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      Interferon-γ acts as a regulator in the trade-off between phagocytosis and production performance in dwarf chickens

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          Abstract

          Background

          Interferon-γ (IFN-γ) is critical for innate and adaptive immunity against viral and bacterial infections. IFN-γ reportedly affects the phagocytic ability of monocytes and macrophages as well as regulates pituitary function in humans and mice. The present study analyzed the impact of IFN-γ on monocyte and macrophage phagocytosis, production performance, and pituitary function in vivo and in vitro (in dwarf chickens). IFN-γ was injected into dwarf chickens through a vein, and then, the laying rate, average egg weight, and levels of follicle-stimulating hormone (FSH) and IFN-γ were measured in treatment and control groups. For the in vitro experiment, the pituitary tissues were supplemented with IFN-γ, and the mRNA expression levels of follicle-stimulating hormone beta subunit ( FSH-β), interferon gamma receptor 1 ( IFNGR1), and interferon gamma receptor 2 ( IFNGR2) in the pituitary were assessed.

          Results

          Monocyte and macrophage phagocytosis product (PP) was decreased by IFN-γ treatment in a dose-dependent manner in vitro. In the in vivo experiment, the level of IFN-γ in the treatment group was higher than that in the control group at 7 d ( P < 0.05), 14 d ( P < 0.01), and 21 d ( P < 0.01) post-injection. Compared with the control group, monocyte and macrophage PP was lower in the treatment group after injection ( P < 0.01). The laying rate was higher in the treatment group than in the control group at 2 and 3 wk post-injection ( P < 0.05). There was a significant difference between the treatment and control groups in the levels of FSH at 1, 3, 7, and 14 d post-injection ( P < 0.01). In the in vitro experiment, increased mRNA expression levels of FSH-β, IFNGR1, and IFNGR2 were observed in the treatment group after stimulation with 100 U/mL IFN-γ for 24 h compared to those in the control group ( P < 0.05).

          Conclusions

          IFN-γ inhibited the phagocytosis of monocytes and macrophages; up-regulated the mRNA expression levels of the FSH-β, IFNGR1, and IFNGR2; enhanced the secretion of FSH; and improved the laying rate. IFN-γ might be an important regulator in the trade-off between the immune effect and production performance in dwarf chickens.

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          Most cited references40

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          Inhibition of pulmonary antibacterial defense by interferon-gamma during recovery from influenza infection.

          Secondary bacterial infection often occurs after pulmonary virus infection and is a common cause of severe disease in humans, yet the mechanisms responsible for this viral-bacterial synergy in the lung are only poorly understood. We now report that pulmonary interferon-gamma (IFN-gamma) produced during T cell responses to influenza infection in mice inhibits initial bacterial clearance from the lung by alveolar macrophages. This suppression of phagocytosis correlates with lung IFN-gamma abundance, but not viral burden, and leads to enhanced susceptibility to secondary pneumococcal infection, which can be prevented by IFN-gamma neutralization after influenza infection. Direct inoculation of IFN-gamma can mimic influenza infection and downregulate the expression of the class A scavenger receptor MARCO on alveolar macrophages. Thus, IFN-gamma, although probably facilitating induction of specific anti-influenza adaptive immunity, suppresses innate protection against extracellular bacterial pathogens in the lung.
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            Trade-off between growth and immune function: a meta-analysis of selection experiments

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              Phagocytosis--the mighty weapon of the silent warriors.

              Professional phagocytes, comprising polymorphonuclear neutrophils and monocyte/macrophage cells, play an important role in the host defense. Any defect in their function exposes the organism to microbial intruders terminating in fatal diseases. The functional responses of the phagocytes to bacterial and fungal infections include chemotaxis, actin assembly, migration, adhesion, aggregation, phagocytosis, degranulation, and reactive oxygen species production. Superoxide generation by phagocytic NADPH oxidase is an imperative step toward bacterial killing. Phagocytes participate in inflammatory reactions and exert tumoricidal activity. They are supported by serum factors such as immunoglobulins, cytokines, complement, the acute phase reactant C-reactive protein, production of antibacterial proteins, and others. In addition to their principal task to eliminate bacteria, they are engaged in removing damaged, senescent, and apoptotic cells. Engulfed cell debris, large particles such as latex beads, fat, and oil droplets, are examples of phagocytic activity illustrated in the present review with transmission and scanning electron microscope micrographs. Numerous factors, such as diseases and stressful conditions, affect the engulfing activity of the professional phagocytes. Our experience regarding the impaired phagocytic capacity of cells in patients with diabetes and chronic renal failure is discussed. The results obtained in our laboratory from experiments detecting the effect of strenuous physical exercise, hypothermia, fasting, and abdominal photon irradiation on the phagocytic capacity of human polymorphonuclear neutrophils and rat peritoneal macrophages are hereby summarized and the reports on those subjects in the recent literature are reviewed. A variety of assays are applied for quantifying phagocytosis. Flow cytometry based on incubation of phagocytic cells with fluorescent conjugated particles and measuring the amount of fluorescence as an indicator of the engulfing capacity of the cells is a useful method. A direct visualization of the ingested particles using light or electron microscopy is a valuable tool for estimation of phagocytic function. In our hands, the use of semithin sections of embedded phagocytes following their incubation with latex particles provided satisfactory results for measuring the total number of phagocytic cells, as well as the internalizing capacity of each individual cell. Microbiological assays, the nitroblue tetrazolium test, quantitation of antibody- and antigen-mediated phagocytosis, as well as methods reviewed in detail in other reports are additional applications for determination of this intricate process. Copyright 2002 Wiley-Liss, Inc.
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                Author and article information

                Contributors
                +86 10 62732681 , yuanyitong@cau.edu.cn
                +86 10 62732681 , jinjin890203@163.com
                +86 10 62732681 , zhaoyuetx@126.com
                +86 10 62731256 , lianlinglara@126.com
                +86 10 62732463 , lianzhxcau@126.com
                Journal
                J Anim Sci Biotechnol
                J Anim Sci Biotechnol
                Journal of Animal Science and Biotechnology
                BioMed Central (London )
                1674-9782
                2049-1891
                23 May 2018
                23 May 2018
                2018
                : 9
                : 40
                Affiliations
                [1 ]ISNI 0000 0004 0530 8290, GRID grid.22935.3f, Key Laboratory of Animal Genetics and Breeding of the Ministry of Agriculture, Beijing Key Laboratory for Animal Genetic Improvement, Department of Animal Genetics and Breeding, College of Animal Science and Technology, , China Agricultural University, ; Beijing, 100193 China
                [2 ]ISNI 0000 0004 0530 8290, GRID grid.22935.3f, Department of Animal Genetics and Breeding, College of Animal Science and Technology, , China Agricultural University, ; Beijing, 100193 China
                Author information
                http://orcid.org/0000-0002-5208-0511
                Article
                256
                10.1186/s40104-018-0256-y
                5964881
                79a82855-3166-469b-a0c8-33d4ed244e1c
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 20 October 2017
                : 19 April 2018
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 3157130570
                Award Recipient :
                Funded by: Young Scientist Supporting Project
                Funded by: Program for Changjiang Scholars and Innovative Research Team in University
                Award ID: IRT_15R62
                Award Recipient :
                Funded by: Farm Animals Germplasm Resource Platform
                Funded by: National Transgenic Creature Breeding Grand Project
                Award ID: 2016ZX08008-003
                Award Recipient :
                Funded by: Innovation Base Cultivation and Development Project-research on precise genetic modify in sheep
                Award ID: Z171100002217072
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Animal science & Zoology
                dwarf chicken,interferon-γ,macrophage,monocyte,phagocytosis product,production performance

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