4.7 Article

Bacteroidetes Species Are Correlated with Disease Activity in Ulcerative Colitis

期刊

JOURNAL OF CLINICAL MEDICINE
卷 10, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/jcm10081749

关键词

ulcerative colitis; microbiota; Bacteroidetes species; biomarker; Alistipes putredinis; Bacteroides stercoris; Bacteroides uniformis; Bacteroides rodentium; Parabacteroides merdae; Bacteroides thetaiotaomicron

资金

  1. Japan Society for the Promotion of Science, KAKENHI [JP16K09328]
  2. Kyowa Kirin Co., Ltd.
  3. Kyowa Hakko Bio Co., Ltd.

向作者/读者索取更多资源

Fecal microbiota transplantation following antibiotic therapy can improve dysbiosis in ulcerative colitis (UC) patients. The reduced abundance of Bacteroidetes species is correlated with UC activity, and certain key species may serve as potential biomarkers for disease activity.
Fecal microbiota transplantation following triple-antibiotic therapy (amoxicillin/fosfomycin/metronidazole) improves dysbiosis caused by reduced Bacteroidetes diversity in patients with ulcerative colitis (UC). We investigated the correlation between Bacteroidetes species abundance and UC activity. Fecal samples from 34 healthy controls and 52 patients with active UC (Lichtiger's clinical activity index >= 5 or Mayo endoscopic subscore >= 1) were subjected to next-generation sequencing with HSP60 as a target in bacterial metagenome analysis. A multiplex gene expression assay using colonoscopy-harvested mucosal tissues determined the involvement of Bacteroidetes species in the mucosal immune response. In patients with UC, six Bacteroides species exhibited significantly lower relative abundance, and twelve Bacteroidetes species were found significantly correlated with at least one metric of disease activity. The abundance of five Bacteroidetes species (Alistipes putredinis, Bacteroides stercoris, Bacteroides uniformis, Bacteroides rodentium, and Parabacteroides merdae) was correlated with three metrics, and their cumulative relative abundance was strongly correlated with the sum of Mayo endoscopic subscore (R = -0.71, p = 2 x 10(-9)). Five genes (TARP, C10ORF54, ITGAE, TNFSF9, and LCN2) associated with UC pathogenesis were expressed by the 12 key species. The loss of key species may exacerbate UC activity, serving as potential biomarkers.

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