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Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle

The response of the abomasal transcriptome to gastrointestinal parasites was evaluated in parasite-susceptible and parasite-resistant Angus cattle using RNA-seq at a depth of 23.7 million sequences per sample. These cattle displayed distinctly separate resistance phenotypes as assessed by fecal egg...

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Autores principales: Li, Robert W, Rinaldi, Manuela, Capuco, Anthony V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260172/
https://www.ncbi.nlm.nih.gov/pubmed/22129081
http://dx.doi.org/10.1186/1297-9716-42-114
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author Li, Robert W
Rinaldi, Manuela
Capuco, Anthony V
author_facet Li, Robert W
Rinaldi, Manuela
Capuco, Anthony V
author_sort Li, Robert W
collection PubMed
description The response of the abomasal transcriptome to gastrointestinal parasites was evaluated in parasite-susceptible and parasite-resistant Angus cattle using RNA-seq at a depth of 23.7 million sequences per sample. These cattle displayed distinctly separate resistance phenotypes as assessed by fecal egg counts. Approximately 65.3% of the 23 632 bovine genes were expressed in the fundic abomasum. Of these, 13 758 genes were expressed in all samples tested and likely represent core components of the bovine abomasal transcriptome. The gene (BT14427) with the most abundant transcript, accounting for 10.4% of sequences in the transcriptome, is located on chromosome 29 and has unknown functions. Additionally, PIGR (1.6%), Complement C3 (0.7%), and Immunoglobulin J chain (0.5%) were among the most abundant transcripts in the transcriptome. Among the 203 genes impacted, 64 were significantly over-expressed in resistant animals at a stringent cutoff (FDR < 5%). Among the 94 224 splice junctions identified, 133 were uniquely present: 90 were observed only in resistant animals, and 43 were present only in susceptible animals. Gene Ontology (GO) enrichment of the genes under study uncovered an association with lipid metabolism, which was confirmed by an independent pathway analysis. Several pathways, such as FXR/RXR activation, LXR/RXR activation, LPS/IL-1 mediated inhibition of RXR function, and arachidonic acid metabolism, were impacted in resistant animals, which are potentially involved in the development of parasite resistance in cattle. Our results provide insights into the development of host immunity to gastrointestinal nematode infection and will facilitate understanding of mechanism underlying host resistance.
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spelling pubmed-32601722012-01-18 Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle Li, Robert W Rinaldi, Manuela Capuco, Anthony V Vet Res Research The response of the abomasal transcriptome to gastrointestinal parasites was evaluated in parasite-susceptible and parasite-resistant Angus cattle using RNA-seq at a depth of 23.7 million sequences per sample. These cattle displayed distinctly separate resistance phenotypes as assessed by fecal egg counts. Approximately 65.3% of the 23 632 bovine genes were expressed in the fundic abomasum. Of these, 13 758 genes were expressed in all samples tested and likely represent core components of the bovine abomasal transcriptome. The gene (BT14427) with the most abundant transcript, accounting for 10.4% of sequences in the transcriptome, is located on chromosome 29 and has unknown functions. Additionally, PIGR (1.6%), Complement C3 (0.7%), and Immunoglobulin J chain (0.5%) were among the most abundant transcripts in the transcriptome. Among the 203 genes impacted, 64 were significantly over-expressed in resistant animals at a stringent cutoff (FDR < 5%). Among the 94 224 splice junctions identified, 133 were uniquely present: 90 were observed only in resistant animals, and 43 were present only in susceptible animals. Gene Ontology (GO) enrichment of the genes under study uncovered an association with lipid metabolism, which was confirmed by an independent pathway analysis. Several pathways, such as FXR/RXR activation, LXR/RXR activation, LPS/IL-1 mediated inhibition of RXR function, and arachidonic acid metabolism, were impacted in resistant animals, which are potentially involved in the development of parasite resistance in cattle. Our results provide insights into the development of host immunity to gastrointestinal nematode infection and will facilitate understanding of mechanism underlying host resistance. BioMed Central 2011 2011-11-30 /pmc/articles/PMC3260172/ /pubmed/22129081 http://dx.doi.org/10.1186/1297-9716-42-114 Text en Copyright ©2011 Li et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Li, Robert W
Rinaldi, Manuela
Capuco, Anthony V
Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle
title Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle
title_full Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle
title_fullStr Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle
title_full_unstemmed Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle
title_short Characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle
title_sort characterization of the abomasal transcriptome for mechanisms of resistance to gastrointestinal nematodes in cattle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3260172/
https://www.ncbi.nlm.nih.gov/pubmed/22129081
http://dx.doi.org/10.1186/1297-9716-42-114
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