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Global gene expression and systems biology analysis of bovine monocyte-derived macrophages in response to in vitro challenge with Mycobacterium bovis
- Source :
- PLoS ONE, PLoS ONE, Vol 7, Iss 2, p e32034 (2012)
- Publication Year :
- 2011
-
Abstract
- peer-reviewed Background Mycobacterium bovis, the causative agent of bovine tuberculosis, is a major cause of mortality in global cattle populations. Macrophages are among the first cell types to encounter M. bovis following exposure and the response elicited by these cells is pivotal in determining the outcome of infection. Here, a functional genomics approach was undertaken to investigate global gene expression profiles in bovine monocyte-derived macrophages (MDM) purified from seven age-matched non-related females, in response to in vitro challenge with M. bovis (multiplicity of infection 2:1). Total cellular RNA was extracted from non-challenged control and M. bovis-challenged MDM for all animals at intervals of 2 hours, 6 hours and 24 hours post-challenge and prepared for global gene expression analysis using the Affymetrix® GeneChip® Bovine Genome Array. Results Comparison of M. bovis-challenged MDM gene expression profiles with those from the non-challenged MDM controls at each time point identified 3,064 differentially expressed genes 2 hours post-challenge, with 4,451 and 5,267 differentially expressed genes detected at the 6 hour and 24 hour time points, respectively (adjusted P-value threshold ≤0.05). Notably, the number of downregulated genes exceeded the number of upregulated genes in the M. bovis-challenged MDM across all time points; however, the fold-change in expression for the upregulated genes was markedly higher than that for the downregulated genes. Systems analysis revealed enrichment for genes involved in: (1) the inflammatory response; (2) cell signalling pathways, including Toll-like receptors and intracellular pathogen recognition receptors; and (3) apoptosis. Conclusions The increased number of downregulated genes is consistent with previous studies showing that M. bovis infection is associated with the repression of host gene expression. The results also support roles for MyD88-independent signalling and intracellular PRRs in mediating the host response to M. bovis. Science Foundation Ireland (www.sfi.ie) Investigator grants (Nos: SFI/01/F.1/B028 and SFI/08/IN.1/B2038); Department of Agriculture, Fisheries and Food (www.agriculture.ie) Research Stimulus Grant (No: RSF 06 405); European Union Framework 7 (http://cordis.europa.eu/fp7) Project Grant (No: KBBE-211602-MACROSYS); Irish Research Council for Science, Engineering and Technology (IRCSET) funded Bioinformatics and Systems Biology PhD Programme (http://bioinfo-casl.ucd.ie/PhD).
- Subjects :
- lcsh:Medicine
Monocytes
Transcriptome
0302 clinical medicine
Multiplicity of infection
Gene expression
Molecular Cell Biology
bovine tuberculosis
lcsh:Science
Oligonucleotide Array Sequence Analysis
2. Zero hunger
Regulation of gene expression
0303 health sciences
Mycobacterium bovis
Multidisciplinary
Genome
Granuloma
biology
monocyte-derived macrophages
Systems Biology
Genomics
Signaling in Selected Disciplines
Female
Functional genomics
Signal Transduction
Research Article
global gene expression analysis
Immunology
In Vitro Techniques
Microbiology
03 medical and health sciences
Genetics
Animals
Gene
Biology
030304 developmental biology
Gene Expression Profiling
Macrophages
lcsh:R
Immunity
biology.organism_classification
Molecular biology
Gene expression profiling
Gene Expression Regulation
Immune System
RNA
lcsh:Q
Cattle
Tuberculosis, Bovine
030215 immunology
Subjects
Details
- ISSN :
- 19326203
- Volume :
- 7
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- PloS one
- Accession number :
- edsair.doi.dedup.....4fec705bf88115b4e93f4bd6ec6aefb1