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تأثیر جنسیت بر ریخت‌شناسی روده، جمعیت میکروبی روده و فراسنجه‌های خونی جوجه‌های گوشتی | ||
| علوم دامی | ||
| دوره 39، شماره 150، خرداد 1405، صفحه 61-76 اصل مقاله (2.3 M) | ||
| نوع مقاله: مقاله پژوهشی | ||
| شناسه دیجیتال (DOI): 10.22092/asj.2025.368586.2466 | ||
| نویسندگان | ||
| مطلب ابراهیمی1؛ محسن دانشیار* 1؛ حامد احمدی2؛ سینا پیوستگان1؛ محمد افروزیه3 | ||
| 1گروه علوم دامی، دانشکده کشاورزی، دانشگاه ارومیه، ایران | ||
| 2گروه علوم دامی، دانشکده کشاورزی، دانشگاه تربیت مدرس،ایران | ||
| 3گروه کشاورزی، خوراک و منابع طبیعی، دانشگاه آلبرتا، ادمنتون، کانادا | ||
| چکیده | ||
| هدف این مطالعه ارزیابی تفاوت بین جوجه‌های گوشتی نر و ماده و بررسی تأثیر جنسیت بر عملکرد، ریخت‌شناسی روده، جمعیت میکروبی روده و فراسنجه‌های خونی جوجه‌های گوشتی بود. بدین منظور تعداد 120 قطعه جوجه گوشتی راس 308 یک روزه نر و ماده تعیین جنسیت شدند و به 2 گروه (60 نر و 60 ماده) با 6 تکرار و 10 پرنده در هر تکرار تقسیم شدند. نتایج نشان داد که مصرف خوراک در دوره رشد، پایانی و کل دوره و افزایش وزن بدن در دوره رشد و کل دوره در جوجه‌های گوشتی نر بیشتر از جوجه‌های گوشتی ماده بود (05/0>P). ارتفاع پرز دئودنوم و ژژونوم و نسبت ارتفاع پرز به عمق کریپت ژژنوم در جوجه‌های گوشتی نر نسبت به پرندگان ماده بیشتر بود (05/0>P). جوجه‌های گوشتی ماده عمق کریپت بیشتری در بخش ژژنوم داشتند. غلظت گلوکز، اسید اوریک، آلبومین و پروتئین کل خون در پرندگان نر به طور معنی‌داری بیشتر از پرندگان ماده بود (05/0>P). اما غلظت تری‌گلیسیرید، کلسترول و T3 خون در جوجه‌های گوشتی ماده بیشتر بود (05/0>P). جمعیت باکتری‌های لاکتوباسیلوس در ایلئوم و سکوم جوجه‌های گوشتی نر بیشتر از جوجه‌های گوشتی ماده بود (05/0>P). به طور کلی جوجه‌های گوشتی نر و ماده در اکثر پارامترهای بررسی شده با هم تفاوت دارند و استفاده از پرندگان نر یا ماده نتایج تحقیقات را تحت تاثیر قرار می‌دهد. بنابراین توصیه می‌شود که محققان به دلیل تفاوت‌های موجود و مشکلات تعیین جنسیت در سن یک روزگی به دنبال روش‌های جایگزین از جمله برآورد اثر جنسیت با استفاده از روش‌های هوشمند محاسباتی باشند. | ||
| کلیدواژه‌ها | ||
| اثر جنسیت؛ ارتفاع پرز؛ پرندگان نر؛ عملکرد؛ جوجه گوشتی | ||
| عنوان مقاله [English] | ||
| Effect of gender on intestinal morphology, gut microbial population and blood parameters of broiler chickens | ||
| نویسندگان [English] | ||
| Motaleb Ebrahimi1؛ M. Daneshyar1؛ Hamed Ahmadi2؛ Sina Payvastegan1؛ Mohammad Afrouziyeh3 | ||
| 1Department of Animal Science, Faculty of Agriculture, Urmia University, Urmia, Iran | ||
| 2Department of Poultry Science, Faculty of Agriculture, Tarbiat Modarres University, Tehran, Iran | ||
| 3Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB T6G 2P5, Canada | ||
| چکیده [English] | ||
| The aim of this study was to evaluate the differences between male and female broilers and to determine the gender effect on performance, intestinal morphology, intestinal microbial population and blood parameters of broilers. For this purpose, 120 one-day-old male and female Ross 308 chicks were sexed and divided into 2 groups (60 males and 60 females) with 6 replicates and 10 birds each. The results showed that feed intake of grower finisher and whole experimental periods and body weight gain of grower and whole experimental periods were greater in male broilers than in female ones (P<0.05). The height of the duodenum and jejunum villus and the ratio of villus height to jejunum crypt depth were higher in male broiler chickens than in female birds (P<0.05). Female broilers had greater crypt depth in the jejunum. Blood glucose, uric acid, albumin, and total protein concentrations were significantly higher in male birds than in female birds (P<0.05). However, blood triglyceride, cholesterol, and T3 concentrations were higher in female broilers (P<0.05). Lactobacillus bacterial populations in the ileum and cecum of male broilers were higher than in female broilers (P<0.05). In general, male and female broilers differ in most of the parameters studied, and the use of male or female birds affects the results of the research. Therefore, it is recommended that researchers seek alternative methods, including estimating the sex effect using intelligent computational methods, due to the existing differences and difficulties in determining sex at day one of age. | ||
| کلیدواژه‌ها [English] | ||
| Sex effect, Villus height, male birds, Performance, Broiler chickens | ||
| مراجع | ||
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Abdi-Hachesoo, B., Talebi, A. and Asri-Rezaei, S. (2011). Comparative study on blood profiles of indigenous and Ross-308 broiler breeders. Global Veterinaria, 7(3), 238-241. Adeleye, O. O., Otakoya, I. O., Fafiolu, A. O., Alabi, J. O., Egbeyale, L. T. and Idowu, O. M. O. (2018). Serum chemistry and gut morphology of two strains of broiler chickens to varying interval of post hatch feeding. Veterinary and Animal Science, 5, 20-25. Alrekabi, M. M., Ali, N. A., Aldulaimi, I. H., Alobaidi, O. S., Aldulaimi, K. I. and Alziadi, H. A. (2018). The effect of sex and slaughter age in some blood traits of broiler chicks Ross 308. In International Conference Food and Agricultural Sciences, Mashhad, 361-366. Apajalahti, J. and Vienola, K. (2016). Interaction between chicken intestinal microbiota and protein digestion. Animal Feed Science and Technology, 221, 323-330. Arab, J. P., Martin-Mateos, R. M. and Shah, V. H. (2018). Gut–liver axis, cirrhosis and portal hypertension: the chicken and the egg. Hepatology International, 12(1), 24-33. Ballou, A. L., Ali, R. A., Mendoza, M. A., Ellis, J. C., Hassan, H. M., Croom, W. J. and Koci, M. D. (2016). Development of the chick microbiome: how early exposure influences future microbial diversity. Frontiers in Veterinary Science, 3, 2-19. Ban, Z., Chen, S., Li, L., Zhang, Q., Zhao, X., Liang, H. and Guo, Y. (2025). Effects of dietary net energy/lysine ratio and sex on growth performance, digestive organ development, and cecal microbiota of broiler chickens. Animals, 15(11), 1572. Barasch, I. B. and Grimes, J. L. (2021). The effect of a heat-stable xylanase on digesta viscosity, apparent metabolizable energy and growth performance of broiler chicks fed a wheat-based diet. Poultry Science, 100(9), 101275. Benyi, K., Tshilate, T. S., Netshipale, A. J. and Mahlako, K. T. (2015). Effects of genotype and sex on the growth performance and carcass characteristics of broiler chickens. Tropical Animal Health and Production, 47, 1225-1231. Bjerrum, L. E. R. M., Engberg, R. M., Leser, T. D., Jensen, B. B., Finster, K. and Pedersen, K. (2006). Microbial community composition of the ileum and cecum of broiler chickens as revealed by molecular and culture-based techniques. Poultry Science, 85(7), 1151-1164. Campbell, J. (2015). Malondialdehyde (MDA): Structure, Biochemistry and Role in Disease, Biochemistry Research Trends. Nova Science Publishers, Inc, New York. Da Costa, M. J., Colson, G., Frost, T. J., Halley, J. and Pesti, G. M. (2017). Straight-run vs. sex separate rearing for two broiler genetic lines Part 2: Economic analysis and processing advantages. Poultry Science, 96(7), 2127-2136. Delfani, N., Daneshyar, M., Farhoomand, P., Alijoo, Y. A., Payvastegan, S., & Najafi, G. (2022). Effects of arginine and guanidinoacetic acid supplementation with or without phenylalanine on performance and ascites susceptibility in cold-stressed broilers fed canola meal-based diet. Journal of Animal Science and Technology, 64(6), 69-95. Delfani, N., Daneshyar, M., Farhoomand, P., Payvastegan, S., Alijoo, Y. A. and Najafi, G. (2024). Attenuating susceptibility to ascites in cold‐stressed broiler chickens fed canola meal‐based diets by supplementing arginine or guanidinoacetic acid, either alone or in combination with phenylalanine. Veterinary Medicine and Science, 10(6), e70011. Elwahesh, R. M., Ben-Elhaj, K. M. and Draid, M. M. (2016). Relationship between body weight performance and plasma thyroid hormones in broiler hens. International Journal of Medical Research Professionals. 2(6), 98-102. England, A. D., de Las Heras-Saldana, S., Gharib-Naseri, K., Kheravii, S. K. and Wu, S. B. (2024). The effect of sex and dietary crude protein level on nutrient transporter gene expression and cecal microbiota populations in broiler chickens. Poultry Science, 103(2), 103268. England, A. D., Kheravii, S. K., Musigwa, S., Kumar, A., Daneshmand, A., Sharma, N. K. and Wu, S. B. (2021). Sexing chickens (Gallus gallus domesticus) with high-resolution melting analysis using feather crude DNA. Poultry Science, 100(3), 100924. England, A., Gharib-Naseri, K., Kheravii, S. K. and Wu, S. B. (2023). Influence of sex and rearing method on performance and flock uniformity in broilers—implications for research settings. Animal Nutrition, 12, 276-283. Filipovic, N., Stojevic, Z., Milinkovic-Tur, S., Ljubic, B. B. and Zdelar-Tuk, M. (2007). Changes in concentration and fractions of blood serum proteins of chickens during fattening. Veterinarski Arhiv, 77(4), 319-334. Goo, D., Kim, J. H., Choi, H. S., Park, G. H., Han, G. P. and Kil, D. Y. (2019). Effect of stocking density and sex on growth performance, meat quality, and intestinal barrier function in broiler chickens. Poultry science, 98(3), 1153-1160. Gous, R. M. (2018). Nutritional and environmental effects on broiler uniformity. World's Poultry Science Journal, 74(1), 21-34. Harr, K. E. (2002). Clinical chemistry of companion avian species: a review. Veterinary Clinical Pathology, 31(3), 140-151. Henry, M. H. and Burke, W. H. (1998). Sexual dimorphism in broiler chick embryos and embryonic muscle development in late incubation. Poultry Science, 77(5), 728-736. Hernawan, E., Wahyuni, S. and Suprapti, H. (2012). The levels of blood glucose, triglyceride, final body weight and abdominal fat percentage of broiler under sex-separated and straight run rearing system. Lucrări Ştiinţifice-Seria Zootehnie, 57(17), 28-33. Hirst, C. E., Major, A. T. and Smith, C. A. (2018). Sex determination and gonadal sex differentiation in the chicken model. International Journal of Developmental Biology, 62(1), 153-166. Humer, E., Rohrer, E., Windisch, W., Wetscherek, W., Schwarz, C., Jungbauer, L. and Schedle, K. (2015). Gender‐specific effects of a phytogenic feed additive on performance, intestinal physiology and morphology in broiler chickens. Journal of Animal Physiology and Animal Nutrition, 99(4), 788-800. Incharoen, T. and Maneechote, P. (2013). The effects of dietary whole rice hull as insoluble fiber on the flock uniformity of pullets and on the egg performance and intestinal mucosa of laying hens. American Journal of Agricultural and Biological Sciences, 8(4), 323-329. Joat, N., Van, T. T. H., Stanley, D., Moore, R. J. and Chousalkar, K. (2021). Temporal dynamics of gut microbiota in caged laying hens: a field observation from hatching to end of lay. Applied Microbiology and Biotechnology, 105(11), 4719-4730. Kadhim, K. K., Zuki, A. B. Z., Noordin, M. M., Babjee, S. A. and Khamas, W. (2010). Growth evaluation of selected digestive organs from day one to four months post-hatch in two breeds of chicken known to differ greatly in growth rate. Journal of Animal and Veterinary Advances, 9(6), 995-1004. Krishnan, K. C., Mehrabian, M. and Lusis, A. J. (2018). Sex differences in metabolism and cardiometabolic disorders. Current Opinion in Lipidology, 29(5), 404. Lee, K. C., Kil, D. Y. and Sul, W. J. (2017). Cecal microbiome divergence of broiler chickens by sex and body weight. Journal of Microbiology, 55, 939-945. Liu, Z. L., Chen, Y., Xue, J. J., Huang, X. F., Chen, Z. P., Wang, Q. G. and Wang, C. (2022). Effects of ambient temperature on the growth performance, fat deposition, and intestinal morphology of geese from 28 to 49 days of age. Poultry Science, 101(5), 101814. Livingston, M. L., Cowieson, A. J., Crespo, R., Hoang, V., Nogal, B., Browning, M. and Livingston, K. A. (2020). Effect of broiler genetics, age, and gender on performance and blood chemistry. Heliyon, 6(7), 39-54. Lopez, K. P., Schilling, M. W. amd Corzo, A. (2011). Broiler genetic strain and sex effects on meat characteristics. Poultry Science, 90(5), 1105-1111. Lumpkins, B. S., Batal, A. B. and Lee, M. (2008). The effect of gender on the bacterial community in the gastrointestinal tract of broilers. Poultry Science, 87(5), 964-967. Lysko, S. B., Baturina, O. A., Naumova, N. B., Lescheva, N. A., Pleshakova, V. I. and Kabilov, M. R. (2021). No-antibiotic-pectin-based treatment differently modified cloaca bacteriobiome of male and female broiler chickens. Agriculture, 12(1), 24. Madilindi, M. A., Mokobane, A., Letwaba, P. B., Tshilate, T. S., Banga, C. B., Rambau, M. D. and Benyi, K. (2018). Effects of sex and stocking density on the performance of broiler chickens in a sub-tropical environment. South African Journal of Animal Science, 48(3), 459-468. Maliwan, P., Khempaka, S. and Molee, W. (2017). Evaluation of various feeding programmes on growth performance, carcass and meat qualities of Thai indigenous crossbred chickens. South African Journal of Animal Science, 47(1), 16-25. Markle, J. G., Frank, D. N., Mortin-Toth, S., Robertson, C. E., Feazel, L. M., Rolle-Kampczyk, U. and Danska, J. S. (2013). Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity. Science, 339(6123), 1084-1088. May, J. D. and Lott, B. D. (2001). Relating weight gain and feed: gain of male and female broilers to rearing temperature. Poultry Science, 80(5), 581-584. Mullur, R., Liu, Y. Y. and Brent, G. A. (2014). Thyroid hormone regulation of metabolism. Physiological reviews. Newcombe, M., Cartwright, A. L., Harter‐Dennis, J. M. and McMurtry, J. P. (1992). The effect of increasing photoperiod and food restriction in sexed, broiler‐type birds. II. plasma thyroxine, triiodothyronine, insulin‐like growth factor‐I and insulin. British Poultry Science, 33(2), 427-436. Niu, Q., Li, P., Hao, S., Zhang, Y., Kim, S. W., Li, H. and Huang, R. (2015). Dynamic distribution of the gut microbiota and the relationship with apparent crude fiber digestibility and growth stages in pigs. Scientific Reports, 5(1), 9938-9952. Rajman, M., Juráni, M., Lamošová, D., Máčajová, M., Sedlačková, M., Košťál, Ľ. and Výboh, P. (2006). The effects of feed restriction on plasma biochemistry in growing meat type chickens (Gallus gallus). Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 145(3), 363-371. Ren, C. and Sylvia, K. (2018). Sexual dimorphism in the gut microbiome. IU Journal of Undergraduate Research, 4(1), 12-16. Rezende, M. S., Fonseca, B. B., de Sousa Braga, P. F., Guimarães, E. C. and Mundim, A. V. (2021). Influence of age and sex on the blood biochemical constituent values of broiler breeders during the egg-laying stage. Tropical Animal Health and Production, 53(6), 540-556. Salim, H. M., Lee, H. R., Jo, C., Lee, S. K. and Lee, B. D. (2012). Effect of sex and dietary organic zinc on growth performance, carcass traits, tissue mineral content, and blood parameters of broiler chickens. Biological Trace Element Research, 147, 120-129. Shafey, T. M., Alodan, M. A., Hussein, E. O. S. and Al-Batshan, H. A. (2013). The effect of sex on the accuracy of predicting carcass composition of Ross broiler chickens. The Journal of Animal & Plant Sciences, 23(4), 975-980. Seifert, J., Chen, Y., Schöning, W., Mai, K., Tacke, F., Spranger, J. and Wirth, E. K. (2023). Hepatic energy metabolism under the local control of the thyroid hormone system. International Journal of Molecular Sciences, 24(5), 4861. Siaga, R., Baloyi, J. J., Rambau, M. D. and Benyi, K. (2017). Research Article Effects of Stocking Density and Genotype on the Growth Performance of Male and Female Broiler Chickens. Asian Journal of Poultry Science, 11(2), 96-104 Singh, P., Karimi, A., Devendra, K., Waldroup, P. W., Cho, K. K. and Kwon, Y. M. (2013). Influence of penicillin on microbial diversity of the cecal microbiota in broiler chickens. Poultry Science, 92(1), 272-276. Stanley, D., Denman, S. E., Hughes, R. J., Geier, M. S., Crowley, T. M., Chen, H. and Moore, R. J. (2012). Intestinal microbiota associated with differential feed conversion efficiency in chickens. Applied Microbiology and Biotechnology, 96, 1361-1369. Sturkie, P. D. (2000). Avian Physiology. 5th ed. New York, Heidelberg, Barlin, Springer Verlag Tomaszewska, E., Dobrowolski, P., Muszyński, S., Kwiecień, M., Kasperek, K., Knaga, S. and Grela, E. R. (2018). Intestinal mucosa develops in a sex-dependent manner in Japanese quail (Coturnix japonica) fed Saccharomyces cerevisiae. British Poultry Science, 59(6), 689-697. Torok, V., Dyson, C., McKay, A. and Ophel-Keller, K. (2013). Quantitative molecular assays for evaluating changes in broiler gut microbiota linked with diet and performance. Animal Production Science, 53(12), 1260-1268. Ucan-Marin, F., Arukwe, A., Mortensen, A., Gabrielsen, G. W., Fox, G. A. and Letcher, R. J. (2009). Recombinant transthyretin purification and competitive binding with organohalogen compounds in two gull species (Larus argentatus and Larus hyperboreus). Toxicological sciences, 107(2), 440-450. You, L., Nishio, K., Kowata, K., Horikawa, M., Fukuchi, H., Ogoshi, M. and Takeuchi, S. (2024). Revisiting the hormonal control of sexual dimorphism in chicken feathers. General and Comparative Endocrinology, 357, 114601. Yuan, C., Jiang, Y., Wang, Z., Chen, G., Chang, G. and Bai, H. (2024). Effects of Sex on Growth Performance, Carcass Traits, Blood Biochemical Parameters, and Meat Quality of XueShan Chickens. Animals, 14(11), 1556. Yurkovetskiy, L., Burrows, M., Khan, A. A., Graham, L., Volchkov, P., Becker, L. and Chervonsky, A. V. (2013). Gender bias in autoimmunity is influenced by microbiota. Immunity, 39(2), 400-412. Zerehdaran, S., Vereijken, A. L. J., Arendonk, J. V. and Van der Waaij, E. H. (2005). Effect of age and housing system on genetic parameters for broiler carcass traits. Poultry Science, 84(6), 833-838. | ||
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