Fecal microbiota transplantation for the decolonization of mucosal adherent-invasive Escherichia coli in Crohn’s disease: an open-label pilot study

Abstract Adherent-invasive Escherichia coli (AIEC) is implicated in Crohn’s disease (CD) pathogenesis, but whether fecal microbiota transplantation (FMT) clears mucosal AIEC and alters fecal and mucosal microbiomes has not been studied. In this open-label pilot study, thirty adults with CD and seropositivity for serum anti- E.coli antibody (AEcAb) received a single colonoscopic FMT from one of two donors (ClinicalTrials.gov identifier NCT05611866). The primary outcome was adverse events (AEs) within 12 weeks after FMT; secondary outcomes included changes in mucosal AIEC, clinical measures, and fecal and mucosal microbiome profiles. Shotgun metagenomic sequencing for fecal samples and 16S rRNA sequencing for ileal mucosal samples were performed at baseline and after FMT. Baseline AEcAb levels were higher in patients with mucosal AIEC colonization ( p = 0.019) and remained elevated after FMT. No FMT-related serious adverse events were reported. FMT was associated with mucosal AIEC decolonization in all 8 evaluable baseline-positive patients. Mucosal alpha diversity increased after FMT ( p = 0.023), which correlated with reduced fecal calprotectin ( p = 0.034). Microbial pathway profiles in CD patients resembled those of their respective donors with reduced donor-recipient dissimilarity post-FMT ( p = 0.030), particularly among recipients with mucosal AIEC decolonization ( p = 0.039). In conclusion, this open-label pilot study demonstrates the feasibility of FMT for modulating mucosal AIEC colonization in CD and highlights the importance of capturing microbial changes at the disease site that may be undetectable in fecal samples.

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Journal
Nature Communications
Published
2026-09-10
DOI
https://doi.org/10.1038/s41467-026-77455-7
Primary Topic
Clostridium difficile and Clostridium perfringens research
Type
article
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article

Fecal microbiota transplantation for the decolonization of mucosal adherent-invasive Escherichia coli in Crohn’s disease: an open-label pilot study

Ting Ting Chan, Siew C. Ng, Wenli Huang, Caroline Chevarin et al.
Nature Communications
Clostridium difficile and Clostridium perfringens research
article

Fecal microbiota transplantation for the decolonization of mucosal adherent-invasive Escherichia coli in Crohn’s disease: an open-label pilot study

Ting Ting Chan, Siew C. Ng, Wenli Huang, Caroline Chevarin, Marc T. Wong, Joyce W.Y. Mak, Yu Lin, Francis K. L. Chan, Anthony Buisson, Rashid N. Lui, Zhilu Xu, Jean-Frédéric Colombel, Alicia Chan, Hui Jiang
article en

Abstract

Abstract Adherent-invasive Escherichia coli (AIEC) is implicated in Crohn’s disease (CD) pathogenesis, but whether fecal microbiota transplantation (FMT) clears mucosal AIEC and alters fecal and mucosal microbiomes has not been studied. In this open-label pilot study, thirty adults with CD and seropositivity for serum anti- E.coli antibody (AEcAb) received a single colonoscopic FMT from one of two donors (ClinicalTrials.gov identifier NCT05611866). The primary outcome was adverse events (AEs) within 12 weeks after FMT; secondary outcomes included changes in mucosal AIEC, clinical measures, and fecal and mucosal microbiome profiles. Shotgun metagenomic sequencing for fecal samples and 16S rRNA sequencing for ileal mucosal samples were performed at baseline and after FMT. Baseline AEcAb levels were higher in patients with mucosal AIEC colonization ( p = 0.019) and remained elevated after FMT. No FMT-related serious adverse events were reported. FMT was associated with mucosal AIEC decolonization in all 8 evaluable baseline-positive patients. Mucosal alpha diversity increased after FMT ( p = 0.023), which correlated with reduced fecal calprotectin ( p = 0.034). Microbial pathway profiles in CD patients resembled those of their respective donors with reduced donor-recipient dissimilarity post-FMT ( p = 0.030), particularly among recipients with mucosal AIEC decolonization ( p = 0.039). In conclusion, this open-label pilot study demonstrates the feasibility of FMT for modulating mucosal AIEC colonization in CD and highlights the importance of capturing microbial changes at the disease site that may be undetectable in fecal samples.

Nature Communications
Inserm (FR), Chinese University of Hong Kong (HK), Université Clermont Auvergne (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Microbe, Intestine, Inflammation and Host Susceptibility (FR), Centre Hospitalier Universitaire de Clermont-Ferrand (FR), Icahn School of Medicine at Mount Sinai (US)
Openalex Percentile: Top 11%
Clostridium difficile and Clostridium perfringens research
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