15
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Microbiota Changes Due to Grape Seed Extract Diet Improved Intestinal Homeostasis and Decreased Fatness in Parental Broiler Hens

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In poultry, the selection of broilers for growth performance has induced a deterioration in the health of the parental hens associated with poor reproductive efficiency. To improve these parameters, we administered to laying parental broiler hens a regular diet supplemented or not (Control) with a moderate (1%) or a high level (2%) of grape seed extract (GSE). The 1% GSE diet was administered from a young age (from 4 to 40 weeks of age) and the high level of 2% GSE was administered only during a 2-week period (from 38 to 40 weeks of age) in the laying period. The analysis of 40-week-old hens showed that 2% GSE displayed a reduction in the fat tissue and an improvement in fertility with heavier and more resistant eggs. Seven monomer phenolic metabolites of GSE were significantly measured in the plasma of the 2% GSE hens. GSE supplementation increased the relative abundance of the following bacteria populations: Bifidobacteriaceae, Lactobacilliaceae and Lachnospiraceae. In conclusion, a supplementation period of only 2 weeks with 2% GSE is sufficient to improve the metabolic and laying parameters of breeder hens through a modification in the microbiota.

          Related collections

          Most cited references59

          • Record: found
          • Abstract: found
          • Article: not found

          Control of apoptosis by p53.

          The p53 tumor suppressor acts to integrate multiple stress signals into a series of diverse antiproliferative responses. One of the most important p53 functions is its ability to activate apoptosis, and disruption of this process can promote tumor progression and chemoresistance. p53 apparently promotes apoptosis through transcription-dependent and -independent mechanisms that act in concert to ensure that the cell death program proceeds efficiently. Moreover, the apoptotic activity of p53 is tightly controlled, and is influenced by a series of quantitative and qualitative events that influence the outcome of p53 activation. Interestingly, other p53 family members can also promote apoptosis, either in parallel or in concert with p53. Although incomplete, our current understanding of p53 illustrates how apoptosis can be integrated into a larger tumor suppressor network controlled by different signals, environmental factors, and cell type. Understanding this network in more detail will provide insights into cancer and other diseases, and will identify strategies to improve their therapeutic treatment.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Bifidobacteria and Their Role as Members of the Human Gut Microbiota

            Members of the genus Bifidobacterium are among the first microbes to colonize the human gastrointestinal tract and are believed to exert positive health benefits on their host. Due to their purported health-promoting properties, bifidobacteria have been incorporated into many functional foods as active ingredients. Bifidobacteria naturally occur in a range of ecological niches that are either directly or indirectly connected to the animal gastrointestinal tract, such as the human oral cavity, the insect gut and sewage. To be able to survive in these particular ecological niches, bifidobacteria must possess specific adaptations to be competitive. Determination of genome sequences has revealed genetic attributes that may explain bifidobacterial ecological fitness, such as metabolic abilities, evasion of the host adaptive immune system and colonization of the host through specific appendages. However, genetic modification is crucial toward fully elucidating the mechanisms by which bifidobacteria exert their adaptive abilities and beneficial properties. In this review we provide an up to date summary of the general features of bifidobacteria, whilst paying particular attention to the metabolic abilities of this species. We also describe methods that have allowed successful genetic manipulation of bifidobacteria.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Mucus enhances gut homeostasis and oral tolerance by delivering immunoregulatory signals.

              A dense mucus layer in the large intestine prevents inflammation by shielding the underlying epithelium from luminal bacteria and food antigens. This mucus barrier is organized around the hyperglycosylated mucin MUC2. Here we show that the small intestine has a porous mucus layer, which permitted the uptake of MUC2 by antigen-sampling dendritic cells (DCs). Glycans associated with MUC2 imprinted DCs with anti-inflammatory properties by assembling a galectin-3-Dectin-1-FcγRIIB receptor complex that activated β-catenin. This transcription factor interfered with DC expression of inflammatory but not tolerogenic cytokines by inhibiting gene transcription through nuclear factor κB. MUC2 induced additional conditioning signals in intestinal epithelial cells. Thus, mucus does not merely form a nonspecific physical barrier, but also constrains the immunogenicity of gut antigens by delivering tolerogenic signals.
                Bookmark

                Author and article information

                Journal
                Microorganisms
                Microorganisms
                microorganisms
                Microorganisms
                MDPI
                2076-2607
                28 July 2020
                August 2020
                : 8
                : 8
                : 1141
                Affiliations
                [1 ]INRAE UMR85 Physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France; jeremy.grandhaye@ 123456inrae.fr (J.G.); alix.barbe@ 123456inrae.fr (A.B.); christelle.rame@ 123456inrae.fr (C.R.); joelle.dupont@ 123456inrae.fr (J.D.)
                [2 ]Micalis Institute, INRAE, AgroParisTech, Université Paris-Saclay, 78350 Jouy-en-Josas, France; veronique.douard@ 123456inrae.fr (V.D.); catherine.philippe@ 123456inrae.fr (C.P.); magali.monnoye@ 123456inrae.fr (M.M.)
                [3 ]Department of Nutritional Sciences, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King’s College London, London SE1 7EH, UK; ana.rodriguez-mateos@ 123456kcl.ac.uk (A.R.-M.); yifan.yu@ 123456kcl.ac.uk (Y.X.); alex.cheok@ 123456kcl.ac.uk (A.C.)
                [4 ]INDENA, 38 Avenue Gustave Eiffel, 37095 Tours, France; antonella.riva@ 123456indena.com
                [5 ]Infection and Innate Immunity in Monogastric Livestock, Centre INRAE Val de Loire, ISP UMR1282, 37380 Nouzilly, France; rodrigo.guabiraba-brito@ 123456inrae.fr
                [6 ]UMR 1388 GenPhySE, Université de Toulouse, INRAE, INPT, ENVT, 31320 Castanet Tolosan, France; olivier.zemb@ 123456inrae.fr
                [7 ]INRAE Unité Expérimentale de Physiologie Animale de l’Orfrasière UEPAO 1297, 37380 Nouzilly, France; christophe.staub@ 123456inrae.fr (C.S.); eric.venturi@ 123456inrae.fr (E.V.)
                Author notes
                [* ]Correspondence: pascal.froment@ 123456inrae.fr ; Tel.: +33-2-47-42-78-08
                Author information
                https://orcid.org/0000-0002-0909-837X
                https://orcid.org/0000-0003-2819-943X
                https://orcid.org/0000-0003-4005-1753
                https://orcid.org/0000-0003-3900-5522
                https://orcid.org/0000-0002-7388-9598
                Article
                microorganisms-08-01141
                10.3390/microorganisms8081141
                7465624
                32731511
                2982bf6d-39f7-4872-8bd1-e69ea6b6624b
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 01 July 2020
                : 27 July 2020
                Categories
                Article

                broiler,grape seed,microbiota,adipose tissue
                broiler, grape seed, microbiota, adipose tissue

                Comments

                Comment on this article