首页> 外文期刊>Veterinary Immunology and Immunopathology >Expression profiling reveals differences in immuno-inflammatory gene expression between the two disease forms of sheep paratuberculosis
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Expression profiling reveals differences in immuno-inflammatory gene expression between the two disease forms of sheep paratuberculosis

机译:表达谱显示绵羊副结核病的两种疾病形式之间的免疫炎性基因表达差异

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摘要

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 <= 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.
机译:副结核病是由鸟分枝杆菌副种副结核病(MAP)引起的反刍动物的慢性肠病。绵羊感染会导致两种疾病,即与免疫反应的差异极化相关的腺杆菌(结核)和多菌(麻风)。此外,大多数被MAP感染的动物没有病理表现,并且没有症状。使用微阵列和实时RT-qPCR分析来比较两种疾病形式的绵羊和无症状绵羊在回肠中的基因表达,以进一步了解病理的分子基础。微阵列在至少一项比较中鉴定出36个折叠倍数大于1.5且P <= 0.05的基因。选择了八个候选物用于RT-qPCR验证。对两个候选基因CXCR4和IGFBP6进行序列分析,每个序列中鉴定出三个SNP。在所有三种疾病中均发现了5种,并且与病理类型没有显着关系。在无症状的绵羊中未检测到IGFBP6 G(3743)A SNP。数据显示这两种疾病与趋化因子和趋化因子受体转录物的差异表达所突出的不同分子特征有关,趋化因子和趋化因子受体转录物的差异表达可能与疾病的不同细胞浸润有关。病变内的细胞也显示异常激活的迹象。它们表达高水平的细胞因子转录物,但与T细胞受体相关分子的转录物表达水平降低。

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