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Gut Microbiota in Health, Diverticular Disease, Irritable Bowel Syndrome, and Inflammatory Bowel Diseases: Time for Microbial Marker of Gastrointestinal Disorders

机译:肠道微生物在健康,憩室疾病,肠易激综合征和炎症肠疾病中:胃肠道疾病的微生物标记时间

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摘要

Few data exist on differences in gut microbiota composition among principal gastrointestinal (GI) diseases. We evaluated the differences in gut microbiota composition among uncomplicated diverticular disease (DD), irritable bowel syndrome (IBS) and inflammatory bowel diseases (IBD) patients. DD, IBS, and IBD patients along with healthy controls (CT) were enrolled in our Italian GI outpatient clinic. Stool samples were collected. Microbiota composition was evaluated through a metagenomic gene-targeted approach. GI pathology represented a continuous spectrum of diseases where IBD displayed one extreme, while CT displayed the other. Among Phyla, Biplot PC2/PC3 and dendogram plot showed major differences in samples from IBS and IBD. DD resembled species CT composition, but not for Bacteroides fragilis . In IBS, Dialister spp. and then Faecalibacterium prausnitzii were the most representative species. Ulcerative colitis showed a reduced concentration of Clostridium difficile and an increase of Bacteroides fragilis . In Crohn's disease, Parabacteroides distasonis was the most represented, while Faecalibacterium prausnitzii and Bacteroides fragilis were significantly reduced. Each disorder has its definite overall microbial signature, which produces a clear differentiation from the others. On the other hand, shared alterations constitute the “core dysbiosis” of GI diseases. The assessment of these microbial markers represents a parameter that may complete the diagnostic assessment.
机译:在主胃肠道(GI)疾病中,肠道微生物群组成的差异存在少数数据。我们在简单的憩室疾病(DD),肠易肠综合征(IBS)和炎症性肠病(IBD)患者中评估了肠道微生物群组合物的差异。 DD,IBS和IBD患者以及健康的对照(CT)注册了我们的意大利GI门诊诊所。收集粪便样品。通过偏见基因靶向方法评估微生物群组合物。 GI病理学代表了IBD显示一个极端的连续疾病,而CT显示另一个。在Phyla中,Biplot PC2 / PC3和Dendograph曲线表显示了IBS和IBD的样品中的主要差异。 DD类似于物种CT组合物,但不适用于Bragilites Fragilis。在IBS中,拨号SPP。然后粪便杆菌Prausnitzii是最具代表性的物种。溃疡性结肠炎表现出浓度降低的梭菌差异浓度和脆弱的Brageiles胰蛋白酶。在克罗恩疾病中,ParaMacteroides Distasonis最代表,而Prausnitzii和Bractoides Fragilis显着降低。每种疾病都有其确定的总体微生物签名,它产生了与其他疾病的明显分化。另一方面,共同的改变构成了GI疾病的“核心缺陷症”。这些微生物标记的评估代表了可以完成诊断评估的参数。

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