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Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis
Mycobacterium bovis is an intracellular pathogen that causes tuberculosis in cattle. Following infection, the pathogen resides and persists inside host macrophages by subverting host immune responses via a diverse range of mechanisms. Here, a high-density bovine microarray platform was used to exami...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181336/ https://www.ncbi.nlm.nih.gov/pubmed/25324841 http://dx.doi.org/10.3389/fimmu.2014.00422 |
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author | Killick, Kate E. Magee, David A. Park, Stephen D. E. Taraktsoglou, Maria Browne, John A. Conlon, Kevin M. Nalpas, Nicolas C. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. Hokamp, Karsten |
author_facet | Killick, Kate E. Magee, David A. Park, Stephen D. E. Taraktsoglou, Maria Browne, John A. Conlon, Kevin M. Nalpas, Nicolas C. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. Hokamp, Karsten |
author_sort | Killick, Kate E. |
collection | PubMed |
description | Mycobacterium bovis is an intracellular pathogen that causes tuberculosis in cattle. Following infection, the pathogen resides and persists inside host macrophages by subverting host immune responses via a diverse range of mechanisms. Here, a high-density bovine microarray platform was used to examine the bovine monocyte-derived macrophage transcriptome response to M. bovis infection relative to infection with the attenuated vaccine strain, M. bovis Bacille Calmette–Guérin. Differentially expressed genes were identified (adjusted P-value ≤0.01) and interaction networks generated across an infection time course of 2, 6, and 24 h. The largest number of biological interactions was observed in the 24-h network, which exhibited scale-free network properties. The 24-h network featured a small number of key hub and bottleneck gene nodes, including IKBKE, MYC, NFKB1, and EGR1 that differentiated the macrophage response to virulent and attenuated M. bovis strains, possibly via the modulation of host cell death mechanisms. These hub and bottleneck genes represent possible targets for immuno-modulation of host macrophages by virulent mycobacterial species that enable their survival within a hostile environment. |
format | Online Article Text |
id | pubmed-4181336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41813362014-10-16 Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis Killick, Kate E. Magee, David A. Park, Stephen D. E. Taraktsoglou, Maria Browne, John A. Conlon, Kevin M. Nalpas, Nicolas C. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. Hokamp, Karsten Front Immunol Immunology Mycobacterium bovis is an intracellular pathogen that causes tuberculosis in cattle. Following infection, the pathogen resides and persists inside host macrophages by subverting host immune responses via a diverse range of mechanisms. Here, a high-density bovine microarray platform was used to examine the bovine monocyte-derived macrophage transcriptome response to M. bovis infection relative to infection with the attenuated vaccine strain, M. bovis Bacille Calmette–Guérin. Differentially expressed genes were identified (adjusted P-value ≤0.01) and interaction networks generated across an infection time course of 2, 6, and 24 h. The largest number of biological interactions was observed in the 24-h network, which exhibited scale-free network properties. The 24-h network featured a small number of key hub and bottleneck gene nodes, including IKBKE, MYC, NFKB1, and EGR1 that differentiated the macrophage response to virulent and attenuated M. bovis strains, possibly via the modulation of host cell death mechanisms. These hub and bottleneck genes represent possible targets for immuno-modulation of host macrophages by virulent mycobacterial species that enable their survival within a hostile environment. Frontiers Media S.A. 2014-10-01 /pmc/articles/PMC4181336/ /pubmed/25324841 http://dx.doi.org/10.3389/fimmu.2014.00422 Text en Copyright © 2014 Killick, Magee, Park, Taraktsoglou, Browne, Conlon, Nalpas, Gormley, Gordon, MacHugh and Hokamp. http://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) or licensor 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 | Immunology Killick, Kate E. Magee, David A. Park, Stephen D. E. Taraktsoglou, Maria Browne, John A. Conlon, Kevin M. Nalpas, Nicolas C. Gormley, Eamonn Gordon, Stephen V. MacHugh, David E. Hokamp, Karsten Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis |
title | Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis |
title_full | Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis |
title_fullStr | Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis |
title_full_unstemmed | Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis |
title_short | Key Hub and Bottleneck Genes Differentiate the Macrophage Response to Virulent and Attenuated Mycobacterium bovis |
title_sort | key hub and bottleneck genes differentiate the macrophage response to virulent and attenuated mycobacterium bovis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181336/ https://www.ncbi.nlm.nih.gov/pubmed/25324841 http://dx.doi.org/10.3389/fimmu.2014.00422 |
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