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Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice

Entamoeba histolytica is a protozoan that causes amoebiasis. Recent studies demonstrated that natural killer T lymphocytes (NKT) are critical for preventing the development of amoebic liver abscess. In spite of that, there are only a handful of studies in the area. Herein, we explored the role of NK...

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Autores principales: Oliveira, Fabrício M.S., Horta, Bernardo C., Prata, Luana O., Santiago, Andrezza F., Alves, Andréa C., Faria, Ana M.C., Gomes, Maria A., Caliari, Marcelo V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892629/
https://www.ncbi.nlm.nih.gov/pubmed/24470941
http://dx.doi.org/10.4081/idr.2012.e27
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author Oliveira, Fabrício M.S.
Horta, Bernardo C.
Prata, Luana O.
Santiago, Andrezza F.
Alves, Andréa C.
Faria, Ana M.C.
Gomes, Maria A.
Caliari, Marcelo V.
author_facet Oliveira, Fabrício M.S.
Horta, Bernardo C.
Prata, Luana O.
Santiago, Andrezza F.
Alves, Andréa C.
Faria, Ana M.C.
Gomes, Maria A.
Caliari, Marcelo V.
author_sort Oliveira, Fabrício M.S.
collection PubMed
description Entamoeba histolytica is a protozoan that causes amoebiasis. Recent studies demonstrated that natural killer T lymphocytes (NKT) are critical for preventing the development of amoebic liver abscess. In spite of that, there are only a handful of studies in the area. Herein, we explored the role of NKT cells in E. histolytica infection using C57BL/6 wild-type and CD1(−/−) mice. Animals were inoculated with E. histolytica and sacrificed 48 hours later to collect caecum samples that were used for quantitative analyses of lesions, trophozoites, NK1.1(+) T lymphocytes and expression of the mucus protein MUC-2 by immunohistochemistry technique. Quantitative analyses confirmed that the frequency of NK1.1(+) T cells was significantly lower in samples from C57BL/6 CD1(−/−) mice as compared to their wild type (WT) counterparts. The extension of necrotic mucosa was larger and the number of trophozoites higher in Entamoeba (Eh)-infected CD1(−/−) mice when compared with Eh-infected WT mice. In mice from both groups, non-infected (CTRL) and Eh-infected CD1(−/−), there was a reduction in the thickness of the caecal mucosa and in the MUC-2-stained area in comparison with CTRL- and Eh-WT mice. Our results showed that NKT lymphocytes contribute to resistance against Entamoeba histolytica infection and to the control of inflammation in the colitis induced by infection. The presence of a normal epithelial layer containing appropriate levels of mucus had also a protective role against infection.
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spelling pubmed-38926292014-01-27 Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice Oliveira, Fabrício M.S. Horta, Bernardo C. Prata, Luana O. Santiago, Andrezza F. Alves, Andréa C. Faria, Ana M.C. Gomes, Maria A. Caliari, Marcelo V. Infect Dis Rep Article Entamoeba histolytica is a protozoan that causes amoebiasis. Recent studies demonstrated that natural killer T lymphocytes (NKT) are critical for preventing the development of amoebic liver abscess. In spite of that, there are only a handful of studies in the area. Herein, we explored the role of NKT cells in E. histolytica infection using C57BL/6 wild-type and CD1(−/−) mice. Animals were inoculated with E. histolytica and sacrificed 48 hours later to collect caecum samples that were used for quantitative analyses of lesions, trophozoites, NK1.1(+) T lymphocytes and expression of the mucus protein MUC-2 by immunohistochemistry technique. Quantitative analyses confirmed that the frequency of NK1.1(+) T cells was significantly lower in samples from C57BL/6 CD1(−/−) mice as compared to their wild type (WT) counterparts. The extension of necrotic mucosa was larger and the number of trophozoites higher in Entamoeba (Eh)-infected CD1(−/−) mice when compared with Eh-infected WT mice. In mice from both groups, non-infected (CTRL) and Eh-infected CD1(−/−), there was a reduction in the thickness of the caecal mucosa and in the MUC-2-stained area in comparison with CTRL- and Eh-WT mice. Our results showed that NKT lymphocytes contribute to resistance against Entamoeba histolytica infection and to the control of inflammation in the colitis induced by infection. The presence of a normal epithelial layer containing appropriate levels of mucus had also a protective role against infection. PAGEPress Publications 2012-04-27 /pmc/articles/PMC3892629/ /pubmed/24470941 http://dx.doi.org/10.4081/idr.2012.e27 Text en ©Copyright F.M.S. Oliveira et al., 2012 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy
spellingShingle Article
Oliveira, Fabrício M.S.
Horta, Bernardo C.
Prata, Luana O.
Santiago, Andrezza F.
Alves, Andréa C.
Faria, Ana M.C.
Gomes, Maria A.
Caliari, Marcelo V.
Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice
title Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice
title_full Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice
title_fullStr Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice
title_full_unstemmed Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice
title_short Susceptibility to Entamoeba histolytica intestinal infection is related to reduction in natural killer T-lymphocytes in C57BL/6 mice
title_sort susceptibility to entamoeba histolytica intestinal infection is related to reduction in natural killer t-lymphocytes in c57bl/6 mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892629/
https://www.ncbi.nlm.nih.gov/pubmed/24470941
http://dx.doi.org/10.4081/idr.2012.e27
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