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Xylanase enhances gut microbiota-derived butyrate to exert immune-protective effects in a histone deacetylase-dependent manner.
- Source :
-
Microbiome [Microbiome] 2024 Oct 21; Vol. 12 (1), pp. 212. Date of Electronic Publication: 2024 Oct 21. - Publication Year :
- 2024
-
Abstract
- Background: Commensal bacteria in the intestine release enzymes to degrade and ferment dietary components, producing beneficial metabolites. However, the regulatory effects of microbial-derived enzymes on the intestinal microbiota composition and the influence on host health remain elusive. Xylanase can degrade xylan into oligosaccharides, showing wide application in feed industry.<br />Results: To validate the immune-protective effects of xylanase, Nile tilapia was used as the model and fed with xylanase. The results showed that dietary xylanase improved the survival rate of Nile tilapia when they were challenged with Aeromonas hydrophila. The transcriptome analysis showed significant enrichment of genes related to interleukin-17d (il-17d) signaling pathway in the xylanase treatment group. High-throughput sequencing revealed that dietary xylanase altered the composition of the intestinal microbiota and directly promoted the proliferation of Allobaculum stercoricanis which could produce butyrate in vitro. Consequently, dietary xylanase supplementation increased the butyrate level in fish gut. Further experiment verified that butyrate supplementation enhanced the expression of il-17d and regenerating islet-derived 3 gamma (reg3g) in the gut. The knockdown experiment of il-17d confirmed that il-17d is necessary for butyrate to protect Nile tilapia from pathogen resistance. Flow cytometry analysis indicated that butyrate increased the abundance of IL-17D <superscript>+</superscript> intestinal epithelial cells in fish. Mechanistically, butyrate functions as an HDAC3 inhibitor, enhancing il-17d expression and playing a crucial role in pathogen resistance.<br />Conclusion: Dietary xylanase significantly altered the composition of intestinal microbiota and increased the content of butyrate in the intestine. Butyrate activated the transcription of il-17d in intestinal epithelial cells by inhibiting histone deacetylase 3, thereby protecting the Nile tilapia from pathogen infection. This study elucidated how microbial-derived xylanase regulates host immune function, providing a theoretical basis for the development and application of functional enzymes. Video Abstract.<br /> (© 2024. The Author(s).)
- Subjects :
- Animals
Animal Feed
Dietary Supplements
Interleukin-17 metabolism
Gram-Negative Bacterial Infections prevention & control
Gram-Negative Bacterial Infections immunology
Gram-Negative Bacterial Infections microbiology
Fish Proteins metabolism
Fish Proteins genetics
Intestines microbiology
Intestines immunology
Gastrointestinal Microbiome drug effects
Butyrates metabolism
Histone Deacetylases metabolism
Cichlids microbiology
Cichlids metabolism
Cichlids immunology
Aeromonas hydrophila
Endo-1,4-beta Xylanases metabolism
Fish Diseases microbiology
Fish Diseases prevention & control
Fish Diseases immunology
Subjects
Details
- Language :
- English
- ISSN :
- 2049-2618
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Microbiome
- Publication Type :
- Academic Journal
- Accession number :
- 39434145
- Full Text :
- https://doi.org/10.1186/s40168-024-01934-6