References
- Afewerki S., Asche F., Misund B., Thorvaldsen T., Tveteras R. (2023). Innovation in the Norwegian aquaculture industry. Rev. Aquacult., 15: 759–771.
- Alajaji S.A., El-Adawy T.A. (2006). Nutritional composition of chick-pea (Cicer arietinum L.) as affected by microwave cooking and other traditional cooking methods. J. Food. Comp. Analys., 19: 806–812.
- Al-Masri M.R., Guenther K.D. (1999). Changes in digestibility and cell-wall constituents of some agricultural by-products due to gamma irradiation and urea treatments. Radi. Phys. Chem., 55: 323–329.
- Asche F., Eggert H., Oglend A., Roheim C.A., Smith M.D. (2022). Aquaculture: externalities and policy options. Rev. Environ. Econom. Policy., 16: 282–305.
- Bagheri S., Gholamhosseini A., Banaee M. (2023). Investigation of different nutritional effects of dietary chromium in fish: a literature review. Biol. Trace Elem. Res., 201: 2546–2554.
- Borrely S.I., Del Mastro N.L., Sampa M.H.O. (1998). Improvement of municipal wastewaters by electron beam accelerator in Brazil. Radi. Phys. Chem., 52: 333–337.
- Choudhury T.G., Kamilya D. (2019). Paraprobiotics: An aquaculture perspective. Rev. Aquac., 11: 1258–1270.
- Chaudhary N., Kumar G. (2023). Mutagenic radiations: X-rays, ionizing particles, and ultraviolet. In Biotechnologies and genetics in plant mutation breeding. Apple Academic Press, pp. 45–67.
- Chung H.-J., Lee S.-Y., Kim J.-H., Lee J.-W., Byun M.-W., Lim S.-T. (2010). Pasting characteristics and in vitro digestibility of γ-irradiated RS4 waxy maize starches. J. Cere. Sci., 52: 53–58.
- Chung M.-S., Ko Y.-T., Kim W.-S. (2000). Survival of Pseudomonas fluorescens and Salmonella typhimurium after electron beam and gamma irradiation of refrigerated beef. J. Food. Prot., 63: 162–166.
- Ciji A., Akhtar M.S. (2021). Stress management in aquaculture: A review of dietary interventions. Rev. Aquac., 13: 2190–2247.
- de Almada C.N., Almada C.N., Martinez R.C.R., Sant’Ana A.S. (2016). Paraprobiotics: Evidences on their ability to modify biological responses, inactivation methods and perspectives on their application in foods. Tren. Food. Sci. Tech., 58: 96–114.
- del Valle J.C., Bonadero M.C., Gimenez A.V.F. (2023). Saccha- romyces cerevisiae as probiotic, prebiotic, synbiotic, postbiotics and parabiotics in aquaculture: An overview. Aquaculture, 739342.
- Ebrahimi S.R., Nikkhah A., Sadeghi A.A., Raisali G. (2009). Chemical composition, secondary compounds, ruminal degradation and in vitro crude protein digestibility of gamma irradiated canola seed. Anim. Feed. Sci. Tech., 151: 184–193.
- Falco A., Bello-Perez M., Díaz-Puertas R., Mold M., Adamek M. (2021). Update on the inactivation procedures for the vaccine development prospects of a new highly virulent RGNNV isolate. Vaccines (Basel), 9: 1441.
- Grasso V., Padilla D., Bravo J., Román L., Rosario I., Acosta B., Vega B., El Aamri F., Escuela O., Ramos-Vivas J. (2015). Immunization of sea bream (Sparus aurata) juveniles against Photobacterium damselae subsp. piscicida by short bath: Effect on some pro-inflammatory molecules and the Mx gene expression. Fish. Shellfish Immunol., 46: 292–296.
- Hahor W., Thongprajukaew K., Nuntapong N., Saekhow S., Rungruangsak-Torrissen K., Dumrongrittamatt T., Phonchai A. (2022). Partial pretreatment of ingredient mixture effectively improved feed chemical composition, physicochemical properties and in vitro digestibility. Anim. Feed. Sci. Tech., 285: 115216.
- Heidarieh M., Rad M.H., Mirvaghefi A.R., Diallo A., Mousavi S., Sheikhzadeh N., Shahbazfar A.A. (2014). Effect of gamma irradiation on inactivation of Ichthyophthirius multifiliis trophonts and its efficacy on host response in experimentally immunized rainbow trout (Oncorhynchus mykiss). Turk. J. Vet. Anim. Sci., 38: 388–393.
- Heidarieh M., Moodi S., Katuli K.K., Unger H. (2015). Biochemical effects of encapsulated radiovaccine via alginate nanoparticles as useful strategy for booster in immunized rainbow trout against Ichthyophytirius multifiliis. Acta Sci. Vet., 43: 1330.
- Heidarieh M., Moodi S., Safari O. (2019). Variations of kidney, liver and spleen total sialic acid levels in immunized rainbow trout (Oncorhynchus mykiss) against Ichthyophthirius multifiliis. Vet. Arhiv., 89: 223–232.
- Heidarieh M., Akbari M., Unger H. (2021). Differential MHC-П, IL-8 and IgM genes expression in the liver, head kidney and gill tissues of juvenile rainbow trout (Oncorhynchus mykiss) immunized by inactive trophonts of Ichthyophthirius multifiliis. Inter. J. Radi. Rese., 19: 955–962.
- Heidarieh M., Banaee M., Heidarieh H., Gholamhosseini A. (2022). Effects of gamma-irradiated ethanolic extract of Iranian propolis on growth performance, immunological and haematological parameters in juvenile common carp (Cyprinus carpio L.). Inter. J. Aquac. Biol., 9: 393–402.
- Heidarieh M., Nowrozani F.R., Banaee M., Gholamhosseini A., Heidarieh H., Shahbazfar A.A., Karimi M. (2023 a). Histopathological changes in the skin and gut mucus layers of rainbow trout (Oncorhynchus mykiss) challenged with Ichthyophthirius multifiliis inactivated by gamma rays and formalin. Inter. J. Aqua. Biol., 11: 431–438.
- Heidarieh M., Gholamhosseini A., Sheikhzadeh N., Esteban M.A. (2023 b). Effects of γ-irradiated date (Phoenix dactylifera) fruit on growth, immunological and antioxidant parameters of goldfish (Carassius auratus). Fishes, 8: 251.
- Heidarieh M., Naeimi S., Resae A., Heidarieh T. (2023 c). Changes in juvenile rainbow trout (Oncorhynchus mykiss) growth performance, digestive enzyme activity, hematological profile and serum biochemical markers after dietary administration of γ-irradiated cinnamon (Cinnamomum verum) ethanolic extract. Turk. J. Fish. Aqua. Sci., 23: 22229.
- Hoseinifar S.H., Maradonna F., Faheem M., Harikrishnan R., Devi G., Ringø E., Van Doan H., Ashouri G., Gioacchini G., Carnevali O. (2023). Sustainable ornamental fish aquaculture: The implication of microbial feed additives. Animals, 13: 1583.
- Hu Z., Wen Z. (2008). Enhancing enzymatic digestibility of switch-grass by microwave-assisted alkali pretreatment. Biol. Engin. J., 38: 369–378.
- Jørgensen L. von G. (2020). Zebrafish as a model for fish diseases in aquaculture. Pathogens, 9: 609.
- Kamilya D., Baruah A., Sangma T., Chowdhury S., Pal P. (2015) Inactivated probiotic bacteria stimulate cellular immune responses of catla, Catla catla (Hamilton) in vitro. Prob. Antimocrob Prot., 7: 101–106.
- Kamiya T., Wang L., Forsythe P., Goettsche G., Mao Y., Wang Y., Tougas G., Bienenstock J. (2006). Inhibitory effects of Lactobacillus reuteri on visceral pain induced by colorectal distension in Sprague-Dawley rats. Gut, 55: 191–196.
- Kilcast D. (1995). Food irradiation: Current problems and future potential. Inter. Biodeteriorat. Biodegrad., 36: 279–296.
- Kim H.J., Ham J.S., Lee J.W., Kim K., Ha S.D., Jo C. (2010). Effects of gamma and electron beam irradiation on the survival of pathogens inoculated into sliced and pizza cheeses. Radiat. Physics Chem., 79: 731–734.
- Knopf K., Lucius R. (2008). Vaccination of eels (Anguilla japonica and Anguilla anguilla) against Anguillicola crassus with irradiated L3. Parasitology, 135: 633–640.
- Knopf K., Lucius R. (2008). Vaccination of eels (Anguilla japonica and Anguilla anguilla) against Anguillicola crassus with irradiated L3. Parasitology, 135: 633–640.
- Kyung H., Ramakrishnan S.R., Kwon J. (2019). Dose rates of electron beam and gamma-ray irradiation affect microbial decontamination and quality changes in dried red pepper (Capsicum annuum L.) powder. J. Sci. Food. Agric., 99: 632–638.
- Li B., Chen J., Huang P., Weng T., Wen Y., Yang H., Liu Y., Xia L. (2022). Induction of attenuated Nocardia seriolae and their use as live vaccine trials against fish nocardiosis. Fish. Shellfish Immunol., 131: 10–20.
- Lopez M., Li N., Kataria, J., Russell, M., Neu, J. (2008). Live and ultraviolet-inactivated Lactobacillus rhamnosus GG decrease flagellin-induced interleukin-8 production in Caco-2 cells. J. Nutr., 138: 2264–2268.
- López-González V., Murano P.S., Brennan R.E., Murano E.A. (1999). Influence of various commercial packaging conditions on survival of Escherichia coli O157: H7 to irradiation by electron beam versus gamma rays. J. Food. Prot., 62: 10–15.
- Ma H., Liu W.-W., Chen X., Wu Y.-J., Yu Z.-L. (2009). Enhanced enzymatic saccharification of rice straw by microwave pretreatment. Biores. Technol., 100: 1279–1284.
- Miccoli A., Manni M., Picchietti S., Scapigliati G. (2021). State-of the-art vaccine research for aquaculture use: The case of three economically relevant fish species. Vaccines (Basel), 9: 140.
- Miller R.B. (2005). Food irradiation using electron beams. Elec. Irra. Foods: Intro. Tech., 43–73.
- Naas C., Kappe A., Schmidt-Posthaus H., Lichtenecker M. (2023). Application of UV-C irradiation prevented a severe outbreak of proliferative kidney disease in rainbow trout aquaculture. Diseas. Aquat. Organisms, 155: 103–108.
- Naylor R., Fang S., Fanzo J. (2023). A global view of aquaculture policy. Food Policy, 116: 102422.
- Nguyen N.D., Van Dang P., Le A.Q., Nguyen T.K.L., Pham D.H., Van Nguyen N., Nguyen Q.H. (2017). Effect of oligochitosan and oligo-β-glucan supplementation on growth, innate immunity, and disease resistance of striped catfish (Pangasianodon hypophthalmus). Biotechnol. Appl. Biochem., 64: 564–571.
- Ou C., Lin S., Tsai J., Lin M. (2011). Heat-killed lactic acid bacteria enhance immunomodulatory potential by skewing the immune response toward Th1 polarization. J. Food. Sci., 76: M260–M267.
- Pasnik D.J., Evans J.J., Klesius P.H. (2014). A microwave-irradiated Streptococcus agalactiae vaccine provides partial protection against experimental challenge in Nile tilapia, Oreochromis niloticus. Wor. J. Vac., 4: 184–189.
- Perelberg A., Ronen A., Hutoran M., Smith Y., Kotler M. (2005). Protection of cultured Cyprinus carpio against a lethal viral disease by an attenuated virus vaccine. Vaccine, 23: 3396–3403.
- Rasco B., Ovissipour M. (2015). Electrolyzed water applications in aquaculture and the seafood industry. J. Aquacult. Res. Develop., 6.
- Reid G.K., Gurney-Smith H.J., Flaherty M., Garber A.F., Forster I., Brewer-Dalton K., Knowler D., Marcogliese D.J., Chopin T., Moccia R.D. (2019). Climate change and aquaculture: considering adaptation potential. Aquacult. Environ. Interact., 11: 603–624.
- Rivas-Aravena A., Fuentes Y., Cartagena J., Brito T., Poggio V., La Torre J., Mendoza H., Gonzalez-Nilo F., Sandino A.M., Spencer E. (2015). Development of a nanoparticle-based oral vaccine for Atlantic salmon against ISAV using an alphavirus replicon as adjuvant. Fish. Shellfish Immunol., 45: 157–166.
- Roushdy H.M. (1977). Status of radiation applications in developing countries. Radi. Phys. Chem., 14: 141–154.
- Sakai M., Atsuta S., Kobayashi M. (1993). The immune response of rainbow trout (Oncorhynchus mykiss) injected with five Renibacterium salmoninarum bacterins. Aquaculture, 113: 11–18.
- Sampa M.H.O., Borrely S.I., Silva B.L., Vieira J.M., Rela P.R., Calvo W.A.P., Nieto R.C., Duarte C.L., Perez H.E.B., Somessari E.S. (1995). The use of electron beam accelerator for the treatment of drinking water and wastewater in Brazil. Radi. Phys. Chem., 46: 1143–1146.
- Sánchez B., Delgado S., Blanco-Míguez A., Lourenço A., Gueimonde M., Margolles A. (2017). Probiotics, gut microbiota, and their influence on host health and disease. Mol. Nutr. Food Res., 61: 1600240.
- Sheikhzadeh N., Chehrara F., Heidarieh M., Nofouzi K., Baradaran B. (2017). Impact of irradiated alginic acid on the growth performance and mucus components of rainbow trout (Oncorhynchus mykiss). J. Oceanol. Limnol., 34: 13–18.
- Shin H.S., Park S.Y., Lee D.K., Kim S.A., An H.M., Kim J.R., Kim M.J., Cha M.G., Lee S.W., Kim K.J. (2010). Hypocholesterolemic effect of sonication-killed Bifidobacterium longum isolated from healthy adult Koreans in high cholesterol fed rats. Arch. Pharm. Res., 33: 1425–1431.
- Summerfelt S.T. (2003). Ozonation and UV irradiation –an introduction and examples of current applications. Aquacult. Eng., 28: 21–36.
- Syaifudin M., Tetriana D., Nurhayati S. (2011). The feasibility of gamma irradiation for developing malaria vaccine. Atom. Indonesia, 37: 91–101.
- Tayefi Nasrabadi H., Heidarieh M., Sheikhzadeh N., Niksefat zendeh S., Karimi P. (2021). Effects of irradiated Ergosan on growth performance, serum biochemical parameters and skin mucosal immune responses in crucian carp (Carassius carassius). Aquacult. Physiol. Biol., 9: 107–124.
- Thongprajukaew K., Rodjaroen S., Yoonram K., Sornthong P., Hutcha N., Tantikitti C., Kovitvadhi U. (2015). Effects of dietary modified palm kernel meal on growth, feed utilization, radical scavenging activity, carcass composition and muscle quality in sex reversed Nile tilapia (Oreochromis niloticus). Aquaculture, 439: 45–52.
- Valero Y., Mokrani D., Chaves-Pozo E., Arizcun M., Oumouna M., Meseguer J., Esteban M.Á., Cuesta A. (2018). Vaccination with UV-inactivated nodavirus partly protects European sea bass against infection, while inducing few changes in immunity. Dev. Comp. Immunol., 86: 171–179.
- Yoon H.-S., Yoo J.-Y., Kim J.-H., Lee J.-W., Byun M.-W., Baik B.-K., Lim S.-T. (2010). In vitro digestibility of gamma-irradiated corn starches. Carbohydr. Polym., 81: 961–963.
- Yue K., Shen Y. (2022). An overview of disruptive technologies for aquaculture. Aquac. Fish., 7: 111–120.
- Zhang L., Li N., Caicedo R., Neu J. (2005). Alive and dead Lactobacillus rhamnosus GG decrease tumor necrosis factor-α–induced interleukin-8 production in caco-2 cells. J. Nutr., 135: 1752–1756.
- Zhang Y.Q., Wu Y.B., Jiang D.L., Qin J.G., Wang Y. (2014). Gamma-irradiated soybean meal replaced more fish meal in the diets of Japanese seabass (Lateolabrax japonicus). Anim. Feed Sci. Tech., 197: 155–163.