Literature DB >> 14573671

Evidence for a novel gene expression program in peripheral blood mononuclear cells from Mycobacterium avium subsp. paratuberculosis-infected cattle.

Paul M Coussens1, Christopher J Colvin, Guilherme J M Rosa, Juliana Perez Laspiur, Michael D Elftman.   

Abstract

A bovine-specific cDNA microarray system was used to compare gene expression profiles of peripheral blood mononuclear cells (PBMCs) from control uninfected (n = 4) and Johne's disease-positive (n = 6) Holstein cows. Microarray experiments were designed so that for each animal, a direct comparison was made between PBMCs stimulated in vitro with Mycobacterium avium subsp. paratuberculosis and PBMCs stimulated with phosphate-buffered saline (nil-stimulated PBMCs). As expected, M. avium subsp. paratuberculosis stimulation of infected cow PBMCs enhanced expression of gamma interferon transcripts. In addition, expression of 15 other genes was significantly affected (>1.25-fold change; P < 0.05) by in vitro stimulation with M. avium subsp. paratuberculosis. Similar treatment of control cow PBMCs with M. avium subsp. paratuberculosis resulted in significant changes in expression of 13 genes, only 2 of which were also affected in PBMCs from the infected cow PBMCs. To compare gene expression patterns in the two cow infection groups (infected cows and uninfected cows), a mixed-model analysis was performed with the microarray data. This analysis indicated that there were major differences in the gene expression patterns between cells isolated from the two groups of cows, regardless of in vitro stimulation. A total of 86 genes were significantly differentially expressed (P < 0.01) in M. avium subsp. paratuberculosis-stimulated PBMCs from infected cows compared to expression in similarly treated PBMCs from control cows. Surprisingly, a larger number of genes (110 genes) were also found to be significantly differentially expressed (P < 0.01) in nil-stimulated cells from the two infection groups. The expression patterns of selected genes were substantiated by quantitative real-time reverse transcriptase PCR. Flow cytometric analysis indicated that there were no gross differences in the relative populations of major immune cell types in PBMCs from infected and control cows. Thus, data presented in this report indicate that the gene expression program of PBMCs from M. avium subsp. paratuberculosis-infected cows is inherently different from that of cells from control uninfected cows.

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Year:  2003        PMID: 14573671      PMCID: PMC219592          DOI: 10.1128/IAI.71.11.6487-6498.2003

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  44 in total

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5.  A comparison of the interferon gamma assay with the absorbed ELISA for the diagnosis of Johne's disease in cattle.

Authors:  H Billman-Jacobe; M Carrigan; F Cockram; L A Corner; I J Gill; J F Hill; T Jessep; A R Milner; P R Wood
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6.  Evaluation of a commercial enzyme-linked immunosorbent assay for Johne's disease.

Authors:  M T Collins; D C Sockett; S Ridge; J C Cox
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9.  Cytokine regulation of the intracellular growth of Mycobacterium paratuberculosis in bovine monocytes.

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Authors:  R J Chiodini; W C Davis
Journal:  Microb Pathog       Date:  1992-12       Impact factor: 3.738

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  23 in total

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Authors:  Paul M Coussens
Journal:  Infect Immun       Date:  2004-06       Impact factor: 3.441

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4.  Analysis of the immune response to Mycobacterium avium subsp. paratuberculosis in experimentally infected calves.

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Authors:  Abraham D Aho; Amanda M McNulty; Paul M Coussens
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Review 7.  Oligonucleotide microarray technology and its application to Mycobacterium avium subsp. paratuberculosis research: a review.

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Review 10.  Anti-inflammatory and antiapoptotic responses to infection: a common denominator of human and bovine macrophages infected with Mycobacterium avium subsp. paratuberculosis.

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