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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
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.
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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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