Abstracts
The understanding of fish immune system structure and function is essential for the development of new technologies and products to improve productivity. This is the first review on immune system of fish with Brazilian studies. Aquaculture in Brazil has shown massive growth in recent years due to methods of culture intensification. However, these procedures led to disease outbreaks, as well as the chemotherapy and the misuse of antibiotics. A viable alternative to avoid the use of chemicals and prevent economic losses is the administration of immunostimulants and prebiotcs, which act by increasing the innate immune system. In Brazil there is a lack of studies on fish immune system, except by some groups that have studied the effects of the immunostimulants administration in various species.
innate immune system; acquired immune system; immunostimulant; prebiotic
O estudo das estruturas e o funcionamento do sistema imune de peixes são fundamentais para o desenvolvimento de novas tecnologias e produtos para a melhoria da produtividade. Esta é a primeira revisão sobre o sistema imune de peixe ressaltando os estudos realizados no Brasil. A aquicultura no Brasil apresentou grande crescimento nos últimos anos, devido aos métodos de intensificação da cultura. Entretanto estes procedimentos levaram ao aparecimento de diversas enfermidades, bem como ao uso indiscriminado de quimioterápicos e antibióticos. Uma alternativa viável para evitar o uso de fármacos e prevenir as perdas econômicas provocadas por diversos agentes etiológicos é o uso de imunoestimulantes e prebióticos, que atuam aumentando as defesas inespecíficas de peixes. No Brasil os estudos sobre o sistema imune de peixes é escasso, mas alguns grupos já demonstraram benefícios com uso destes compostos em diversas espécies.
sistema imune inato; sistema imune adquirido; imunoestimulante; prebiótico
INTRODUCTION
The Innate and Acquire Immune System of Bony Fish
The immune system is a set of cellular and humoral components to defend the body against foreign substances, such as microorganisms, toxins or malignant cells, responding to factors such as endogenous or exogenous components that stimulate this system. The fish immune system is divided into innate and adaptive (memory), both divided into cell mediated defense and humoral factors (soluble substances), although today it is known that these two systems work together in order to destroy invaders or to trigger defense processes. The innate system includes all components present in the body before the appearance of the pathologic agent, as the first line of defense that acts faster than the specific system. Among these components there is the skin as a physical barrier, the complement system, the antimicrobial enzymes, the interleukins, the interferon and the organic defense cells, such as granulocytes, monocytes, macrophages and natural killers cells (Bayne and Gerwick 2001Bayne CJ and Gerwick L. 2001. The acute phase response and innate immunity of fish. Dev Comp Immunol 25: 725-743., Ellis 1999Ellis AE. 1999. Immunity to bacteria in fish. Fish Shellfish Immunol 9: 291-308., Magnadottir et al. 2011Magnadottir B, Audunsdottir SS, Bragason BTH, Gisladottir B, Jonsson ZO and Gudmundsdottir S. 2011. The acute phase response of Atlantic cod (Gadus morhua): Humoral and cellular responses. Fish Shellfish Imunnol 30: 1124-1130.).
The inflammation is also considered an innate mechanism of immune response, mediated by complex interactions of cellular and humoral compounds. Once a tissue has been penetrated by an infectious agent, mediator factors are released in order to extend and make blood capillaries more permeable, allowing the migration of the defense cells. The granulocytes are the first cell type to arrive at the inflammation focus, being responsible for the destruction of pathogens. On the other hand, the remaining pathogenic cells and cellular debris are phagocytosed by macrophages (Magnadottir 2006Magnadottir B. 2006. Innate immunity of fish (overview). Fish Shellfish Immunol 20: 137-151.).
The innate immunity is the oldest system in the phylogenetic scale and probably originated in unicellular organisms during the evolutionary period. By definition, this system recognizes regions in molecules called Pamps - Pathogen Associated Molecular Patterns - from infectious agents or microorganisms of normal microbiota, such as lipopolysaccharide, peptidoglycan, bacterial DNA or viral RNA, or other molecules found in multicellular organisms membranes known as “non-self”. The Pamps are usually highly preserved portions during the evolution of species and are found in the greater part of microorganisms. Conversely, the specific system first appeared around 450 million years ago, and can be found in all vertebrates except in fish of the Agnatha class. The acquired system receptors are responsible for detecting the pathogenic agent, and can be found in the cell membrane of T lymphocytes (TCR - T cell receptor) and B lymphocytes (BCR - B cell receptor, also called as well as membrane immunoglobulin) or in serum as free antibody (Abbas and Litchman 2004, Boltaña et al. 2011Boltaña S, Rohera N, Goetz FW and Mackenzie SA. 2011. PAMPs, PRRs and the genomics of gram negative bacterial recognition in fish. Dev Comp Immunol 35: 1195-1203., Elward and Gasque 2003Elward K and Gasque P. 2003. “Eat me” and “don't eat me” signals govern the innate immune response and tissue repair in the CNS: emphasis on the critical role of the complement system. Molecular Immunology 40: 85-94., Goldsby et al. 2002Goldsby RA, Kindt TJ, Osborne BA and Kuby J. 2002. In: Immunology, 5th ed., WH Freeman & Company Publisher, 554 p., Holland and Lambris 2002Holland MCH and Lambris JD. 2002. The complement system in teleosts. Fish Shellfish Immunol 12: 399-420.).
The specific system of defense requires the presence of an antigen, which is a strange molecule or cell that will initiate reactions and culminate in the increase of circulation of specific antibodies, besides promoting immune memory. Antigens that enter the body will be recognized and processed by the innate system by antigen presenting cells (APC - macrophages, dendritic cells and B lymphocytes), to process microorganisms in molecular units, and at first trigger immune response of proliferation, and in a second moment, the response of memory. As a result, the antigen processed by APC will be presented to the T lymphocytes which are the cells of the specific system. T lymphocytes carry the ability to recognize the antigen strictly in the presence of a specific humoral component called major histocompatibility complex molecules, which are glycoprotein receptors coded by genes in a major histocompatibility complex (MHC). After this recognition, the T cell secretes cytokines, which are proteins that activate other cells such as B lymphocytes (responsible for the production of antibodies), cytotoxic lymphocytes, macrophages and other cells in order to destroy the invading agent (Abbas and Lichman 2004, Bernstein et al. 1998Bernstein RM, Schluter SF and Marchalonis JJ. 1998. Immunity. In: EVANS DH (Ed), The physiology of fishes. 2nd ed., Boca Raton: CRC Press, p. 215-242., Goldsby et al. 2002Goldsby RA, Kindt TJ, Osborne BA and Kuby J. 2002. In: Immunology, 5th ed., WH Freeman & Company Publisher, 554 p., Salinas et al. 2011Salinas I, Zhang YA and Sunyer JO. 2011. Mucosal immunoglobulins and B cells of teleost fish. Dev Comp Immunol 35: 1346-1365.).
The antibodies recognize and connect to specific microorganisms and consequently activate phagocytosis (component of the innate system, indicating that the specific and innate systems act together). Antibodies may promote agent neutralization or opsonization and may bind to extracellular antigens in addition to complement system. However, if the antigen is established in the intracellular compartment, the defense is conducted by cytotoxic T lymphocytes (Ellis 2001Ellis AE. 2001. Innate host defense mechanism of fish against virus and bacteria. Dev Comp Immunol 25: 827-839., Goldsby et al. 2002Goldsby RA, Kindt TJ, Osborne BA and Kuby J. 2002. In: Immunology, 5th ed., WH Freeman & Company Publisher, 554 p., Salinas et al. 2011Salinas I, Zhang YA and Sunyer JO. 2011. Mucosal immunoglobulins and B cells of teleost fish. Dev Comp Immunol 35: 1346-1365.).
The Ontogeny of the Immune System
The tissues and organs that structure the immune system of bony fish are classified as lymphoid, and there is no myeloid classification, such as in mammals, because fish lack bone marrow and lymph nodes. The lymphoid organs are the kidneys (the largest lymphoid organ), thymus, spleen and gut associated lymphoid tissues (GALT), formed during larval development. It is known that there are approximately 24,000 fish species thus morphological differences have been found (Nelson 1994Nelson JS. 1994. Fishes of the World. 3rd ed., New York: J Wiley & Sons, 600 p., Press and Evensen 1999Press CMCL and Evensen O. 1999. The morphology of the immune system in teleost fishes. Fish Shellfish Immunol 9: 309-318., Rombout et al. 2010Rombout JHWM, Abelli L, Picchietti S, Scapigliati G and Kiron V. 2010. Teleost intestinal immunology. Fish Shellfish Immunol 31: 616-626.). The lymphoid tissues and organs are usually arranged by reticular cell networks in order to build a structure for the cells of the innate and specific defense, such as lymphocytes, monocytes, macrophages, granulocytes and thrombocytes, mast cells, NK cells, cytotoxic cells and dendritic cells. This arrangement is responsible for the production of the immune system components (Miller et al. 1985Miller NW, Sizemore RC and Clem LW. 1985. Phylogeny of lymphocyte heterogeneity: the cellular requirements for in vitro antibody responses of channel catfish leukocytes. J Immunol 134: 2884-2888., Ellis 1977Ellis AE. 1977. The leucocytes of fish: a review. J Fish Biol 11: 453-491., Salinas et al. 2011Salinas I, Zhang YA and Sunyer JO. 2011. Mucosal immunoglobulins and B cells of teleost fish. Dev Comp Immunol 35: 1346-1365.).
Thymus is a double organ located behind the operculum in the dorsolateral position of gills. The thymus ontogeny and histology differ according to species, however, in general, their origin occurs 24 hours after fertilization. It is considered an important tissue of T lymphocytes development and maturation (Bowden 2005, Fishelson 1995Fishelson L. 1995. Cytological and morphological ontogenesis and involution of the thymus in cichlid fishes (Cichlidae, Teleostei). J Morphol 223: 175-190.). Although the involution of the thymus occurs in adult vertebrates, it can differ in bony fish depending on the species. The kidney is very important for fish hematopoiesis and immunity, and could even be compared to the marrow of mammals. It has the function of formation and maturation of red and white blood cells. The kidney displays differences between the anterior and posterior section, both with haemopoietic function. However, the first portion of the organ is more important for the production of defense cells, in addition to differentiation and maturation of leukocytes, including B lymphocytes, monocytes, macrophages and granulocytes (Meseguer et al. 1994Meseguer J, Esteban AM, Lopez-Ruiz A and Bielek E. 1994. Ultrastructure of nonspecific cytotoxic cells in teleosts. I. Effector-target cell binding in a marine and a freshwater species (seabream: Sparus aurata L., and carp: Cyprinus carpio L.). The Anat Rec 239: 468-474., Torroba and Zapata 2003Torroba M and Zapata AG. 2003. Aging of the vertebrate immune system. Microsc Res Technol 62: 477-481.).
The fish spleen contains a white pulp that promotes haematopoiesis with formation of defense cells, and a red pulp that causes phagocytosis of old or defective cells. However, different from mammals, this division in fish is not organized, although it is possible to identify each pulp in various species. The organ concentrates lymphocytes and macrophages, most of which are macrophages arranged in centers that are responsible for phagocytosis that will culminate in immune memory. Once blood flows through spleen, antigens are kept in these centers in order to be processed and presented for T lymphocytes (Press and Evensen 1999Press CMCL and Evensen O. 1999. The morphology of the immune system in teleost fishes. Fish Shellfish Immunol 9: 309-318., Solem and Stenvik 2006Solem ST and Stenvik J. 2006. Antibody repertoire development in teleosts—a review with emphasis on salmonids and Gadus morhua L. Dev Comp Immunol 30: 57-76.).
GALT includes gastrointestinal mucosa, gills, and skin. These tissues produce mucus containing soluble defense components, such as lysozyme, complement system proteins and immunoglobulins in order to promote the first barrier against pathogen agent. These lymphoid tissues are scattered throughout the mucosa in clusters of defense cells, including macrophages, lymphocytes, mast cells and granulocytes (Georgopoulou and Vernier 1986Georgopoulou U and Vernier JM. 1986. Local immunological response in the posterior intestinal segment of the rainbow trout after oral administration of macromolecules. Dev Comp Immunol 10: 529-537., Rombout et al. 2010Rombout JHWM, Abelli L, Picchietti S, Scapigliati G and Kiron V. 2010. Teleost intestinal immunology. Fish Shellfish Immunol 31: 616-626.). These cells capture the antigen in order to process and promote immune memory. The liver has the same function as in mammals, of producing humoral compounds such as proteins of the complement system and acute phase proteins of the inflammatory response (Davidson et al. 1997Davidson GA, Lin SH, Secombes CJ and Ellis AE. 1997. Detection of specific and constitutive antibody secreting cells in the gills, head kidney and peripheral blood leucocytes of dab (Limanda limanda). Vete Immunology Immunopath 58: 363-374., Salinas et al. 2011Salinas I, Zhang YA and Sunyer JO. 2011. Mucosal immunoglobulins and B cells of teleost fish. Dev Comp Immunol 35: 1346-1365.).
Humoral and Cellular Mediated Immunity
The fish immune system is responsible for destroying microorganisms through acquired and innate components, with humoral and cellular process that perform together in an attempt to prevent the outbreak of diseases. The humoral innate system functions through several soluble components in body fluids, while the humoral specific system acts only through antibodies. Fish are susceptible to viral, bacterial, fungal and parasite agents, however, they can resist microbial invasion because of specific and innate mechanisms. The unspecific mechanisms includes the production of numerous antibacterial compounds, proteins of inflammation acute phase, complement activated by alternative pathway, cytokines, phagocytosis and inflammation (Bayne and Gerwick 2001Bayne CJ and Gerwick L. 2001. The acute phase response and innate immunity of fish. Dev Comp Immunol 25: 725-743., Ellis 1999Ellis AE. 1999. Immunity to bacteria in fish. Fish Shellfish Immunol 9: 291-308., 2001Ellis AE. 2001. Innate host defense mechanism of fish against virus and bacteria. Dev Comp Immunol 25: 827-839., Lin et al. 2011Lin S, Pan Y, Luo L and Luo L. 2011. Effects of dietary b-1,3-glucan, chitosan or raffinose on the growth, innate immunity and resistance of koi (Cyprinus carpio koi). Fish Shellfish Immunol 31: 788-794.).
Among the humoral innate components are the inhibitory factors of bacteria growth, such as transferrin, antiproteases, lysozyme, C-reactive protein, antibacterial peptides and complement system proteins, activated through alternative and lectin pathways. The complement system is one of the most important mechanisms since it has lytic activity, chemotaxic, pro-inflammatory and opsonization functions. Defense cells represented by phagocytes, neutrophils and macrophages are very important due to their large quantities of enzymes in lysosomes and reactive oxygen species produced during phagocytosis (Ellis 1999Ellis AE. 1999. Immunity to bacteria in fish. Fish Shellfish Immunol 9: 291-308., Magnadottir et al. 2011Magnadottir B, Audunsdottir SS, Bragason BTH, Gisladottir B, Jonsson ZO and Gudmundsdottir S. 2011. The acute phase response of Atlantic cod (Gadus morhua): Humoral and cellular responses. Fish Shellfish Imunnol 30: 1124-1130.).
Antiproteases are blood proteins which act against microorganism proteolytic proteins, those ones that make lysis in fish tissues in order to obtain amino acids as sources of energy. Lectins are proteins found in eggs, mucus and blood that promote agglutination due to their high affinity for carbohydrates of the pathogens cell wall. Lysins present in mucus are peptides that attack the membranes of pathogens. Lysozyme is produced by leukocytes (mainly monocytes and neutrophils) and it is found in mucus, eggs, blood and tissues and acts on the peptidoglycan of pathogens cell wall (Arason 1996Arason GJ. 1996. Lectins as defence molecules in vertebrates and invertebrates. Fish Shellfish Immunol 6: 277-289., Braun et al. 1990Braun R, Arnesen JA, Rinne A and Hjelmeland K. 1990. Immunohistological localisation of trypsin in mucussecreting layers of Atlantic salmon, Salmo salar L. J Fish Dis 13: 233-238., Ellis 1999Ellis AE. 1999. Immunity to bacteria in fish. Fish Shellfish Immunol 9: 291-308., 2001Ellis AE. 2001. Innate host defense mechanism of fish against virus and bacteria. Dev Comp Immunol 25: 827-839., Murray and Fletcher 1976Murray CK and Fletcher TC. 1976. The immunohistochemical localization of lysozyme in plaice (Pleuronectes platessa L.) tissues. J Fish Biol 9: 329-334., Magnadottir 2006Magnadottir B. 2006. Innate immunity of fish (overview). Fish Shellfish Immunol 20: 137-151., Ohta et al. 1990Ohta M, Okada M and Yamashita I. 1990. The mechanism of carbohydrate-mediated complement activation by the serum mannose-binding protein. J Biol Chem 265: 1980-1984.). C-reactive protein from the pentraxin family is found in large concentrations in the blood, egg and mucus. The protein recognize and connect to phosphoryl colin, a component usually found on the walls of various microorganisms such as bacteria, fungi and parasites. The C-reactive protein and the mannose binding lectin are considered inflammation acute phase proteins and receptors of soluble microbial components so that they have ability to connecting and promoting pathogen opsonization, complement activation and phagocytosis. The concentration of acute phase proteins may increase after heat shock (high temperatures), infectious agents and in warm periods of the year (Goldsby et al. 2002Goldsby RA, Kindt TJ, Osborne BA and Kuby J. 2002. In: Immunology, 5th ed., WH Freeman & Company Publisher, 554 p., Magnadottir et al. 2011Magnadottir B, Audunsdottir SS, Bragason BTH, Gisladottir B, Jonsson ZO and Gudmundsdottir S. 2011. The acute phase response of Atlantic cod (Gadus morhua): Humoral and cellular responses. Fish Shellfish Imunnol 30: 1124-1130., Nakanishi et al. 1991Nakanishi Y, Kodama H, Murai T, Mikami T and Izawa H. 1991. Activation of rainbow trout complement by C-reactive protein. Am J Vet Res 52: 397-401., Szalai et al. 1994Szalai AJ, Bly JE and Clem LW. 1994. Changes in serum concentration of channel catfish (Ictalurus punctatus Rafinesque) phosphorylcholine – reactive protein (PRP) in response to inflammatory agents, low temperature shock and infection by the fungus Saprolegnia sp. Fish Shellfish Immunol 4: 323-336.).
The complement system of fish is considered more effective than that of mammals and is one of the most important innate compounds for host protection due to its production of inflammatory mediators (Nonaka et al. 1981Nonaka M, Yamaguchi N, Natsuume-Sakai S and Takahashi M. 1981. The complement system of rainbow trout (Salmo gairdneri). I. Identification of the serum lytic system homologous to mammalian complement. The J Immunol 126: 1489-1494., Boshra et al. 2006Boshra H, Li J and Sunyer JO. 2006. Recent advances on the complement system of teleost fish. Fish Shellfish Immunol 20: 239-262.). The complement system is comprised of soluble and membrane proteins in inactive form or in low levels of spontaneous activation and they are triggered by sequential pathway since the initial stimulus contributes to the proteolysis of the next component. Activation can be triggered by three pathways: i) classical pathway, an antibody-dependent activation by antigen-antibody complex, ii) alternative pathway, prompted by microorganisms Pamps or antigen-antibody complex, iii) lectin pathway, triggered by bacterial surface carbohydrates. The alternative pathway is very efficient on innate recognition and is considered the most important among the three activation pathways, besides it can be easily trigged by various gram-negative bacteria lipopolysaccharide and cause cytolysis. Alternatively, the classic pathway performs interaction between innate and specific systems (Boltaña et al. 2011Boltaña S, Rohera N, Goetz FW and Mackenzie SA. 2011. PAMPs, PRRs and the genomics of gram negative bacterial recognition in fish. Dev Comp Immunol 35: 1195-1203., Boshra et al. 2006Boshra H, Li J and Sunyer JO. 2006. Recent advances on the complement system of teleost fish. Fish Shellfish Immunol 20: 239-262., Holland and Lambris 2002Holland MCH and Lambris JD. 2002. The complement system in teleosts. Fish Shellfish Immunol 12: 399-420.).
Two complement system components C5a and C3b play a central role in the recruitment of phagocytes and inflammation. C5a and C3b are chemotaxic proteins for neutrophils and macrophages because they remain linked to bacterial wall triggering biological processes of opsonization, phagocytosis, chemotaxis of leukocytes and inactivation of the released bacteria toxin. The complement system is widely used as an immune status indicator due to its contribution to host protection. The function of the complement system regarding cellular activation, phagocytosis, chemotaxis, inflammatory reaction and lise of pathogens cells are well known mainly for their ability to destroy pathogens through membrane injuries, commonly characterized by pores (Bayne and Gerwick 2001Bayne CJ and Gerwick L. 2001. The acute phase response and innate immunity of fish. Dev Comp Immunol 25: 725-743., Boshra et al. 2006Boshra H, Li J and Sunyer JO. 2006. Recent advances on the complement system of teleost fish. Fish Shellfish Immunol 20: 239-262., Ellis 2001Ellis AE. 2001. Innate host defense mechanism of fish against virus and bacteria. Dev Comp Immunol 25: 827-839., Secombes 1996Secombes CJ. 1996. The nonspecific immune system: cellular defenses. In: IWAMA G and NAKANISHI T (Eds), The fish immune system. London: Academic Press, p. 95-103.).
Innate humoral components increase after outbreak of pathogens such as bacteria, viruses, parasites and fungi, as well as in trauma, necroses, chemicals, heat shock, tumor cells and in some cases increase up to 1000 folds, such as C-reactive protein. These compounds are called acute phase proteins and most of them are synthesized by the liver, however, they can also be synthesized by the brain and leukocytes. The C-reactive protein, serum amyloid A, transferrin, α-2 macroglobulin, C3 complement, lysozyme and lectins are commonly used for the diagnosis of diseases (Bayne and Gerwick 2001Bayne CJ and Gerwick L. 2001. The acute phase response and innate immunity of fish. Dev Comp Immunol 25: 725-743., Magnadottir et al. 2011Magnadottir B, Audunsdottir SS, Bragason BTH, Gisladottir B, Jonsson ZO and Gudmundsdottir S. 2011. The acute phase response of Atlantic cod (Gadus morhua): Humoral and cellular responses. Fish Shellfish Imunnol 30: 1124-1130.).
The bony fish defense cells are produced by lymphoid tissues such as kidney, thymus, spleen and GALT since they have the same cellular precursor called pluripotent cell. The lymphoid cells production is recognized as hematopoiesis that results in the formation and differentiation of a large quantity of cell types such as erythrocytes, granulocytes, monocytes, lymphocytes, mast cells and thrombocytes (Metcalf and Nicola 1995Metcalf D and Nicola NA. 1995. The hematopoietis colonystimulating factors: From biological to clinical applications. New York: Cambridge University Press, USA, 329 p., Evans 1997Evans T. 1997. Developmental biology of hematopoieses. Hematol Oncol Clinic North Am 11: 1115-1147., Chettri et al. 2011Chettri JK, Raida MK, Andersen LH, Kania PW and Buchmann K. 2011. PAMP induced expression of immune relevant genes in head kidney leukocytes of rainbow trout (Oncorhynchus mykiss). Dev Comp Immunol 35: 476-482.). The hematopoiesis is regulated by cytokines that act on pluripotent cell receptors controlling their survival, proliferation, differentiation, maturation and function (Hanington et al. 2009Hanington PC, Tamb J, Katzenback BA, Hitchen SJ, Barreda DR and Belosevic M. 2009. Development of macrophages of cyprinid fish. Dev Comp Immunol 33: 411-429.). The hematological parameters assessment can be an indicator of physical condition and diseases outbreak of the fish (Stoskopf 1993, Barreda and Belosevic 2009Barreda DR and Belosevic M. 2009. Development of macrophages of cyprinid fish. Dev Comp Immunol 33: 411-429.).
Among the defense cells of fish, thrombocytes have phagocytosis capacity besides coagulation function. They have acid phosphatase what leads the cell to be in inflammatory site (Tavares-Dias et al. 1999Tavares-Dias M, Schalch SHC, Martins ML, Silva ED, Moraes FR and Perecin D. 1999. Hematologia de teleósteos brasileiros com infecção parasitaria. I. Variáveis do Leporinus macrocephalus Garavello & Britski, 1988 (Anostomidae) e Piaractus mesopotamicus Holmberg, 1887 (Characidae). Acta Sci Anim Sci 21: 337-342.). Monocytes show phagocytosis and unspecific citotoxic activities and are considered transitory cells in blood because during the inflammatory process they migrate through the connective tissue and turn into macrophages (Mesenguer et al. 1994, Witten et al. 1998Witten PE, Villwock W and Renwrantz L. 1998. Haematogram of the tilapia Oreochromis niloticus (Cichlidae, Teleostei) and application of a putative phenoloxidase for differentiating between neutrophilic granulocytes and monocytes. Can J Zool 76: 310-319., Cuesta et al. 1999Cuesta A, Angeles Esteban M and Meseguer J. 1999. Natural cytotoxic activity of gilthead seabream (Sparus aurata L.) leucocytes assessment by flow cytometry and microscopy. Vet Immunology Immunopath 71: 161-171.). Neutrophils are polymorphonuclear cells found in the blood, lymphoid tissues and peritoneal cavity that can phagocytosis foreign particles or cells and produce superoxide anions that are a bactericidal compound (Plyzycz et al. 1989Plyzycz B, Flory CM, Galvan I and Bayne CJ. 1989. Leucocytes of rainbow trout (Oncorhynchus mykiss) pronephros: cell types producing superoxide anion. Dev Comp Immunol 13: 217-224., Secombes 1996Secombes CJ. 1996. The nonspecific immune system: cellular defenses. In: IWAMA G and NAKANISHI T (Eds), The fish immune system. London: Academic Press, p. 95-103.). Eosinophils are distributed by connective tissue, especially in the gastrointestinal tract, gills and bloodstream and provide degranulation when there are parasites infestations. Basophils are unusual in most fish (Hine 1992Hine PM. 1992. The granulocytes of fish. Fish Shellfish Immunol 2: 79-88.). The special granulocytic cell are polymorphonuclear cells found in the blood mainly in parasitized fish or injected with inflammatory agents but their exact function is still unknown (Ranzani-Paiva 1996Ranzani-Paiva MJT. 1996. Células sanguíneas e contagem diferencial de leucócitos em Piratinga do Sul, Brycon sp., sob condições experimentais de criação intensiva. Rev Ceres 43: 685-696., Martins et al. 2000Martins ML, Moraes FR, Moraes JRE and Malheiros EB. 2000. Falha na resposta do cortisol estresse por captura e por carreginina em Piaractus mesopotamicus Holmberg (Osteichthyes, Characidae). Rev Bras Zool 12: 545-552.). The phagocytes described below play an important role in innate immune system modulation since they have phagocytosis ability with consequent pathogen destruction (Chettri et al. 2011Chettri JK, Raida MK, Andersen LH, Kania PW and Buchmann K. 2011. PAMP induced expression of immune relevant genes in head kidney leukocytes of rainbow trout (Oncorhynchus mykiss). Dev Comp Immunol 35: 476-482., Verlhac and Gabaudan 1997Verlhac V and Gabaudan J. 1997. The effect of vitamin C on Fish Health. Roche Technical Bulletin, Hoffmann-La Roche Ltd, Basel, Switzerland, 30 p.).
T and B lymphocytes are the adaptive immune system cells, however, there are distinct populations of lymphocyte called natural killers or T cytotoxic that have been classified as an innate immune compound and relies on the ability to destroy injured somatic cells (tumor or viruses infected cells) and produce immune modulation cytokines. (Tizard 2002Tizard IR. 2002. Imunologia Veterinária. Uma introdução. Editora Roca, São Paulo, 532 p., Raulet 2004Raulet DH. 2004. Interplay of natural killer cells and their receptors with the adaptive immune response. Nature Immunol 5: 996-1002.).
Some cells are able to trigger phagocytosis of invading particles, such as microorganisms, cells, cell debris and macromolecules aggregates, in order to destroy or present them to the specific system cells. Phagocytosis is initiated by the connection between the agent and the phagocyte receptor membrane (Neumann et al. 2001Neumann NF, Stafford JL, Barreda D, Ainsworth AJ and Belosevic M. 2001. Antimicrobial mechanisms of fish phagocytes and their role in host defense. Dev Comp Immunol 25: 807-825.). Monocytes, macrophages, dendritic cells and granulocytes are professional phagocytes that may be mobilized to the inflammation site by molecular signals of inflammation (cytokines) released by injured tissue (Stuart and Ezekowitz 2005Stuart LM and Ezekowitz RAB. 2005. Phagocytosis: elegant complexity. Immunity 22: 539-550.).
Neutrophils and macrophages destroy microorganisms through phagocytosis with hydrolytic enzymes and reactive oxygen species (ROS). The inflammatory tissue liberates chemotaxis factors that promote cell migration. Neutrophils are the first granulocytes to appear at the injured site, followed by macrophages. Neutrophils migrate from the bloodstream and macrophages are originated from blood monocytes. At the site of injury, these cells trigger the phagocytosis process, in order to destruct invading agents (Hanington et al. 2009Hanington PC, Tamb J, Katzenback BA, Hitchen SJ, Barreda DR and Belosevic M. 2009. Development of macrophages of cyprinid fish. Dev Comp Immunol 33: 411-429., Rowley 1996Rowley AF. 1996. The evolution of inflammatory mediators. Mediators of Inflammation 5: 3-13., Secombes 1996Secombes CJ. 1996. The nonspecific immune system: cellular defenses. In: IWAMA G and NAKANISHI T (Eds), The fish immune system. London: Academic Press, p. 95-103.).
During the phagocytosis there is increased oxygen consumption in a molecular mechanism known as leukocyte respiratory burst which result in oxygen reduction with superoxide anion production. The superoxide dismutase enzyme acts over the superoxide anion and generates hydrogen peroxide, in addition myeloperoxidase enzyme released by granular leukocytes react with hydrogen peroxide in order to produce hypochlorite that lead to the production of cloramins. All of these compounds are oxidative substances and can attack microorganism membranes (Verlhac and Gabaudan 1997Verlhac V and Gabaudan J. 1997. The effect of vitamin C on Fish Health. Roche Technical Bulletin, Hoffmann-La Roche Ltd, Basel, Switzerland, 30 p., Caipang et al. 2012Caipang CMA, Lazaro CC, Brinchmann MF and Kiron V. 2012. Transcription of selected immune-related genes in spleen cells of cod, Gadus morhua following incubation with alginic acid and β-glucan. J Exp Mar Biol Ecol 416-417: 202-207.).
The relationship between innate and acquired immune system is made by antigen-presenting cells (dendritic cells and macrophages) that after processing microorganism introduce the processed molecule to T lymphocytes with the help of major histocompatibility complex (MHC), class 2 receptors, thus initiating the acquired response cell mediated (Tizard 2002Tizard IR. 2002. Imunologia Veterinária. Uma introdução. Editora Roca, São Paulo, 532 p.). Histocompatibility molecules are glycoprotein receptors encoded by a gene complex, which are expressed in almost all organism cells. MHC plays an important role for endogenous and exogenous antigens recognition but lacks in specificity and may recognize several related antigens (Goldsby et al. 2002Goldsby RA, Kindt TJ, Osborne BA and Kuby J. 2002. In: Immunology, 5th ed., WH Freeman & Company Publisher, 554 p.).
On the other hand, antibodies are glycoproteins, known as well as immunoglobulins (Ig), expressed in the membrane of the B lymphocyte (BCR) or free in body fluids, secreted by plasma cells (B lymphocytes activated by antigen connection) (Goldsby et al. 2002Goldsby RA, Kindt TJ, Osborne BA and Kuby J. 2002. In: Immunology, 5th ed., WH Freeman & Company Publisher, 554 p.). The immunoglobulin IgM is a tetrameric protein with four sites for antigen recognition well known in fish. However, researchers have observed other immunoglobulins in some species of fish, such as the IgD (Wilson et al. 1997Wilson M, Bengte NE, Miller N, Clem LW, Du Pasquier L and Warr GW. 1997. A novel chimeric Ig heavy chain from a teleost fish shares similarities to IgD. Proc Natl Acad Sci USA 94: 4593-4597.), IgZ (Danilova et al. 2005Danilova N, Bussmann J, Jekosch K and Steiner LA. 2005. The immunoglobulin heavy-chain locus in zebrafish: identification and expression of a previously unknown isotype, immunoglobulin. Nature Immunol 6: 295-302.) and the IgT (Hansen et al. 2005Hansen JD, Landis ED and Phillips RB. 2005. Discovery of a unique Ig heavy-chain isotype (IgT) in rainbow trout: implications for a distinctive B cell developmental pathway in teleost fish. Proc Natl Acad Sci USA 102: 6919-6924.). Immunoglobulins can be found in the serum, body fluids, mucus, eggs and in the gastrointestinal mucosa (Davidson et al. 1993Davidson GA, Ellis AE and Secombes CJ. 1993. Route of immunization influences the generation of antibody secreting cells in the gut of rainbow trout (Oncorhynchus mykiss). Dev Comp Immunol 17: 373-376., Ellis 2001Ellis AE. 2001. Innate host defense mechanism of fish against virus and bacteria. Dev Comp Immunol 25: 827-839., Solem and Stenvik 2006Solem ST and Stenvik J. 2006. Antibody repertoire development in teleosts—a review with emphasis on salmonids and Gadus morhua L. Dev Comp Immunol 30: 57-76.).
The antibodies may develop several roles such as anti-adhesin function which mainly occurs in the epithelium of digestive system surface (Davidson et al. 1993Davidson GA, Ellis AE and Secombes CJ. 1993. Route of immunization influences the generation of antibody secreting cells in the gut of rainbow trout (Oncorhynchus mykiss). Dev Comp Immunol 17: 373-376.), gills (Davidson et al. 1997Davidson GA, Lin SH, Secombes CJ and Ellis AE. 1997. Detection of specific and constitutive antibody secreting cells in the gills, head kidney and peripheral blood leucocytes of dab (Limanda limanda). Vete Immunology Immunopath 58: 363-374., Joosten et al. 1997Joosten PHM, Tiemersma E, Threels A, Caumartin-Dhieux C and Rombout JHWM. 1997. Oral vaccination of fish against Vibrio anguillarum using alginate microparticles. Fish Shellfish Immunol 7: 471-485.) and skin (Rombout et al. 1993Rombout JHWM, Taverne N, Van De Kamp M and Taverne-Thiele AJ. 1993. Differences in mucus and serum immunoglobulin of carp (Cyprinus carpio L.). Dev Comp Immunol 17: 309-317.) so that these antibodies prevent bacteria adherence (Ellis 2001Ellis AE. 2001. Innate host defense mechanism of fish against virus and bacteria. Dev Comp Immunol 25: 827-839.). Antitoxins antibodies neutralize toxins produced by countless bacteria (Gudmundsdottir and Magnadottir 1997Gudmundsdottir B and Magnadottir B. 1997. Protection of Atlantic salmon (Salmo salar L.) against an experimental infection of Aeromonas salmonicida ssp. achromogenes. Fish Shellfish Immunol 7: 55-69.). Anti-invasins antibodies avoid bacteria infiltration into unprotected cells (Magarinos et al. 1996Magarinos B, Romalde JL, Noya M, Barja JL and Toranzo AE. 1996. Adherence and invasive capacities of the fish pathogen Pasteurella piscicida. FEMS Microbio Let 138: 29-34.).
Regarding specific immune response, once antigen have been recognized by immunoglobulins receptor of B lymphocyte, it will stimulate endocytosis and proliferation of memory B cells, which activate T lymphocytes, resulting in cytokines release and triggering of B cells, macrophages, among others cells (Tizard 2002Tizard IR. 2002. Imunologia Veterinária. Uma introdução. Editora Roca, São Paulo, 532 p.). The serum antibodies concentration may differ according to species, age, sexual maturity and physiological events (natural or artificial incident – as smoltification, cortisol boost, etc) and may be increased by artificial immunization or due to chronic infection (Miller et al. 1985Miller NW, Sizemore RC and Clem LW. 1985. Phylogeny of lymphocyte heterogeneity: the cellular requirements for in vitro antibody responses of channel catfish leukocytes. J Immunol 134: 2884-2888., White et al. 1985White MB, Shen AL, Word CJ, Tucker PW and Blattner FR. 1985. Human immunoglobulin D: genomic sequence of the delta heavy chain. Science 228: 733-737., Hordvik et al. 1992Hordvik I, Voie AM, Glette J, Male R and Endresen C. 1992. Cloning and sequence analysis of two isotypic IgM heavy chain genes from Atlantic salmon, Salmon salar L. Eur J Immunol 22: 2957-2962., van Ginkel et al. 1994, Wilson et al. 1997Wilson M, Bengte NE, Miller N, Clem LW, Du Pasquier L and Warr GW. 1997. A novel chimeric Ig heavy chain from a teleost fish shares similarities to IgD. Proc Natl Acad Sci USA 94: 4593-4597., Rycyzyn et al. 1996Rycyzyn MA, Wilson MR, Warr GW, Clem LW and Miller NW. 1996. Membrane immunoglobulin-associated molecules on channel catfish B lymphocytes. Dev Comp Immunol 20: 341-351., Wilson et al. 1997Wilson M, Bengte NE, Miller N, Clem LW, Du Pasquier L and Warr GW. 1997. A novel chimeric Ig heavy chain from a teleost fish shares similarities to IgD. Proc Natl Acad Sci USA 94: 4593-4597., Zhao et al. 2002Zhao Y, Kacskovics I, Pan Q, Liberles DA, Geli J and Davis SK. 2002. Artiodactyl IgD: the missing link. J Immunol 169: 4408-4416.).
The Modification and Manipulation of the Innate Immune System
Immunostimulants and prebiotics
In Brazil, intensive aquaculture has lead to outbreaks of diseases with substantial damage in production and economic losses (Biller et al. 2013). The misuse of antibiotics in order to reduce diseases has lead to unsatisfactory results, since the prevention and health restore after any chemical uses depends on the appropriate administration and interaction with pathogens. In an attempt to prevent or ban the excessive use of antibiotics and consequent bacterial resistance, several studies have evaluated an alternative to antibiotics administration, such as immunostimulants, probiotics and prebiotics to prevent and control diseases (Verschuere et al. 2000Verschuere L, Heang H, Criel G, Sorgeloos P and Verstraete W. 2000. Selected bacterial strains protect Artemia spp. from the pathogenic effects of Vibrio proteolyticus CW8T2. Appl Environ Microbiol 66: 1139-1146., Nayak 2010Nayak SK. 2010. Probiotics and immunity: A fish perspective. Fish Shellfish Immunol 29: 2-14., Nikoskelainen et al. 2001Nikoskelainen S, Salminen S, Bylund G and Ouwehand AC. 2001. Characterization of the properties of human and dairy-derived probiotics for prevention of infectious diseases in fish. Appl Environ Microbiol 67: 2430-2435.).
Among them, there are synthetic chemicals (levamisole, FK-565 – isolated from Streptomyces olivaceogriseus cultures), biological substances (bacteria derivates, polysaccharides, animal and plant extract), nutritional factors (C and E vitamins), hormones (prolactin and growth hormone) and cytokines (polypeptides and glycoprotein). These immunostimulants, synthetic or biological extracts enhance the immune system by increasing cellular and humoral production (Raa 1996Raa J. 1996. The use of immunostimulatory substances in fish and shellfish farming. Rev Fish Biol Fisheries 4: 229-288., Sakai 1999Sakai M. 1999. Current research status of fish immunostimulants. Aquaculture 172: 63-92., Fujimoto et al. 2013Fujimoto RY, Santos RFB and Carneiro DJ. 2013. Morphological deformities in the osseous structure in spotted sorubim Pseudoplatystoma coruscans (Agassiz & Spix, 1829) with vitamin c deficiency. An Acad Bras Cienc 85: 379-384., Sinha et al. 2011Sinha AK, Kumar V, Makkar HPS, Boeck G and Becker K. 2011. Non-starch polysaccharides and their role en fish nutrition – A review. Food Chem 127: 1409-1426., Sado et al. 2013Sado RY, Bicudo AJA and Cyrino JEP. 2013. Growth and hematology of juvenile pacu Piaractus mesopotamicus (Holmberg 1887) fed with increasing levels of vitamin E (DL-α-tocopheryl acetate). An Acad Bras Cienc 85: 385-393.).
Among the immunostimulants, β-glucan has been defined as a linear polyglucose chain derived from yeast, fungi or fungal mycelium that has demonstrated immune modulation function with anti-tumor, anti-microbial, anti-viral and anti-parasite properties (Caipang et al. 2012Caipang CMA, Lazaro CC, Brinchmann MF and Kiron V. 2012. Transcription of selected immune-related genes in spleen cells of cod, Gadus morhua following incubation with alginic acid and β-glucan. J Exp Mar Biol Ecol 416-417: 202-207., Wasser and Weis 1999Wasser SP and Weis AL. 1999. Therapeutic effects of substances occurring in higher basidiomycetes mushrooms: A modern perspective. Critic Rev Immunol 19: 65-96.). β-glucan with a structure composed of glucose units connected by β 1-3 links and lateral chains by β 1-6 links facilitated the stimulation of mammal and fish innate immune system. β-glucan has activated several functions such as hematopoiesis, lytic proteins production such as lysozyme and complement system protein in addition to promoting phagocytosis activity (Caipang et al. 2012Caipang CMA, Lazaro CC, Brinchmann MF and Kiron V. 2012. Transcription of selected immune-related genes in spleen cells of cod, Gadus morhua following incubation with alginic acid and β-glucan. J Exp Mar Biol Ecol 416-417: 202-207., Di-Luzio 1985Di-Luzio NR. 1985. Update on the immunomodulating activities of glucans. Springer Semin Immun 8: 387-400., Kiron 2012, Ortuno et al. 2001).
Macrophages play an important role in specific immune response because of the phagocytosis and lymphocyte activation. Macrophages also have specific receptors able to recognize β-glucan so that the immunostimulants increase leukocytes respiratory burst which releases reactive oxygen species, most of them with bactericidal activity (Caipang et al. 2012Caipang CMA, Lazaro CC, Brinchmann MF and Kiron V. 2012. Transcription of selected immune-related genes in spleen cells of cod, Gadus morhua following incubation with alginic acid and β-glucan. J Exp Mar Biol Ecol 416-417: 202-207., Secombes and Fletcher 1992Secombes CJ and Fletcher TC. 1992. The role of phagocytes in the protective mechanisms of fish. A Rev Fish Dis 2: 53-71.). According to Lin et al. (2012) β-glucan feed inclusion has enhanced growth, survival and immune response of Cyprinus carpio. Anderson (1992)Anderson DP. 1992. Immunostimulants, adjuvants and vaccine carriers in fish: applications to aquaculture. Ann Rev Fish Dis 20: 281-307., Sahoo and Mukherjee (1999)Sahoo PK and Mukherjee SC. 1999. Immunostimulants in aquaculture. In: MOHAPATRA BC, INGOLE PG and BHARAD GM (Eds), Aquaculture with Special Reference to Vidarbha, Maharasthra State, India. Akola, p. 282-293. and Sakai (1999)Sakai M. 1999. Current research status of fish immunostimulants. Aquaculture 172: 63-92. have reported healthy improvement, including increased specific and innate immunity parameters, even after stressor, resulting in protection against pathogen. However, factors such as pathway, dosage and period of immunostimulant administration and species of fish may compromise its efficiency. Regarding the pathway, injection is considered more efficient, yet more invasive, consequently the oral pathway, mainly supplemented in food is the standard process chosen (Raa et al. 1992Raa J, Rostad G, Engstad R and Robertson B. 1992. The use of immunostimulants to increase resistance of aquatic organisms to microbial infections. In: SHARIFF M, SUBASINGHE RP and ARTHUR JR (Eds), Diseases in Asian Aquaculture. Manila: Fish Health Section. Asian Fisheries Society, p. 3-50., Duncan and Klesius 1996Duncan PL and Klesius PH. 1996. Dietary immunostimulants enhanced non-specific immune response in channel catfish but not resistance to Edwardsiella ictaluri. J Aquat An Health 8: 1-7., Sakai 1999Sakai M. 1999. Current research status of fish immunostimulants. Aquaculture 172: 63-92., Gannam and Schrock 2001Gannam AL and Schrock RM. 2001. Immunostimulants in fish diets. In: LIM C and WEBSTER CD (Eds), Nutrition and fish health. Binghamton: The Haworth Press Inc., p. 235-266., Lin et al. 2011Lin S, Pan Y, Luo L and Luo L. 2011. Effects of dietary b-1,3-glucan, chitosan or raffinose on the growth, innate immunity and resistance of koi (Cyprinus carpio koi). Fish Shellfish Immunol 31: 788-794.)
The mannan oligosaccharide (MOS) is an oligosaccharide characterized as a carbohydrate complex derived from glucomannan proteins of yeast wall (Abraham and Beachey 1985Abraham SN and Beachey EH. 1985. Host Defense Mechanisms. In: Gallin and Fauci (Eds), 1st ed., Raven Press, New York, USA, 284 p.). Other oligosaccharides have been used as prebiotics, such as xylo oligosaccharide (XOS), fructo oligosaccharide (FOS), galacto oligosaccharide (GOS), transgalactosylated oligosaccharides (TOS) and inulin. MOS is a component of yeast wall found in the external section, corresponding to approximately 40% of this cellular structure (Hough 1990Hough JS. 1990. Biotecnologia de la cerveza y de malta. Zaragoza: Acribia, 98 p.). Over the last few years several researchers have noted its ability to promote better growth rate, prevent colonization of pathogenic bacteria in the gastrointestinal tract and increase survival rates in a wide variety of species. The results of MOS on growth, systemic immunity and gut mucosa are considered sufficient to avoid the costs of curative measures besides decrease the microbiological problem of the misuse of antibiotics (Newman 1994Newman K. 1994. Mannan-oligosaccharides: natural polymers with significant impact on the gastrointestinal microflora and the immune system. In: Lyons TP and Jacques KA (Eds), Biotechnology in the feed industry. Proceedings of Alltech's tenth annual symposium. NottinghamUniversity Press, Nottingham, UK, p. 167-174., Devegowda et al. 1997Devegowda G, Aravind BIR and Morton MG. 1997. Immunosupression in poultry caused by aflatoxins and its alleviation by Saccaromyces cerevisiae and mannanoligosaccharides. In: Lyons TP and Jacques KA (Eds), Biotechnology in the feed industry. Proceedings of Alltech's thirteenth annual symposium. Nottingham University Press, Nottingham, UK, p. 205-215., Spring 1999Spring P. 1999. The move away from antibiotic growth promoters in Europe. In: Lyons TP and Jacques KA (Eds), Biotechnology in the feed industry. Proceedings of Alltech's fifteenth annual symposium. Nottingham University Press, Nottingham, UK, p 173-183., Spring et al. 2000Spring P, Wenk C, Dawson KA and Newman KE. 2000. The effects of dietary mannanoligosaccharides on cecal parameters and the concentrations of enteric bacteria in the ceca of salmonella-challenged broiler chicks. Poult Sci 79: 205-211., Liu et al. 2013Liu B, Xu L, Ge X, Xie J, Xu P, Zhou Q, Pan L and Zhang YY. 2013. Effects of mannan oligosaccharide on the physiological responses, HSP70 gene expression and disease resistance of Allogynogenetic crucian carp (Carassius auratus gibelio) under Aeromonas hydrophila infection. Fish Shellfish Immunol 34: 1395-1403.).
MOS is defined as a prebiotic because it is a nondigestible food ingredient which positively influences the host organism by stimulating growth and activity of one or more bacteria in gut, promoting growth, nutrient utilization and health improvement (Gibson and Roberfroid 1995Gibson GR and Roberfroid MB. 1995. Dietary modulation of the human colonic microbiota: Introducing the concept of prebiotics. J Nutr 125: 1401-1412.).
The MOS is a mannose source that has high affinity for gram-negative bacteria. Once bacteria connect to MOS complex, it prevents the colonization of gastrointestinal tract and decrease outbreaks of diseases and the toxins effects, resulting in intact gut with maximum capacity of nutrients absorption and modulation of gut immunity (Ballou 1977Ballou CE. 1977. A study of the immunochemistry of three yeast mannans. J Biol Chem 245: 1197-1203., Spring 2000, Ferket et al. 2002Ferket PR, Parks CW and Grimes JL. 2002. Mannan oligosaccharides versus antibiotics for turkeys. In: Alltech's eighteenth annual symposium, Nottingham. Nutritional biotechnology in the feed and food industry: proceedings… Nottingham: Nottingham University Press, p. 43-63.).
Brazilian Studies
In Brazil, there is a lack of studies on the manipulation of fish innate immune system, however some groups have already evaluated some growth performance and immunology parameters after the application of immunostimulants and prebiotics.
Abreu (2007)Abreu JS. 2007. Suplementação alimentar de pacu (Piaractus mesopotamicus Holmberg, 1887) com β 1,3 glicano: atividade respiratória de leucócitos, lisozima e estresse por captura. Tese de Doutorado,– Centro de Aqüicultura, Universidade Estadual Paulista, Jaboticabal. has assessed the effects of β-glucan on innate immunity and in prevention of stress responses in Pacu (Piaractus mesopotamicus), and the author has concluded that 100 µg of β-glucan per 100 g body weight injection (Macrogard®), or 0.5% β-glucan in food can stimulate components of the pacu innate immune system. Furthermore, Biller (2008)Biller JD. 2008. Respostas fisio-patológicas e desafio por Aeromonas hydrophila em pacu alimentado com ração suplementada com 1,3 β-glucano. Dissertação de Mestrado. Universidade Estadual Paulista, Jaboticabal. (Unpublished). has evaluated the physiological and immunological effects of β-glucan (Macrogard®) in pacu challenged by Aeromonas hydrophila. The β-glucan administration has shown immunity stimulation and decreased mortality from opportunistic pathogens, promoting increased survival in the treated groups, in addition to increasing the immunological parameters such as the number of white blood cells, leucocytes respiratory burst activity, lyzosyme and complement system.
Schorer (2008)Schorer M. 2008. Utilização do β-glucano sobre o desempenho produtivo, indicadores de estresse, perfil hematológico e sobrevivência de pacu (Piaractus mesopotamicus). Dissertação de Mestrado, Centro de Aqüicultura, Universidade Estadual Paulista, Jaboticabal. (Unpublished). has observed pacu fed β-glucan in order to evaluate growth performance, stress indicators, blood profile and survival. Pacu supplied with 0.3% of β-glucan per kg/diet presented greater weight gain, specific growth rate and final weight. In addition 0.1% of β-glucan per kg/diet has led to increased survival after bacterial challenge, as well as the influence on physiopathologic and stress indicators. Conversely, Sado (2008)Sado RY. 2008. Imunoestimulantes dietéticos e respostas biológicas, bioquímicas e hematológicas de juvenis de Piaractus mesopotamicus (Holmberg, 1887). Tese de Doutorado, Universidade de São Paulo. has utilized mannan oligossacharide and β-glucan supplement (Active-MOS ®) during 60 days in order to assess biological, haematological and biochemical responses of juvenile pacu, and found changes in growth performance, hematology and intestinal morphology of treated fish.
Chagas (2010)Chagas EC. 2010. β-glucano e nucleotídeos para tambaquis (Colossoma macropomum) vacinados e desafiados com Aeromonas hydrophila: desempenho produtivo e respostas fisiopatológicas. Tese de Doutorado. Centro de Aquicultura, Universidade Estadual Paulista, Jaboticabal. has observed the productive performance and physiopathologic responses of tambaqui (Colossoma macropomum) fed with β-glucan (Macrogard®) and nucleotides (Biotide®) after Aeromonas hydrophila vaccination and challenge and has concluded that the 0.1% of immunostimulant administration increased the resistance against bacterial infection, with survival of 95 to 100% in the treated groups.
Sousa (2010)Sousa ADL. 2010. Mananoligossacarídeo e β-glucano na suplementação dietária para juvenis de tilápia do Nilo mantidos em tanques-rede. Tese de Doutorado, Centro de Aquicultura, Universidade Estadual Paulista, Jaboticabal. has assessed the feed supplementation with 0.1% mannan oligossacharide (Active-MOS®) and 0.03% of β-glucan (Macrogard®) for up to 90 days for tilapia in cage. The author found that these compounds promoted improvement on immune system and gut, with increased enzymatic activity and nutrients absorption mainly in β-glucan treated groups. Garcia (2008)Garcia F. 2008. Suplementação alimentar com β-glucano e mananoligossacarídeo para tilápias do Nilo em tanquesrede. Tese de Doutorado, Centro de Aquicultura, Universidade Estadual Paulista, Jaboticabal. has evaluated the homogeneity, growth performance, intestinal structures morphology and the efficiency of food supplementation with 0, 500, 1000 e 2000 mg per kg/diet of mannan oligossacharide and β-glucan supplement (Active-MOS®) in Nile tilapia. Best results were found after administration of 500 mg/kg in the diet of the compound during at least 37 days for cage production due to its improvement in protein utilization and greater integrity of the intestinal surface than the control group. In addition Falcon (2007)Falcon DR. 2007. β-glucano e vitamina C no desempenho produtivo e parâmetros fisiopatológicos em juvenil de tilápia do Nilo: nível de suplementação e tempo de administração. Tese de Doutorado, Centro de Aqüicultura, Universidade Estadual Paulista, Jaboticabal. has also tested the administration of β-glucan (Macrogard®) for tilapia and determined the best concentration and period of time in order to promote immune stimulation in this species. In his study growth performance, hematologic and immune responses of fish were assessed, and revealed that 0.1% of β-glucan and 600 mg/kg vitamin C in diet for at least 15 days promoted better responses after cold temperature and A. hydrophila challenge.
CONCLUSIONS
The knowledge of the structure and function of Brazilian fish immune system is essential for promoting the aquaculture as an economic activity, since the intensification of production often leads to immune suppression, disease outbreak and even death. However, once knowing the immune system, there is a possibility of promoting appropriate stimuli, such as immunostimulants and prebiotcs administration in order to prevent losses during critical periods of cultivation and to avoid the misuse of antibiotics. The study on the modification and manipulation of the innate immune system in Brazil is scarce but this area of knowledge is in successful development because it is crucial for the expansion of Brazilian sustainable aquaculture.
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Publication Dates
-
Publication in this collection
Sept 2014
History
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Received
22 Apr 2013 -
Accepted
9 Sept 2013