important parasite and establish effective preventive or palliative measures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3007-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-31 /pmc/articles/PMC6069777/ /pubmed/30064468 http://dx.doi.org/10.1186/s13071-018-3007-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Piazzon, M. Carla Estensoro, Itziar Calduch-Giner, Josep A. del Pozo, Raquel Picard-Sánchez, Amparo Pérez-Sánchez, Jaume Sitjà-Bobadilla, Ariadna Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status |
title | Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status |
title_full | Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status |
title_fullStr | Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status |
title_full_unstemmed | Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status |
title_short | Hints on T cell responses in a fish-parasite model: Enteromyxum leei induces differential expression of T cell signature molecules depending on the organ and the infection status |
title_sort | hints on t cell responses in a fish-parasite model: enteromyxum leei induces differential expression of t cell signature molecules depending on the organ and the infection status |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069777/ https://www.ncbi.nlm.nih.gov/pubmed/30064468 http://dx.doi.org/10.1186/s13071-018-3007-1 |
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