# Modulation of the nutritional, metabolomic and microRNA profile of colostrum and piglet performance via a high-energy, high-lysine transition diet in sows

**Authors:** Diana Luise, Silvia Bencivenni, Antonio Zurru, Andrea Serra, Luca Laghi, Federico Correa, Francesco Palumbo, Paolo Trevisi

PMC · DOI: 10.1186/s40104-026-01355-5 · Journal of Animal Science and Biotechnology · 2026-03-09

## TL;DR

A high-energy, high-lysine diet for sows during the transition period improves colostrum quality and piglet growth, possibly through changes in energy metabolism and microRNA profiles.

## Contribution

This study demonstrates that a high-energy, high-lysine transition diet improves sow and piglet outcomes by modulating colostrum composition and microRNA expression.

## Key findings

- The TRT diet reduced stillbirths and improved piglet body weight at weaning.
- TRT colostrum had higher fat content and specific metabolites linked to energy metabolism.
- The TRT diet increased expression of ssc-miR-143-3p, associated with reduced inflammation and oxidative stress.

## Abstract

The transition period is a critical phase for the sow due to physiological changes and nutritional requirements. A diet balanced in energy and amino acid (AA) content could improve reproductive performance, colostrum quality and piglets' growth. This study evaluated the efficacy of a transition diet (TRT) with higher energy (12.97 MJ/kg of metabolizable energy (ME)) and SID lysine (Lys; 0.85%), compared to a standard (CO) diet (12.33 MJ/kg of ME and 0.70% SID Lys), on the composition and quality of colostrum and on sow and piglet performance. The AA/SID Lys ratio was maintained in both diets. Sows (50 sows/group) were fed the CO or TRT diet from 6 d prepartum to d 4 postpartum. At farrowing, sow performance (50 sows/group) and piglet vitality (12 sows/group) were recorded, and colostrum (20 sows/group) was collected to analyze its composition and microRNAs. Piglet performances were collected d 6 and weaning (d 24).

The diet did not affect sow feed intake, body condition score, backfat and muscle loss, nor farrowing duration and time interval between piglets. The TRT group had fewer stillbirths (P = 0.002). Piglets of TRT litters had higher body weight at d 24 (P = 0.032) and tended to have higher average daily gain from d 0 to d 24 (P = 0.080). Colostrum from the TRT group tended to be higher in somatic cell count (P = 0.07), higher in fat percentage (P = 0.036), and higher in C18:2 9cis,12cis, C18:4 6cis,9cis,12cis,15cis, C20:0, UDP-glucuronate and carnitine (P < 0.05); moreover, it had a lower concentration of citrate (P < 0.05). The 208 microRNAs were detected in colostrum, 13 of which were differentially expressed (P < 0.05). The TRT group had a higher ssc-miR-143-3p expression, which is associated with increased phagocytosis and reduced inflammation and oxidative stress. This, together with the increase in fat and specific metabolites related to energy metabolism, could potentially benefit piglet performance.

These results suggest that the TRT diet improves sow parturition and lactation performance by modifying sow energy metabolism and colostrum quality. This highlights the importance of a properly designed transition diet for sows.

The online version contains supplementary material available at 10.1186/s40104-026-01355-5.

## Linked entities

- **Chemicals:** lysine (PubChem CID 866), UDP-glucuronate (PubChem CID 17473), carnitine (PubChem CID 288), citrate (PubChem CID 31348)
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** KRT6B (keratin 6B) [NCBI Gene 3854] {aka CK-6B, CK6B, K6B, KRTL1, PC2, PC4}, LOC102167096 (immunoglobulin lambda-like polypeptide 1) [NCBI Gene 102167096] {aka IgM}, IGHA (immunoglobulin alpha heavy chain constant region) [NCBI Gene 100568455] {aka IGA}, VIP (vasoactive intestinal peptide) [NCBI Gene 7432] {aka PHM27}, OXT (oxytocin/neurophysin I prepropeptide) [NCBI Gene 5020] {aka OT, OT-NPI, OXT-NPI}, IGG (Immunoglobulin G level) [NCBI Gene 102658792], PCSK1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 5122] {aka BMIQ12, NEC1, PC1, PC1/3, PC3, SPC3}
- **Diseases:** Ear lesions (MESH:D004427), swelling (MESH:D004487), SCC (MESH:D013001), inflammation (MESH:D007249), hypoxic (MESH:D002534), lesions (MESH:D009059), scarring (MESH:D002921), tail lesions (MESH:C562903), health (OMIM:603663), virus infection (MESH:D014777), deficiency (MESH:D007153), TRT (MESH:D008579), brain disorder (MESH:D001927), SID (MESH:D007077), stillbirths (MESH:D050497), aggressive (MESH:D010554), CO (MESH:C536209), muscle loss (MESH:D009135)
- **Chemicals:** vitamin E (MESH:D014810), orotate (MESH:D009963), bilirubin (MESH:D001663), lactose (MESH:D007785), Gabbrostim (MESH:C038354), C (MESH:D002244), essential fatty acids (MESH:D005228), vitamin K3 (MESH:D024483), methanol (MESH:D000432), linoleic acid (MESH:D019787), methionine (MESH:D008715), ammonia (MESH:D000641), zinc (MESH:D015032), uridine (MESH:D014529), Phosphorus (MESH:D010758), phosphate (MESH:D010710), Cu (MESH:D003300), C12:0 (MESH:C030358), biotin (MESH:D001710), PGF2alpha (MESH:D015237), ethyl alcohol (MESH:D000431), vitamin PP (MESH:D009536), alpha-linolenic acid (MESH:D017962), NaN3 (MESH:D019810), water (MESH:D014867), D2O (MESH:D017666), palm oil (MESH:D000073878), vitamin A (MESH:D014801), iron (MESH:D007501), UDP-glucose (MESH:D014532), vitamin D3 (MESH:D002762), AA (MESH:D000596), vitamin B1 (MESH:D013831), urea (MESH:D014508), coconut oil (MESH:D000074263), sodium selenite (MESH:D018038), Fatty acid (MESH:D005227), oils (MESH:D009821), selenium (MESH:D012643), creatine phosphate (MESH:D010725), vitamin B2 (MESH:D012256), TCA (MESH:D014238), Helium (MESH:D006371), C18:2 9cis,12cis (-), glucuronic acid (MESH:D020723), Carnitine (MESH:D002331), soybean oil (MESH:D013024), PUFA (MESH:D005231), silica (MESH:D012822), hexane (MESH:D006586), oleic acid (MESH:D019301), UMP (MESH:D014542), vitamin B6 (MESH:D025101), KCl (MESH:D011189), Lys (MESH:D008239), folic acid (MESH:D005492), Mn (MESH:D008345), glucose (MESH:D005947), ribose (MESH:D012266), Citrate (MESH:D019343)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Sus scrofa (pig, species) [taxon 9823], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]
- **Mutations:** DGR 165 del, C at 2
- **Cell lines:** IPEC-J2 — Sus scrofa (Pig), Spontaneously immortalized cell line (CVCL_2246)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12969886/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12969886/full.md

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Source: https://tomesphere.com/paper/PMC12969886