[
Afewerki S., Asche F., Misund B., Thorvaldsen T., Tveteras R. (2023). Innovation in the Norwegian aquaculture industry. Rev. Aquacult., 15: 759–771.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Choudhury T.G., Kamilya D. (2019). Paraprobiotics: An aquaculture perspective. Rev. Aquac., 11: 1258–1270.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Ciji A., Akhtar M.S. (2021). Stress management in aquaculture: A review of dietary interventions. Rev. Aquac., 13: 2190–2247.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Hu Z., Wen Z. (2008). Enhancing enzymatic digestibility of switch-grass by microwave-assisted alkali pretreatment. Biol. Engin. J., 38: 369–378.
]Search in Google Scholar
[
Jørgensen L. von G. (2020). Zebrafish as a model for fish diseases in aquaculture. Pathogens, 9: 609.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Kilcast D. (1995). Food irradiation: Current problems and future potential. Inter. Biodeteriorat. Biodegrad., 36: 279–296.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Knopf K., Lucius R. (2008). Vaccination of eels (Anguilla japonica and Anguilla anguilla) against Anguillicola crassus with irradiated L3. Parasitology, 135: 633–640.
]Search in Google Scholar
[
Knopf K., Lucius R. (2008). Vaccination of eels (Anguilla japonica and Anguilla anguilla) against Anguillicola crassus with irradiated L3. Parasitology, 135: 633–640.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Miller R.B. (2005). Food irradiation using electron beams. Elec. Irra. Foods: Intro. Tech., 43–73.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Naylor R., Fang S., Fanzo J. (2023). A global view of aquaculture policy. Food Policy, 116: 102422.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Rasco B., Ovissipour M. (2015). Electrolyzed water applications in aquaculture and the seafood industry. J. Aquacult. Res. Develop., 6.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Roushdy H.M. (1977). Status of radiation applications in developing countries. Radi. Phys. Chem., 14: 141–154.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Summerfelt S.T. (2003). Ozonation and UV irradiation –an introduction and examples of current applications. Aquacult. Eng., 28: 21–36.
]Search in Google Scholar
[
Syaifudin M., Tetriana D., Nurhayati S. (2011). The feasibility of gamma irradiation for developing malaria vaccine. Atom. Indonesia, 37: 91–101.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
Yue K., Shen Y. (2022). An overview of disruptive technologies for aquaculture. Aquac. Fish., 7: 111–120.
]Search in Google Scholar
[
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.
]Search in Google Scholar
[
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.
]Search in Google Scholar