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Differentially Abundant Bacterial Taxa Associated with Prognostic Variables of Crohn's Disease: Results from the IMPACT Study

Authors :
Jong Pil Im
Dong Il Park
Jae Myung Cha
Hyung Lae Kim
Chang Hwan Choi
Han-Na Kim
Hyun Gun Kim
Soo-Kyung Park
Dong Soo Han
Hyuk Yoon
Kwang-Sung Ahn
Yunho Jung
Tae Oh Kim
Sang-Bum Kang
Chang Soo Eun
Chil-Woo Lee
Ki Bae Bang
Source :
Journal of Clinical Medicine, Vol 9, Iss 1748, p 1748 (2020), Journal of Clinical Medicine, Volume 9, Issue 6
Publication Year :
2020
Publisher :
MDPI AG, 2020.

Abstract

Limited studies have examined the intestinal microbiota composition in relation to Crohn&rsquo<br />s disease (CD) prognosis. We analyzed the differences in microbial communities and relevant metabolic pathways associated with prognostic variables in patients with CD. We applied 16S rRNA gene sequencing to analyze a cohort of 1110 CD and healthy control (HC) fecal samples. We categorized patients with CD into good (CD-G), intermediate (CD-I) and poor (CD-P) prognosis groups, according to the history of using biologics and intestinal resection. Microbiota &alpha<br />diversity decreased more in CD-P than CD-G and CD-I. Microbiota &szlig<br />diversity in CD-P differed from that in CD-G and CD-I. Thirteen genera and 10 species showed differential abundance between CD-G and CD-P groups. Escherichia coli (p = 0.001) and species Producta (p = 0.01) and genera Lactobacillus (p = 0.003) and Coprococcus (p = 0.01) consistently showed differences between CD-G and CD-P groups after adjusting for confounding variables. Functional profiling suggested that the microbial catabolic pathways and pathways related to enterobacterial common antigen and lipopolysaccharide biosynthesis were better represented in the CD-P group than in the CD-G group, and E. coli were the top contributors to these pathways. CD prognosis is associated with altered microbiota composition and decreased diversity, and E. coli might be causally involved in CD progression, and may have adapted to live in inflammatory environments.

Details

Language :
English
ISSN :
20770383
Volume :
9
Issue :
1748
Database :
OpenAIRE
Journal :
Journal of Clinical Medicine
Accession number :
edsair.doi.dedup.....670cba8de3a3cf6d23a95277c98545cf