Exclusive Enteral Nutrition Mediates Beneficial Gut Microbiome Enrichment in Acute Severe Colitis

Author:

Bajaj Aditya1,Markandey Manasvini1,Singh Mukesh1,Sahu Pabitra1,Vuyyuru Sudheer K1,Kante Bhaskar1,Kumar Peeyush1,Verma Mahak1,Makharia Govind1,Kedia Saurabh1,Travis Simon P L23,Ahuja Vineet1ORCID

Affiliation:

1. Department of Gastroenterology, All India Institute of Medical Sciences , New Delhi , India

2. Translational Gastroenterology Unit, University of Oxford and Oxford Biomedical Research Centre , Oxford , United Kingdom

3. Kennedy Institute of Rheumatology, University of Oxford and Oxford Biomedical Research Centre , Oxford , United Kingdom

Abstract

Abstract Background Exclusive enteral nutrition (EEN) supplementation of the standard of care (SOC) augments steroid responsiveness in patients with acute severe ulcerative colitis (ASUC). EEN is known to alter gut microbial composition. The present study investigates EEN-driven gut microbial alterations in patients with ASUC and examines their correlations with clinical parameters. Methods Stool samples from patients with ASUC (n = 44) who received either EEN-supplemented SOC (EEN group; n = 20) or SOC alone (SOC group; n = 24) for 7 days were collected at baseline (day 0) and postintervention (day 7). Microbiome analysis was carried out using 16S ribosomal RNA gene sequencing followed by data processing using QIIME2 and R packages. Results Seven-day EEN-conjugated corticosteroid therapy in patients with ASUC enhanced the abundances of beneficial bacterial genera Faecalibacterium and Veillonella and reduced the abundance of Sphingomonas (generalized linear model fitted with Lasso regularization with robustness of 100%), while no such improvements in gut microbiota were observed in the SOC group. The EEN-associated taxa correlated with the patient’s clinical parameters (serum albumin and C-reactive protein levels). Unlike the SOC group, which retained its preintervention core microbiota, EEN contributed Faecalibacterium prausnitzii, a beneficial gut bacterial taxon, to the gut microbial core. EEN responders showed enhancement of Ligilactobacillus and Veillonella and reduction in Prevotella and Granulicatella. Analysis of baseline gut microbiota showed relative enhancement of certain microbial genera being associated with corticosteroid response and baseline clinical parameters and that this signature could conceivably be used as a predictive tool. Conclusions Augmentation of clinical response by EEN-conjugated corticosteroid therapy is accompanied by beneficial gut microbial changes in patients with ASUC.

Funder

Indian Council of Medical Research

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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