Chiba M, Fukushima T, Horie Y, Iizuka M, Masamune O
First Department of Internal Medicine, Akita University School of Medicine, Japan.
J Gastroenterol. 1998 Aug;33(4):482-7. doi: 10.1007/s005350050119.
To clarify the etiologic significance of Mycobacterium paratuberculosis in Crohn's disease, we investigated whether M. paratuberculosis was detected in intestinal tissues, including Peyer's patches, where M. paratuberculosis invades, and colonic lymph follicles, where early lesions appear. Fifty-one samples of intestinal tissues, either therapeutically resected or biopsied, including 34 specimens from 30 patients with Crohn's disease, were studied. Four Peyer's patches and eight lymph follicles were included in the intestinal tissue samples of Crohn's disease. They were visualized by acetic acid fixation. DNA extracted from intestinal tissues by proteinase K treatment was used for nested polymerase chain reaction (PCR) for detection of IS900, which is specific for M. paratuberculosis. PCR products were analyzed by agarose gel electrophoresis and subsequent Southern blot analysis. Our amplification system could detect 7.5 fg of M. paratuberculosis DNA. None of the tissue samples showed positive IS900 amplification, whereas they all showed amplification of the positive control human leukocyte antigen (HLA)-DQA DNA. Spiked experiments of tissue samples with M. paratuberculosis demonstrated that inhibitors of IS900 amplification were not present in the samples. Our study does not support the etiologic significance of M. paratuberculosis in Crohn's disease.
为阐明副结核分枝杆菌在克罗恩病中的病因学意义,我们研究了在副结核分枝杆菌侵入的肠道组织(包括派尔集合淋巴结)以及出现早期病变的结肠淋巴滤泡中是否能检测到副结核分枝杆菌。我们研究了51份经治疗性切除或活检的肠道组织样本,其中包括来自30例克罗恩病患者的34份标本。克罗恩病肠道组织样本中包括4个派尔集合淋巴结和8个淋巴滤泡。通过乙酸固定使其可视化。经蛋白酶K处理从肠道组织中提取的DNA用于巢式聚合酶链反应(PCR)以检测对副结核分枝杆菌具有特异性的IS900。PCR产物通过琼脂糖凝胶电泳及随后的Southern印迹分析进行检测。我们的扩增系统能够检测到7.5 fg的副结核分枝杆菌DNA。所有组织样本均未显示IS900扩增阳性,而它们均显示阳性对照人白细胞抗原(HLA)-DQA DNA扩增。用副结核分枝杆菌对组织样本进行加标实验表明样本中不存在IS900扩增抑制剂。我们的研究不支持副结核分枝杆菌在克罗恩病中的病因学意义。