# Modulation of Milk Source Differences on Immunity, Nutritional Physiology and Intestinal Microbiota in Neonatal Piglets

**Authors:** Junhong Liu, Miaomiao Bai, Shanshan Wang, Yihui Zhang, Changfeng Peng, Yirui Shao, Xia Xiong, Yueyao Xing, Hongnan Liu

PMC · DOI: 10.3390/ani15213104 · Animals : an Open Access Journal from MDPI · 2025-10-25

## TL;DR

This study shows that goat milk formula improves immunity, nutrient metabolism, and gut health in neonatal piglets compared to cow milk formula.

## Contribution

The study demonstrates that goat milk formula has superior effects on immunity and gut microbiota in neonatal piglets compared to cow milk.

## Key findings

- Goat milk formula increased piglet weight, immune markers, and intestinal trypsin content.
- Goat milk improved amino acid and fatty acid levels and modulated gut microbiota diversity.
- Goat milk enhanced intestinal microbial richness and short-chain fatty acid concentrations.

## Abstract

Differences in milk sources exert a considerable influence on the early digestive and absorptive processes, allergy susceptibility, and nutritional utilization in neonatal piglets. The nutritional profile and digestive properties of goat milk powder are more close to those of breast milk, facilitating easier digestion and absorption in infants. Utilizing neonatal piglets as an animal model, the present study aims to investigate the effects of different milk sources on immune function, amino acid and fatty acid metabolism, and intestinal microbiota. Findings indicate that goat milk formula powder showed promising trends in neonatal piglets’ growth performance by augmenting immune responses, promoting amino acid metabolism, and modulating the intestinal microbiota, thereby demonstrating its superiority over cow milk formula powder.

Milk sources directly influence digestion, absorption, and overall nutrient utilization during early infant nutrition. Goat milk features a nutritional composition and digestive properties that are more similar to human breast milk. This study aimed to investigate the effects of different milk sources on the immunity, amino acid and fatty acid metabolism, and intestinal microbiota in neonatal piglets. Sixteen 7-day-old suckling piglets were randomly allocated into two groups (eight replicates/group, one piglet/replicate) and fed with standard formula milk powder (CON) and goat milk formula powder (GMF). The formal experiment lasted for 14 days. Results showed that compared with the CON group, the GMF group showed a significant increase (p < 0.05) in the final weight, the serum levels of immunoglobulin A (IgA), IgG, IgM and C-reactive protein (CRP4), and intestinal trypsin content. Additionally, the GMF group had higher (p < 0.05) serum essential and non-essential amino acid and fatty acid levels, and had trends toward upregulation (0.05 < p < 0.1) in hepatic mRNA expression of spermine N1-acetyltransferase 1 (SAT1), duodenal peptide transporter 1 (PePT1), and jejunal cationic amino acid transporter 1 (CAT1). Microbiome sequencing revealed that GMF enhanced intestinal microbial richness and diversity and increased concentrations of acetic and propionic acids (p < 0.05). In conclusion, GMF suggests a potential improvement in the growth performance by enhancing immunity, amino acid and fatty acid metabolism and optimizing intestinal microbiota composition in neonatal piglets. These findings further support the favorable nutritional properties and tolerability of GMF in early-life nutrition.

## Linked entities

- **Genes:** SAT1 (spermidine/spermine N1-acetyltransferase 1) [NCBI Gene 6303], SLC15A1 (solute carrier family 15 member 1) [NCBI Gene 6564], CRAT (carnitine O-acetyltransferase) [NCBI Gene 1384]
- **Proteins:** prss1.L (serine protease 1 L homeolog), PTR1 (peptide transporter 1), AAT1 (amino acid transporter 1)
- **Chemicals:** acetic acid (PubChem CID 176), propionic acid (PubChem CID 1032)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** SLC7A1 (solute carrier family 7 member 1) [NCBI Gene 6541] {aka ATRC1, CAT-1, ERR, HCAT1, REC1L}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, SAT1 (spermidine/spermine N1-acetyltransferase 1) [NCBI Gene 6303] {aka DC21, KFSD, KFSDX, SAT, SSAT, SSAT-1}, SLC15A1 (solute carrier family 15 member 1) [NCBI Gene 6564] {aka HPECT1, HPEPT1, PEPT1}
- **Chemicals:** amino acid (MESH:D000596), fatty acid (MESH:D005227), acetic and propionic acids (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12607554/full.md

## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC12607554/full.md

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Source: https://tomesphere.com/paper/PMC12607554