# Gestational and lactational dietary supplementation with live yeast partially attenuates inflammatory responses to lipopolysaccharide challenge in newly weaned piglets

**Authors:** Yuechi Fu, Abiola S Lawal, Timothy A Johnson, Theresa M Casey, Jun Xie, Olayiwola Adeola, Kolapo M Ajuwon

PMC · DOI: 10.1093/jas/skaf435 · Journal of Animal Science · 2025-12-15

## TL;DR

Adding live yeast to the diets of pregnant and nursing sows may help reduce inflammation in piglets after weaning when they are exposed to bacterial toxins.

## Contribution

This study shows maternal live yeast supplementation can partially reduce inflammation in piglets after weaning.

## Key findings

- YLPS piglets had lower rectal temperatures and reduced TNF-α levels in the ileal mucosa compared to CLPS piglets.
- Piglets from LY-supplemented sows showed higher mRNA levels of several cytokines and E-cadherin protein in the ileal and jejunal mucosa.
- YLPS piglets had reduced NF-κB and TLR4 mRNA in the liver and lower NF-κB and MyD88 gene expression in the mesenteric lymph node.

## Abstract

Weaning is an abrupt event in the life of piglets that adversely affects metabolic homeostasis, leading to poor nutrient absorption, increased susceptibility to enteric pathogens, and reduced growth performance. Few studies have examined the effects of maternal dietary live yeast (LY) supplementation on the responses of piglets subjected to an immunological challenge immediately after weaning. The aim of this study was to evaluate the effects of gestational and lactational dietary LY supplementation on inflammatory and antioxidant markers in newly weaned piglets challenged with lipopolysaccharide (LPS). On day 77 of gestation, 40 sows were randomly assigned to two dietary treatments: without (CON) or with LY supplementation at 0.05% of the diet during gestation and 0.1% during lactation. Within 24 h postweaning, 16 piglets with similar weights were selected from each maternal group and intraperitoneally injected with sterile saline or LPS, resulting in four treatment groups (n = 8): 1) CON + saline (CS), 2) LY + saline (YS), 3) CON+ LPS (CLPS), and 4) LY + LPS (YLPS). Rectal temperature was measured hourly for 4 h post-injection, after which piglets were euthanized. Samples of the mesenteric lymph node, liver, muscle, and intestinal mucosa were collected at 4 h post-injection to detect maternal LY-induced physiological changes in piglets. Results showed that YLPS piglets tended to have a lower rectal temperature than CLPS piglets at 3 h post-injection (P = 0.09). Levels of tumor necrosis factor (TNF)-α were decreased in the ileal mucosa of YLPS piglets compared with CLPS piglets (P < 0.05). Additionally, piglets from LY-supplemented sows had higher mRNA abundance of interleukin (IL)-6, IL-10, TNF-α, and IL-1β in the ileal mucosa, with higher protein abundance of E-cadherin in the jejunal mucosa than those from CON sows (P < 0.05). In the liver, YLPS piglets had lower mRNA abundance of nuclear factor kappa B (NF-κB) and toll-like receptor 4 than CLPS piglets (P < 0.05). In the mesenteric lymph node, piglets from LY-supplemented sows had lower gene expression of NF-κB and myeloid differentiation factor 88 than those from CON sows (P < 0.05). These results suggest that maternal dietary LY supplementation may confer protective effects against bacterial endotoxin exposure by attenuating inflammatory responses in newly weaned piglets, with implications for improved resilience to certain gram-negative bacterial infections, such as Escherichia coli, after weaning.

Gestational and lactational dietary supplementation with live yeast partially attenuates lipopolysaccharide-induced inflammation in offspring.

## Linked entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124], IL6 (interleukin 6) [NCBI Gene 3569], IL10 (interleukin 10) [NCBI Gene 3586], IL1B (interleukin 1 beta) [NCBI Gene 3553], shg (shotgun) [NCBI Gene 37386], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], TLR4 (toll like receptor 4) [NCBI Gene 7099], MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615]
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Diseases:** gram-negative bacterial infections (MESH:D016905), inflammatory (MESH:D007249)
- **Chemicals:** LPS (MESH:D008070), LY (-)
- **Species:** Escherichia coli (E. coli, species) [taxon 562], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Full text

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## Figures

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## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12863951/full.md

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Source: https://tomesphere.com/paper/PMC12863951