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Effect of different forms of lysine and methionine in broiler diets on the key genes transcriptional profile

https://doi.org/10.32634/0869-8155-2025-391-02-87-94

Abstract

The. aim of the. study was to evaluate the effect of compound feeds with reduced (by 5%) nutritional content of lysine, methionine and metabolic energy when lysine and methionine are included in them in various forms during their interaction with broiler sex on the transcription profile of key genes regulating antioxidant protection, the immune system, inflammation and apoptosis, productivity and barrier function of the gastrointestinal epithelium.

Methods. The experiment was carried out at the “Zagorskoye” in 2024 on a poultry meat of the “Smena 9” cross from 1 to 35 days of age.

Results. The live weight of rooster and hens in experimental groups II and IV was slightly higher compared to control I, whereas in group III it was lower. In many cases, changes in the composition of the diet of rooster and hens had a significant impact on the expression of a number of key genes. In roosters, PTGS2 expression in experimental groups II–IV increased sharply (from 4.9 to 52.0 times) compared with control I, whereas in hens it increased only 1.5–2.3 times. The expression of the Muc2 gene mRNA in hens decreased in experimental group II by 1.9 times compared with group I, whereas in roosters, on the contrary, it increased by 3.1 times.

About the Authors

E. A. Yildirim
«BIOTROF+» Ltd; Saint Petersburg State Agrarian University
Russian Federation

Elena Alexandrovna Yildirim - Doctor of Biological Sciences, Chief Biotechnologist of the Molecular Genetic Laboratory; Doctor of Biological Sciences, Professor of the Department of Large Animal Husbandry.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284; Peterburgskoe Highway, Pushkin, St. Petersburg, 196601



L. A. Ilyina
«BIOTROF+» Ltd; Saint Petersburg State Agrarian University
Russian Federation

Larisa Alexandrovna Ilyina - Doctor of Biological Sciences, Head of the Molecular Genetic Laboratory; Doctor of Biological Sciences, Professor of the Department of Large Animal Husbandry.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284; Peterburgskoe Highway, Pushkin, St. Petersburg, 196601



G. Yu. Laptev
«BIOTROF+» Ltd
Russian Federation

Georgy Yurievich Laptev - Doctor of Biological Sciences, CEO of “BIOTROF+”.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284



V. A. Filippova
«BIOTROF+» Ltd; Saint Petersburg State Agrarian University
Russian Federation

Valentina Anatolyevna Filippova - Senior Biotechnologist of the Molecular Genetic Laboratory; Head of the Laboratory of the Department of Large Animal Husbandry.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284; Peterburgskoe Highway, Pushkin, St. Petersburg, 196601



A. V. Dubrovin
«BIOTROF+» Ltd
Russian Federation

Andrey Valeryevich Dubrovin - Candidate of Veterinary Sciences, Biotechnologist of the Molecular Genetic Laboratory; Candidate of Veterinary Sciences, Senior Researcher at the Department of Large Animal Husbandry.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284; Peterburgskoe Highway, Pushkin, St. Petersburg, 196601



D. G. Turina
«BIOTROF+» Ltd
Russian Federation

Daria Georgievna Tyurina - Candidate of Economic Sciences, Chief Biotechnologist of the Molecular Genetic Laboratory.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284



K. A. Sokolova
«BIOTROF+» Ltd; Saint Petersburg State Agrarian University
Russian Federation

Ksenia Andreevna Sokolova - Biotechnologist of the Molecular Genetic Laboratory; Assistant of the Department of Large animal Husbandry.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284; Peterburgskoe Highway, Pushkin, St. Petersburg, 196601



V. A. Zaikin
«BIOTROF+» Ltd
Russian Federation

Vasily Alexandrovich Zaikin - Biotechnologist of the Molecular Genetic Laboratory.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284



E. S. Ponomareva
«BIOTROF+» Ltd
Russian Federation

Ekaterina Sergeevna Ponomareva - Biotechnologist of the Molecular Genetic Laboratory.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284



I. A. Klyuchnikova
«BIOTROF+» Ltd; Saint Petersburg State Agrarian University
Russian Federation

Irina Alexandrovna Klyuchnikova - Biotechnologist of the Molecular Genetic Laboratory; Graduate Student.

19/1 Zagrebskiy Аve., Saint Petersburg, 1192284; Peterburgskoe Highway, Pushkin, St. Petersburg, 196601



V. I. Fisinin
All-Russian Scientific Research and Technological Institute of Poultry Farming
Russian Federation

Vladimir Ivanovich Fisinin - Doctor of Agricultural Sciences, Professor, Academician of the Russian Academy of Sciences, Scientific Supervisor.

10 Ptitsegradskaya Str., Sergiev Posad, Moscow region, 141311



I. A. Еgorov
All-Russian Scientific Research and Technological Institute of Poultry Farming
Russian Federation

Ivan Afanasievich Egorov - Doctor of Biological Sciences, Professor, Academician of the Russian Academy of Sciences.

10 Ptitsegradskaya Str., Sergiev Posad, Moscow region, 141311



T. A. Еgorova
All-Russian Scientific Research and Technological Institute of Poultry Farming
Russian Federation

Tatyana Anatolyevna Egorova - Doctor of Agricultural Sciences, Deputy Director for Research.

10 Ptitsegradskaya Str., Sergiev Posad, Moscow region, 141311



V. A. Manukyan
All-Russian Scientific Research and Technological Institute of Poultry Farming
Russian Federation

Vardges Aghavardovich Manukyan - Doctor of Agricultural Sciences, Chief Researcher, Head of the Poultry Nutrition Department.

10 Ptitsegradskaya Str., Sergiev Posad, Moscow region, 141311



T. N. Lenkova
All-Russian Scientific Research and Technological Institute of Poultry Farming
Russian Federation

Tatyana Nikolaevna Lenkova - Doctor of Agricultural Sciences, Professor.

10 Ptitsegradskaya Str., Sergiev Posad, Moscow region, 141311



O. N. Degtyareva
All-Russian Scientific Research and Technological Institute of Poultry Farming
Russian Federation

Olga Nikolaevna Degtyareva - Candidate of Agricultural Sciences, Researcher.

10 Ptitsegradskaya Str., Sergiev Posad, Moscow region, 141311



References

1. Muharlien, Nursita I.W., Pangestu V.M. The Effect of Feed Protein Level on Feed Consumption, Body Weight Gain and Feed Conversion of Finisher Java Super Male Chicken. IOP Conference Series: Earth and Environmental Science.2020; 478: 012044. https://doi.org/10.1088/1755-1315/478/1/012044

2. Pakiding W., Hakim M.R., Daryatmo, Linggi T.R., Elis. The influence of protein levels on body weight, body dimensions, and reproductive characteristics of local chickens treated in-ovo feeding L-Arginine for two generations. IOP Conference Series: Earth and Environmental Science.2021; 788: 012188. https://doi.org/10.1088/1755-1315/788/1/012188

3. Houshmand M., Azhar K., Zulkifli I., Bejo M.H., Kamyab A. Effects of non-antibiotic feed additives on performance, immunity and intestinal morphology of broilers fed different levels of protein. South African Journal of Animal Science. 2012; 42(1): 22–32. https://doi.org/10.4314/sajas.v42i1.3

4. Hernández F., López M., Martínez S., Megías M.D., Catalá P., Madrid J. Effect of low-protein diets and single sex on production performance, plasma metabolites, digestibility, and nitrogen excretion in 1to 48-day-old broilers. Poultry Science. 2012; 91(3): 683–692. https://doi.org/10.3382/ps.2011-01735

5. Awad E.A. et al. Response of broiler to reduced-protein diets under heat stress conditions. World’s.Poultry Science Journal.2019; 75(4): 583–598. https://doi.org/10.1017/S0043933919000576

6. Kidd M.T., McDaniel C.D., Branton S.L., Miller E.R., Boren B.B., Fancher B.I. Increasing Amino Acid Density Improves Live Performance and Carcass Yields of Commercial Broilers. Journal of Applied Poultry Research. 2004; 13(4): 593–604. https://doi.org/10.1093/japr/13.4.593

7. Waldroup P.W., Oviedo-Rondon E.O. Models to Estimate Amino Acid Requirements for Broiler Chickens: A Review International Journal of Poultry Science. 2002; 1(5): 106–113. https://doi.org/10.3923/ijps.2002.106.113

8. Smiricky-Tjardes M.R., Mavromichalis I., Albin D.M., Wubben J.E., Rademacher M., Gabert V.M. Bioefficacy of L-lysine sulfate compared with feed-grade L-lysine•HCl in young pigs. Journal of animal science. 2004; 82(9): 2610–2614. https://doi.org/10.2527/2004.8292610x

9. Ahmad G., Mushtaq T., Aslam Mirza M., Ahmed Z. Comparative Bioefficacy of Lysine from l-Lysine Hydrochloride or l-Lysine Sulfate in Basal Diets Containing Graded Levels of Canola Meal for Female Broiler Chickens. Poultry Science. 2007; 86(3): 525–530. https://doi.org/10.1093/ps/86.3.525

10. Sauer N., Emrich K., Piepho H.-P., Lemme A., Redshaw M.S., Mosenthin R. Meta-Analysis of the Relative Efficiency of Methionine-Hydroxy-Analogue-Free-Acid Compared with dl-Methionine in Broilers Using Nonlinear Mixed Models. Poultry Science. 2008; 87(10): 2023–2031. https://doi.org/10.3382/ps.2007-00514

11. Kluge H., Gessner D.K., Herzog E., Eder K. Efficacy of DL-methionine hydroxy analogue-free acid in comparison to DL-methionine in growing male white Pekin ducks. Poultry Science. 2016; 95(3): 590–594. https://doi.org/10.3382/ps/pev355

12. Martín-Venegas R., Geraert P.A., Ferrer R. Conversion of the Methionine Hydroxy Analogue dl-2-Hydroxy-(4-Methylthio) Butanoic Acid to Sulfur-Containing Amino Acids in the Chicken Small Intestine. Poultry Science. 2006; 85(11): 1932–1938. https://doi.org/10.1093/ps/85.11.1932

13. Zarghi H., Ghavi S. Relative biological efficacy of methionine hydroxy analogue-free acid compared to dl-methionine in the broiler chickens. Veterinary Medicine and Science. 2024; 10(3): e1460. https://doi.org/10.1002/vms3.1460

14. Gelli M., Duo Y., Konda A.R., Zhang C., Holding D., Dweikat I. Identification of differentially expressed genes between sorghum genotypes with contrasting nitrogen stress tolerance by genome-wide transcriptional profiling. BMC Genomics. 2014; 15: 179. https://doi.org/10.1186/1471-2164-15-179

15. Pauletto M. et al. Nutrigenomic Effects of Long-Term Grape Pomace Supplementation in Dairy Cows. Animals. 2020; 10(4): 714. https://doi.org/10.3390/ani10040714

16. Vázquez-AñÓn M., Kratzer D., González-Esquerra R., Yi I.G., Knight C.D. A Multiple Regression Model Approach to Contrast The Performance of 2-Hydroxy-4-Methylthio Butanoic Acid and DL-Methionine Supplementation Tested in Broiler Experiments and Reported in the Literature. Poultry Science. 2006; 85(4): 693–705. https://doi.org/10.1093/ps/85.4.693

17. Surai P.F. Integrated Antioxidant Defence Network in Animals. EC. Nutrition. 2023; 18(6): 18–20.

18. Surai F. Vitagenes in avian biology and poultry health. Wageningen, The Netherlands: Wageningen Academic Publishers. 2020; 544. ISBN 978-90-8686-353-2 https://doi.org/10.3920/978-90-8686-906-0

19. Martín-Vázquez E., Cobo-Vuilleumier N., López-Noriega L., Lorenzo P.I., Gauthier B.R. The PTGS2/COX2-PGE signaling cascade in inflammation: Pro or anti? A case study with type 1 diabetes mellitus. International Journal of Biological Sciences. 2023; 19(13): 4157–4165. https://doi.org/10.7150/ijbs.86492

20. Surai P.F., Kochish I.I., Kidd M.T. Redox Homeostasis in Poultry: Regulatory Roles of NF-κB. Antioxidants. 2021; 10(2): 186. https://doi.org/10.3390/antiox10020186

21. Burdick Sanchez N.C., Broadway P.R., Carroll J.A. Influence of Yeast Products on Modulating Metabolism and Immunity in Cattle and Swine. Animals. 2021; 11(2): 371. https://doi.org/10.3390/ani11020371

22. Kern L., Mittenbühler M.J., Vesting A.J., Ostermann A.L., Wunderlich C.M., Wunderlich F.T. Obesity-Induced TNFα and IL-6 Signaling: The Missing Link between Obesity and Inflammation— Driven Liver and Colorectal Cancers. Cancers. 2019; 11(1): 24. https://doi.org/10.3390/cancers11010024

23. Ghezzi C., Loo D.D.F., Wright E.M. Physiology of renal glucose handling via SGLT1, SGLT2 and GLUT2. Diabetologia.2018; 61(10): 2087–2097. https://doi.org/10.1007/s00125-018-4656-5

24. Weintraut M.L., Kim S., Dalloul R.A., Wong E.A. Expression of small intestinal nutrient transporters in embryonic and posthatch turkeys. Poultry Science. 2016; 95(1): 90–98. https://doi.org/10.3382/ps/pev310

25. Uni Z., Smirnov A., Sklan D. Preand posthatch development of goblet cells in the broiler small intestine: effect of delayed access to feed. Poultry Science. 2003; 82(2): 320–327. https://doi.org/10.1093/ps/82.2.320

26. Horn N.L., Donkin S.S., Applegate T.J., Adeola O. Intestinal mucin dynamics: response of broiler chicks and White Pekin ducklings to dietary threonine. Poultry Science. 2009; 88(9): 1906–1914. https://doi.org/10.3382/ps.2009-00009

27. Celi P., Verlhac V., Pérez Calvo E., Schmeisser J., Kluenter A.-M. Biomarkers of gastrointestinal functionality in animal nutrition and health. Animal Feed Science and Technology. 2019; 250: 9–13. https://doi.org/10.1016/J.ANIFEEDSCI.2018.07.012

28. Faure M., Moënnoz D., Montigon F., Mettraux C., Breuillé D., Ballèvre O. Dietary Threonine Restriction Specifically Reduces Intestinal Mucin Synthesis in Rats The Journal of Nutrition. 2005; 135(3): 486–491. https://doi.org/10.1093/jn/135.3.486

29. Conde-Aguilera J.A., Cholet J.C.G., Lessire M., Mercier Y., Tesseraud S., van Milgen J. The level and source of free-methionine affect body composition and breast muscle traits in growing broilers. Poultry Science.2016; 95(10): 2322–2331. https://doi.org/10.3382/ps/pew105


Review

For citations:


Yildirim E.A., Ilyina L.A., Laptev G.Yu., Filippova V.A., Dubrovin A.V., Turina D.G., Sokolova K.A., Zaikin V.A., Ponomareva E.S., Klyuchnikova I.A., Fisinin V.I., Еgorov I.A., Еgorova T.A., Manukyan V.A., Lenkova T.N., Degtyareva O.N. Effect of different forms of lysine and methionine in broiler diets on the key genes transcriptional profile. Agrarian science. 2025;(2):87-94. (In Russ.) https://doi.org/10.32634/0869-8155-2025-391-02-87-94

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