# Birth Season and Breed Effects on Newborn Longissimus Thoracis and Semimembranosus Muscles: Insights from the Nero Di Lomellina Piglets

**Authors:** Margherita Pallaoro, Giorgio Mirra, Lucia Aidos, Mirko Sergio, Mauro Di Giancamillo, Raffaella Rossi, Annamaria Costa, Eleonora Buoio, Silvia Michela Mazzola, Silvia Clotilde Modina, Alessia Di Giancamillo

PMC · DOI: 10.3390/ani16040655 · Animals : an Open Access Journal from MDPI · 2026-02-18

## TL;DR

This study shows that summer-born piglets, especially a local Italian breed, have more developed muscles at birth compared to winter-born piglets.

## Contribution

The study reveals breed and seasonal effects on muscle development in newborn piglets through gene expression and morphology analysis.

## Key findings

- Summer-born piglets had larger muscle fiber cross-sectional areas in both Longissimus thoracis and Semimembranosus muscles.
- MYF6 and heat shock protein genes were more expressed in summer-born Nero di Lomellina piglets.
- Winter-born piglets showed higher expression of MYF5, MYOD, and MYOG genes in Semimembranosus muscles.

## Abstract

Muscle development and growth can be influenced by several factors. This study investigated how the season of birth (winter or summer) and the breed affect muscle development in newborn piglets. We compared a local Italian pig breed, Nero di Lomellina, with a widely used commercial crossbreed. We considered the muscles Longissimus thoracis and Semimembranosus and assessed their morphology and the expression of genes related to muscle growth and stress response. Piglets born in summer showed more developed muscle tissue, especially in the local breed. These findings suggest that muscle development at birth may vary between seasons of birth and breeds. This information could be useful to promote and improve local pig breeds; besides, understanding how early muscle growth is affected by season can support more sustainable and effective breeding strategies in traditional farming systems.

Background: Understanding the factors influencing muscle development is essential for the livestock industry. This study aims to evaluate the effect of birth season and breed on the muscles Longissimus thoracis (LT) and Semimembranosus (SM) from newborn piglets of the local Italian breed Nero di Lomellina (NL) and the Commercial Hybrid Large WhitexDuroc (CH), born in winter (W) and summer (S). Methods: Muscles’ morphological features were evaluated, and the expression of Myogenic Regulatory Factors (MRFs: MYF5, MYOD, MYOG, MYF6) and heat and cold shock proteins (HSP27, HSP70, HSP90, CIRBP, RMB3) was assessed by quantitative PCR. Results: Both muscles showed a larger fiber cross-sectional area (LT: NL/S > NL/W, p = 0.035. SM: NL/S > NL/W, p = 0.035; CH/S > CH/W, p = 0.05) and a lower total number of fibers in summer piglets (LT: NL/S < NL/W, p = 0.05. SM: NL/S < NL/W, p = 0.033). In LT, MYF6 was higher, mainly in NL, in S (NL/S > NL/W, p < 0.0001; NL/S > CH/S, p = 0.0002), as well as HSP27 (NL/S > NL/W, p = 0.0001; NL/S > CH/S, p = 0.0018), HSP70 (NL/S > NL/W, p = 0.044. CH/S > CH/W, p = 0.0018), HSP90 (NL/S > NL/W, p < 0.0001; NL/S > CH/S, p = 0.023; CH/S > CH/W, p = 0.027), CIRBP NL/S > NL/W, p = 0.003; CH/S > CH/W, p = 0.0008), and RBM3 (NL/S > NL/W, p = 0.01; NL/S > CH/S, p = 0.036). In SM, MYF5 was higher in W in both breeds (NL/W > NL/S, p = 0.008; CH/W > CH/S, p < 0.0001; CH/W > NL/S, p = 0.012). Similarly, MYOD (NL/W > NL/S, p = 0.045), MYOG (NL/W > NL/S, p = 0.002; CH/W > CH/S, p = 0.025), and CIRBP (NL/W > NL/S, p = 0.003; NL/W > CH/W, p = 0.004) were mainly expressed in winter, while HSP90 was expressed in summer in CH. Conclusions: Our results demonstrate that muscle development in piglets at birth can vary between breeds and along different birth seasons, with an enhanced development observed mainly in summer newborns. These results could be helpful for improvement programs for NL and other local breeds by linking muscle development at birth to seasonal adaptation.

## Linked entities

- **Genes:** MYF5 (myogenic factor 5) [NCBI Gene 4617], MYOD1 (myogenic differentiation 1) [NCBI Gene 4654], MYOG (myogenin) [NCBI Gene 4656], MYF6 (myogenic factor 6) [NCBI Gene 4618], HSPB1 (heat shock protein family B (small) member 1) [NCBI Gene 3315], HSPA1A (heat shock protein family A (Hsp70) member 1A) [NCBI Gene 3303], HSP90AA1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 3320], CIRBP (cold inducible RNA binding protein) [NCBI Gene 1153], RBM3 (RNA binding motif protein 3) [NCBI Gene 5935]

## Full-text entities

- **Genes:** HSP90AA1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 397028] {aka HSP90, HSP90A, Hspca}, HSPB1 (heat shock protein family B (small) member 1) [NCBI Gene 3315] {aka CMT2F, HEL-S-102, HMN2B, HMND3, HS.76067, HSP27}, HSPA6 (heat shock protein family A (Hsp70) member 6) [NCBI Gene 396906] {aka HSP70, HSP70B'}, HSP90AA1 (heat shock protein 90 alpha family class A member 1) [NCBI Gene 3320] {aka EL52, HEL-S-65p, HSP86, HSP89A, HSP90A, HSP90N}, MYF5 (myogenic factor 5) [NCBI Gene 100153269] {aka MYF-5}, CIRBP (cold inducible RNA binding protein) [NCBI Gene 100522851] {aka CIRP}, MYOG (myogenin) [NCBI Gene 497618], ACTA2 (actin alpha 2, smooth muscle) [NCBI Gene 733615] {aka ACT-4, actin}, RBM3 (RNA binding motif protein 3) [NCBI Gene 5935] {aka IS1-RNPL, RNPL}, RBM3 (RNA binding motif protein 3) [NCBI Gene 100627807], DRAP1 (DR1 associated protein 1) [NCBI Gene 100525028], MYF6 (myogenic factor 6) [NCBI Gene 4618] {aka CNM3, MRF4, bHLHc4, myf-6}, MYOG (myogenin) [NCBI Gene 4656] {aka MYF4, bHLHc3, myf-4}, MYF5 (myogenic factor 5) [NCBI Gene 4617] {aka EORVA, bHLHc2}, MYOD1 (myogenic differentiation 1) [NCBI Gene 407604] {aka MUF3, MYF-3, MYOD}, MYF6 (myogenic factor 6) [NCBI Gene 397005] {aka Myf-6}, HSPB1 (heat shock protein family B (small) member 1) [NCBI Gene 493184] {aka HSP27}, CIRBP (cold inducible RNA binding protein) [NCBI Gene 1153] {aka CIRP}, HSPA4 (heat shock protein family A (Hsp70) member 4) [NCBI Gene 3308] {aka APG-2, HEL-S-5a, HS24/P52, HSPH2, RY, hsp70}, PAX7 [NCBI Gene 494466], MYOD1 (myogenic differentiation 1) [NCBI Gene 4654] {aka CMYO17, CMYP17, MYF3, MYOD, MYODRIF, PUM}
- **Diseases:** malformations (MESH:C564254), CH (MESH:D015456), bone fractures (MESH:D050723), injury to (MESH:D014947), muscle atrophy (MESH:D009133)
- **Chemicals:** Ethanol (MESH:D000431), Eosin (MESH:D004801), agarose (MESH:D012685), SYBR Green (MESH:C098022), isopentane (MESH:C067038), nitrogen (MESH:D009584), Xylene (MESH:D014992), oxygen (MESH:D010100), Hematoxylin (MESH:D006416), DPX (MESH:C027512), ANCTIN (-)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Gallus gallus (bantam, species) [taxon 9031], Ursus arctos (brown bear, species) [taxon 9644], Bos taurus (bovine, species) [taxon 9913], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937204/full.md

## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937204/full.md

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Source: https://tomesphere.com/paper/PMC12937204