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首页> 外文期刊>Journal of Pathology: Journal of the Pathological Society of Great Britain and Ireland >Validation of 16S rDNA sequencing in microdissected bowel biopsies from Crohn's disease patients to assess bacterial flora diversity.
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Validation of 16S rDNA sequencing in microdissected bowel biopsies from Crohn's disease patients to assess bacterial flora diversity.

机译:在来自克罗恩病患者的显微解剖肠活检中验证16S rDNA序列以评估细菌菌群多样性。

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摘要

The bowel flora is implicated in Crohn's disease (CD) pathogenesis but its precise role is still unclear. Several non-mutually exclusive hypotheses have been proposed: an unidentified persistent pathogen; excessive bacterial translocation; an immune system abnormality in response to normal bacteria; or a breakdown in the balance between protective and harmful bacteria. These hypotheses can be tested by identifying bacteria in specific microscopic bowel structures or lesions. The present paper describes a novel technique to assess bacterial flora diversity in bowel biopsies, by combining laser capture microdissection with broad-range 16S rDNA sequencing. Fifty-four samples comprising histologically normal and pathological mucosa, MALT, ulcers, submucosal lymphangiectasias, epithelioid granulomas, and lymph nodes were microdissected out of 30 bowel biopsies from five CD patients. Bacterial 16S rDNA was successfully amplified by PCR in all samples, and PCR products from 15 samples were selected for cloning and sequence analysis. A total of 729 bacterial DNA sequences were analysed, which could be attributed to six different phyla (Proteobacteria, Firmicutes, Bacteroidetes, Actinobacteria, Fusobacteria, and Planctomycetes). DNA from typical bowel bacteria (Enterobacteriaceae, Clostridiales, Bacteroidetes, Fusobacteria) was detected in all microdissected areas. It was thus convincingly demonstrated that 16S rDNA sequencing can be combined with microdissection to study the bowel flora. However, no specific persistent pathogen causal for CD was identified. The results suggest that Enterobacteriaceae may initiate or colonize ulcers in CD. Translocation of bacteria through established mucosal lesions or as a result of increased permeability may be involved in the evolution towards chronic inflammation and in the establishment of persistent lesions. Further study is needed to confirm these preliminary findings.
机译:肠道菌群与克罗恩病(CD)发病机理有关,但其确切作用仍不清楚。已经提出了几种非互斥的假设:一种未知的持久性病原体;细菌过度移位;对正常细菌有反应的免疫系统异常;或保护性细菌与有害细菌之间的平衡失衡。这些假设可以通过鉴定特定微观肠结构或病变中的细菌来检验。本文介绍了一种新技术,通过结合激光捕获显微切割技术和广泛的16S rDNA测序技术来评估肠道活检中的细菌菌群多样性。从五名CD患者的30份肠活检样本中,对包括组织学正常和病理性粘膜,MALT,溃疡,粘膜下淋巴管扩张,上皮样肉芽肿和淋巴结在内的54个样本进行了解剖。通过PCR在所有样品中成功扩增了细菌16S rDNA,并从15个样品中选择了PCR产物进行克隆和序列分析。总共分析了729条细菌DNA序列,这可归因于6种不同的门(变形杆菌,硬毛菌,拟杆菌,放线菌,梭菌和浮游菌)。在所有显微解剖区域中检测到典型肠细菌(肠杆菌科,梭菌,拟杆菌,梭菌)的DNA。因此,令人信服地证明了16S rDNA测序可以与显微解剖相结合来研究肠道菌群。但是,未发现CD的特定持续性病原体原因。结果表明肠杆菌科细菌可引发或定殖于CD中的溃疡。细菌通过已建立的粘膜病变或由于通透性增加而发生的移位可能与向慢性炎症的发展以及持续性病变的形成有关。需要进一步研究以确认这些初步发现。

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