Smeed J A, Watkins C A, Gossner A G, Hopkins J
The Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Summerhall, Edinburgh EH9 1QH, UK.
Vet Immunol Immunopathol. 2010 Jun 15;135(3-4):218-25. doi: 10.1016/j.vetimm.2009.11.015. Epub 2009 Dec 5.
Paratuberculosis is a chronic enteropathy of ruminants caused by Mycobacterium avium subspecies paratuberculosis (MAP); infection of sheep results in two disease forms - paucibacillary (tuberculoid) and multibacillary (lepromatous) associated with the differential polarization of the immune response. In addition the majority of MAP-infected animals show no pathology and remain asymptomatic. Microarray and real-time RT-qPCR analyses were used to compare gene expression in ileum from sheep with the two disease forms and asymptomatic sheep, to further understand the molecular basis of the pathologies. Microarrays identified 36 genes with fold-change of >1.5 and P< or = 0.05 in at least one comparison; eight candidates were chosen for RT-qPCR validation. Sequence analysis of two candidates, CXCR4 and IGFBP6, identified three SNPs in each; five were found in all three forms of disease and showed no significant relationship to pathological type. The IGFBP6 G(3743) A SNP was not detected in asymptomatic sheep. The data show that the two forms of disease are associated with distinct molecular profiles highlighted by the differential expression of chemokine and chemokine receptor transcripts, the protein products of which might be implicated in the different cell infiltrates of the pathologies. The cells within the lesions also show evidence of abnormal activation; they express high levels of cytokine transcripts but have reduced expression levels of transcripts for T cell receptor associated molecules.
副结核病是由副结核分枝杆菌(MAP)引起的反刍动物慢性肠病;绵羊感染会导致两种疾病形式——少菌型(结核样型)和多菌型(瘤型),这与免疫反应的不同极化有关。此外,大多数感染MAP的动物没有病理学变化且保持无症状。使用微阵列和实时逆转录定量聚合酶链反应(RT-qPCR)分析来比较患有两种疾病形式的绵羊和无症状绵羊回肠中的基因表达,以进一步了解病理学的分子基础。微阵列在至少一次比较中鉴定出36个基因,其变化倍数>1.5且P≤0.05;选择了8个候选基因进行RT-qPCR验证。对两个候选基因CXCR4和IGFBP6的序列分析在每个基因中鉴定出3个单核苷酸多态性(SNP);在所有三种疾病形式中发现了5个,且与病理类型无显著关系。在无症状绵羊中未检测到IGFBP6 G(3743)A SNP。数据表明,两种疾病形式与不同的分子谱相关,趋化因子和趋化因子受体转录本的差异表达突出了这一点,其蛋白质产物可能与病理学中不同的细胞浸润有关。病变内的细胞也显示出异常激活的证据;它们表达高水平的细胞因子转录本,但T细胞受体相关分子的转录本表达水平降低。