Gut Microbiota-mediated Alleviation of Dextran Sulfate Sodium-induced Colitis in Mice.

DSS IBD Roseburia SCFA butyrate

Journal

Gastro hep advances
ISSN: 2772-5723
Titre abrégé: Gastro Hep Adv
Pays: Netherlands
ID NLM: 9918350485906676

Informations de publication

Date de publication:
2024
Historique:
received: 21 08 2023
accepted: 29 01 2024
medline: 12 8 2024
pubmed: 12 8 2024
entrez: 12 8 2024
Statut: epublish

Résumé

Gut dysbiosis characterized by an imbalanced microbiota is closely involved in the pathogenesis of a widespread gastrointestinal inflammatory disorder, inflammatory bowel disease. However, it is unclear how the complex intestinal microbiota affects development or resistant of mucosal inflammation. Our aim was to investigate the impact of the gut microbiota on susceptibility in a mouse model of ulcerative colitis. We compared the susceptibility to dextran sulfate sodium (DSS)-induced colitis of inbred BALB/c mice obtained from the 3 main distributors of laboratory animals in Japan. Clinical symptoms of the colitis and the faecal microbiota were assessed. Cohousing approach was used to identify whether the gut microbiota is a primary factor determining disease susceptibility. Here, we showed differences in the susceptibility of BALB/c mice from the vendors to DSS colitis. Analysis of the gut microbiota using 16S ribosomal RNA sequencing revealed clear separation of the gut microbial composition among mice from the vendors. Notably, the abundance of the phylum A BALB/c substrain that was resistant to DSS-induced colitis was observed, and the severity of DSS-induced colitis was mainly influenced by the gut microbiota. Targeting butyrate-producing bacteria could have therapeutic potential for ulcerative colitis.

Sections du résumé

Background and Aims UNASSIGNED
Gut dysbiosis characterized by an imbalanced microbiota is closely involved in the pathogenesis of a widespread gastrointestinal inflammatory disorder, inflammatory bowel disease. However, it is unclear how the complex intestinal microbiota affects development or resistant of mucosal inflammation. Our aim was to investigate the impact of the gut microbiota on susceptibility in a mouse model of ulcerative colitis.
Methods UNASSIGNED
We compared the susceptibility to dextran sulfate sodium (DSS)-induced colitis of inbred BALB/c mice obtained from the 3 main distributors of laboratory animals in Japan. Clinical symptoms of the colitis and the faecal microbiota were assessed. Cohousing approach was used to identify whether the gut microbiota is a primary factor determining disease susceptibility.
Results UNASSIGNED
Here, we showed differences in the susceptibility of BALB/c mice from the vendors to DSS colitis. Analysis of the gut microbiota using 16S ribosomal RNA sequencing revealed clear separation of the gut microbial composition among mice from the vendors. Notably, the abundance of the phylum
Conclusion UNASSIGNED
A BALB/c substrain that was resistant to DSS-induced colitis was observed, and the severity of DSS-induced colitis was mainly influenced by the gut microbiota. Targeting butyrate-producing bacteria could have therapeutic potential for ulcerative colitis.

Identifiants

pubmed: 39131720
doi: 10.1016/j.gastha.2024.01.016
pii: S2772-5723(24)00016-5
pmc: PMC11308119
doi:

Types de publication

Journal Article

Langues

eng

Pagination

461-470

Informations de copyright

© 2024 The Authors.

Auteurs

Eri Ikeda (E)

Department of Microbiology, Graduates School of Dentistry, Osaka University, Suita, Osaka, Japan.
Department of Molecular Immunology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

Masaya Yamaguchi (M)

Department of Microbiology, Graduates School of Dentistry, Osaka University, Suita, Osaka, Japan.
Bioinformatics Research Unit, Graduates School of Dentistry, Osaka University, Suita, Osaka, Japan.
Center for Infectious Disease Education and Research (CiDER), Osaka University, Suita, Osaka, Japan.
Bioinformatics Center, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.

Shigetada Kawabata (S)

Department of Microbiology, Graduates School of Dentistry, Osaka University, Suita, Osaka, Japan.
Center for Infectious Disease Education and Research (CiDER), Osaka University, Suita, Osaka, Japan.

Classifications MeSH