Microbiome mismatches from microbiota transplants lead to persistent off-target metabolic and immunomodulatory effects

Fecal microbiota transplant (FMT) is an increasingly used intervention, but its suitability to restore regional gut microbiota, particularly in the small bowel (SB), must be questioned because of its predominant anaerobic composition. In human subjects receiving FMT by upper endoscopy, duodenal engr...

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Published inCell Vol. 188; no. 15; pp. 3927 - 3941.e13
Main Authors DeLeon, Orlando, Mocanu, Mora, Tan, Alan, Sidebottom, Ashley M., Koval, Jason, Ceccato, Hugo D., Kralicek, Sarah, Colgan, John J., St. George, Marissa M., Lake, Joash M., Cooper, Michael, Xu, Jingwen, Moore, Julia, Su, Qi, Xu, Zhilu, Ng, Siew C., Chan, Francis K.L., Tun, Hein M., Cham, Candace M., Liu, Cambrian Y., Rubin, David T., Martinez-Guryn, Kristina, Chang, Eugene B.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 24.07.2025
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Online AccessGet full text
ISSN0092-8674
1097-4172
1097-4172
DOI10.1016/j.cell.2025.05.014

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Abstract Fecal microbiota transplant (FMT) is an increasingly used intervention, but its suitability to restore regional gut microbiota, particularly in the small bowel (SB), must be questioned because of its predominant anaerobic composition. In human subjects receiving FMT by upper endoscopy, duodenal engraftment of anaerobes was observed after 4 weeks. We hypothesized that peroral FMTs create host-microbe mismatches that impact SB homeostasis. To test this, antibiotic-treated specific-pathogen-free (SPF) mice were given jejunal, cecal, or fecal microbiota transplants (JMTs, CMTs, or FMTs, respectively) and studied 1 or 3 months later. JMT and FMT altered regional microbiota membership and function, energy balance, and intestinal and hepatic transcriptomes; JMT favored host metabolic pathways and FMT favored immune pathways. MTs drove regional intestinal identity (Gata4, Gata6, and Satb2) and downstream differentiation markers. RNA sequencing (RNA-seq) of metabolite-exposed human enteroids and duodenal biopsies post-FMT confirmed transcriptional changes in mice. Thus, regional microbial mismatches after FMTs can lead to unintended consequences and require rethinking of microbiome-based interventions. [Display omitted] •Microbes alter regional intestinal environments to enhance fitness and engraftment•Mismatches alter metabolic and immune states of host tissues and regional microbiomes•Engraftment of FMT (anaerobic) microbes in the small bowel is persistent•Regionally matched microbiota in the small and large bowel restore homeostasis Fecal microbiota transplants (FMTs) may not always effectively restore small bowel microbiota due to regional differences in gut environments, potentially causing unintended effects on metabolism and immune function. This research suggests that personalized, intestinal-region-specific microbiome therapies are needed to improve outcomes and avoid mismatches that could impact gut health and disease.
AbstractList Fecal microbiota transplant (FMT) is an increasingly used intervention, but its suitability to restore regional gut microbiota, particularly in the small bowel (SB), must be questioned because of its predominant anaerobic composition. In human subjects receiving FMT by upper endoscopy, duodenal engraftment of anaerobes was observed after 4 weeks. We hypothesized that peroral FMTs create host-microbe mismatches that impact SB homeostasis. To test this, antibiotic-treated specific-pathogen-free (SPF) mice were given jejunal, cecal, or fecal microbiota transplants (JMTs, CMTs, or FMTs, respectively) and studied 1 or 3 months later. JMT and FMT altered regional microbiota membership and function, energy balance, and intestinal and hepatic transcriptomes; JMT favored host metabolic pathways and FMT favored immune pathways. MTs drove regional intestinal identity (Gata4, Gata6, and Satb2) and downstream differentiation markers. RNA sequencing (RNA-seq) of metabolite-exposed human enteroids and duodenal biopsies post-FMT confirmed transcriptional changes in mice. Thus, regional microbial mismatches after FMTs can lead to unintended consequences and require rethinking of microbiome-based interventions.Fecal microbiota transplant (FMT) is an increasingly used intervention, but its suitability to restore regional gut microbiota, particularly in the small bowel (SB), must be questioned because of its predominant anaerobic composition. In human subjects receiving FMT by upper endoscopy, duodenal engraftment of anaerobes was observed after 4 weeks. We hypothesized that peroral FMTs create host-microbe mismatches that impact SB homeostasis. To test this, antibiotic-treated specific-pathogen-free (SPF) mice were given jejunal, cecal, or fecal microbiota transplants (JMTs, CMTs, or FMTs, respectively) and studied 1 or 3 months later. JMT and FMT altered regional microbiota membership and function, energy balance, and intestinal and hepatic transcriptomes; JMT favored host metabolic pathways and FMT favored immune pathways. MTs drove regional intestinal identity (Gata4, Gata6, and Satb2) and downstream differentiation markers. RNA sequencing (RNA-seq) of metabolite-exposed human enteroids and duodenal biopsies post-FMT confirmed transcriptional changes in mice. Thus, regional microbial mismatches after FMTs can lead to unintended consequences and require rethinking of microbiome-based interventions.
Fecal microbiota transplant (FMT) is an increasingly used intervention, but its suitability to restore regional gut microbiota, particularly in the small bowel (SB), must be questioned because of its predominant anaerobic composition. In human subjects receiving FMT by upper endoscopy, duodenal engraftment of anaerobes was observed after 4 weeks. We hypothesized that peroral FMTs create host-microbe mismatches that impact SB homeostasis. To test this, antibiotic-treated specific-pathogen-free (SPF) mice were given jejunal, cecal, or fecal microbiota transplants (JMTs, CMTs, or FMTs, respectively) and studied 1 or 3 months later. JMT and FMT altered regional microbiota membership and function, energy balance, and intestinal and hepatic transcriptomes; JMT favored host metabolic pathways and FMT favored immune pathways. MTs drove regional intestinal identity (Gata4, Gata6, and Satb2) and downstream differentiation markers. RNA sequencing (RNA-seq) of metabolite-exposed human enteroids and duodenal biopsies post-FMT confirmed transcriptional changes in mice. Thus, regional microbial mismatches after FMTs can lead to unintended consequences and require rethinking of microbiome-based interventions. [Display omitted] •Microbes alter regional intestinal environments to enhance fitness and engraftment•Mismatches alter metabolic and immune states of host tissues and regional microbiomes•Engraftment of FMT (anaerobic) microbes in the small bowel is persistent•Regionally matched microbiota in the small and large bowel restore homeostasis Fecal microbiota transplants (FMTs) may not always effectively restore small bowel microbiota due to regional differences in gut environments, potentially causing unintended effects on metabolism and immune function. This research suggests that personalized, intestinal-region-specific microbiome therapies are needed to improve outcomes and avoid mismatches that could impact gut health and disease.
Fecal microbiota transplant (FMT) is an increasingly used intervention, but its suitability to restore regional gut microbiota, particularly in the small bowel (SB), must be questioned because of its predominant anaerobic composition. In human subjects receiving FMT by upper endoscopy, duodenal engraftment of anaerobes was observed after 4 weeks. We hypothesized that peroral FMTs create host-microbe mismatches that impact SB homeostasis. To test this, antibiotic-treated specific-pathogen-free (SPF) mice were given jejunal, cecal, or fecal microbiota transplants (JMTs, CMTs, or FMTs, respectively) and studied 1 or 3 months later. JMT and FMT altered regional microbiota membership and function, energy balance, and intestinal and hepatic transcriptomes; JMT favored host metabolic pathways and FMT favored immune pathways. MTs drove regional intestinal identity (Gata4, Gata6, and Satb2) and downstream differentiation markers. RNA sequencing (RNA-seq) of metabolite-exposed human enteroids and duodenal biopsies post-FMT confirmed transcriptional changes in mice. Thus, regional microbial mismatches after FMTs can lead to unintended consequences and require rethinking of microbiome-based interventions.
Author Ceccato, Hugo D.
Koval, Jason
Kralicek, Sarah
Rubin, David T.
Tun, Hein M.
Martinez-Guryn, Kristina
Tan, Alan
Mocanu, Mora
Colgan, John J.
Lake, Joash M.
Su, Qi
Ng, Siew C.
DeLeon, Orlando
Chang, Eugene B.
St. George, Marissa M.
Xu, Zhilu
Moore, Julia
Cham, Candace M.
Liu, Cambrian Y.
Xu, Jingwen
Sidebottom, Ashley M.
Cooper, Michael
Chan, Francis K.L.
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Keywords regional ecosystem
engraftment
intestine
small bowel microbiota
metabolism
jejunum
FMT
microbiome
mucosa
regional mismatch
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Snippet Fecal microbiota transplant (FMT) is an increasingly used intervention, but its suitability to restore regional gut microbiota, particularly in the small bowel...
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SubjectTerms Animals
Anti-Bacterial Agents - pharmacology
Duodenum - microbiology
engraftment
Fecal Microbiota Transplantation - adverse effects
Fecal Microbiota Transplantation - methods
Female
FMT
Gastrointestinal Microbiome - immunology
Humans
intestine
jejunum
Male
metabolism
Mice
Mice, Inbred C57BL
microbiome
mucosa
regional ecosystem
regional mismatch
small bowel microbiota
Specific Pathogen-Free Organisms
Transcriptome
Title Microbiome mismatches from microbiota transplants lead to persistent off-target metabolic and immunomodulatory effects
URI https://dx.doi.org/10.1016/j.cell.2025.05.014
https://www.ncbi.nlm.nih.gov/pubmed/40482640
https://www.proquest.com/docview/3216696155
Volume 188
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