Coussens Paul M, Colvin Christopher J, Rosa Guilherme J M, Perez Laspiur Juliana, Elftman Michael D
Department of Animal Science and Center for Animal Functional Genomics, Michigan State University, East Lansing, Michigan 48824, USA.
Infect Immun. 2003 Nov;71(11):6487-98. doi: 10.1128/IAI.71.11.6487-6498.2003.
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.
使用牛特异性cDNA微阵列系统比较了未感染对照(n = 4)和患有副结核病的荷斯坦奶牛(n = 6)外周血单个核细胞(PBMC)的基因表达谱。设计微阵列实验,以便对每只动物在体外分别用副结核分枝杆菌亚种刺激的PBMC与用磷酸盐缓冲盐水刺激的PBMC(未刺激的PBMC)进行直接比较。正如预期的那样,副结核分枝杆菌亚种刺激感染奶牛的PBMC会增强γ干扰素转录本的表达。此外,用副结核分枝杆菌亚种进行体外刺激会显著影响(变化>1.25倍;P < 0.05)其他15个基因的表达。用副结核分枝杆菌亚种对对照奶牛的PBMC进行类似处理,导致13个基因的表达发生显著变化,其中只有2个基因在感染奶牛的PBMC中也受到影响。为了比较两个奶牛感染组(感染奶牛和未感染奶牛)的基因表达模式,对微阵列数据进行了混合模型分析。该分析表明,无论体外刺激如何,两组奶牛分离的细胞之间的基因表达模式存在主要差异。与对照奶牛经类似处理的PBMC相比,感染奶牛经副结核分枝杆菌亚种刺激的PBMC中共有86个基因显著差异表达(P < 0.01)。令人惊讶的是,在两个感染组未刺激的细胞中也发现大量基因(110个基因)显著差异表达(P < 0.01)。通过定量实时逆转录PCR证实了所选基因的表达模式。流式细胞术分析表明,感染奶牛和对照奶牛的PBMC中主要免疫细胞类型的相对比例没有明显差异。因此,本报告中的数据表明,副结核分枝杆菌亚种感染奶牛的PBMC的基因表达程序与未感染对照奶牛的细胞的基因表达程序本质上不同。