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Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum
Neospora caninum is a protozoan parasite that causes neurological disorders in dogs and cattle. It can cause nonsuppurative meningoencephalitis and a variety of neuronal symptoms are observed, particularly in dogs. However, the pathogenic mechanism, including the relationship between the parasite di...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300462/ https://www.ncbi.nlm.nih.gov/pubmed/25604996 http://dx.doi.org/10.1038/srep07936 |
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author | Nishimura, Maki Tanaka, Sachi Ihara, Fumiaki Muroi, Yoshikage Yamagishi, Junya Furuoka, Hidefumi Suzuki, Yutaka Nishikawa, Yoshifumi |
author_facet | Nishimura, Maki Tanaka, Sachi Ihara, Fumiaki Muroi, Yoshikage Yamagishi, Junya Furuoka, Hidefumi Suzuki, Yutaka Nishikawa, Yoshifumi |
author_sort | Nishimura, Maki |
collection | PubMed |
description | Neospora caninum is a protozoan parasite that causes neurological disorders in dogs and cattle. It can cause nonsuppurative meningoencephalitis and a variety of neuronal symptoms are observed, particularly in dogs. However, the pathogenic mechanism, including the relationship between the parasite distribution and the clinical signs, is unclear. In this study, to understand the pathogenic mechanism of neosporosis, parasite distribution and lesions were assessed in the brain of mice infected with N. caninum (strain Nc-1). Host gene expression was also analyzed with RNA sequencing (RNA-Seq). The histopathological lesions in the frontal lobe and the medulla oblongata were significantly more severe in symptomatic mice than in asymptomatic mice, although no association between the severity of the lesions and parasite numbers was found. In infected mice, the expression of 772 mouse brain genes was upregulated. A GOstat analysis predicted that the upregulated genes were involved in the host immune response. Genes whose expression correlated positively and negatively with parasite numbers were involved in the host immune response, and neuronal morphogenesis and lipid metabolic processes, respectively. These results suggest that changes in the gene expression profile associated with neuronal functions as well as immune responses can contribute to the pathogenesis in N. caninum-infected animals. |
format | Online Article Text |
id | pubmed-4300462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43004622015-01-27 Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum Nishimura, Maki Tanaka, Sachi Ihara, Fumiaki Muroi, Yoshikage Yamagishi, Junya Furuoka, Hidefumi Suzuki, Yutaka Nishikawa, Yoshifumi Sci Rep Article Neospora caninum is a protozoan parasite that causes neurological disorders in dogs and cattle. It can cause nonsuppurative meningoencephalitis and a variety of neuronal symptoms are observed, particularly in dogs. However, the pathogenic mechanism, including the relationship between the parasite distribution and the clinical signs, is unclear. In this study, to understand the pathogenic mechanism of neosporosis, parasite distribution and lesions were assessed in the brain of mice infected with N. caninum (strain Nc-1). Host gene expression was also analyzed with RNA sequencing (RNA-Seq). The histopathological lesions in the frontal lobe and the medulla oblongata were significantly more severe in symptomatic mice than in asymptomatic mice, although no association between the severity of the lesions and parasite numbers was found. In infected mice, the expression of 772 mouse brain genes was upregulated. A GOstat analysis predicted that the upregulated genes were involved in the host immune response. Genes whose expression correlated positively and negatively with parasite numbers were involved in the host immune response, and neuronal morphogenesis and lipid metabolic processes, respectively. These results suggest that changes in the gene expression profile associated with neuronal functions as well as immune responses can contribute to the pathogenesis in N. caninum-infected animals. Nature Publishing Group 2015-01-21 /pmc/articles/PMC4300462/ /pubmed/25604996 http://dx.doi.org/10.1038/srep07936 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Nishimura, Maki Tanaka, Sachi Ihara, Fumiaki Muroi, Yoshikage Yamagishi, Junya Furuoka, Hidefumi Suzuki, Yutaka Nishikawa, Yoshifumi Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum |
title | Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum |
title_full | Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum |
title_fullStr | Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum |
title_full_unstemmed | Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum |
title_short | Transcriptome and Histopathological Changes in Mouse Brain Infected with Neospora caninum |
title_sort | transcriptome and histopathological changes in mouse brain infected with neospora caninum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300462/ https://www.ncbi.nlm.nih.gov/pubmed/25604996 http://dx.doi.org/10.1038/srep07936 |
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