What question did this study set out to answer?

This research aims to evaluate how combining butyrate with niacin affects intestinal barrier repair in weaned piglets infected with ETEC.

May 14, 2026Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology2 citationsOpen Access

Butyrate combined with niacin enhances intestinal barrier function repair in weaned piglets infected with ETEC by promoting colonic metabolism and antimicrobial peptide expression

QTQingsong Tang RZRui Zhen BYBijing Yang

Key Points

This research aims to evaluate how combining butyrate with niacin affects intestinal barrier repair in weaned piglets infected with ETEC.
Conducted two 14-day animal experiments to assess the effects of butyrate and niacin.
Implemented a supplementation ratio of 100:2 (2,000 mg/kg butyrate and 40 mg/kg niacin).
Measured growth performance, antimicrobial peptide expression, and metabolic changes.
BN2 treatment increased average daily gain and reduced diarrhea incidence in weaned piglets.
Enhanced expression of antimicrobial peptides pBD1, pBD2, and PR39 noted, alongside improved colonic microbiome composition.
Elevated acetylation of histone 3 lysine 27 linked to increased binding of acH3K27 to promoter regions of antimicrobial peptide genes.

Abstract

Abstract Background Weaning piglets are highly susceptible to enterotoxigenic Escherichia coli (ETEC) infections, which can cause intestinal barrier function dysfunction and death. However, there is still a lack of efficient, economical, and safe nutritional interventions. This study aimed to investigate the effects of combining butyrate with niacin on intestinal barrier function repair and resistance to ETEC infection in weaned piglets. In this study, two 14-d animal experiments were designed to observe the optimal butyrate-to-niacin ratio and assess their responses to the ETEC challenge. Results Supplementation with butyrate and niacin at a ratio of 100:2 (2,000 mg/kg butyrate and 40 mg/kg niacin, BN2) increased the average daily gain (ADG) and reduced the diarrhea incidence. We also observed an increase in the levels of nicotinamide adenine dinucleotide (NAD) in the colon of weaned piglets. Notably, BN2 promoted amino acid anabolism in the colon and enhanced glycolysis and the tricarboxylic acid (TCA) cycle by increasing the acetylation of key enzymes in the TCA. Furthermore, BN2 enhanced the expression of indispensable genes for the colonic mucosal barrier, including antimicrobial peptides such as porcine β defensin 1 ( pBD1 ), porcine β defensin 2 ( pBD2 ), and proline-arginine rich 39-amino acid peptide ( PR39 ), tight junction proteins, and improved colonic microbiome composition. Based on these findings, we found that BN2 alleviated growth restriction and diarrhea, and modulated the expression of antimicrobial peptides, tight junction proteins, and cytokines to reduce colonic barrier function dysfunction in weaned piglets challenged with ETEC. Mechanistically, we confirmed that BN2 elevated the protein expression of acetylation of histone 3 lysin 27 (H3K27ac) and enhanced the binding of acH3K27 to the promoter regions of pBD1 and PR39 . Conclusions Supplementation with BN2 improved growth performance, supported colonic barrier function repair, and enhanced disease resistance in weaned piglets challenged with ETEC. This offers new insights into nutritional strategies for intestinal barrier function repair of piglets infected with ETEC.

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