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Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing
Gastrointestinal nematode (GIN) infections are considered the most important disease of grazing sheep and due to increasing anthelmintic resistance, chemical control alone is inadequate. Resistance to Gastrointestinal nematode infection is a heritable trait, and through natural selection many sheep...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981634/ https://www.ncbi.nlm.nih.gov/pubmed/36873933 http://dx.doi.org/10.3389/fgene.2023.1111426 |
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author | Dixon, Samantha Karrow, Niel A. Borkowski, Emma Suarez-Vega, Aroa Menzies, Paula I. Kennedy, Delma Peregrine, Andrew S. Mallard, Bonnie A. Cánovas, Ángela |
author_facet | Dixon, Samantha Karrow, Niel A. Borkowski, Emma Suarez-Vega, Aroa Menzies, Paula I. Kennedy, Delma Peregrine, Andrew S. Mallard, Bonnie A. Cánovas, Ángela |
author_sort | Dixon, Samantha |
collection | PubMed |
description | Gastrointestinal nematode (GIN) infections are considered the most important disease of grazing sheep and due to increasing anthelmintic resistance, chemical control alone is inadequate. Resistance to Gastrointestinal nematode infection is a heritable trait, and through natural selection many sheep breeds have higher resistance. Studying the transcriptome from GIN-exposed and GIN-unexposed sheep using RNA-Sequencing technology can provide measurements of transcript levels associated with the host response to Gastrointestinal nematode infection, and these transcripts may harbor genetic markers that can be used in selective breeding programs to enhance disease resistance. The objective of this study was to compare liver transcriptomes of sheep naturally exposed to Gastrointestinal nematode s, with either high or low parasite burdens, to GIN-unexposed control sheep in order to identify key regulator genes and biological processes associated with Gastrointestinal nematode infection. Differential gene expression analysis revealed no significant differentially expressed genes (DEG) between sheep with a high or low parasite burden (p-value ≤0.01; False Discovery Rate (FDR) ≤ 0.05; and Fold-Change (FC) of > ±2). However, when compared to the control group, low parasite burden sheep showed 146 differentially expressed genes (64 upregulated and 82 downregulated in the low parasite burden group relative to the control), and high parasite burden sheep showed 159 differentially expressed genes (57 upregulated and 102 downregulated in the low parasite burden group relative to the control) (p-value ≤0.01; FDR ≤0.05; and FC of > ±2). Among these two lists of significant differentially expressed genes, 86 differentially expressed genes (34 upregulated, 52 downregulated in the parasited group relative to the control) were found in common between the two parasite burden groups compared to the control (GIN-unexposed sheep). Functional analysis of these significant 86 differentially expressed genes found upregulated genes involved in immune response and downregulated genes involved in lipid metabolism. Results of this study offer insight into the liver transcriptome during natural Gastrointestinal nematode exposure that helps provide a better understanding of the key regulator genes involved in Gastrointestinal nematode infection in sheep. |
format | Online Article Text |
id | pubmed-9981634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99816342023-03-04 Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing Dixon, Samantha Karrow, Niel A. Borkowski, Emma Suarez-Vega, Aroa Menzies, Paula I. Kennedy, Delma Peregrine, Andrew S. Mallard, Bonnie A. Cánovas, Ángela Front Genet Genetics Gastrointestinal nematode (GIN) infections are considered the most important disease of grazing sheep and due to increasing anthelmintic resistance, chemical control alone is inadequate. Resistance to Gastrointestinal nematode infection is a heritable trait, and through natural selection many sheep breeds have higher resistance. Studying the transcriptome from GIN-exposed and GIN-unexposed sheep using RNA-Sequencing technology can provide measurements of transcript levels associated with the host response to Gastrointestinal nematode infection, and these transcripts may harbor genetic markers that can be used in selective breeding programs to enhance disease resistance. The objective of this study was to compare liver transcriptomes of sheep naturally exposed to Gastrointestinal nematode s, with either high or low parasite burdens, to GIN-unexposed control sheep in order to identify key regulator genes and biological processes associated with Gastrointestinal nematode infection. Differential gene expression analysis revealed no significant differentially expressed genes (DEG) between sheep with a high or low parasite burden (p-value ≤0.01; False Discovery Rate (FDR) ≤ 0.05; and Fold-Change (FC) of > ±2). However, when compared to the control group, low parasite burden sheep showed 146 differentially expressed genes (64 upregulated and 82 downregulated in the low parasite burden group relative to the control), and high parasite burden sheep showed 159 differentially expressed genes (57 upregulated and 102 downregulated in the low parasite burden group relative to the control) (p-value ≤0.01; FDR ≤0.05; and FC of > ±2). Among these two lists of significant differentially expressed genes, 86 differentially expressed genes (34 upregulated, 52 downregulated in the parasited group relative to the control) were found in common between the two parasite burden groups compared to the control (GIN-unexposed sheep). Functional analysis of these significant 86 differentially expressed genes found upregulated genes involved in immune response and downregulated genes involved in lipid metabolism. Results of this study offer insight into the liver transcriptome during natural Gastrointestinal nematode exposure that helps provide a better understanding of the key regulator genes involved in Gastrointestinal nematode infection in sheep. Frontiers Media S.A. 2023-02-17 /pmc/articles/PMC9981634/ /pubmed/36873933 http://dx.doi.org/10.3389/fgene.2023.1111426 Text en Copyright © 2023 Dixon, Karrow, Borkowski, Suarez-Vega, Menzies, Kennedy, Peregrine, Mallard and Cánovas. https://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 | Genetics Dixon, Samantha Karrow, Niel A. Borkowski, Emma Suarez-Vega, Aroa Menzies, Paula I. Kennedy, Delma Peregrine, Andrew S. Mallard, Bonnie A. Cánovas, Ángela Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing |
title | Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing |
title_full | Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing |
title_fullStr | Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing |
title_full_unstemmed | Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing |
title_short | Identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using RNA-Sequencing |
title_sort | identifying hepatic genes regulating the ovine response to gastrointestinal nematodes using rna-sequencing |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981634/ https://www.ncbi.nlm.nih.gov/pubmed/36873933 http://dx.doi.org/10.3389/fgene.2023.1111426 |
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