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Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis

Both in vitro and in vivo studies were conducted to evaluate the beneficial effects of green tea extract (GT), cinnamon oil (CO), and pomegranate extract (PO) on avian coccidiosis. In experiment (EXP) 1, an in vitro culture system was used to investigate the individual effects of GT, CO, and PO on t...

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Autores principales: Park, Inkyung, Nam, Hyoyoun, Wickramasuriya, Samiru S., Lee, Youngsub, Wall, Emma H., Ravichandran, Sripathy, Lillehoj, Hyun S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272459/
https://www.ncbi.nlm.nih.gov/pubmed/37334385
http://dx.doi.org/10.3389/fimmu.2023.1145367
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author Park, Inkyung
Nam, Hyoyoun
Wickramasuriya, Samiru S.
Lee, Youngsub
Wall, Emma H.
Ravichandran, Sripathy
Lillehoj, Hyun S.
author_facet Park, Inkyung
Nam, Hyoyoun
Wickramasuriya, Samiru S.
Lee, Youngsub
Wall, Emma H.
Ravichandran, Sripathy
Lillehoj, Hyun S.
author_sort Park, Inkyung
collection PubMed
description Both in vitro and in vivo studies were conducted to evaluate the beneficial effects of green tea extract (GT), cinnamon oil (CO), and pomegranate extract (PO) on avian coccidiosis. In experiment (EXP) 1, an in vitro culture system was used to investigate the individual effects of GT, CO, and PO on the proinflammatory cytokine response and integrity of tight junction (TJ) in chicken intestinal epithelial cells (IEC), on the differentiation of quail muscle cells and primary chicken embryonic muscle cells, and anticoccidial and antibacterial activities against Eimeria tenella sporozoites and Clostridium perfringens bacteria, respectively. In EXP 2 and 3, in vivo trials were carried out to study the dose-dependent effect of blended phytochemicals (GT, CO, PO) on coccidiosis in broiler chickens infected with E. maxima. For EXP 2, one hundred male broiler chickens (0-day-old) were allocated into the following five treatment groups: Control group for non-infected chickens (NC), Basal diet group for E. maxima-infected chickens (PC), PC group supplemented with phytochemicals at 50 (Phy 50), 100 (Phy 100), and 200 (Phy 200) mg/kg feed diets for E. maxima-infected chickens. For EXP 3, one hundred twenty male broiler chickens (0-day-old) were allocated into the following six treatment groups: NC, PC, PC supplemented with phytochemicals at 10 (Phy 10), 20 (Phy 20), 30 (Phy 30), and 100 (Phy 100) mg/kg feed for E. maxima-infected chickens. Body weights (BW) were measured on days 0, 7, 14, 20, and 22, and jejunum samples were used to measure cytokine, TJ protein, and antioxidant enzyme responses at 8 days post-infection (dpi). Fecal samples for oocyst enumeration were collected from 6 to 8 dpi. In vitro, CO and PO reduced LPS-induced IL-1β and IL-8 in IEC, respectively, and GT enhanced the gene expression of occludin in IEC. PO at 1.0 and 5.0 mg/mL exerted antimicrobial effect against E. tenella sporozoites and C. perfringens bacteria, respectively. In vivo, chickens fed a diet supplemented with phytochemicals showed enhanced BW, reduced oocyst shedding, and decreased proinflammatory cytokines following E. maxima challenge. In conclusion, the combination of GT, CO, and PO in the diet of broiler chickens infected with E. maxima induced enhanced host disease resistance including innate immunity and gut health, which contributed to improved growth and reduced disease responses. These findings provide scientific support for the development of a novel phytogenic feed additive formula that enhances the growth and intestinal health of broiler chickens infected with coccidiosis.
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spelling pubmed-102724592023-06-17 Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis Park, Inkyung Nam, Hyoyoun Wickramasuriya, Samiru S. Lee, Youngsub Wall, Emma H. Ravichandran, Sripathy Lillehoj, Hyun S. Front Immunol Immunology Both in vitro and in vivo studies were conducted to evaluate the beneficial effects of green tea extract (GT), cinnamon oil (CO), and pomegranate extract (PO) on avian coccidiosis. In experiment (EXP) 1, an in vitro culture system was used to investigate the individual effects of GT, CO, and PO on the proinflammatory cytokine response and integrity of tight junction (TJ) in chicken intestinal epithelial cells (IEC), on the differentiation of quail muscle cells and primary chicken embryonic muscle cells, and anticoccidial and antibacterial activities against Eimeria tenella sporozoites and Clostridium perfringens bacteria, respectively. In EXP 2 and 3, in vivo trials were carried out to study the dose-dependent effect of blended phytochemicals (GT, CO, PO) on coccidiosis in broiler chickens infected with E. maxima. For EXP 2, one hundred male broiler chickens (0-day-old) were allocated into the following five treatment groups: Control group for non-infected chickens (NC), Basal diet group for E. maxima-infected chickens (PC), PC group supplemented with phytochemicals at 50 (Phy 50), 100 (Phy 100), and 200 (Phy 200) mg/kg feed diets for E. maxima-infected chickens. For EXP 3, one hundred twenty male broiler chickens (0-day-old) were allocated into the following six treatment groups: NC, PC, PC supplemented with phytochemicals at 10 (Phy 10), 20 (Phy 20), 30 (Phy 30), and 100 (Phy 100) mg/kg feed for E. maxima-infected chickens. Body weights (BW) were measured on days 0, 7, 14, 20, and 22, and jejunum samples were used to measure cytokine, TJ protein, and antioxidant enzyme responses at 8 days post-infection (dpi). Fecal samples for oocyst enumeration were collected from 6 to 8 dpi. In vitro, CO and PO reduced LPS-induced IL-1β and IL-8 in IEC, respectively, and GT enhanced the gene expression of occludin in IEC. PO at 1.0 and 5.0 mg/mL exerted antimicrobial effect against E. tenella sporozoites and C. perfringens bacteria, respectively. In vivo, chickens fed a diet supplemented with phytochemicals showed enhanced BW, reduced oocyst shedding, and decreased proinflammatory cytokines following E. maxima challenge. In conclusion, the combination of GT, CO, and PO in the diet of broiler chickens infected with E. maxima induced enhanced host disease resistance including innate immunity and gut health, which contributed to improved growth and reduced disease responses. These findings provide scientific support for the development of a novel phytogenic feed additive formula that enhances the growth and intestinal health of broiler chickens infected with coccidiosis. Frontiers Media S.A. 2023-06-02 /pmc/articles/PMC10272459/ /pubmed/37334385 http://dx.doi.org/10.3389/fimmu.2023.1145367 Text en Copyright © 2023 Park, Nam, Wickramasuriya, Lee, Wall, Ravichandran and Lillehoj https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Park, Inkyung
Nam, Hyoyoun
Wickramasuriya, Samiru S.
Lee, Youngsub
Wall, Emma H.
Ravichandran, Sripathy
Lillehoj, Hyun S.
Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis
title Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis
title_full Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis
title_fullStr Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis
title_full_unstemmed Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis
title_short Host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis
title_sort host-mediated beneficial effects of phytochemicals for prevention of avian coccidiosis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272459/
https://www.ncbi.nlm.nih.gov/pubmed/37334385
http://dx.doi.org/10.3389/fimmu.2023.1145367
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