Research Article
BibTex RIS Cite

Synergistic Effects of Cyanus depressus and Schizochytrium sp. Extracts on Growth Indices and The Expression Levels of Antioxidant and Immunity-Related Genes in Common Carp (Cyprinus carpio)

Year 2025, Volume: 12 Issue: 1, 111 - 121

Abstract

This study aimed to assess the combined effects of Cyanus depressus and Schizochytrium sp. extracts on growth indices and the expression of genes linked to antioxidant activity and immunity in carp (Cyprinus carpio). Fish, averaging 3.71 ± 0.16 g in weight, were assigned to three dietary groups over a 60-day period: a control group (0 g/kg extract) and two test groups receiving extract mixtures at 0.5 g/kg (CS05) and 1 g/kg (CS1). The supplemented groups, particularly those at 0.5 and 1 g/kg, showed significant increases in final body weight, weight gain, and specific growth rate. The highest superoxide dismutase (SOD) and catalase (CAT) gene expression levels were seen in fish on the 0.5 g/kg CS-supplemented diet, and CS-fed groups displayed the greatest expression of the immune-related gene interleukin-1 beta (IL-1β) relative to the control. Collectively, these findings indicate that Cyanus depressus and Schizochytrium sp. extracts, especially at a dosage of 0.5 g/kg, have promising potential as dietary supplements for enhancing the physiological health and growth of carp.

Ethical Statement

This experiment was approved by the Van Yüzüncü Yıl University Local Ethics Committee for Animal Experiments (protocol no: 2023/13-31) and conducted in accordance with established ethical guidelines.

Supporting Institution

Van Yüzüncü Yıl University, Scientific Research Projects Department

Project Number

FHD-2024-10941

Thanks

This research was supported by the Van Yüzüncü Yıl University, Scientific Research Projects Department (FHD-2024-10941). The author thanks the Van Yuzuncu Yıl University Scientific Research Projects Department for their support.

References

  • Ababouch, L., Nguyen, K. A. T., Castro de Souza, M., & Fernandez‐Polanco, J. (2023). Value chains and market access for aquaculture products. Journal of the World Aquaculture Society, 54(2), 527-553. https://doi.org/10.1111/jwas.12964
  • Abu-Elala, N. M., Galal, M. K., Abd-Elsalam, R. M., Mohey-Elsaeed, O., & Ragaa, N. M. (2016). Effects of dietary supplementation of Spirulina platensis and garlic on the growth performance and expression levels of immune-related genes in Nile tilapia (Oreochromis niloticus). Journal of Aquaculture Research and Development, 7(7), 433-442.
  • Ahmadifar, E., Kalhor, N., Yousefi, M., Adineh, H., Moghadam, M. S., Sheikhzadeh, N., Moonmanee, T., Hoseinifar, S. H., & Van Doan, H. (2023). Effects of dietary Plantago ovata seed extract administration on growth performance and immune function of common carp (Cyprinus carpio) fingerling exposed to ammonia toxicity. Veterinary Research Communications, 47(2), 731-744. https://doi.org/10.1007/s11259-022-10034-5
  • Ahmadifar, E., Pourmohammadi Fallah, H., Yousefi, M., Dawood, M. A., Hoseinifar, S. H., Adineh, H., Yilmaz, S., Paolucci, M., & Doan, H. V. (2021a). The gene regulatory roles of herbal extracts on the growth, immune system, and reproduction of fish. Animals, 11(8), 2167. https://doi.org/10.3390/ani11082167
  • Ahmadifar, E., Yousefi, M., Karimi, M., Fadaei Raieni, R., Dadar, M., Yilmaz, S., Dawood, M. A., & Abdel-Latif, H. M. (2021b). Benefits of dietary polyphenols and polyphenol-rich additives to aquatic animal health: an overview. Reviews in Fisheries Science & Aquaculture, 29(4), 478-511. https://doi.org/10.1080/23308249.2020.1818689
  • Bahi, A., Ramos‐Vega, A., Angulo, C., Monreal‐Escalante, E., & Guardiola, F. A. (2023). Microalgae with immunomodulatory effects on fish. Reviews in Aquaculture, 15(4), 1522-1539. https://doi.org/10.1111/raq.12792
  • Bélanger, A., Sarker, P. K., Bureau, D. P., Chouinard, Y., & Vandenberg, G. W. (2021). Apparent digestibility of macronutrients and fatty acids from microalgae (Schizochytrium sp.) fed to rainbow trout (Oncorhynchus mykiss): A potential candidate for fish oil substitution. Animals, 11(2), 456. https://doi.org/10.3390/ani11020456
  • Bi, Z. Q., Ren, L. J., Hu, X. C., Sun, X. M., Zhu, S. Y., Ji, X. J., & Huang, H. (2018). Transcriptome and gene expression analysis of docosahexaenoic acid producer Schizochytrium sp. under different oxygen supply conditions. Biotechnology for Biofuels, 11, 1-13. https://doi.org/10.1186/s13068-018-1250-5
  • Boyd, C. E., D'Abramo, L. R., Glencross, B. D., Huyben, D. C., Juarez, L. M., Lockwood, G. S., McNevin, A. A., Tacon, A. G. J., Teletchea, F., Tomasso Jr, J. R., Tucker, C. S., & Valenti, W. C. (2020). Achieving sustainable aquaculture: Historical and current perspectives and future needs and challenges. Journal of the World Aquaculture Society, 51(3), 578-633. https://doi.org/10.1111/jwas.12714
  • Ciji, A., & Akhtar, M. S. (2021). Stress management in aquaculture: A review of dietary interventions. Reviews in Aquaculture, 13(4), 2190-2247. https://doi.org/10.1111/raq.12565
  • das Neves, S. C., da Silva, S. M., Costa, G. K., Correia, E. S., Santos, A. L., da Silva, L. C., & Bicudo, Á. J. (2021) Dietary supplementation with fumaric acid improves growth performance in nile tilapia juveniles. Animals, 12(1), 8. https://doi.org/10.3390/ani12010008
  • Dawood, M. A., Koshio, S., & Esteban, M. Á. (2018). Beneficial roles of feed additives as immunostimulants in aquaculture: a review. Reviews in Aquaculture, 10(4), 950-974. https://doi.org/10.1111/raq.12209
  • Dos Santos, S. K. A., Schorer, M., Moura, G. D. S., Lanna, E. A. T., & Pedreira, M. M. (2019). Evaluation of growth and fatty acid profile of Nile tilapia (Oreochromis niloticus) fed with Schizochytrium. Aquaculture research, 50(4), 1068-1074. https://doi.org/10.1111/are.13979
  • Duman, K. E., Dogan, A., & Kaptaner, B. (2022). Ameliorative role of Cyanus depressus (M. Bieb.) Soják plant extract against diabetes‐associated oxidative‐stress‐induced liver, kidney, and pancreas damage in rats. Journal of Food Biochemistry, 46(10), e14314. https://doi.org/10.1111/jfbc.14314
  • Eroldoğan, O. T., Glencross, B., Novoveska, L., Gaudêncio, S. P., Rinkevich, B., Varese, G. C., Carvalho, M. F., Tasdemir, D., Safarik, I., Nielsen, S. L., Rebours, C., Lada, L. B., Robbens, J., Strode, E., Haznedaroğlu, B. Z., Kotta, J., Evliyaoğlu, E., Oliveira, J., Girao, M., Vasquez, M. I., Cabarkapa, I., Rakita, S., Klun, K., & Rotter, A. (2023). From the sea to aquafeed: A perspective overview. Reviews in aquaculture, 15(3), 1028-1057. https://doi.org/10.1111/raq.12740
  • Escher, G. B., Santos, J. S., Rosso, N. D., Marques, M. B., Azevedo, L., do Carmo, M. A. V., Daguer, H., Molognoni, L., do Prado-Silva, L., Sant'Ana, A. S., da Silva, M. C., & Granato, D. (2018). Chemical study, antioxidant, anti-hypertensive, and cytotoxic/cytoprotective activities of Centaurea cyanus L. petals aqueous extract. Food and chemical toxicology, 118, 439-453. https://doi.org/10.1016/j.fct.2018.05.046
  • Estim, A., Shapawi, R., Shaleh, S. R. M., Fui-Fui, C., & Mustafa, S. (2024). Transformative Research in Aquaculture for Sustainable Seafood Security. In SDGs in the Asia and Pacific Region (pp. 415-444). Cham: Springer International Publishing. https://doi.org/10.1007/978-3-031-17463-6_118
  • Fattaheian-Dehkordi, S., Hojjatifard, R., Saeedi, M., & Khanavi, M. (2021). A review on antidiabetic activity of Centaurea spp.: A new approach for developing herbal remedies. Evidence‐Based Complementary and Alternative Medicine, 2021(1), 5587938. https://doi.org/10.1155/2021/5587938
  • Fazelan, Z., Hoseini, S. M., Yousefi, M., Khalili, M., Hoseinifar, S. H., & Van Doan, H. (2020). Effects of dietary eucalyptol administration on antioxidant and inflammatory genes in common carp (Cyprinus carpio) exposed to ambient copper. Aquaculture, 520, 734988. https://doi.org/10.1016/j.aquaculture.2020.734988
  • Gawlik-Dziki, U., Wrzesińska-Krupa, B., Nowak, R., Pietrzak, W., Zyprych-Walczak, J., & Obrępalska-Stęplowska, A. (2023). Herbicide resistance status impacts the profile of non-anthocyanin polyphenolics and some phytomedical properties of edible cornflower (Centaurea cyanus L.) flowers. Scientific Reports, 13(1), 11538. https://doi.org/10.1038/s41598-023-38520-z
  • Gephart, J. A., Golden, C. D., Asche, F., Belton, B., Brugere, C., Froehlich, H. E., Fry, J. P., Halpern, B. S., Hicks, C. C., Jones, R. C., Klinger, D. H., Little, D. C., McCauley, D. J., Thilsted, S. H., Troell, M., & Allison, E. H. (2020). Scenarios for global aquaculture and its role in human nutrition. Reviews in Fisheries Science & Aquaculture, 29(1), 122-138. https://doi.org/10.1080/23308249.2020.1782342
  • Ghafarifarsani, H, Hoseinifar, S. H., Adhami, B., Rohani, M. F., & Van Doan, H. (2023). Dietary gallic acid influences serum enzymatic parameters and immunological responses in Cyprinus carpio exposed to crowding stress. Aquaculture Reports, 30, 101630. https://doi.org/10.1016/j.aqrep.2023.101630
  • Ghafarifarsani, H., Hoseinifar, S. H., Adorian, T. J., Ferrigolo, F. R. G., Raissy, M., & Van Doan, H. (2021). The effects of combined inclusion of Malvae sylvestris, Origanum vulgare, and Allium hirtifolium boiss for common carp (Cyprinus carpio) diet: Growth performance, antioxidant defense, and immunological parameters. Fish & Shellfish Immunology, 119, 670-677. https://doi.org/10.1016/j.fsi.2021.10.014
  • Hashimoto, M., Hossain, S., Al Mamun, A., Matsuzaki, K., & Arai, H. (2017). Docosahexaenoic acid: one molecule diverse functions. Critical reviews in biotechnology, 37(5), 579-597. https://doi.org/10.1080/07388551.2016.1207153
  • Hoseini, S. M., Khalili, M., Rajabiesterabadi, H., Hoseinifar, S. H., & Van Doan, H. (2020). Effects of dietary monoterpene, myrcene, administration on immune-and health-related genes expression in common carp gill following exposure to copper sulfate. Fish & shellfish immunology, 98, 438-445. https://doi.org/10.1016/j.fsi.2020.01.027
  • Hoseini, S. M., Mirghaed, A. T., Iri, Y., Hoseinifar, S. H., Van Doan, H., & Reverter, M. (2021). Effects of dietary Russian olive, Elaeagnus angustifolia, leaf extract on growth, hematological, immunological, and antioxidant parameters in common carp, Cyprinus carpio. Aquaculture, 536, 736461. https://doi.org/10.1016/j.aquaculture.2021.736461
  • Hoseinifar, S. H., Fazelan, Z., Bayani, M., Yousefi, M., Van Doan, H., & Yazici, M. (2022). Dietary red macroalgae (Halopithys incurva) improved systemic an mucosal immune and antioxidant parameters and modulated related gene expression in zebrafish (Danio rerio). Fish & Shellfish Immunology, 123, 164-171. https://doi.org/10.1016/j.fsi.2022.02.047
  • Hoseinifar, S. H., Ghafarifarsani, H., Raeisi, M., Raissy, M., Safari, R., Khosraviani, K., Yousefi, M., & Van Doan, H. (2023). Effect of dietary nutmeg (Myristica fragrans) on growth performance, antioxidant status, immune response, and gene expression of common carp (Cyprinus carpio). Aquaculture Reports, 33, 101787. https://doi.org/10.1016/j.aqrep.2023.101787
  • Hoseinifar, S. H., Zou, H. K., Miandare, H. K., Van Doan, H., Romano, N., & Dadar, M. (2017). Enrichment of common carp (Cyprinus carpio) diet with medlar (Mespilus germanica) leaf extract: Effects on skin mucosal immunity and growth performance. Fish & shellfish immunology, 67, 346-352. https://doi.org/10.1016/j.fsi.2017.06.023
  • Idenyi, J. N., Eya, J. C., Nwankwegu, A. S., & Nwoba, E. G. (2022). Aquaculture sustainability through alternative dietary ingredients: Microalgal value-added products. Engineering Microbiology, 2(4), 100049. https://doi.org/10.1016/j.engmic.2022.100049
  • Ivanova, S., Sukhikh, S., Popov, A., Shishko, O., Nikonov, I., Kapitonova, E., Krol, O., Larina, V., Noskova, S., & Babich, O. (2024). Medicinal plants: a source of phytobiotics for the feed additives. Journal of Agriculture and Food Research, 101172. https://doi.org/10.1016/j.jafr.2024.101172
  • Jeney G, Wet LD, Jeney Z, & Yin G (2015) Plant extracts. Dietary nutrients, additives, and fish health, 321-332. https://doi.org/10.1002/9781119005568.ch16
  • Ji, S., Xue, R., Zhou, L., Sun, J., & Ji, H. (2025). The individual and combined effect of DHA and high-fat diet on flesh quality, antioxidant capacity and myofiber characteristics of grass carp (Ctenopharyngodon idellus). Aquaculture, 595, 741487. https://doi.org/10.1016/j.aquaculture.2024.741487
  • Jin, X., Su, M., Liang, Y., & Li, Y. (2023) Effects of chlorogenic acid on growth, metabolism, antioxidation, immunity, and intestinal flora of crucian carp (Carassius auratus). Frontiers in Microbiology, 13, 1084500. https://doi.org/10.3389/fmicb.2022.1084500
  • Jitendrasinh, R. R., Kotiya, A. S., & Dipakbhai, J. M. (2024). Bioactive Feed Ingredients used in Aquaculture: A Review. Journal of Scientific Research and Reports, 30(5), 399-414. https://doi.org/10.9734/jsrr/2024/v30i51956
  • Kalaiselvan, P., Malarvizhi, K., & Ranjan, A. (2024). Exploring phytobiotics in aquaculture: sources, mode of action, effects, administration, and its bioavailability in fish. Aquaculture International, 1-63. https://doi.org/10.1007/s10499-024-01444-0
  • Karataş, B. (2024). Dietary Cyanus depressus (M. Bieb.) Soják plant extract enhances growth performance, modulates intestinal microbiota, and alters gene expression associated with digestion, antioxidant, stress, and immune responses in rainbow trout (Oncorhynchus mykiss). Aquacult Int 32, 7929–7951. https://doi.org/10.1007/s10499-024-01548-7
  • Khammar, A., & Djeddi, S. (2012). Pharmacological and biological properties of some Centaurea species. Eur J Sci Res, 84(3), 398-416.
  • Kiadaliri, M., Firouzbakhsh, F., & Deldar, H. (2020). Effects of feeding with red algae (Laurencia caspica) hydroalcoholic extract on antioxidant defense, immune responses, and immune gene expression of kidney in rainbow trout (Oncorhynchus mykiss) infected with Aeromonas hydrophila. Aquaculture, 526, 735361. https://doi.org/10.1016/j.aquaculture.2020.735361
  • Kousoulaki, K., Sveen, L., Norén, F., & Espmark, Å. (2022). Atlantic salmon (Salmo salar) performance fed low trophic ingredients in a fish meal and fish oil free diet. Frontiers in Physiology, 13, 884740. https://doi.org/10.3389/fphys.2022.884740
  • Koven, W., Yanowski, E., Gardner, L., Nixon, O., & Block, B. (2024). Docosahexaenoic acid (DHA) is a driving force regulating gene expression in bluefin tuna (Thunnus thynnus) larvae development. Scientific Reports, 14(1), 23191. https://doi.org/10.1038/s41598-024-74152-7
  • Kuebutornye, F. K. A., Roy, K., Folorunso, E. A., & Mraz, J. (2024). Plant‐based feed additives in Cyprinus carpio aquaculture. Reviews in Aquaculture, 16(1), 309-336. https://doi.org/10.1111/raq.12840
  • Li, Y., Le, Q., Zhang, M., Xu, S., He, S., Yan, X., Hu, J., & Wang, Y. (2023). The effect of Schizochytrium on growth, fatty acid profile and gut microbiota of Silver Pomfret (Pampus argenteus). Journal of Marine Science and Engineering, 11(2), 414. https://doi.org/10.3390/jmse11020414
  • Lin, Y., Li, S., Li, Y., Fang, L., Zhang, H., Wang, Q., & Ruan, G. (2024). Effects of luteolin supplementation on growth, histology, antioxidant capacity, non− specific immunity and intestinal microbiota of the red swamp crayfish (Procambarus clarkii). Animal Feed Science and Technology, 313, 115986. https://doi.org/10.1016/j.anifeedsci.2024.115986
  • Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. methods, 25(4), 402-408. https://doi.org/10.1006/meth.2001.1262
  • Magalhães, R., Guardiola, F. A., Guerreiro, I., Fontinha, F., Moutinho, S., Olsen, R. E., Peres, H., & Oliva-Teles, A. (2021). Effect of different dietary arachidonic, eicosapentaenoic, and docosahexaenoic acid content on selected immune parameters in gilthead sea bream (Sparus aurata). Fish and Shellfish Immunology Reports, 2, 100014. https://doi.org/10.1016/j.fsirep.2021.100014
  • Martos-Sitcha, J. A., Mancera, J. M., Prunet, P., & Magnoni, L. J. (2020). Welfare and stressors in fish: Challenges facing aquaculture. Frontiers in physiology, 11, 162. https://doi.org/10.3389/fphys.2020.00162
  • Mugwanya, M., Dawood, M. A., Kimera, F., & Sewilam, H. (2023). Replacement of fish meal with fermented plant proteins in the aquafeed industry: A systematic review and meta‐analysis. Reviews in Aquaculture, 15(1), 62-88. https://doi.org/10.1111/raq.12701
  • Nagarajan, D., Varjani, S., Lee, D. J., & Chang, J. S. (2021). Sustainable aquaculture and animal feed from microalgae–nutritive value and techno-functional components. Renewable and Sustainable Energy Reviews, 150, 111549. https://doi.org/10.1016/j.rser.2021.111549
  • Naiel, M. A., El-Kholy, A. I., Negm, S. S., Ghazanfar, S., Shukry, M., Zhang, Z., Ahmadifar, E., & Abdel-Latif, H. M. (2023). A mini-review on plant-derived phenolic compounds with particular emphasis on their possible applications and beneficial uses in aquaculture. Annals of Animal Science, 23(4), 971-977. https://doi.org/10.2478/aoas-2023-0007
  • Onomu, A. J., & Okuthe, G. E. (2024). The Role of Functional Feed Additives in Enhancing Aquaculture Sustainability. Fishes, 9(5), 167. https://doi.org/10.3390/fishes9050167
  • Önalan, Ş. (2019). Expression differences of stress and immunity genes in rainbow trout (Oncorhynchus mykiss, Walbaum 1792) with different bacterial fish diseases. Israeli Journal of Aquaculture-Bamidgeh, 71.
  • Pradhan, B., Patra, S., Dash, S. R., Nayak, R., Behera, C., & Jena, M. (2021). Evaluation of the anti-bacterial activity of methanolic extract of Chlorella vulgaris Beyerinck [Beijerinck] with special reference to antioxidant modulation. Future Journal of Pharmaceutical Sciences, 7, 1-11. https://doi.org/10.1186/s43094-020-00172-5
  • Rajabiesterabadi, H., Yousefi, M., & Hoseini, S. M. (2020). Enhanced haematological and immune responses in common carp Cyprinus carpio fed with olive leaf extract‐supplemented diets and subjected to ambient ammonia. Aquaculture Nutrition, 26(3), 763-771. https://doi.org/10.1111/anu.13035
  • Rashidian, G., Zare, M., Tabibi, H., Stejskal, V., & Faggio, C. (2023). The synergistic effects of four medicinal plant seeds and chelated minerals on the growth, immunity, and antioxidant capacity of rainbow trout (Oncorhynchus mykiss). Fish & Shellfish Immunology, 139, 108930. https://doi.org/10.1016/j.fsi.2023.108930
  • Reverter, M., Tapissier‐Bontemps, N., Sarter, S., Sasal, P., & Caruso, D. (2021). Moving towards more sustainable aquaculture practices: a meta‐analysis on the potential of plant‐enriched diets to improve fish growth, immunity and disease resistance. Reviews in Aquaculture, 13(1), 537-555. https://doi.org/10.1111/raq.12485
  • Rombenso, A., Araujo, B., & Li, E. (2022). Recent advances in fish nutrition: Insights on the nutritional implications of modern formulations. Animals, 12(13), 1705. https://doi.org/10.3390/ani12131705
  • Sarker, P. K. (2023). Microorganisms in fish feeds, technological innovations, and key strategies for sustainable aquaculture. Microorganisms, 11(2), 439. https://doi.org/10.3390/microorganisms11020439
  • Sattanathan, G., Liu, W. C., Padmapriya, S., Pushparaj, K., Sureshkumar, S., Lee, J. W., Balasubramanian, B., & Kim, I. H. (2022). Effects of Dietary Blend of Algae Extract Supplementation on Growth, Biochemical, Haemato-Immunological Response, and Immune Gene Expression in Labeo rohita with Aeromonas hydrophila Post-Challenges. Fishes, 8(1), 7. https://doi.org/10.3390/fishes8010007
  • Serrano, E., Simpfendorfer, R., Medina, A., Sandoval, C., Martínez, A., Morales, R., & Davies, S. J. (2021). Partially replacing fish oil with microalgae (Schizochytrium limacinum and Nannochloropsis oceanica) in diets for rainbow trout (Oncorhynchus mykiss) reared in saltwater with reference to growth performance, muscle fatty acid composition and liver ultrastructure. Aquaculture Research, 52(9), 4401-4413. https://doi.org/10.1111/are.15279
  • Shang, G. J., Liu, S. Y., Zhu, R., Li, D. L., Meng, S. T., Wang, Y. T., & Wu, L. F. (2024). Chlorogenic acid improves common carp (Cyprinus carpio) liver and intestinal health through Keap-1/Nrf2 and NF-κB signaling pathways: Growth performance, immune response and antioxidant capacity. Fish & Shellfish Immunology, 146, 109378.https://doi.org/10.1016/j.fsi.2024.109378
  • Song, C., Sun, C., Liu, B., & Xu, P. (2023). Oxidative stress in aquatic organisms. Antioxidants, 12(6), 1223. https://doi.org/10.3390/antiox12061223
  • Souza, F. P. D., Lima, E. C. S. D., Urrea-Rojas, A. M., Suphoronski, S. A., Facimoto, C. T., Bezerra Junior, J. D. S., de Oliveira, T. E. S., Pereira, U. P., Di Santis, G. W., de Oliveira, C. A. L., & Lopera-Barrero, N. M. (2020). Effects of dietary supplementation with a microalga (Schizochytrium sp.) on the hemato-immunological, and intestinal histological parameters and gut microbiota of Nile tilapia in net cages. PloS one, 15(1), e0226977. https://doi.org/10.1371/journal.pone.0226977
  • Tadese, D. A., Song, C., Sun, C., Liu, B., Liu, B., Zhou, Q., Xu, P., Ge, X., Liu, M., Tamiru, M., Zhou, Z., Lakew, A., & Kevin, N. T. (2022). The role of currently used medicinal plants in aquaculture and their action mechanisms: A review. Reviews in Aquaculture, 14(2), 816-847. https://doi.org/10.1111/raq.12626
  • Trevi, S., Uren Webster, T., Consuegra, S., & Garcia de Leaniz, C. (2023). Benefits of the microalgae Spirulina and Schizochytrium in fish nutrition: a meta-analysis. Scientific Reports, 13(1), 2208. https://doi.org/10.1038/s41598-023-29183-x
  • Vijayaram, S., Ringø, E., Ghafarifarsani, H., Hoseinifar, S. H., Ahani, S., & Chou, C. C. (2024). Use of Algae in Aquaculture: A Review. Fishes, 9(2), 63. https://doi.org/10.3390/fishes9020063
  • Vijayaram, S., Sun, Y. Z., Zuorro, A., Ghafarifarsani, H., Van Doan, H., & Hoseinifar, S. H. (2022). Bioactive immunostimulants as health-promoting feed additives in aquaculture: A review. Fish & Shellfish Immunology, 130, 294-308. https://doi.org/10.1016/j.fsi.2022.09.011
  • Wang, J., Deng, L., Chen, M., Che, Y., Li, L., Zhu, L., Chen, G., & Feng, T. (2024). Phytogenic feed additives as natural antibiotic alternatives in animal health and production: A review of the literature of the last decade. Animal Nutrition. https://doi.org/10.1016/j.aninu.2024.01.012
  • Xie, J., Fang, H., Liao, S., Guo, T., Yin, P., Liu, Y., Tian, L., & Niu, J. (2019). Study on Schizochytrium improving the growth performance and non-specific immunity of golden pompano (Trachinotus ovatus) while not affecting the antioxidant capacity. Fish & shellfish immunology, 95, 617-623. https://doi.org/10.1016/j.fsi.2019.10.028
  • Xu, G., Xing, W., Yu, H., Jiang, N., Ma, Z., Luo, L., & Li, T. (2022). Evaluation of chlorogenic acid supplementation in koi (Cyprinus carpio) diet: growth performance, body color, antioxidant activity, serum biochemical parameters, and immune response. Aquaculture Nutrition, (1), 2717003. https://doi.org/10.1155/2022/2717003
  • Yousefi, M., Farsani, M. N., Ghafarifarsani, H., Hoseinifar, S. H., & Van Doan, H. (2021). The effects of dietary supplementation of mistletoe (Viscum album) extract on the growth performance, antioxidant, and innate, immune responses of rainbow trout (Oncorhynchus mykiss). Aquaculture, 536, 736385. https://doi.org/10.1016/j.aquaculture.2021.736385 Yousefi, M., Ahmadifar, M., Mohammadzadeh, S., Kalhor, N., Esfahani, D. E., Bagheri, A., Mashhadizadeh, N., Moghadam, M. S., & Ahmadifar, E. (2022). Individual and combined effects of the dietary Spirulina platensis and Bacillus licheniformis supplementation on growth performance, antioxidant capacity, innate immunity, relative gene expression and resistance of goldfish, Carassius auratus to Aeromonas hydrophila. Fish & Shellfish Immunology, 127, 1070-1078. https://doi.org/10.1016/j.fsi.2022.07.015
  • Zhang, J., Wang, Z., Shi, Y., Xia, L., Hu, Y., & Zhong, L. (2023). Protective effects of chlorogenic acid on growth, intestinal inflammation, hepatic antioxidant capacity, muscle development and skin color in channel catfish Ictalurus punctatus fed an oxidized fish oil diet. Fish & Shellfish Immunology, 134, 108511. https://doi.org/10.1016/j.fsi.2022.108511
  • Zhang, T. T., Xu, J., Wang, Y. M., & Xue, C. H. (2019). Health benefits of dietary marine DHA/EPA-enriched glycerophospholipids. Progress in lipid research, 75, 100997. https://doi.org/10.1016/j.plipres.2019.100997
  • Zhang, X., Zhang, Y., Zhang, Q., Liu, P., Guo, R., Jin, S., Liu, J., Chen, L., Ma, Z., & Liu, Y. (2020). Evaluation and analysis of water quality of marine aquaculture area. International Journal of Environmental Research and Public Health, 17(4), 1446. https://doi.org/10.3390/ijerph17041446
  • Zhou, L., Li, K., Duan, X., Hill, D., Barrow, C., Dunshea, F., Martin, G., & Suleria, H. (2022) Bioactive compounds in microalgae and their potential health benefits. Food Bioscience, 49, 101932. https://doi.org/10.1016/j.fbio.2022.101932

Cyanus depressus ve Schizochytrium sp. Ekstraktlarının Sazan Balığında (Cyprinus carpio) Büyüme Endeksleri, Antioksidan ve Bağışıklık İlgili Genlerin İfade Düzeyleri Üzerindeki Sinerjik Etkileri

Year 2025, Volume: 12 Issue: 1, 111 - 121

Abstract

Bu çalışmanın amacı Cyanus depressus ve Schizochytrium sp. özütlerinin sazan balığında büyüme performansı ile antioksidan ve bağışıklıkla ilgili genlerin ifade düzeyleri üzerindeki sinerjik etkilerini değerlendirmektir. Ortalama ağırlığı 3,71 ± 0,16 g olan balıklar 60 günlük bir süre boyunca 0 (Kontrol), 0,5 (CS05), ve 1 (CS1) g/kg seviyelerinde ekstrakt karışımı (CS) içeren diyetler alan üç besleme grubuna ayrıldı. Sonuçlar, 0,5 ve 1 g/kg CS ekstresi ile desteklenen gruplarda son vücut ağırlığında, kilo alımında ve özgül büyüme hızında önemli iyileşmeler olduğunu ortaya koydu. Süperoksit dismutaz (SOD), ve katalaz (CAT) gen ekspresyon düzeylerindeki en önemli artış 0,5 g/kg CS özütü ile beslenen balıklarda gözlendi. Tedaviler arasında bağışıklık ile ilgili interlökin-1 beta (IL-1β)'nın en yüksek ekspresyon düzeyi, kontrol grubuna göre CS özütü ile zenginleştirilmiş diyetle beslenen gruplarda bulundu. Sonuç olarak çalışmamız, Cyanus depressus ve Schizochytrium sp. özlerinin özellikle 0,5 g/kg dozunda diyet takviyesi olarak birleştirilmesi sazan balığının çeşitli fizyolojik ve sağlık yönlerini iyileştirmede önemli bir potansiyele sahip olduğunu göstermektedir.

Ethical Statement

This experiment was approved by the Van Yüzüncü Yıl University Local Ethics Committee for Animal Experiments (protocol no: 2023/13-31) and conducted in accordance with established ethical guidelines.

Supporting Institution

Van Yüzüncü Yıl University, Scientific Research Projects Department

Project Number

FHD-2024-10941

Thanks

This research was supported by the Van Yüzüncü Yıl University, Scientific Research Projects Department (FHD-2024-10941). The author thanks the Van Yuzuncu Yıl University Scientific Research Projects Department for their support.

References

  • Ababouch, L., Nguyen, K. A. T., Castro de Souza, M., & Fernandez‐Polanco, J. (2023). Value chains and market access for aquaculture products. Journal of the World Aquaculture Society, 54(2), 527-553. https://doi.org/10.1111/jwas.12964
  • Abu-Elala, N. M., Galal, M. K., Abd-Elsalam, R. M., Mohey-Elsaeed, O., & Ragaa, N. M. (2016). Effects of dietary supplementation of Spirulina platensis and garlic on the growth performance and expression levels of immune-related genes in Nile tilapia (Oreochromis niloticus). Journal of Aquaculture Research and Development, 7(7), 433-442.
  • Ahmadifar, E., Kalhor, N., Yousefi, M., Adineh, H., Moghadam, M. S., Sheikhzadeh, N., Moonmanee, T., Hoseinifar, S. H., & Van Doan, H. (2023). Effects of dietary Plantago ovata seed extract administration on growth performance and immune function of common carp (Cyprinus carpio) fingerling exposed to ammonia toxicity. Veterinary Research Communications, 47(2), 731-744. https://doi.org/10.1007/s11259-022-10034-5
  • Ahmadifar, E., Pourmohammadi Fallah, H., Yousefi, M., Dawood, M. A., Hoseinifar, S. H., Adineh, H., Yilmaz, S., Paolucci, M., & Doan, H. V. (2021a). The gene regulatory roles of herbal extracts on the growth, immune system, and reproduction of fish. Animals, 11(8), 2167. https://doi.org/10.3390/ani11082167
  • Ahmadifar, E., Yousefi, M., Karimi, M., Fadaei Raieni, R., Dadar, M., Yilmaz, S., Dawood, M. A., & Abdel-Latif, H. M. (2021b). Benefits of dietary polyphenols and polyphenol-rich additives to aquatic animal health: an overview. Reviews in Fisheries Science & Aquaculture, 29(4), 478-511. https://doi.org/10.1080/23308249.2020.1818689
  • Bahi, A., Ramos‐Vega, A., Angulo, C., Monreal‐Escalante, E., & Guardiola, F. A. (2023). Microalgae with immunomodulatory effects on fish. Reviews in Aquaculture, 15(4), 1522-1539. https://doi.org/10.1111/raq.12792
  • Bélanger, A., Sarker, P. K., Bureau, D. P., Chouinard, Y., & Vandenberg, G. W. (2021). Apparent digestibility of macronutrients and fatty acids from microalgae (Schizochytrium sp.) fed to rainbow trout (Oncorhynchus mykiss): A potential candidate for fish oil substitution. Animals, 11(2), 456. https://doi.org/10.3390/ani11020456
  • Bi, Z. Q., Ren, L. J., Hu, X. C., Sun, X. M., Zhu, S. Y., Ji, X. J., & Huang, H. (2018). Transcriptome and gene expression analysis of docosahexaenoic acid producer Schizochytrium sp. under different oxygen supply conditions. Biotechnology for Biofuels, 11, 1-13. https://doi.org/10.1186/s13068-018-1250-5
  • Boyd, C. E., D'Abramo, L. R., Glencross, B. D., Huyben, D. C., Juarez, L. M., Lockwood, G. S., McNevin, A. A., Tacon, A. G. J., Teletchea, F., Tomasso Jr, J. R., Tucker, C. S., & Valenti, W. C. (2020). Achieving sustainable aquaculture: Historical and current perspectives and future needs and challenges. Journal of the World Aquaculture Society, 51(3), 578-633. https://doi.org/10.1111/jwas.12714
  • Ciji, A., & Akhtar, M. S. (2021). Stress management in aquaculture: A review of dietary interventions. Reviews in Aquaculture, 13(4), 2190-2247. https://doi.org/10.1111/raq.12565
  • das Neves, S. C., da Silva, S. M., Costa, G. K., Correia, E. S., Santos, A. L., da Silva, L. C., & Bicudo, Á. J. (2021) Dietary supplementation with fumaric acid improves growth performance in nile tilapia juveniles. Animals, 12(1), 8. https://doi.org/10.3390/ani12010008
  • Dawood, M. A., Koshio, S., & Esteban, M. Á. (2018). Beneficial roles of feed additives as immunostimulants in aquaculture: a review. Reviews in Aquaculture, 10(4), 950-974. https://doi.org/10.1111/raq.12209
  • Dos Santos, S. K. A., Schorer, M., Moura, G. D. S., Lanna, E. A. T., & Pedreira, M. M. (2019). Evaluation of growth and fatty acid profile of Nile tilapia (Oreochromis niloticus) fed with Schizochytrium. Aquaculture research, 50(4), 1068-1074. https://doi.org/10.1111/are.13979
  • Duman, K. E., Dogan, A., & Kaptaner, B. (2022). Ameliorative role of Cyanus depressus (M. Bieb.) Soják plant extract against diabetes‐associated oxidative‐stress‐induced liver, kidney, and pancreas damage in rats. Journal of Food Biochemistry, 46(10), e14314. https://doi.org/10.1111/jfbc.14314
  • Eroldoğan, O. T., Glencross, B., Novoveska, L., Gaudêncio, S. P., Rinkevich, B., Varese, G. C., Carvalho, M. F., Tasdemir, D., Safarik, I., Nielsen, S. L., Rebours, C., Lada, L. B., Robbens, J., Strode, E., Haznedaroğlu, B. Z., Kotta, J., Evliyaoğlu, E., Oliveira, J., Girao, M., Vasquez, M. I., Cabarkapa, I., Rakita, S., Klun, K., & Rotter, A. (2023). From the sea to aquafeed: A perspective overview. Reviews in aquaculture, 15(3), 1028-1057. https://doi.org/10.1111/raq.12740
  • Escher, G. B., Santos, J. S., Rosso, N. D., Marques, M. B., Azevedo, L., do Carmo, M. A. V., Daguer, H., Molognoni, L., do Prado-Silva, L., Sant'Ana, A. S., da Silva, M. C., & Granato, D. (2018). Chemical study, antioxidant, anti-hypertensive, and cytotoxic/cytoprotective activities of Centaurea cyanus L. petals aqueous extract. Food and chemical toxicology, 118, 439-453. https://doi.org/10.1016/j.fct.2018.05.046
  • Estim, A., Shapawi, R., Shaleh, S. R. M., Fui-Fui, C., & Mustafa, S. (2024). Transformative Research in Aquaculture for Sustainable Seafood Security. In SDGs in the Asia and Pacific Region (pp. 415-444). Cham: Springer International Publishing. https://doi.org/10.1007/978-3-031-17463-6_118
  • Fattaheian-Dehkordi, S., Hojjatifard, R., Saeedi, M., & Khanavi, M. (2021). A review on antidiabetic activity of Centaurea spp.: A new approach for developing herbal remedies. Evidence‐Based Complementary and Alternative Medicine, 2021(1), 5587938. https://doi.org/10.1155/2021/5587938
  • Fazelan, Z., Hoseini, S. M., Yousefi, M., Khalili, M., Hoseinifar, S. H., & Van Doan, H. (2020). Effects of dietary eucalyptol administration on antioxidant and inflammatory genes in common carp (Cyprinus carpio) exposed to ambient copper. Aquaculture, 520, 734988. https://doi.org/10.1016/j.aquaculture.2020.734988
  • Gawlik-Dziki, U., Wrzesińska-Krupa, B., Nowak, R., Pietrzak, W., Zyprych-Walczak, J., & Obrępalska-Stęplowska, A. (2023). Herbicide resistance status impacts the profile of non-anthocyanin polyphenolics and some phytomedical properties of edible cornflower (Centaurea cyanus L.) flowers. Scientific Reports, 13(1), 11538. https://doi.org/10.1038/s41598-023-38520-z
  • Gephart, J. A., Golden, C. D., Asche, F., Belton, B., Brugere, C., Froehlich, H. E., Fry, J. P., Halpern, B. S., Hicks, C. C., Jones, R. C., Klinger, D. H., Little, D. C., McCauley, D. J., Thilsted, S. H., Troell, M., & Allison, E. H. (2020). Scenarios for global aquaculture and its role in human nutrition. Reviews in Fisheries Science & Aquaculture, 29(1), 122-138. https://doi.org/10.1080/23308249.2020.1782342
  • Ghafarifarsani, H, Hoseinifar, S. H., Adhami, B., Rohani, M. F., & Van Doan, H. (2023). Dietary gallic acid influences serum enzymatic parameters and immunological responses in Cyprinus carpio exposed to crowding stress. Aquaculture Reports, 30, 101630. https://doi.org/10.1016/j.aqrep.2023.101630
  • Ghafarifarsani, H., Hoseinifar, S. H., Adorian, T. J., Ferrigolo, F. R. G., Raissy, M., & Van Doan, H. (2021). The effects of combined inclusion of Malvae sylvestris, Origanum vulgare, and Allium hirtifolium boiss for common carp (Cyprinus carpio) diet: Growth performance, antioxidant defense, and immunological parameters. Fish & Shellfish Immunology, 119, 670-677. https://doi.org/10.1016/j.fsi.2021.10.014
  • Hashimoto, M., Hossain, S., Al Mamun, A., Matsuzaki, K., & Arai, H. (2017). Docosahexaenoic acid: one molecule diverse functions. Critical reviews in biotechnology, 37(5), 579-597. https://doi.org/10.1080/07388551.2016.1207153
  • Hoseini, S. M., Khalili, M., Rajabiesterabadi, H., Hoseinifar, S. H., & Van Doan, H. (2020). Effects of dietary monoterpene, myrcene, administration on immune-and health-related genes expression in common carp gill following exposure to copper sulfate. Fish & shellfish immunology, 98, 438-445. https://doi.org/10.1016/j.fsi.2020.01.027
  • Hoseini, S. M., Mirghaed, A. T., Iri, Y., Hoseinifar, S. H., Van Doan, H., & Reverter, M. (2021). Effects of dietary Russian olive, Elaeagnus angustifolia, leaf extract on growth, hematological, immunological, and antioxidant parameters in common carp, Cyprinus carpio. Aquaculture, 536, 736461. https://doi.org/10.1016/j.aquaculture.2021.736461
  • Hoseinifar, S. H., Fazelan, Z., Bayani, M., Yousefi, M., Van Doan, H., & Yazici, M. (2022). Dietary red macroalgae (Halopithys incurva) improved systemic an mucosal immune and antioxidant parameters and modulated related gene expression in zebrafish (Danio rerio). Fish & Shellfish Immunology, 123, 164-171. https://doi.org/10.1016/j.fsi.2022.02.047
  • Hoseinifar, S. H., Ghafarifarsani, H., Raeisi, M., Raissy, M., Safari, R., Khosraviani, K., Yousefi, M., & Van Doan, H. (2023). Effect of dietary nutmeg (Myristica fragrans) on growth performance, antioxidant status, immune response, and gene expression of common carp (Cyprinus carpio). Aquaculture Reports, 33, 101787. https://doi.org/10.1016/j.aqrep.2023.101787
  • Hoseinifar, S. H., Zou, H. K., Miandare, H. K., Van Doan, H., Romano, N., & Dadar, M. (2017). Enrichment of common carp (Cyprinus carpio) diet with medlar (Mespilus germanica) leaf extract: Effects on skin mucosal immunity and growth performance. Fish & shellfish immunology, 67, 346-352. https://doi.org/10.1016/j.fsi.2017.06.023
  • Idenyi, J. N., Eya, J. C., Nwankwegu, A. S., & Nwoba, E. G. (2022). Aquaculture sustainability through alternative dietary ingredients: Microalgal value-added products. Engineering Microbiology, 2(4), 100049. https://doi.org/10.1016/j.engmic.2022.100049
  • Ivanova, S., Sukhikh, S., Popov, A., Shishko, O., Nikonov, I., Kapitonova, E., Krol, O., Larina, V., Noskova, S., & Babich, O. (2024). Medicinal plants: a source of phytobiotics for the feed additives. Journal of Agriculture and Food Research, 101172. https://doi.org/10.1016/j.jafr.2024.101172
  • Jeney G, Wet LD, Jeney Z, & Yin G (2015) Plant extracts. Dietary nutrients, additives, and fish health, 321-332. https://doi.org/10.1002/9781119005568.ch16
  • Ji, S., Xue, R., Zhou, L., Sun, J., & Ji, H. (2025). The individual and combined effect of DHA and high-fat diet on flesh quality, antioxidant capacity and myofiber characteristics of grass carp (Ctenopharyngodon idellus). Aquaculture, 595, 741487. https://doi.org/10.1016/j.aquaculture.2024.741487
  • Jin, X., Su, M., Liang, Y., & Li, Y. (2023) Effects of chlorogenic acid on growth, metabolism, antioxidation, immunity, and intestinal flora of crucian carp (Carassius auratus). Frontiers in Microbiology, 13, 1084500. https://doi.org/10.3389/fmicb.2022.1084500
  • Jitendrasinh, R. R., Kotiya, A. S., & Dipakbhai, J. M. (2024). Bioactive Feed Ingredients used in Aquaculture: A Review. Journal of Scientific Research and Reports, 30(5), 399-414. https://doi.org/10.9734/jsrr/2024/v30i51956
  • Kalaiselvan, P., Malarvizhi, K., & Ranjan, A. (2024). Exploring phytobiotics in aquaculture: sources, mode of action, effects, administration, and its bioavailability in fish. Aquaculture International, 1-63. https://doi.org/10.1007/s10499-024-01444-0
  • Karataş, B. (2024). Dietary Cyanus depressus (M. Bieb.) Soják plant extract enhances growth performance, modulates intestinal microbiota, and alters gene expression associated with digestion, antioxidant, stress, and immune responses in rainbow trout (Oncorhynchus mykiss). Aquacult Int 32, 7929–7951. https://doi.org/10.1007/s10499-024-01548-7
  • Khammar, A., & Djeddi, S. (2012). Pharmacological and biological properties of some Centaurea species. Eur J Sci Res, 84(3), 398-416.
  • Kiadaliri, M., Firouzbakhsh, F., & Deldar, H. (2020). Effects of feeding with red algae (Laurencia caspica) hydroalcoholic extract on antioxidant defense, immune responses, and immune gene expression of kidney in rainbow trout (Oncorhynchus mykiss) infected with Aeromonas hydrophila. Aquaculture, 526, 735361. https://doi.org/10.1016/j.aquaculture.2020.735361
  • Kousoulaki, K., Sveen, L., Norén, F., & Espmark, Å. (2022). Atlantic salmon (Salmo salar) performance fed low trophic ingredients in a fish meal and fish oil free diet. Frontiers in Physiology, 13, 884740. https://doi.org/10.3389/fphys.2022.884740
  • Koven, W., Yanowski, E., Gardner, L., Nixon, O., & Block, B. (2024). Docosahexaenoic acid (DHA) is a driving force regulating gene expression in bluefin tuna (Thunnus thynnus) larvae development. Scientific Reports, 14(1), 23191. https://doi.org/10.1038/s41598-024-74152-7
  • Kuebutornye, F. K. A., Roy, K., Folorunso, E. A., & Mraz, J. (2024). Plant‐based feed additives in Cyprinus carpio aquaculture. Reviews in Aquaculture, 16(1), 309-336. https://doi.org/10.1111/raq.12840
  • Li, Y., Le, Q., Zhang, M., Xu, S., He, S., Yan, X., Hu, J., & Wang, Y. (2023). The effect of Schizochytrium on growth, fatty acid profile and gut microbiota of Silver Pomfret (Pampus argenteus). Journal of Marine Science and Engineering, 11(2), 414. https://doi.org/10.3390/jmse11020414
  • Lin, Y., Li, S., Li, Y., Fang, L., Zhang, H., Wang, Q., & Ruan, G. (2024). Effects of luteolin supplementation on growth, histology, antioxidant capacity, non− specific immunity and intestinal microbiota of the red swamp crayfish (Procambarus clarkii). Animal Feed Science and Technology, 313, 115986. https://doi.org/10.1016/j.anifeedsci.2024.115986
  • Livak, K. J., & Schmittgen, T. D. (2001). Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. methods, 25(4), 402-408. https://doi.org/10.1006/meth.2001.1262
  • Magalhães, R., Guardiola, F. A., Guerreiro, I., Fontinha, F., Moutinho, S., Olsen, R. E., Peres, H., & Oliva-Teles, A. (2021). Effect of different dietary arachidonic, eicosapentaenoic, and docosahexaenoic acid content on selected immune parameters in gilthead sea bream (Sparus aurata). Fish and Shellfish Immunology Reports, 2, 100014. https://doi.org/10.1016/j.fsirep.2021.100014
  • Martos-Sitcha, J. A., Mancera, J. M., Prunet, P., & Magnoni, L. J. (2020). Welfare and stressors in fish: Challenges facing aquaculture. Frontiers in physiology, 11, 162. https://doi.org/10.3389/fphys.2020.00162
  • Mugwanya, M., Dawood, M. A., Kimera, F., & Sewilam, H. (2023). Replacement of fish meal with fermented plant proteins in the aquafeed industry: A systematic review and meta‐analysis. Reviews in Aquaculture, 15(1), 62-88. https://doi.org/10.1111/raq.12701
  • Nagarajan, D., Varjani, S., Lee, D. J., & Chang, J. S. (2021). Sustainable aquaculture and animal feed from microalgae–nutritive value and techno-functional components. Renewable and Sustainable Energy Reviews, 150, 111549. https://doi.org/10.1016/j.rser.2021.111549
  • Naiel, M. A., El-Kholy, A. I., Negm, S. S., Ghazanfar, S., Shukry, M., Zhang, Z., Ahmadifar, E., & Abdel-Latif, H. M. (2023). A mini-review on plant-derived phenolic compounds with particular emphasis on their possible applications and beneficial uses in aquaculture. Annals of Animal Science, 23(4), 971-977. https://doi.org/10.2478/aoas-2023-0007
  • Onomu, A. J., & Okuthe, G. E. (2024). The Role of Functional Feed Additives in Enhancing Aquaculture Sustainability. Fishes, 9(5), 167. https://doi.org/10.3390/fishes9050167
  • Önalan, Ş. (2019). Expression differences of stress and immunity genes in rainbow trout (Oncorhynchus mykiss, Walbaum 1792) with different bacterial fish diseases. Israeli Journal of Aquaculture-Bamidgeh, 71.
  • Pradhan, B., Patra, S., Dash, S. R., Nayak, R., Behera, C., & Jena, M. (2021). Evaluation of the anti-bacterial activity of methanolic extract of Chlorella vulgaris Beyerinck [Beijerinck] with special reference to antioxidant modulation. Future Journal of Pharmaceutical Sciences, 7, 1-11. https://doi.org/10.1186/s43094-020-00172-5
  • Rajabiesterabadi, H., Yousefi, M., & Hoseini, S. M. (2020). Enhanced haematological and immune responses in common carp Cyprinus carpio fed with olive leaf extract‐supplemented diets and subjected to ambient ammonia. Aquaculture Nutrition, 26(3), 763-771. https://doi.org/10.1111/anu.13035
  • Rashidian, G., Zare, M., Tabibi, H., Stejskal, V., & Faggio, C. (2023). The synergistic effects of four medicinal plant seeds and chelated minerals on the growth, immunity, and antioxidant capacity of rainbow trout (Oncorhynchus mykiss). Fish & Shellfish Immunology, 139, 108930. https://doi.org/10.1016/j.fsi.2023.108930
  • Reverter, M., Tapissier‐Bontemps, N., Sarter, S., Sasal, P., & Caruso, D. (2021). Moving towards more sustainable aquaculture practices: a meta‐analysis on the potential of plant‐enriched diets to improve fish growth, immunity and disease resistance. Reviews in Aquaculture, 13(1), 537-555. https://doi.org/10.1111/raq.12485
  • Rombenso, A., Araujo, B., & Li, E. (2022). Recent advances in fish nutrition: Insights on the nutritional implications of modern formulations. Animals, 12(13), 1705. https://doi.org/10.3390/ani12131705
  • Sarker, P. K. (2023). Microorganisms in fish feeds, technological innovations, and key strategies for sustainable aquaculture. Microorganisms, 11(2), 439. https://doi.org/10.3390/microorganisms11020439
  • Sattanathan, G., Liu, W. C., Padmapriya, S., Pushparaj, K., Sureshkumar, S., Lee, J. W., Balasubramanian, B., & Kim, I. H. (2022). Effects of Dietary Blend of Algae Extract Supplementation on Growth, Biochemical, Haemato-Immunological Response, and Immune Gene Expression in Labeo rohita with Aeromonas hydrophila Post-Challenges. Fishes, 8(1), 7. https://doi.org/10.3390/fishes8010007
  • Serrano, E., Simpfendorfer, R., Medina, A., Sandoval, C., Martínez, A., Morales, R., & Davies, S. J. (2021). Partially replacing fish oil with microalgae (Schizochytrium limacinum and Nannochloropsis oceanica) in diets for rainbow trout (Oncorhynchus mykiss) reared in saltwater with reference to growth performance, muscle fatty acid composition and liver ultrastructure. Aquaculture Research, 52(9), 4401-4413. https://doi.org/10.1111/are.15279
  • Shang, G. J., Liu, S. Y., Zhu, R., Li, D. L., Meng, S. T., Wang, Y. T., & Wu, L. F. (2024). Chlorogenic acid improves common carp (Cyprinus carpio) liver and intestinal health through Keap-1/Nrf2 and NF-κB signaling pathways: Growth performance, immune response and antioxidant capacity. Fish & Shellfish Immunology, 146, 109378.https://doi.org/10.1016/j.fsi.2024.109378
  • Song, C., Sun, C., Liu, B., & Xu, P. (2023). Oxidative stress in aquatic organisms. Antioxidants, 12(6), 1223. https://doi.org/10.3390/antiox12061223
  • Souza, F. P. D., Lima, E. C. S. D., Urrea-Rojas, A. M., Suphoronski, S. A., Facimoto, C. T., Bezerra Junior, J. D. S., de Oliveira, T. E. S., Pereira, U. P., Di Santis, G. W., de Oliveira, C. A. L., & Lopera-Barrero, N. M. (2020). Effects of dietary supplementation with a microalga (Schizochytrium sp.) on the hemato-immunological, and intestinal histological parameters and gut microbiota of Nile tilapia in net cages. PloS one, 15(1), e0226977. https://doi.org/10.1371/journal.pone.0226977
  • Tadese, D. A., Song, C., Sun, C., Liu, B., Liu, B., Zhou, Q., Xu, P., Ge, X., Liu, M., Tamiru, M., Zhou, Z., Lakew, A., & Kevin, N. T. (2022). The role of currently used medicinal plants in aquaculture and their action mechanisms: A review. Reviews in Aquaculture, 14(2), 816-847. https://doi.org/10.1111/raq.12626
  • Trevi, S., Uren Webster, T., Consuegra, S., & Garcia de Leaniz, C. (2023). Benefits of the microalgae Spirulina and Schizochytrium in fish nutrition: a meta-analysis. Scientific Reports, 13(1), 2208. https://doi.org/10.1038/s41598-023-29183-x
  • Vijayaram, S., Ringø, E., Ghafarifarsani, H., Hoseinifar, S. H., Ahani, S., & Chou, C. C. (2024). Use of Algae in Aquaculture: A Review. Fishes, 9(2), 63. https://doi.org/10.3390/fishes9020063
  • Vijayaram, S., Sun, Y. Z., Zuorro, A., Ghafarifarsani, H., Van Doan, H., & Hoseinifar, S. H. (2022). Bioactive immunostimulants as health-promoting feed additives in aquaculture: A review. Fish & Shellfish Immunology, 130, 294-308. https://doi.org/10.1016/j.fsi.2022.09.011
  • Wang, J., Deng, L., Chen, M., Che, Y., Li, L., Zhu, L., Chen, G., & Feng, T. (2024). Phytogenic feed additives as natural antibiotic alternatives in animal health and production: A review of the literature of the last decade. Animal Nutrition. https://doi.org/10.1016/j.aninu.2024.01.012
  • Xie, J., Fang, H., Liao, S., Guo, T., Yin, P., Liu, Y., Tian, L., & Niu, J. (2019). Study on Schizochytrium improving the growth performance and non-specific immunity of golden pompano (Trachinotus ovatus) while not affecting the antioxidant capacity. Fish & shellfish immunology, 95, 617-623. https://doi.org/10.1016/j.fsi.2019.10.028
  • Xu, G., Xing, W., Yu, H., Jiang, N., Ma, Z., Luo, L., & Li, T. (2022). Evaluation of chlorogenic acid supplementation in koi (Cyprinus carpio) diet: growth performance, body color, antioxidant activity, serum biochemical parameters, and immune response. Aquaculture Nutrition, (1), 2717003. https://doi.org/10.1155/2022/2717003
  • Yousefi, M., Farsani, M. N., Ghafarifarsani, H., Hoseinifar, S. H., & Van Doan, H. (2021). The effects of dietary supplementation of mistletoe (Viscum album) extract on the growth performance, antioxidant, and innate, immune responses of rainbow trout (Oncorhynchus mykiss). Aquaculture, 536, 736385. https://doi.org/10.1016/j.aquaculture.2021.736385 Yousefi, M., Ahmadifar, M., Mohammadzadeh, S., Kalhor, N., Esfahani, D. E., Bagheri, A., Mashhadizadeh, N., Moghadam, M. S., & Ahmadifar, E. (2022). Individual and combined effects of the dietary Spirulina platensis and Bacillus licheniformis supplementation on growth performance, antioxidant capacity, innate immunity, relative gene expression and resistance of goldfish, Carassius auratus to Aeromonas hydrophila. Fish & Shellfish Immunology, 127, 1070-1078. https://doi.org/10.1016/j.fsi.2022.07.015
  • Zhang, J., Wang, Z., Shi, Y., Xia, L., Hu, Y., & Zhong, L. (2023). Protective effects of chlorogenic acid on growth, intestinal inflammation, hepatic antioxidant capacity, muscle development and skin color in channel catfish Ictalurus punctatus fed an oxidized fish oil diet. Fish & Shellfish Immunology, 134, 108511. https://doi.org/10.1016/j.fsi.2022.108511
  • Zhang, T. T., Xu, J., Wang, Y. M., & Xue, C. H. (2019). Health benefits of dietary marine DHA/EPA-enriched glycerophospholipids. Progress in lipid research, 75, 100997. https://doi.org/10.1016/j.plipres.2019.100997
  • Zhang, X., Zhang, Y., Zhang, Q., Liu, P., Guo, R., Jin, S., Liu, J., Chen, L., Ma, Z., & Liu, Y. (2020). Evaluation and analysis of water quality of marine aquaculture area. International Journal of Environmental Research and Public Health, 17(4), 1446. https://doi.org/10.3390/ijerph17041446
  • Zhou, L., Li, K., Duan, X., Hill, D., Barrow, C., Dunshea, F., Martin, G., & Suleria, H. (2022) Bioactive compounds in microalgae and their potential health benefits. Food Bioscience, 49, 101932. https://doi.org/10.1016/j.fbio.2022.101932
There are 75 citations in total.

Details

Primary Language English
Subjects Pisciculture
Journal Section Research Article
Authors

Boran Karataş 0000-0003-4353-1293

Project Number FHD-2024-10941
Early Pub Date January 25, 2025
Publication Date
Submission Date November 8, 2024
Acceptance Date November 29, 2024
Published in Issue Year 2025 Volume: 12 Issue: 1

Cite

APA Karataş, B. (n.d.). Synergistic Effects of Cyanus depressus and Schizochytrium sp. Extracts on Growth Indices and The Expression Levels of Antioxidant and Immunity-Related Genes in Common Carp (Cyprinus carpio). Turkish Journal of Agricultural and Natural Sciences, 12(1), 111-121. https://doi.org/10.30910/turkjans.1581615