Abstract:A few studies have illustrated the effects of sodium salt derived from alginic acid on different fish species. However, little is known about the effect of sodium alginate on catfish (Clarias gariepinus). Therefore, this study was performed to assess the use of low molecular weight sodium alginate (LMWSA) in C. gariepinus. A total of 180 apparently healthy C. gariepinus with a mean body weight of 45 g were randomly divided into three equal groups (D1, D2 and D3). D1 the control group received a control diet, w… Show more
“…Recently, the use of natural ingredients as immunomodulators for enhancing resistance and immunity in various live organisms has been proposed (Abdallah, Nasr El‐Deen, Neamat‐Allah, & Abd El‐Aziz, ; Badr et al, ; Hashem, Neamat‐Allah, Hammza, & Abou‐Elnaga, ; Neamat‐Allah, El‐Murr, & Abd El‐Hakim, ; Neamat‐Allah, Mahmoud, & Abd El Hakim, ; Prasanna, Ashraf, & Essam, ). β‐glucan (βG) is known as natural immunomodulator.…”
Three hundred Oreochromis niloticus were divided into five groups; the control fish (CNT) were fed a basal diet, beta glucan (βG) group was fed 0.5 g/kg−1 βG, atrazine (ATZ) group was exposed to 1/5 96‐hr LC50 (1.39 mg/L) ATZ, the (βG/ATZ) group was fed βG while being exposed to ATZ, and the (βG then ATZ) group was supplemented with βG for fifteen days before exposed to ATZ. ATZ exposure caused a decline in growth that was ameliorated by βG. ATZ reduced the levels of total and different types of leucocytes. Additionally, ATZ exposure caused reductions in total proteins, globulins, α 1‐globulin, α 2‐globulin, ɤ‐globulin, immunoglobulin M, lysozymes, superoxide dismutase, nitric oxide and catalase but increases in hepatic transaminases and malondialdehyde without any variations in albumin and β‐globulin. Exposure to ATZ also resulted in a rise in the mRNA level of IL‐8. In contrast, expression of IgM, SOD and CAT were decreased in the tilapias exposed to ATZ. Exposure to ATZ increases the susceptibility response to Aeromonas sobria challenge, as indicated by an increase in cumulative mortality post‐challenge. Supplementation with βG fifteen days before (βG then ATZ group), counteracted the adverse effects of ATZ on the immune, biochemical and antioxidants values, though only slight alleviation was observed with simultaneous treatment (βG/ATZ group). Our results established that ATZ has adverse impacts on immune responses, antioxidant equilibrium and its related genes. While, supplementation with βG before exposure to ATZ may be valuable for counteracting the possible damage caused by ATZ water pollution than its simultaneous treatment with ATZ.
“…Recently, the use of natural ingredients as immunomodulators for enhancing resistance and immunity in various live organisms has been proposed (Abdallah, Nasr El‐Deen, Neamat‐Allah, & Abd El‐Aziz, ; Badr et al, ; Hashem, Neamat‐Allah, Hammza, & Abou‐Elnaga, ; Neamat‐Allah, El‐Murr, & Abd El‐Hakim, ; Neamat‐Allah, Mahmoud, & Abd El Hakim, ; Prasanna, Ashraf, & Essam, ). β‐glucan (βG) is known as natural immunomodulator.…”
Three hundred Oreochromis niloticus were divided into five groups; the control fish (CNT) were fed a basal diet, beta glucan (βG) group was fed 0.5 g/kg−1 βG, atrazine (ATZ) group was exposed to 1/5 96‐hr LC50 (1.39 mg/L) ATZ, the (βG/ATZ) group was fed βG while being exposed to ATZ, and the (βG then ATZ) group was supplemented with βG for fifteen days before exposed to ATZ. ATZ exposure caused a decline in growth that was ameliorated by βG. ATZ reduced the levels of total and different types of leucocytes. Additionally, ATZ exposure caused reductions in total proteins, globulins, α 1‐globulin, α 2‐globulin, ɤ‐globulin, immunoglobulin M, lysozymes, superoxide dismutase, nitric oxide and catalase but increases in hepatic transaminases and malondialdehyde without any variations in albumin and β‐globulin. Exposure to ATZ also resulted in a rise in the mRNA level of IL‐8. In contrast, expression of IgM, SOD and CAT were decreased in the tilapias exposed to ATZ. Exposure to ATZ increases the susceptibility response to Aeromonas sobria challenge, as indicated by an increase in cumulative mortality post‐challenge. Supplementation with βG fifteen days before (βG then ATZ group), counteracted the adverse effects of ATZ on the immune, biochemical and antioxidants values, though only slight alleviation was observed with simultaneous treatment (βG/ATZ group). Our results established that ATZ has adverse impacts on immune responses, antioxidant equilibrium and its related genes. While, supplementation with βG before exposure to ATZ may be valuable for counteracting the possible damage caused by ATZ water pollution than its simultaneous treatment with ATZ.
“…niloticus fed with Se nanoparticles demonstrated significantly enhanced lysozyme activity (Dawood et al, 2020). Several other reports indicate immunomodulatory effects of Se nanoparticles as functional supplements in fish diets (Naderi et al, 2019; Neamat‐Allah et al, 2019b, 2019a). Immunostimulants can increase non‐specific immunity by either enhancing/activating phagocytes or increasing the synthesis of molecules involved in the innate immunity such as the complement lysozyme antiprotease.…”
Section: Discussionmentioning
confidence: 93%
“…Immunostimulants are considered as an alternative for antibiotics, which will boost the immune system of the cultured organism, thus effectively countering the assault of pathogens. The use of medicinal plants/natural ingredients (whole plant, roots and leaves) and/or their extracts has been proposed as valuable feed additives to boost fish immunity and an eco‐friendly approach for the control of pathogens (Abdallah et al, 2020; Abdel‐Latif et al, 2020; Ayoub et al, 2019; Badr et al, 2011; Hashem et al, 2019; Neamat‐Allah et al, 2019b, 2019a; Prasanna et al, 2017; Yousefi et al, 2019).…”
Nile tilapia is a cornerstone of fish farming in Egypt, which is the largest aquaculture producer in Africa. With 900,000 tons of tilapia harvested annually, the country has risen to become the seventh aquaculture producer in the world (Feidi, 2018). The progress of this fast-growing industry is impeded by many challenges such as poor water quality and associated bacterial infections (El-Gohary et al., 2020). As a result, the use of antibiotics in the aquafeeds to mitigate infectious diseases or to boost growth performance is commonly practised. The prophylactic use of antibiotics and chemotherapies, however, has been scrutinized which eventually led to their ban in aquaculture by law in many countries (Dawood et al., 2018). In the context of the banning and restrictions of antibiotic use, the need to establish new ways of potentiation of immune reaction in fish is clear. Immunostimulants are considered as an alternative for antibiotics, which will boost the immune system of the cultured organism, thus effectively countering the assault of pathogens. The use of medicinal plants/natural ingredients (whole plant, roots and leaves) and/or their extracts has been proposed as valuable feed additives to boost fish immunity and an eco-friendly approach for the control of pathogens (
“…The seaweeds or seaweed form (e.g. sodium alginate; refined seaweed product) that was tested was often already known to have immunostimulatory action or another specific bioactivity on fish based on previous trials (Fujiki et al 1994; Cheng et al 2012; Neamat‐Allah et al 2019). Given the tremendous diversity and global distribution of seaweeds, and their widespread production of bioactive compounds (most of which are likely still undiscovered; Holdt & Kraan 2011), there is a need to investigate more seaweed species and/or more bioactive extracts.…”
Disease is an enduring threat to aquaculture, with direct costs from outbreaks of more than US$6 billion a year. Efforts to reduce antibiotic use in aquaculture have resulted in a recent shift towards the use of immunostimulants that boost fish immune systems. Seaweeds are a potential source of unique immunostimulants because of their diverse taxonomy (11,353 species) and diverse bioactives, but there has been no synthesis of their effects on fish. A systematic review and meta‐analysis of 142 peer‐reviewed studies was conducted to evaluate the effects of seaweed on the innate immunity, resistance (to stress and pathogens) and growth of farmed fish. Overall, our review indicated that dietary supplementation with seaweeds or their extracts had substantial positive impacts on the health and growth of fish compared with control groups and were comparable to currently utilised immunostimulants. Dramatic effects on survival of fish during challenge experiments were detected, with an average of 33% higher survival of fish fed diets that included seaweeds or their extracts. This study provides broad evidence for the benefits of supplementing fish feed with the reviewed seaweeds or their bioactive extracts, including potential synergistic effects of supplements. However, the meta‐analysis also highlighted considerable variation among studies, and between fish and seaweed species, making it difficult to extrapolate results beyond individual experiments. Future studies should focus on developing synergistic combinations of ingredients and elucidating the mode of action through isolation of seaweed bioactives, together with standardisation of experimental conditions, to fast‐track the benefits of seaweed supplements for aquaculture.
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