Microorganisms (May 2022)

Gut Microbiota Associated with Clinical Relapse in Patients with Quiescent Ulcerative Colitis

  • Hiroaki Kitae,
  • Tomohisa Takagi,
  • Yuji Naito,
  • Ryo Inoue,
  • Yuka Azuma,
  • Takashi Torii,
  • Katsura Mizushima,
  • Toshifumi Doi,
  • Ken Inoue,
  • Osamu Dohi,
  • Naohisa Yoshida,
  • Kazuhiro Kamada,
  • Kazuhiko Uchiyama,
  • Takeshi Ishikawa,
  • Hideyuki Konishi,
  • Yoshito Itoh

DOI
https://doi.org/10.3390/microorganisms10051044
Journal volume & issue
Vol. 10, no. 5
p. 1044

Abstract

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The microbiota associated with relapse in patients with quiescent ulcerative colitis (qUC) remains unclear. Our objective was to analyze the fecal microbiota of Japanese patients with qUC and identify the relapse-associated microbiota. In this study, 59 patients with qUC and 59 healthy controls (HCs) were enrolled (UMIN 000019486), and their fecal microbiota was compared using 16S rRNA gene amplicon sequencing. We followed their clinical course up to 3.5 years and analyzed the relapse-associated microbiota. Potential functional changes in the fecal microbiota were evaluated using PICRUSt software and the Kyoto Encyclopedia of Genes and Genomes database. There were significant differences in fecal microbiota diversity between HC and qUC subjects, with 13 taxa characterizing each subject. Despite no significant difference in variation of microbiota in a single sample (α diversity) between patients in sustained remission and relapsed patients, the variation in microbial communities between samples (β diversity) was significantly different. Prevotella was more abundant in the sustained remission patients, whereas Faecalibacterium and Bifidobacterium were more abundant in the relapsed patients. We clustered the entire cohort into four clusters, and Kaplan–Meier analysis revealed the subsequent clinical course of each cluster was different. We identified 48 metabolic pathways associated with each cluster using linear discriminant analysis effect size. We confirmed the difference in microbiota between patients with qUC and HCs and identified three genera associated with relapse. We found that the clusters based on these genera had different subsequent clinical courses and activated different metabolic pathways.

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