# Evaluation of the effects of microencapsulated DL-methionine on productive performance, immunity, plasma amino acids, and hepatic growth-related gene expression in broilers

**Authors:** Mohammad Ali Khazab, Hossein Ali Ghasemi, Seyed Abdullah Hosseini, Iman Hajkhodadadi, Amir Hossein Alizadeh-Ghamsari

PMC · DOI: 10.1016/j.vas.2026.100593 · Veterinary and Animal Science · 2026-02-06

## TL;DR

This study shows that microencapsulated DL-methionine can reduce the amount needed in broiler diets while maintaining performance and improving immunity and gene expression.

## Contribution

The study demonstrates that microencapsulated DL-methionine can reduce supplementation by 30% without negative effects and enhances immune and growth-related outcomes.

## Key findings

- Microencapsulated DL-methionine at ≥70% of recommended levels maintained body weight gain and feed conversion ratio compared to the control.
- Higher MEM levels increased influenza antibody titers and upregulated growth-related genes like GHR and mTOR.
- Reduced MEM levels (60%) led to lower body weight gain and higher feed conversion ratio.

## Abstract

A 42-day feeding trial was conducted to compare a diet supplemented with crystalline DL-methionine (control) with diets containing microencapsulated DL-methionine (MEM) supplied at 60, 70, 80, 90, or 100 % of the commercially recommended level in broiler chickens. A total of 1260 one-day-old Arian broilers were randomly allotted to six treatments, with seven replicates of 30 birds each. Body weight gain (BWG), feed intake, and feed conversion ratio (FCR) did not differ between birds fed the control diet and those fed MEM diets containing ≥70 % of the recommended level, whereas the 60 % MEM diet reduced BWG and increased FCR. Increasing the dietary MEM level resulted in a quadratic increase in leg yield and a linear decrease in abdominal fat, without affecting hematological traits or leukocyte differential counts. The 100 % MEM diet increased influenza (H9N2) antibody titers, and all MEM levels enhanced Newcastle disease virus titers compared with the 60 % MEM diet; moreover, titers in the 100 % MEM group also exceeded those of the control. Plasma methionine, serine, and total amino acid concentrations were higher in birds fed the 60 % MEM diet than in those fed the 90 % MEM diet, while plasma cysteine showed a quadratic response as MEM level increased. Diets providing 80–100 % MEM upregulated hepatic GHR expression, and diets providing 90–100 % MEM also increased mTOR expression compared with the 60 % MEM diet. Overall, microencapsulated DL-methionine enabled approximately a 30 % reduction in supplemental methionine without impairing performance, while higher inclusion levels (≥80 % of the recommended level) beneficially modulated immune responses and growth-related gene expression.

## Linked entities

- **Genes:** GHR (growth hormone receptor) [NCBI Gene 2690], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475]
- **Chemicals:** DL-methionine (PubChem CID 876), methionine (PubChem CID 876), serine (PubChem CID 5951), cysteine (PubChem CID 594)
- **Diseases:** Newcastle disease (MONDO:0005875)

## Full-text entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 418090] {aka IGF-1, IGF-I}, MTOR (mechanistic target of rapamycin) [NCBI Gene 419455] {aka FRAP1}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 374193] {aka GAPD, KNC-NDS6}, MSTN (myostatin) [NCBI Gene 373964] {aka GDF-8, GDF8}, GHR (growth hormone receptor) [NCBI Gene 408184] {aka GHBP}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, IGF-I (Insulin-like growth factor level) [NCBI Gene 100327329], GH (growth hormone) [NCBI Gene 378781] {aka GH1, cGH}, growth hormone receptor [NCBI Gene 107049315], GHR (growth hormone receptor) [NCBI Gene 2690] {aka GHBP, GHIP}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}
- **Diseases:** AA (MESH:D000592), hyperhomocysteinemia (MESH:D020138), dislocation (MESH:D004204), Met deficiency (MESH:C565394)
- **Chemicals:** glutathione (MESH:D005978), SYBR Green (MESH:C098022), C5H11NO2S (MESH:C013809), lipids (MESH:D008055), Cys (MESH:D003545), Lys (MESH:D008239), sulfur (MESH:D013455), IAA (-), AA (MESH:D000596), creatine (MESH:D003401), trichloroacetic acid (MESH:D014238), Ser (MESH:D012694), luminal (MESH:D010634), Leu (MESH:D007930), lithium (MESH:D008094), DL-Met (MESH:D064697), Indispensable amino acids (MESH:D000601), Met (MESH:D008715), uric acid (MESH:D014527), EDTA (MESH:D004492), nitrogen (MESH:D009584), Ile (MESH:D007532)
- **Species:** Newcastle Disease Virus [taxon 11176], unidentified influenza virus (species) [taxon 11309], Gallus gallus (bantam, species) [taxon 9031], H9N2 subtype (serotype) [taxon 102796], Glycine max (soybean, species) [taxon 3847]

## Full text

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## Figures

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## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914431/full.md

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Source: https://tomesphere.com/paper/PMC12914431