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Investigation of mycobacteria in Crohn's disease tissue by Southern blotting and DNA hybridisation with cloned mycobacterial genomic DNA probes from a Crohn's disease isolated mycobacteria.

机译:通过Southern印迹和与克隆克隆的分枝杆菌基因组DNA探针进行DNA杂交和DNA杂交,研究克罗恩氏病组织中的分枝杆菌。

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摘要

A mycobacterial aetiology for Crohn's disease (CD) has been suggested. Slow growing mycobacteria indistinguishable from M paratuberculosis, the causative agent of enteritis in ruminants (Johne's disease) have been isolated from CD tissues. We have used cloned genomic DNA probes derived from a CD isolated mycobacteria strain Ben, to investigate the presence of mycobacterial DNA sequences in CD tissues. DNA was extracted from total tissue from 17 CD and four control gut specimens. DNA was digested with restriction endonucleases, electrophoresed and transferred to nylon membranes by Southern blotting and hybridised to radiolabelled DNA probes. No mycobacterial DNA was detected in any tissue sample studied. Reconstitution experiments with known numbers of in vitro cultured mycobacteria showed sensitive detection of mycobacterial DNA. DNA extracted from mouse liver, infected with M lepraemurium revealed a strong hybridisation signal and showed the applicability of the experimental approach to the detection of mycobacterial DNA in naturally infected tissues. The results do not provide evidence for the involvement of mycobacteria in the pathogenesis of CD but do not exclude the possibility of low levels of infection in subsets of intestinal cells with spheroplast or cell wall deficient forms of mycobacteria.
机译:已经提出了克罗恩病(CD)的分枝杆菌病因。已经从CD组织中分离出了与副结核分枝杆菌无法区分的缓慢生长的分枝杆菌,这是反刍动物中肠炎的病原体(约翰氏病)。我们已经使用了从CD分离的分枝杆菌菌株Ben衍生的克隆基因组DNA探针,来研究CD组织中分枝杆菌DNA序列的存在。从17个CD和四个对照肠标本的总组织中提取DNA。用限制性核酸内切酶消化DNA,进行电泳并通过Southern印迹转移到尼龙膜上,并与放射性标记的DNA探针杂交。在研究的任何组织样本中均未检测到分枝杆菌DNA。用已知数量的体外培养的分枝杆菌进行的重建实验表明,对分枝杆菌DNA的检测灵敏。从小鼠肝中提取的,感染了肺炎支原体的DNA显示出很强的杂交信号,并表明了该实验方法在自然感染组织中检测分枝杆菌DNA的适用性。结果没有提供分枝杆菌参与CD发病机理的证据,但没有排除原生质球或细胞壁缺陷型分枝杆菌形式的肠道细胞亚群中低水平感染的可能性。

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