# Early-life stages impact later feeding behavior and physiology in light-born piglets

**Authors:** Elizabeth Huenul, Susana M Martín-Orúe, Lluís Fabà, Ruth Forsten, Pau Salgado-López, Ferran Llobet-Cabau, María José Rodríguez-Lagunas, Marta Fornós, José Francisco Pérez

PMC · DOI: 10.1093/jas/skaf437 · Journal of Animal Science · 2025-12-18

## TL;DR

This study shows that early-life growth rates in low birth weight piglets affect their later feeding behavior and physiological markers.

## Contribution

The study reveals that early-life growth during the suckling period has lasting effects on metabolism and feeding behavior in low birth weight piglets.

## Key findings

- Slow-growing piglets spent less time at feeders post-weaning and had altered blood and urine biomarkers.
- Early-life growth rates independently influenced immune and stress-related gene expression in the jejunum.
- Suckling period growth had a stronger impact on later performance than nursery period growth.

## Abstract

Low birth weight (LBW) piglets and those exposed to negative experiences early in life are at higher risk of poor development. This study aimed to investigate the potential imprinting effects of early growth rates on metabolism and feeding behavior in LBW piglets. A total of 128 piglets ([Landrace × Yorkshire] × Pietrain) were selected at weaning 23.1 ± 0.37 d old (5.2 ± 0.94 kg body weight [BW]), including 69 castrated males and 59 females. At 51 d of age, 46 LBW piglets (0.98 ± 0.139 kg) were classified using a 2 × 2 factorial design based on growth rate during the suckling and nursery periods. Average daily gains for fast- and slow-nursery piglets were 315 ± 36.6 and 230 ± 39.0 g/d in the fast-suckling group, and 236 ± 26.9 and 159 ± 21.1 g/d in the slow-suckling group. Thereafter, piglets were euthanized at 58 d-old for sampling of physiological biomarkers in blood and urine, and jejunal gene expression. Postweaning piglet to feeder interactions were recorded daily and BW was measured weekly. Slow-growth piglets during the suckling and nursery periods spent less time at the feeder per day during the first week post-weaning (P < 0.05). Additionally, slow-growing suckling piglets showed a tendency to higher urea (P = 0.087) and lower albumin (P = 0.079) levels, and significantly lower Zn and Gamma-Aminobutyric Acid (P < 0.05) concentrations in blood compared to fast-growth piglets. In urine, the suckling slow-growing piglets had significantly higher urea, sulfur, kynurenine and tryptophan creatinine ratios (P < 0.05), with a trend toward a higher kynurenine/tryptophan ratio (KTR; P = 0.084). Slow-growing nursery piglets presented a low level of Zn in blood, a high level of KYN/Creatinine (P < 0.05) and tended to a high KTR (P = 0.074) in urine. Regarding jejunal gene expression, slow-growing suckling piglets showed a significant higher mRNA abundance of the immune response gene CXCL2 (P = 0.043) with a tendency toward increased mRNA levels of S100A9 and IL-8. Furthermore, there was a tendency to higher mRNA abundance of the protein breakdown gene (SH3RF2) and stress response gene (HSD11β1) (P < 0.10). The results suggest that the effects of the suckling and nursery periods were often independent and early-life experiences in LBW piglets, especially the suckling period, have a significant impact on their overall performance, as reflected in the physiological and behavioral differences observed at the end of the nursery period.

Early-life experiences, especially during the suckling period, significantly influence piglets’ growth, physiology, and behavior by the end of the nursery period.

## Linked entities

- **Genes:** CXCL2 (C-X-C motif chemokine ligand 2) [NCBI Gene 2920], S100A9 (S100 calcium binding protein A9) [NCBI Gene 6280], CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576], SH3RF2 (SH3 domain containing ring finger 2) [NCBI Gene 153769], HSD11B1 (hydroxysteroid 11-beta dehydrogenase 1) [NCBI Gene 3290]
- **Chemicals:** urea (PubChem CID 1176), Zn (PubChem CID 23994), Gamma-Aminobutyric Acid (PubChem CID 119), sulfur (PubChem CID 5362487), kynurenine (PubChem CID 846), tryptophan (PubChem CID 1148), creatinine (PubChem CID 588)

## Full-text entities

- **Genes:** HSD11B1 (hydroxysteroid 11-beta dehydrogenase 1) [NCBI Gene 3290] {aka 11-DH, 11-beta-HSD1, CORTRD2, HDL, HSD11, HSD11B}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, CXCL2 (C-X-C motif chemokine ligand 2) [NCBI Gene 2920] {aka CINC-2a, GRO2, GROb, MGSA-b, MIP-2a, MIP2}, SH3RF2 (SH3 domain containing ring finger 2) [NCBI Gene 153769] {aka HEPP1, POSHER, PPP1R39, RNF158}, S100A9 (S100 calcium binding protein A9) [NCBI Gene 6280] {aka 60B8AG, CAGB, CFAG, CGLB, L1AG, LIAG}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Chemicals:** Zn (MESH:D015032), sulfur (MESH:D013455), urea (MESH:D014508), tryptophan (MESH:D014364), Gamma-Aminobutyric Acid (MESH:D005680), KYN (MESH:D007737), Creatinine (MESH:D003404)

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12863952/full.md

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Source: https://tomesphere.com/paper/PMC12863952