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      Effect of parenteral endotoxin administration on the immuno-haematological responses of catfish , Heteropneustes fossilis

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          Highlights

          • Stinging catfish Heteropneustes fossilis were found to resist endotoxin up to 0.1mg.

          • Endotoxin at 0.05mg per fish enhanced some of the non-specific immune responses while at low dose (0.01mg per fish) failed to stimulate immune responses.

          • Endotoxin at 0.05mg immunostimulatory while at 0.1 mg immunosuppressive for stinging catfish Heteropneustes fossilis.

          • Endotoxin at 0.05mg per fish was found to protect stinging catfish from Aeromonas hydrophila challenge.

          Abstract

          Endotoxin, the outer cell wall membrane lipopolysaccharide component of the Gram-negative bacteria is a factor responsible for a number of complications/disorders and plays important role in the associated with pathophysiological complications and pathogenesis of many diseases in animals. Unlike higher animals which are extremely sensitive to endotoxin, fish are found to be resistant to endotoxic shock and earlier studies though limited have demonstrated the patho-physiological, immuno-endocrinological and immuno-neurological effects of LPS/endotoxin in aquatic animals including fish. Herein in the present investigation, the effect of pure endotoxin on immuno-haematological parameters of stinging catfish , Heteropneustes fossilis ranging from 50–60 g was studied by intraperitoneally injecting 0.1, 0.05 and 0.01 mg endotoxin per fish. H. fossilis yearlings were found to resist the endotoxin concentration up to 0.1 mg without any mortality. While, no change in immune parameters was recorded in stinging catfish injected with low dose of endotoxin (0.01 mg), most of the immune parameters were found to be significantly elevated in catfish injected with 0.05 mg endotoxin. Different serum and immune parameters like protein, globulin, lysozyme, respiratory burst activity, myeloperoxidase activity, natural agglutination titre were found to be significantly high (p < 0.01) at a dose of 0.05 mg endotoxin per fish. On the contrary, most of these parameters were decreased at high dose i.e., 0.1 mg endotoxin per fish, thereby indicating the immuno-suppressive effect of the endotoxin. The findings of the modulation of innate immunity also corroborated with the results of Aeromonas hydrophila pathogen challenge study with highest percent of mortality in group injected with 0.1 mg endotoxin per fish and least percentage in group injected with 0.05 mg endotoxin per fish.

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          Most cited references62

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          Lipopolysaccharide endotoxins.

          Bacterial lipopolysaccharides (LPS) typically consist of a hydrophobic domain known as lipid A (or endotoxin), a nonrepeating "core" oligosaccharide, and a distal polysaccharide (or O-antigen). Recent genomic data have facilitated study of LPS assembly in diverse Gram-negative bacteria, many of which are human or plant pathogens, and have established the importance of lateral gene transfer in generating structural diversity of O-antigens. Many enzymes of lipid A biosynthesis like LpxC have been validated as targets for development of new antibiotics. Key genes for lipid A biosynthesis have unexpectedly also been found in higher plants, indicating that eukaryotic lipid A-like molecules may exist. Most significant has been the identification of the plasma membrane protein TLR4 as the lipid A signaling receptor of animal cells. TLR4 belongs to a family of innate immunity receptors that possess a large extracellular domain of leucine-rich repeats, a single trans-membrane segment, and a smaller cytoplasmic signaling region that engages the adaptor protein MyD88. The expanding knowledge of TLR4 specificity and its downstream signaling pathways should provide new opportunities for blocking inflammation associated with infection.
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            Recognition of pathogen-associated molecular patterns by TLR family.

            Toll-like receptors (TLRs) are type I transmembrane proteins involved in innate immunity by recognizing microbial conserved structures. Recent studies have shown that TLR3 recognizes dsRNA, a viral product, whereas TLR9 recognizes unmethylated CpG motifs frequently found in the genome of bacteria and viruses, but not vertebrates. TLR7 recognizes small synthetic immune modifiers including imiquimod, R-848, loxoribine, and bropirimine, all of which are already applied or promising for clinical use against viral infections and cancers. Plasmacytoid dendritic cells express TLR7 and TLR9, and respond to TLR7 and TLR9 ligands by producing a large amount of interferon (IFN-alpha). These results indicate that TLR3, TLR7 and TLR9 may play an important role in detecting and combating viral infections.
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              Bacterial lipopolysaccharides and innate immunity.

              Bacterial lipopolysaccharides (LPS) are the major outer surface membrane components present in almost all Gram-negative bacteria and act as extremely strong stimulators of innate or natural immunity in diverse eukaryotic species ranging from insects to humans. LPS consist of a poly- or oligosaccharide region that is anchored in the outer bacterial membrane by a specific carbohydrate lipid moiety termed lipid A. The lipid A component is the primary immunostimulatory centre of LPS. With respect to immunoactivation in mammalian systems, the classical group of strongly agonistic (highly endotoxic) forms of LPS has been shown to be comprised of a rather similar set of lipid A types. In addition, several natural or derivatised lipid A structures have been identified that display comparatively low or even no immunostimulation for a given mammalian species. Some members of the latter more heterogeneous group are capable of antagonizing the effects of strongly stimulatory LPS/lipid A forms. Agonistic forms of LPS or lipid A trigger numerous physiological immunostimulatory effects in mammalian organisms, but--in higher doses--can also lead to pathological reactions such as the induction of septic shock. Cells of the myeloid lineage have been shown to be the primary cellular sensors for LPS in the mammalian immune system. During the past decade, enormous progress has been obtained in the elucidation of the central LPS/lipid A recognition and signaling system in mammalian phagocytes. According to the current model, the specific cellular recognition of agonistic LPS/lipid A is initialized by the combined extracellular actions of LPS binding protein (LBP), the membrane-bound or soluble forms of CD14 and the newly identified Toll-like receptor 4 (TLR4)*MD-2 complex, leading to the rapid activation of an intracellular signaling network that is highly homologous to the signaling systems of IL-1 and IL-18. The elucidation of structure-activity correlations in LPS and lipid A has not only contributed to a molecular understanding of both immunostimulatory and toxic septic processes, but has also re-animated the development of new pharmacological and immunostimulatory strategies for the prevention and therapy of infectious and malignant diseases.
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                Author and article information

                Contributors
                Journal
                Fish Shellfish Immunol Rep
                Fish Shellfish Immunol Rep
                Fish and Shellfish Immunology Reports
                Elsevier
                2667-0119
                29 August 2021
                December 2021
                29 August 2021
                : 2
                : 100022
                Affiliations
                [0001]Department of Biotechnology, Maharaja Sriram Chandra Bhanja Deo University, (Erstwhile North Orissa University), Mayurbhanj, Baripada, Odisha 757003, India
                Author notes
                [* ]Corresponding author. sukantanayak@ 123456rediffmail.com
                Article
                S2667-0119(21)00017-7 100022
                10.1016/j.fsirep.2021.100022
                9680051
                36420485
                8c023c20-b732-48df-9527-07dc8bf2d59d
                © 2021 The Authors. Published by Elsevier Ltd.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 9 July 2021
                : 10 August 2021
                : 27 August 2021
                Categories
                Article

                endotoxin,lipopolysachharide,heteropneustes fossilis,immunity,haematology

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