XOS-based prebiotic complex improves laying performance and attenuates inflammation-driven gut injury and dysbiosis under LPS challenge

Xylooligosaccharides (XOS) are prebiotics that promote gut health and microbial balance in poultry, but their efficacy under immune-inflammatory stress such as that induced by lipopolysaccharide (LPS) challenge, remains uncertain. To enhance their functional breadth, a XOS-based prebiotic complex (XOS-PC), combining diverse oligosaccharides and fermentable fibers, was utilized. This study investigated the effects of XOS-PC on productivity, intestinal integrity, and inflammation in laying hens under both basal and lipopolysaccharide (LPS)-challenged conditions. A total of 600 Dawu Jinfeng laying hens (35 weeks) were assigned to five dietary groups receiving 0, 0.05%, 0.1%, 0.2%, or 0.4% XOS-PC for 12 weeks. At the end of the trial, the 0.2% XOS group exhibited optimal laying performance and was selected, along with the control group, for the subsequent LPS challenge. A total of 32 birds were selected from both the control (n = 16) and the 0.2% XOS-PC group (n = 16). Within each group, half of the birds (n = 8) were administered Escherichia coli LPS, while the other half (n = 8) received PBS at a dosage of 1 mg/kg body weight, intravenously. At 6 hours post-injection, samples were collected for intestinal morphology, gene expression, and ileal microbiota profiling. Supplementation of 0.2% XOS-PC significantly improved egg production, feed conversion ratio, and yolk pigmentation, reduced serum AST, and enriched ileal microbial diversity, with marked increases in Lactobacillaceae (P < 0.05). Following LPS exposure, XOS-PC preserved villus architecture, evidenced by increased ileal VH and VH/CD ratio (P < 0.05). In the ileal mucosa, XOS-PC supplementation upregulated CLDN1, CLDN5, TLR2, and TLR4 gene expression while suppressing TNF-α (P < 0.05), indicating enhanced barrier function and attenuated inflammatory signaling. Microbiota analysis revealed increased alpha diversity, distinct beta diversity, elevated Lactobacillaceae, and reduced Fusobacteria and Sphaerochaeta (P < 0.05). Correlation analysis revealed positive association between Lactobacillus with villus height and gut barrier genes, while Fusobacteria and Sphaerochaeta correlated inversely with epithelial integrity and positively with TNF-α. Collectively, this study demonstrates that a structurally enriched XOS-based prebiotic complex enhances productivity, reinforces gut integrity, and reprograms microbiota under both physiological and immune-stressed states, offering a novel precision-nutritional solution for poultry resilience.

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Journal
Poultry Science
Published
2025-11-20
DOI
https://doi.org/10.1016/j.psj.2025.106124
Primary Topic
Animal Nutrition and Physiology
Type
article
Field-Weighted Citation Impact
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article

XOS-based prebiotic complex improves laying performance and attenuates inflammation-driven gut injury and dysbiosis under LPS challenge

Pan Xin, Shugeng Wu, Uchechukwu Edna Obianwuna, Kai Qiu et al.
Poultry Science
Animal Nutrition and Physiology
article

XOS-based prebiotic complex improves laying performance and attenuates inflammation-driven gut injury and dysbiosis under LPS challenge

Pan Xin, Shugeng Wu, Uchechukwu Edna Obianwuna, Kai Qiu, Caihong Xin, Jing Wang, Haijun Zhang, Jianmin Zhou
article en

Abstract

Xylooligosaccharides (XOS) are prebiotics that promote gut health and microbial balance in poultry, but their efficacy under immune-inflammatory stress such as that induced by lipopolysaccharide (LPS) challenge, remains uncertain. To enhance their functional breadth, a XOS-based prebiotic complex (XOS-PC), combining diverse oligosaccharides and fermentable fibers, was utilized. This study investigated the effects of XOS-PC on productivity, intestinal integrity, and inflammation in laying hens under both basal and lipopolysaccharide (LPS)-challenged conditions. A total of 600 Dawu Jinfeng laying hens (35 weeks) were assigned to five dietary groups receiving 0, 0.05%, 0.1%, 0.2%, or 0.4% XOS-PC for 12 weeks. At the end of the trial, the 0.2% XOS group exhibited optimal laying performance and was selected, along with the control group, for the subsequent LPS challenge. A total of 32 birds were selected from both the control (n = 16) and the 0.2% XOS-PC group (n = 16). Within each group, half of the birds (n = 8) were administered Escherichia coli LPS, while the other half (n = 8) received PBS at a dosage of 1 mg/kg body weight, intravenously. At 6 hours post-injection, samples were collected for intestinal morphology, gene expression, and ileal microbiota profiling. Supplementation of 0.2% XOS-PC significantly improved egg production, feed conversion ratio, and yolk pigmentation, reduced serum AST, and enriched ileal microbial diversity, with marked increases in Lactobacillaceae (P < 0.05). Following LPS exposure, XOS-PC preserved villus architecture, evidenced by increased ileal VH and VH/CD ratio (P < 0.05). In the ileal mucosa, XOS-PC supplementation upregulated CLDN1, CLDN5, TLR2, and TLR4 gene expression while suppressing TNF-α (P < 0.05), indicating enhanced barrier function and attenuated inflammatory signaling. Microbiota analysis revealed increased alpha diversity, distinct beta diversity, elevated Lactobacillaceae, and reduced Fusobacteria and Sphaerochaeta (P < 0.05). Correlation analysis revealed positive association between Lactobacillus with villus height and gut barrier genes, while Fusobacteria and Sphaerochaeta correlated inversely with epithelial integrity and positively with TNF-α. Collectively, this study demonstrates that a structurally enriched XOS-based prebiotic complex enhances productivity, reinforces gut integrity, and reprograms microbiota under both physiological and immune-stressed states, offering a novel precision-nutritional solution for poultry resilience.

Poultry ScienceVol. 105(1)
Buchang Pharma (China) (CN), Chinese Academy of Agricultural Sciences (CN), Feed Research Institute (CN), Ministry of Agriculture and Rural Affairs (CN)
Openalex Percentile: Top 59%
Animal Nutrition and Physiology
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