Research Article
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Year 2025, Volume: 40 Issue: 4, 272 - 277, 10.10.2025
https://doi.org/10.26650/ASE.2025.1739592

Abstract

Project Number

NONE

References

  • Adel, M., Safari, R., Soltanian, S., Zorriehzahra, M. J., & Esteban, M. Á. (2018). Antimicrobial activity and enzymes on skin mucus from male and female Caspian kutum (Rutilus frisii kutum Kamensky, 1901) specimens. Slovenian Veterinary Research, 55(4), 235-243. https://doi.org/10.26873/SVR-440-2018 google scholar
  • Baba,E. (2021). Analysis of some immune parameters in the skin mucus of four cultured fish species. The Israeli Journal of Aquaculture, 73, 1-13. https://doi. org/10.46989/001c.29916 google scholar
  • Bromage, E. S., Ye, J., & Kaattari, S. L. (2006). Antibody structural variation in rainbow trout fluids. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 143(1), 61-69. https://doi.org/10.1016/j.cbpb.2005.10.003 google scholar
  • Cunha, M. F., Coscueta, E. R., Brassesco, M. E., Almada, F., Gonçalves, D., & Pintado, M. (2024). Methods for the collection of fish mucus: a systematic google scholar
  • review. Reviews in Fisheries Science and Aquaculture, 32(2), 334-368. https:// doi.org/10.1080/23308249.2023.2289012 google scholar
  • Dash, S., Samal, J., & Thatoi, H. (2014). A comparative study on innate immunity parameters in the epidermal mucus of Indian major carps. Aquaculture International, 22, 411–421. https://doi.org/10.1007/s10499-013-9649-2 google scholar
  • Dawood, M.A.O., Koshio, S., Zaineldin, A.I. Van Doan, H., Moustafa, E. M., Abdel-Daim, M. M., Esteban, A.M., & Hassaan, M. S. (2019). Dietary supplementation of selenium nanoparticles modulated systemic and mucosal immune status and stress resistance of red sea bream (Pagrus major). Fish physiology and biochemistry, 45, 219–230. https://doi.org/10.1007/s10695-018-0556-3 google scholar
  • Erel, Ö. (2005). A new automated colorimetric method for measuring total oxidant status. Clinical Biochemistry, 38(12), 1103-1111. https://doi.org/10.1016/ j.clinbiochem.2005.08.008 google scholar
  • Esteban, Á. (2012). An overview of the immunological defenses in fish skin. International Scholarly Research Notices, 2012, 853470. https://doi.org/10. 5402/2012/853470 google scholar
  • Fast, M. D., Sims, D. E., Burka, J. F., Mustafa, A., & Ross, N. W. (2002). Skin morphology and humoral non-specific defence parameters of mucus and plasma in rainbow trout, coho and Atlantic salmon. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 132(3), 645-657. https://doi.org/10. 1016/S1095-6433(02)00109-5 google scholar
  • Fernández-Alacid, L., Sanahuja, I., Ordóñez-Grande, B., Sánchez-Nuño, S., Herrera, M., & Ibarz, A. (2019). Skin mucus metabolites and cortisol in meagre-fed acute stress-attenuating diets: Correlations between plasma and mucus. Aquaculture, 499, 185-194. https://doi.org/10.1016/j.aquaculture.2018.09.039 google scholar
  • Franco-Martinez, L., Brandts, I., Reyes-López, F., Tort, L., Tvarijonaviciute, A., & Teles, M. (2022). Skin Mucus as a Relevant Low-Invasive Biological Matrix for the Measurement of an Acute Stress Response in Rainbow Trout (Oncorhynchus mykiss). Water, 14(11), 1754. https://doi.org/10.3390/w14111754 google scholar
  • Gan, Q., Chi, H., Dalmo, R. A., Meng, X., Tang, X., Xing, J., Sheng, X., & Zhan, W. (2023). Characterization of myeloperoxidase and its contribution to antimicrobial effect on extracellular traps in flounder (Paralichthys olivaceus). Frontiers in Immunology, 14, 1124813. https://doi.org/10.3389/fimmu.2023.1124813 google scholar
  • Ghafoori, Z., Heidari, B., Farzadfar, F., & Aghamaali, M. (2014). Variations of serum and mucus lysozyme activity and total protein content in the male and female Caspian kutum (Rutilus frisii kutum, Kamensky 1901) during reproductive period. Fish & Shellfish Immunology, 37(1), 139-146. https://doi.org/10.1016/j. fsi.2014.01.016 google scholar
  • Hatten, F., Fredriksen, Å., Hordvik, I., & Endresen, C. (2001). Presence of IgM in cutaneous mucus, but not in gut mucus of Atlantic salmon, Salmo salar. Fish & Shellfish Immunology, 11(3), 257–268. https://doi.org/10.1006/fsim.2000.0313 google scholar
  • Hoole, D., Lewis, J. W., Schuwerack, P. M., Chakravarthy, C., Shrive, A. K., Greenhough, T. J., & Cartwright, J. R. (2003). Inflammatory interactions in fish exposed to pollutants and parasites: A role for apoptosis and C-reactive protein. Parasitology, 126(7), 71–85. https://doi.org/10.1017/s0031182003003779 google scholar
  • Klein, S., Flanagan, K. (2016). Sex differences in immune responses. Nature Reviews Immunology, 16, 626-638. https://doi.org/101038/nri.2Q16.9Q google scholar
  • Kodama, H., Matsuoka, Y., Tanaka, Y., Liu, Y., Iwasaki, T., & Watarai, S. (2004). Changes of C-reactive protein levels in rainbow trout (Oncorhynchus mykiss) sera after exposure to anti-ectoparasitic chemicals used in aquaculture. Fish & Shellfish Immunology, 16(5), 589-597. https://doi.org/10.1016/j.fsi.2003.09.007 google scholar
  • Lowry, O. H., Rosebrough, N. J., Farr, A. L., & Randall, R. J. (1951). Protein measurement with the Folin phenol reagent. The Journal of Biological Chemistry, 193(1), 265-275. google scholar
  • Pelusio, N. F., Bonaldo, A., Gisbert, E., Andree, K. B., Esteban, M. A., Dondi, F., Sabetti, M. C., Gatta, P. P., & Parma, L. (2022). Different fish meal and fish oil dietary levels in European Sea bass: welfare implications after acute confinement stress. Frontiers in Marine Science, 8, 779053. https://doi.org/10.3389/fmars. 2021.779053 google scholar
  • Pepys, M. B., Dash, A. C., Fletcher, T. C., Richardson, N., Munn, E. A., & Feinstein, A. (1978). Analogues in other mammals and in fish of human plasma proteins, C-reactive protein and amyloid P component. Nature, 273(5658), 168–170. https:// doi.org/10.1038/273168a0 google scholar
  • Ramos, F., & Smith, A. C. (1978). The C-reactive protein (CRP) test for the detection of early disease in fishes. Aquaculture, 14(3), 261–266. https://doi.org/10.1016/ 0044-8486(78)90099-6 google scholar
  • Reverter, M., Tapissier-Bontemps, N., Lecchini, D., Banaigs, B., & Sasal, P. (2018). Biological and ecological roles of external fish mucus: a review. Fishes, 3(4), 41. https://doi.org/10.3390/fishes3040041 google scholar
  • Roosta, Z., Falahatkar, B., Sajjadi, M., Paknejad, H., Akbarzadeh, A., & Kestemont, P. (2023). Sex and reproductive development impact skin mucosal epithelium immunity, antimicrobial capacity, and up-regulation of immune-related gene of goldfish (Carassius auratus). Developmental & Comparative Immunology, 138, 104494. https://doi.org/10.1016/j.dci.2022.104494 google scholar
  • Roy, S., Kumar, V., Kumar, V., & Behera, B. K. (2017). Acute phase proteins and their potential role as an indicator for fish health and in diagnosis of fish diseases. Protein and peptide letters, 24(1), 78-89. https://doi.org/10.2174/ 0929866524666161121142221 google scholar
  • Salinas, I., Ding, Y., Fernández-Montero, Á., & Sunyer, J. O. (2022). Mucosal immunity in fish. In Principles of fish immunology: From cells and molecules to host protection (pp. 387-443). Buchmann & C. J. Secombes (Eds.) Cham: Springer International Publishing. google scholar
  • Salinas, I., Zhang, Y. A., & Sunyer, J. O. (2011). Mucosal immunoglobulins and B cells of teleost fish. Developmental & Comparative Immunology, 35(12), 1346-1365. https://doi.org/10.1016/j.dci.2011.11.009 google scholar
  • Shakoori, M., Hoseinifar, S. H., Paknejad, H., Jafari, V., Safari, R., Van Doan, H., & Mozanzadeh, M. T. (2019). Enrichment of rainbow trout (Oncorhynchus mykiss) fingerlings diet with microbial lysozyme: Effects on growth performance, serum and skin mucus immune parameters. Fish & Shellfish Immunology, 86, 480-485. https://doi.org/10.1016/j.fsi.2018.11.077 google scholar
  • Shephard, K. L. (1994). Functions for fish mucus. Reviews in Fish Biology and Fisheries, 4(4), 401-429. google scholar
  • Siwicki, A. K., & Anderson, D. P. (1993). Immunostimulation in fish: measuring the effects of stimulants by serological and immunological methods. Abstract Symposium on Fish Immunology, Lysekil, Sweden. google scholar
  • Tugrul, S., Koçyiğit, A., Doğan, R., Eren, S. B., Senturk, E., Ozturan, O., & Ozar, O. F. (2016). Total antioxidant status and oxidative stress in recurrent aphthous stomatitis. International Journal of Dermatology, 55(S1), e130–e135. https://doi.org/10. 1111/ijd.13101 google scholar
  • Valdenegro-Vega, V. A., Crosbie, P., Bridle, A., Leef, M., Wilson, R., & Nowak, B. F. (2014). Differentially expressed proteins in gill and skin mucus of Atlantic salmon (Salmo salar) affected by amoebic gill disease. Fish & Shellfish Immunology, 40(1), 69–77. https://doi.org/10.1016/j.fsi.2014.06.025 google scholar
  • Valero, Y., Hurtado, C. F., & Mercado, L. (2024). Sexual dimorphism in fish innate immunity: A functional and transcriptional study in yellowtail kingfish. Fish & Shellfish Immunology, 154, 109921. https://doi.org/10.1016/j.fsi.2024.109921 google scholar
  • Whyte, S. K. (2007). The innate immune response of finfish: A review of current knowledge. Fish & Shellfish Immunology, 23(6), 1127–1151. https://doi.org/10. 1016/j.fsi.2007.06.005 google scholar
  • Winkelhake, J. L., & Chang, R. J. (1982). Acute phase (C-reactive) protein-like macromolecules from rainbow trout (Salmo gairdneri). Developmental & Comparative Immunology, 6(3), 481-489. https://doi.org/10.1016/S0145-305X (82)80034-7 google scholar
  • Xu, Z., Parra, D., Gómez, D., Salinas, I., Zhang, Y. A., von Gersdorff Jørgensen, L., Heinecke,R.D., Buchmann, K., LaPatra, S., & Sunyer, J. O. (2013). Teleost skin, an ancient mucosal surface that elicits gut-like immune responses. Proceedings of the National Academy of Sciences, 110(32), 13097-13102. https://doi.org/10. 1073/pnas.1304319110 google scholar
  • Yildiz Yavuzcan, H. (2006). Plasma lysozyme levels and secondary stress response in rainbow trout, Oncorhynchus mykiss (Walbaum) after exposure to Leteux-Meyer mixture. Turkish Journal of Veterinary & Animal Sciences, 30(2), 265-269. google scholar
  • Zavvar, F., Mazandarani, M., Hoseinifar, S. H., Jafari, V., & Lieke, T. (2025). Effects of feed supplementation with fulvic acid on the systemic and mucosal protective mechanisms of juvenile Rainbow Trout (Oncorhynchus mykiss). Journal of Animal Physiology and Animal Nutrition, 109(3), 834-843. https://doi.org/10. 1111/jpn.14100 google scholar

Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus mykiss)

Year 2025, Volume: 40 Issue: 4, 272 - 277, 10.10.2025
https://doi.org/10.26650/ASE.2025.1739592

Abstract

Fish skin mucus plays a critical role in maintaining homeostasis through its various components while serving multiple functions, such as ionic regulation, osmotic balance, immune response, and disease resistance, making it a highly multifunctional material. Since mucus provides a non-invasive means of monitoring fish physiology, health, and welfare, it is important to provide baseline data on its components as biomarkers of immunity. This study assesses the baseline values of various biomarkers, including C-reactive protein (CRP), total protein, total immunoglobulins (Ig), myeloperoxidase (MPO), total antioxidant status (TAS), nitroblue tetrazolium (NBT) and lysozyme activity in rainbow trout (Oncorhynchus mykiss) epidermal mucus, with a focus on sex-based differences. The baseline values for CRP and TAS in the skin mucus of rainbow trout were established for the first time, providing a foundational reference point for mucosal immunity. We observed significant changes in total Ig, lysozyme activity and MPO, with varying responses between sexes. However, no overall differences were observed between females and males based on the other assessed parameters. This study provides baseline data for various innate immunity parameters in the skin mucus of rainbow trout under normal conditions, which can serve as a critical reference for understanding fish health and welfare.

Ethical Statement

All procedures involving animals were conducted in accordance with the ethical standards of the institution and national guidelines for the care and use of laboratory animals. No specific ethical approval is needed for this study.

Supporting Institution

ANKARA UNIVERSITY

Project Number

NONE

Thanks

We appreciate the technical staff of the Diagnostic Laboratory (OTTO Medikal San. ve Tic. Ltd. Şti., Ankara, Turkiye) for their support in measuring some biomarkers.

References

  • Adel, M., Safari, R., Soltanian, S., Zorriehzahra, M. J., & Esteban, M. Á. (2018). Antimicrobial activity and enzymes on skin mucus from male and female Caspian kutum (Rutilus frisii kutum Kamensky, 1901) specimens. Slovenian Veterinary Research, 55(4), 235-243. https://doi.org/10.26873/SVR-440-2018 google scholar
  • Baba,E. (2021). Analysis of some immune parameters in the skin mucus of four cultured fish species. The Israeli Journal of Aquaculture, 73, 1-13. https://doi. org/10.46989/001c.29916 google scholar
  • Bromage, E. S., Ye, J., & Kaattari, S. L. (2006). Antibody structural variation in rainbow trout fluids. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 143(1), 61-69. https://doi.org/10.1016/j.cbpb.2005.10.003 google scholar
  • Cunha, M. F., Coscueta, E. R., Brassesco, M. E., Almada, F., Gonçalves, D., & Pintado, M. (2024). Methods for the collection of fish mucus: a systematic google scholar
  • review. Reviews in Fisheries Science and Aquaculture, 32(2), 334-368. https:// doi.org/10.1080/23308249.2023.2289012 google scholar
  • Dash, S., Samal, J., & Thatoi, H. (2014). A comparative study on innate immunity parameters in the epidermal mucus of Indian major carps. Aquaculture International, 22, 411–421. https://doi.org/10.1007/s10499-013-9649-2 google scholar
  • Dawood, M.A.O., Koshio, S., Zaineldin, A.I. Van Doan, H., Moustafa, E. M., Abdel-Daim, M. M., Esteban, A.M., & Hassaan, M. S. (2019). Dietary supplementation of selenium nanoparticles modulated systemic and mucosal immune status and stress resistance of red sea bream (Pagrus major). Fish physiology and biochemistry, 45, 219–230. https://doi.org/10.1007/s10695-018-0556-3 google scholar
  • Erel, Ö. (2005). A new automated colorimetric method for measuring total oxidant status. Clinical Biochemistry, 38(12), 1103-1111. https://doi.org/10.1016/ j.clinbiochem.2005.08.008 google scholar
  • Esteban, Á. (2012). An overview of the immunological defenses in fish skin. International Scholarly Research Notices, 2012, 853470. https://doi.org/10. 5402/2012/853470 google scholar
  • Fast, M. D., Sims, D. E., Burka, J. F., Mustafa, A., & Ross, N. W. (2002). Skin morphology and humoral non-specific defence parameters of mucus and plasma in rainbow trout, coho and Atlantic salmon. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 132(3), 645-657. https://doi.org/10. 1016/S1095-6433(02)00109-5 google scholar
  • Fernández-Alacid, L., Sanahuja, I., Ordóñez-Grande, B., Sánchez-Nuño, S., Herrera, M., & Ibarz, A. (2019). Skin mucus metabolites and cortisol in meagre-fed acute stress-attenuating diets: Correlations between plasma and mucus. Aquaculture, 499, 185-194. https://doi.org/10.1016/j.aquaculture.2018.09.039 google scholar
  • Franco-Martinez, L., Brandts, I., Reyes-López, F., Tort, L., Tvarijonaviciute, A., & Teles, M. (2022). Skin Mucus as a Relevant Low-Invasive Biological Matrix for the Measurement of an Acute Stress Response in Rainbow Trout (Oncorhynchus mykiss). Water, 14(11), 1754. https://doi.org/10.3390/w14111754 google scholar
  • Gan, Q., Chi, H., Dalmo, R. A., Meng, X., Tang, X., Xing, J., Sheng, X., & Zhan, W. (2023). Characterization of myeloperoxidase and its contribution to antimicrobial effect on extracellular traps in flounder (Paralichthys olivaceus). Frontiers in Immunology, 14, 1124813. https://doi.org/10.3389/fimmu.2023.1124813 google scholar
  • Ghafoori, Z., Heidari, B., Farzadfar, F., & Aghamaali, M. (2014). Variations of serum and mucus lysozyme activity and total protein content in the male and female Caspian kutum (Rutilus frisii kutum, Kamensky 1901) during reproductive period. Fish & Shellfish Immunology, 37(1), 139-146. https://doi.org/10.1016/j. fsi.2014.01.016 google scholar
  • Hatten, F., Fredriksen, Å., Hordvik, I., & Endresen, C. (2001). Presence of IgM in cutaneous mucus, but not in gut mucus of Atlantic salmon, Salmo salar. Fish & Shellfish Immunology, 11(3), 257–268. https://doi.org/10.1006/fsim.2000.0313 google scholar
  • Hoole, D., Lewis, J. W., Schuwerack, P. M., Chakravarthy, C., Shrive, A. K., Greenhough, T. J., & Cartwright, J. R. (2003). Inflammatory interactions in fish exposed to pollutants and parasites: A role for apoptosis and C-reactive protein. Parasitology, 126(7), 71–85. https://doi.org/10.1017/s0031182003003779 google scholar
  • Klein, S., Flanagan, K. (2016). Sex differences in immune responses. Nature Reviews Immunology, 16, 626-638. https://doi.org/101038/nri.2Q16.9Q google scholar
  • Kodama, H., Matsuoka, Y., Tanaka, Y., Liu, Y., Iwasaki, T., & Watarai, S. (2004). Changes of C-reactive protein levels in rainbow trout (Oncorhynchus mykiss) sera after exposure to anti-ectoparasitic chemicals used in aquaculture. Fish & Shellfish Immunology, 16(5), 589-597. https://doi.org/10.1016/j.fsi.2003.09.007 google scholar
  • Lowry, O. H., Rosebrough, N. J., Farr, A. L., & Randall, R. J. (1951). Protein measurement with the Folin phenol reagent. The Journal of Biological Chemistry, 193(1), 265-275. google scholar
  • Pelusio, N. F., Bonaldo, A., Gisbert, E., Andree, K. B., Esteban, M. A., Dondi, F., Sabetti, M. C., Gatta, P. P., & Parma, L. (2022). Different fish meal and fish oil dietary levels in European Sea bass: welfare implications after acute confinement stress. Frontiers in Marine Science, 8, 779053. https://doi.org/10.3389/fmars. 2021.779053 google scholar
  • Pepys, M. B., Dash, A. C., Fletcher, T. C., Richardson, N., Munn, E. A., & Feinstein, A. (1978). Analogues in other mammals and in fish of human plasma proteins, C-reactive protein and amyloid P component. Nature, 273(5658), 168–170. https:// doi.org/10.1038/273168a0 google scholar
  • Ramos, F., & Smith, A. C. (1978). The C-reactive protein (CRP) test for the detection of early disease in fishes. Aquaculture, 14(3), 261–266. https://doi.org/10.1016/ 0044-8486(78)90099-6 google scholar
  • Reverter, M., Tapissier-Bontemps, N., Lecchini, D., Banaigs, B., & Sasal, P. (2018). Biological and ecological roles of external fish mucus: a review. Fishes, 3(4), 41. https://doi.org/10.3390/fishes3040041 google scholar
  • Roosta, Z., Falahatkar, B., Sajjadi, M., Paknejad, H., Akbarzadeh, A., & Kestemont, P. (2023). Sex and reproductive development impact skin mucosal epithelium immunity, antimicrobial capacity, and up-regulation of immune-related gene of goldfish (Carassius auratus). Developmental & Comparative Immunology, 138, 104494. https://doi.org/10.1016/j.dci.2022.104494 google scholar
  • Roy, S., Kumar, V., Kumar, V., & Behera, B. K. (2017). Acute phase proteins and their potential role as an indicator for fish health and in diagnosis of fish diseases. Protein and peptide letters, 24(1), 78-89. https://doi.org/10.2174/ 0929866524666161121142221 google scholar
  • Salinas, I., Ding, Y., Fernández-Montero, Á., & Sunyer, J. O. (2022). Mucosal immunity in fish. In Principles of fish immunology: From cells and molecules to host protection (pp. 387-443). Buchmann & C. J. Secombes (Eds.) Cham: Springer International Publishing. google scholar
  • Salinas, I., Zhang, Y. A., & Sunyer, J. O. (2011). Mucosal immunoglobulins and B cells of teleost fish. Developmental & Comparative Immunology, 35(12), 1346-1365. https://doi.org/10.1016/j.dci.2011.11.009 google scholar
  • Shakoori, M., Hoseinifar, S. H., Paknejad, H., Jafari, V., Safari, R., Van Doan, H., & Mozanzadeh, M. T. (2019). Enrichment of rainbow trout (Oncorhynchus mykiss) fingerlings diet with microbial lysozyme: Effects on growth performance, serum and skin mucus immune parameters. Fish & Shellfish Immunology, 86, 480-485. https://doi.org/10.1016/j.fsi.2018.11.077 google scholar
  • Shephard, K. L. (1994). Functions for fish mucus. Reviews in Fish Biology and Fisheries, 4(4), 401-429. google scholar
  • Siwicki, A. K., & Anderson, D. P. (1993). Immunostimulation in fish: measuring the effects of stimulants by serological and immunological methods. Abstract Symposium on Fish Immunology, Lysekil, Sweden. google scholar
  • Tugrul, S., Koçyiğit, A., Doğan, R., Eren, S. B., Senturk, E., Ozturan, O., & Ozar, O. F. (2016). Total antioxidant status and oxidative stress in recurrent aphthous stomatitis. International Journal of Dermatology, 55(S1), e130–e135. https://doi.org/10. 1111/ijd.13101 google scholar
  • Valdenegro-Vega, V. A., Crosbie, P., Bridle, A., Leef, M., Wilson, R., & Nowak, B. F. (2014). Differentially expressed proteins in gill and skin mucus of Atlantic salmon (Salmo salar) affected by amoebic gill disease. Fish & Shellfish Immunology, 40(1), 69–77. https://doi.org/10.1016/j.fsi.2014.06.025 google scholar
  • Valero, Y., Hurtado, C. F., & Mercado, L. (2024). Sexual dimorphism in fish innate immunity: A functional and transcriptional study in yellowtail kingfish. Fish & Shellfish Immunology, 154, 109921. https://doi.org/10.1016/j.fsi.2024.109921 google scholar
  • Whyte, S. K. (2007). The innate immune response of finfish: A review of current knowledge. Fish & Shellfish Immunology, 23(6), 1127–1151. https://doi.org/10. 1016/j.fsi.2007.06.005 google scholar
  • Winkelhake, J. L., & Chang, R. J. (1982). Acute phase (C-reactive) protein-like macromolecules from rainbow trout (Salmo gairdneri). Developmental & Comparative Immunology, 6(3), 481-489. https://doi.org/10.1016/S0145-305X (82)80034-7 google scholar
  • Xu, Z., Parra, D., Gómez, D., Salinas, I., Zhang, Y. A., von Gersdorff Jørgensen, L., Heinecke,R.D., Buchmann, K., LaPatra, S., & Sunyer, J. O. (2013). Teleost skin, an ancient mucosal surface that elicits gut-like immune responses. Proceedings of the National Academy of Sciences, 110(32), 13097-13102. https://doi.org/10. 1073/pnas.1304319110 google scholar
  • Yildiz Yavuzcan, H. (2006). Plasma lysozyme levels and secondary stress response in rainbow trout, Oncorhynchus mykiss (Walbaum) after exposure to Leteux-Meyer mixture. Turkish Journal of Veterinary & Animal Sciences, 30(2), 265-269. google scholar
  • Zavvar, F., Mazandarani, M., Hoseinifar, S. H., Jafari, V., & Lieke, T. (2025). Effects of feed supplementation with fulvic acid on the systemic and mucosal protective mechanisms of juvenile Rainbow Trout (Oncorhynchus mykiss). Journal of Animal Physiology and Animal Nutrition, 109(3), 834-843. https://doi.org/10. 1111/jpn.14100 google scholar
There are 38 citations in total.

Details

Primary Language English
Subjects Ecology (Other)
Journal Section Research Article
Authors

Hijran Yavuzcan Yıldız 0000-0001-6567-7467

Bilgenur Harmanşa Yılmaz 0000-0003-0679-8327

Project Number NONE
Submission Date July 10, 2025
Acceptance Date September 29, 2025
Publication Date October 10, 2025
Published in Issue Year 2025 Volume: 40 Issue: 4

Cite

APA Yavuzcan Yıldız, H., & Harmanşa Yılmaz, B. (2025). Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus mykiss). Aquatic Sciences and Engineering, 40(4), 272-277. https://doi.org/10.26650/ASE.2025.1739592
AMA Yavuzcan Yıldız H, Harmanşa Yılmaz B. Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus mykiss). Aqua Sci Eng. October 2025;40(4):272-277. doi:10.26650/ASE.2025.1739592
Chicago Yavuzcan Yıldız, Hijran, and Bilgenur Harmanşa Yılmaz. “Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus Mykiss)”. Aquatic Sciences and Engineering 40, no. 4 (October 2025): 272-77. https://doi.org/10.26650/ASE.2025.1739592.
EndNote Yavuzcan Yıldız H, Harmanşa Yılmaz B (October 1, 2025) Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus mykiss). Aquatic Sciences and Engineering 40 4 272–277.
IEEE H. Yavuzcan Yıldız and B. Harmanşa Yılmaz, “Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus mykiss)”, Aqua Sci Eng, vol. 40, no. 4, pp. 272–277, 2025, doi: 10.26650/ASE.2025.1739592.
ISNAD Yavuzcan Yıldız, Hijran - Harmanşa Yılmaz, Bilgenur. “Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus Mykiss)”. Aquatic Sciences and Engineering 40/4 (October2025), 272-277. https://doi.org/10.26650/ASE.2025.1739592.
JAMA Yavuzcan Yıldız H, Harmanşa Yılmaz B. Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus mykiss). Aqua Sci Eng. 2025;40:272–277.
MLA Yavuzcan Yıldız, Hijran and Bilgenur Harmanşa Yılmaz. “Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus Mykiss)”. Aquatic Sciences and Engineering, vol. 40, no. 4, 2025, pp. 272-7, doi:10.26650/ASE.2025.1739592.
Vancouver Yavuzcan Yıldız H, Harmanşa Yılmaz B. Sex-Specific Baseline Levels of Selected Immune Biomarkers in the Skin Mucus of Rainbow Trout (Oncorhynchus mykiss). Aqua Sci Eng. 2025;40(4):272-7.

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