[Abass D. A., Obirikorang K. A., Campion B. B., Edziyie R. E., Skov P. V. (2018). Dietary supplementation of yeast (Saccharomyces cerevisiae) improves growth, stress tolerance, and disease resistance in juvenile Nile tilapia (Oreochromis niloticus). Aquacult. Int., 26: 843–855.]Search in Google Scholar
[Abd El-Kader M. F., El-Bab A. F. F., Abd-Elghany M. F., Abdel-Warith A. -W. A., Younis E. M., Dawood M. A. (2020). Selenium nanoparticles act potentially on the growth performance, hemato-biochemical indices, antioxidative, and immune-related genes of European seabass (Dicentrarchus labrax). Biol. Trace Elem. Res., 1–9.]Search in Google Scholar
[Abdel-Latif H. M. R., Abdel-Tawwab M., Khafaga A. F., Dawood M. A. O. (2020). Dietary oregano essential oil improved the growth performance via enhancing the intestinal morphometry and hepato-renal functions of common carp (Cyprinus carpio L.) fingerlings. Aquaculture, 526: 735432.]Search in Google Scholar
[Abu-Elala N., Marzouk M., Moustafa M. (2013). Use of different Saccharomyces cerevisiae biotic forms as immune-modulator and growth promoter for Oreochromis niloticus challenged with some fish pathogens. Int. J. Vet. Sci. Med., 1: 21–29.]Search in Google Scholar
[Abu-Elala N. M., Younis N. A., Abu Bakr H. O., Ragaa N. M., Borges L. L., Bonato M. A. (2020). Influence of dietary fermented Saccharomyces cerevisiae on growth performance, oxidative stress parameters, and immune response of cultured Oreochromis niloticus. Fish Physiol. Biochem., 46: 533–545.]Search in Google Scholar
[Ahmadifar E., Yousefi M., Karimi M., Fadaei Raieni R., Dadar M., Yilmaz S., Dawood M. A., Abdel-Latif H. M. (2020). Benefits of dietary polyphenols and polyphenolrich additives to aquatic animal health: an overview. Rev. Fish. Sci. Aquac., 1–34.]Search in Google Scholar
[Blaxhall P. C., Daisley K. W. (1973). Routine haematological methods for use with fish blood. J. Fish Biol., 5: 771–781.]Search in Google Scholar
[Brewer M. S. (2011). Natural antioxidants: sources, compounds, mechanisms of action, and potential applications. Compr. Rev. Food Sci. F., 10: 221–247.]Search in Google Scholar
[Cai W. -Q., Li S. -F., Ma J. -Y. (2004). Diseases resistance of Nile tilapia (Oreochromis niloticus), blue tilapia (Oreochromis aureus) and their hybrid (female Nile tilapia×male blue tilapia) to Aeromonas sobria. Aquaculture, 229: 79–87.]Search in Google Scholar
[Cao Y., Liu H., Qin N., Ren X., Zhu B., Xia X. (2020). Impact of food additives on the composition and function of gut microbiota: A review. Trends Food Sci. Technol., 99: 295–310.]Search in Google Scholar
[Dawood M. A. O. (2021). Nutritional immunity of fish intestines: important insights for sustainable aquaculture. Rev. Aquacult., 13: 642–663.]Search in Google Scholar
[Dawood M. A. O., Koshio S. (2016). Recent advances in the role of probiotics and prebiotics in carp aquaculture: A review. Aquaculture, 454: 243–251.]Search in Google Scholar
[Dawood M. A. O., Koshio S. (2020). Application of fermentation strategy in aquafeed for sustainable aquaculture. Rev. Aquacult., 12: 987–1002.]Search in Google Scholar
[Dawood M. A. O., Koshio S., Esteban M.Á. (2018). Beneficial roles of feed additives as immunostimulants in aquaculture: a review. Rev. Aquacult., 10: 950–974.]Search in Google Scholar
[Dawood M. A. O., Koshio S., Abdel-Daim M. M., Van Doan H. (2019). Probiotic application for sustainable aquaculture. Rev. Aquacult., 11: 907–924.]Search in Google Scholar
[Dawood M. A., Abo-Al-Ela H. G., Hasan M. T. (2020 a). Modulation of transcriptomic profile in aquatic animals: Probiotics, prebiotics and synbiotics scenarios. Fish Shellfish Immunol., 97: 268–282.10.1016/j.fsi.2019.12.05431863903]Search in Google Scholar
[Dawood M. A., Eweedah N. M., Moustafa E. M., Farahat E. M. (2020 b). Probiotic effects of Aspergillus oryzae on the oxidative status, heat shock protein, and immune related gene expression of Nile tilapia (Oreochromis niloticus) under hypoxia challenge. Aquaculture, 520: 734669.10.1016/j.aquaculture.2019.734669]Search in Google Scholar
[Dawood M. A. O., Eweedah N. M., Khalafalla M. M., Khalid A., Asely A. E., Fadl S. E., Amin A. A., Paray B. A., Ahmed H. A. (2020 c). Saccharomyces cerevisiae increases the acceptability of Nile tilapia (Oreochromis niloticus) to date palm seed meal. Aquacult. Rep., 17: 100314.10.1016/j.aqrep.2020.100314]Search in Google Scholar
[Doumas B. T., Bayse D. D., Carter R. J., Peters T., Schaffer R. (1981). A candidate reference method for determination of total protein in serum. I. Development and validation. Clin. Chem., 27: 1642–1650.]Search in Google Scholar
[Ellis A., Stolen J., Fletcher T., Anderson D., Robertson B., Van Muiswinkel W. (1990). Lysozyme assay. Tech. Fish Immunol., 1: 101–103.]Search in Google Scholar
[Essa M. A., Mabrouk H. A., Mohamed R. A., Michael F. R. (2011). Evaluating different additive levels of yeast, Saccharomyces cerevisiae, on the growth and production performances of a hybrid of two populations of Egyptian African catfish, Clarias gariepinus. Aquaculture, 320: 137–141.]Search in Google Scholar
[Ethuin F., Delarche C., Benslama S., Gougerot-Pocidalo M. -A., Jacob L., Chollet-Martin S. (2001). Interleukin-12 increases interleukin 8 production and release by human polymorphonuclear neutrophils. J. Leukoc. Biol., 70: 439–446.]Search in Google Scholar
[FAO (2018). Aquaculture Department. The state of world fisheries and aquaculture. Rome.]Search in Google Scholar
[Fiúza L. S., Aragão N. M., Ribeiro Junior H. P., de Moraes M. G., Rocha Í. R. C. B., Lustosa Neto A. D., de Sousa R. R., Madrid R. M. M., de Oliveira E. G., Costa F. H. F. (2015). Effects of salinity on the growth, survival, haematological parameters and osmoregulation of tambaqui Colossoma macropomum juveniles. Aquacult. Res., 46: 1–9.]Search in Google Scholar
[Garlock T., Asche F., Anderson J., Bjørndal T., Kumar G., Lorenzen K., Ropicki A., Smith M. D., Tveterås R. (2020). A global blue revolution: Aquaculture growth across regions, species, and countries. Rev. Fish. Sci. Aquac., 28: 107–116.]Search in Google Scholar
[Gella F. J., Olivella T., Pastor M. C., Arenas J., Moreno R., Durban R., Gomez J. A. (1985). A simple procedure for the routine determination of aspartate aminotransferase and alanine aminotransferase with pyridoxal phosphate. Clin. Chim. Acta., 153: 241–247.]Search in Google Scholar
[Hansen J. Ø., Lagos L., Lei P., Reveco-Urzua F. E., Morales-Lange B., Hansen L. D., Schiavone M., Mydland L. T., Arntzen M. Ø., Mercado L., Benicio R. T., Øverland M. (2021). Down-stream processing of baker’s yeast (Saccharomyces cerevisiae) – Effect on nutrient digestibility and immune response in Atlantic salmon (Salmo salar). Aquaculture, 530: 735707.]Search in Google Scholar
[Hindu S. V., Chandrasekaran N., Mukherjee A., Thomas J. (2019). A review on the impact of seaweed polysaccharide on the growth of probiotic bacteria and its application in aquaculture. Aquacult. Int., 27: 227–238.]Search in Google Scholar
[Hrubec T. C., Smith S. A. (1999). Differences between plasma and serum samples for the evaluation of blood chemistry values in rainbow trout, channel catfish, hybrid tilapias, and hybrid striped bass. J. Aquat. Anim. Health., 11: 116–122.]Search in Google Scholar
[Huang L., Ran C., He S., Ren P., Hu J., Zhao X., Zhou Z. (2015). Effects of dietary Saccharomyces cerevisiae culture or live cells with Bacillus amyloliquefaciens spores on growth performance, gut mucosal morphology, hsp70 gene expression, and disease resistance of juvenile common carp (Cyprinus carpio). Aquaculture, 438: 33–38.]Search in Google Scholar
[Huyben D., Nyman A., Vidaković A., Passoth V., Moccia R., Kiessling A., Dicksved J., Lundh T. (2017). Effects of dietary inclusion of the yeasts Saccharomyces cerevisiae and Wickerhamomyces anomalus on gut microbiota of rainbow trout. Aquaculture, 473: 528–537.]Search in Google Scholar
[Itou T., Lida T., Kawatsut H. (1996). Kinetics of oxygen metabolism during respiratory burst in Japanese eel neutrophils. Dev. Comp. Immunol., 20: 323–330.]Search in Google Scholar
[Iwashita M. K. P., Nakandakare I. B., Terhune J. S., Wood T., Ranzani-Paiva M. J. T. (2015). Dietary supplementation with Bacillus subtilis, Saccharomyces cerevisiae and Aspergillus oryzae enhance immunity and disease resistance against Aeromonas hydrophila and Streptococcus iniae infection in juvenile tilapia Oreochromis niloticus. Fish Shellfish Immunol., 43: 60–66.]Search in Google Scholar
[Kawahara E., Ueda T., Nomura S. (1991). In vitro phagocytic activity of white-spotted char blood cells after injection with Aeromonas salmonicida extracellular products. Fish Path., 26: 213–214.]Search in Google Scholar
[Kuebutornye F. K. A., Abarike E. D., Lu Y. (2019). A review on the application of Bacillus as probiotics in aquaculture. Fish Shellfish Immunol., 87: 820–828.]Search in Google Scholar
[Li X. M., Ma Y. L., Liu X. J. (2007). Effect of the Lycium barbarum polysaccharides on age-related oxidative stress in aged mice. J. Ethnopharmacol., 111: 504–511.]Search in Google Scholar
[Liu J., Cao S., Kim S., Chung E. Y., Homma Y., Guan X., Jimenez V., Ma X. (2005). Interleukin- 12: an update on its immunological activities, signaling and regulation of gene expression. Curr. Immunol. Rev., 1: 119–137.]Search in Google Scholar
[Magalhães R., Sánchez-López A., Leal R. S., Martínez-Llorens S., Oliva-Teles A., Peres H. (2017). Black soldier fly (Hermetia illucens) pre-pupae meal as a fish meal replacement in diets for European seabass (Dicentrarchus labrax). Aquaculture, 476: 79–85.]Search in Google Scholar
[Magnadóttir B. (2006). Innate immunity of fish (overview). Fish Shellfish Immunol., 20: 137–151.]Search in Google Scholar
[Martínez-Álvarez R. M., Morales A. E., Sanz A. (2005). Antioxidant defenses in fish: Biotic and abiotic factors. Rev. Fish Biol. Fish., 15: 75–88.]Search in Google Scholar
[Ming J., Xie J., Xu P., Liu W., Ge X., Liu B., He Y., Cheng Y., Zhou Q., Pan L. (2010). Molecular cloning and expression of two HSP70 genes in the Wuchang bream (Megalobrama amblycephala Yih). Fish Shellfish Immunol., 28: 407–418.]Search in Google Scholar
[Pfaffl M. W. (2001). A new mathematical model for relative quantification in real-time RT-PCR Nucleic Acids Res., 29: e45.]Search in Google Scholar
[Reinhold J. (1953). Total protein, albumin and globulin. Standard Methods of Clinical Chemistry. 1.]Search in Google Scholar
[Reque V. R., de Moraes J. R. E., de Andrade Belo M. A., de Moraes F. R. (2010). Inflammation induced by inactivated Aeromonas hydrophila in Nile tilapia fed diets supplemented with Saccharomyces cerevisiae. Aquaculture, 300: 37–42.]Search in Google Scholar
[Shi X., Li D., Zhuang P., Nie F., Long L. (2006). Comparative blood biochemistry of Amur sturgeon, Acipenser schrenckii, and Chinese surgeon, Acipenser sinensis. Fish Physiol. Biochem., 32: 63.]Search in Google Scholar
[Stoskopf M. (1993). Fish Medicine. WB Saunders Comp. Philadelphia.]Search in Google Scholar
[Takahashi L. S., Biller-Takahashi J. D., Mansano C. F. M., Urbinati E. C., Gimbo R. Y., Saita M. V. (2017). Long-term organic selenium supplementation overcomes the tradeoff between immune and antioxidant systems in pacu (Piaractus mesopotamicus). Fish Shellfish Immunol., 60: 311–317.]Search in Google Scholar
[Tort L., Balasch J., Mackenzie S. (2003). Fish immune system. A crossroads between innate and adaptive responses. Inmunología, 22: 277–286.]Search in Google Scholar
[Uribe C., Folch H., Enríquez R., Moran G. (2011). Innate and adaptive immunity in teleost fish: a review. Vet. Med-Czech, 56: 486–503.]Search in Google Scholar
[Yang X., He Y., Chi S., Tan B., Lin S., Dong X., Yang Q., Liu H., Zhang S. (2020). Supplementation with Saccharomyces cerevisiae hydrolysate in a complex plant protein, low-fishmeal diet improves intestinal morphology, immune function and Vibrio harveyi disease resistance in Epinephelus coioides. Aquaculture, 529: 735655.]Search in Google Scholar
[Yao Y. -Y., Yang Y. -L., Gao C. -C., Zhang F. -L., Xia R., Li D., Hu J., Ran C., Zhang Z., Liu-Clarke J., Zhou Z. -G. (2020). Surface display system for probiotics and its application in aquaculture. Rev. Aquacult. 12: 2333–2350.]Search in Google Scholar
[Yilmaz S., Sova M., Ergün S. (2018). Antimicrobial activity of trans-cinnamic acid and commonly used antibiotics against important fish pathogens and nonpathogenic isolates. J. Appl. Microbiol., 125: 1714–1727.]Search in Google Scholar
[Yılmaz S., Ergun S., Yigit M., Çelik E.Ş. (2020). Effect of combination of dietary Bacillus subtilis and trans-cinnamic acid on innate immune responses and resistance of rainbow trout, Oncorhynchus mykiss to Yersinia ruckeri. Aquacult. Res., 51: 441–454.]Search in Google Scholar
