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Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii
BACKGROUND: Although sexual reproduction of the parasite Toxoplasma gondii exclusively occurs in the cat intestine, knowledge about the alteration of gene expression in the intestine of cats infected with T. gondii is still limited. Here, we investigated the temporal transcriptional changes that occ...
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/PMC6236892/ https://www.ncbi.nlm.nih.gov/pubmed/30428922 http://dx.doi.org/10.1186/s13071-018-3179-8 |
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author | Wang, Meng Zhang, Fu-Kai Elsheikha, Hany M. Zhang, Nian-Zhang He, Jun-Jun Luo, Jian-Xun Zhu, Xing-Quan |
author_facet | Wang, Meng Zhang, Fu-Kai Elsheikha, Hany M. Zhang, Nian-Zhang He, Jun-Jun Luo, Jian-Xun Zhu, Xing-Quan |
author_sort | Wang, Meng |
collection | PubMed |
description | BACKGROUND: Although sexual reproduction of the parasite Toxoplasma gondii exclusively occurs in the cat intestine, knowledge about the alteration of gene expression in the intestine of cats infected with T. gondii is still limited. Here, we investigated the temporal transcriptional changes that occur in the cat intestine during T. gondii infection. METHODS: Cats were infected with 100 T. gondii cysts and their intestines were collected at 6, 12, 18, 24, 72 and 96 hours post-infection (hpi). RNA sequencing (RNA-Seq) Illumina technology was used to gain insight into the spectrum of genes that are differentially expressed due to infection. Quantitative RT-PCR (qRT-PCR) was also used to validate the level of expression of a set of differentially expressed genes (DEGs) obtained by sequencing. RESULTS: Our transcriptome analysis revealed 2363 DEGs that were clustered into six unique patterns of gene expression across all the time points after infection. Our analysis revealed 56, 184, 404, 508, 400 and 811 DEGs in infected intestines compared to uninfected controls at 6, 12, 18, 24, 72 and 96 hpi, respectively. RNA-Seq results were confirmed by qRT-PCR. DEGs were mainly enriched in catalytic activity and metabolic process based on gene ontology enrichment analysis. Kyoto Encyclopedia of Genes and Genomes pathway analysis showed that transcriptional changes in the intestine of infected cats evolve over the course of infection, and the largest difference in the enriched pathways was observed at 96 hpi. The anti-T. gondii defense response of the feline host was mediated by Major Histocompatibility Complex class I, proteasomes, heat-shock proteins and fatty acid binding proteins. CONCLUSIONS: This study revealed novel host factors, which may be critical for the successful establishment of an intracellular niche during T. gondii infection in the definitive feline host. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3179-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6236892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62368922018-11-20 Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii Wang, Meng Zhang, Fu-Kai Elsheikha, Hany M. Zhang, Nian-Zhang He, Jun-Jun Luo, Jian-Xun Zhu, Xing-Quan Parasit Vectors Research BACKGROUND: Although sexual reproduction of the parasite Toxoplasma gondii exclusively occurs in the cat intestine, knowledge about the alteration of gene expression in the intestine of cats infected with T. gondii is still limited. Here, we investigated the temporal transcriptional changes that occur in the cat intestine during T. gondii infection. METHODS: Cats were infected with 100 T. gondii cysts and their intestines were collected at 6, 12, 18, 24, 72 and 96 hours post-infection (hpi). RNA sequencing (RNA-Seq) Illumina technology was used to gain insight into the spectrum of genes that are differentially expressed due to infection. Quantitative RT-PCR (qRT-PCR) was also used to validate the level of expression of a set of differentially expressed genes (DEGs) obtained by sequencing. RESULTS: Our transcriptome analysis revealed 2363 DEGs that were clustered into six unique patterns of gene expression across all the time points after infection. Our analysis revealed 56, 184, 404, 508, 400 and 811 DEGs in infected intestines compared to uninfected controls at 6, 12, 18, 24, 72 and 96 hpi, respectively. RNA-Seq results were confirmed by qRT-PCR. DEGs were mainly enriched in catalytic activity and metabolic process based on gene ontology enrichment analysis. Kyoto Encyclopedia of Genes and Genomes pathway analysis showed that transcriptional changes in the intestine of infected cats evolve over the course of infection, and the largest difference in the enriched pathways was observed at 96 hpi. The anti-T. gondii defense response of the feline host was mediated by Major Histocompatibility Complex class I, proteasomes, heat-shock proteins and fatty acid binding proteins. CONCLUSIONS: This study revealed novel host factors, which may be critical for the successful establishment of an intracellular niche during T. gondii infection in the definitive feline host. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3179-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-14 /pmc/articles/PMC6236892/ /pubmed/30428922 http://dx.doi.org/10.1186/s13071-018-3179-8 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 Wang, Meng Zhang, Fu-Kai Elsheikha, Hany M. Zhang, Nian-Zhang He, Jun-Jun Luo, Jian-Xun Zhu, Xing-Quan Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii |
title | Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii |
title_full | Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii |
title_fullStr | Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii |
title_full_unstemmed | Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii |
title_short | Transcriptomic insights into the early host-pathogen interaction of cat intestine with Toxoplasma gondii |
title_sort | transcriptomic insights into the early host-pathogen interaction of cat intestine with toxoplasma gondii |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236892/ https://www.ncbi.nlm.nih.gov/pubmed/30428922 http://dx.doi.org/10.1186/s13071-018-3179-8 |
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