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      Effects of Lactobacillus reuteri LR1 on the growth performance, intestinal morphology, and intestinal barrier function in weaned pigs

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          Abstract

          <p id="d779938e178">The objective of this study was to investigate the effects of <i>Lactobacillus reuteri</i> LR1, a new strain isolated from the feces of weaned pigs, on the growth performance, intestinal morphology, immune responses, and intestinal barrier function in weaned pigs. A total of 144 weaned pigs (Duroc × Landrace × Yorkshire, 21 d of age) with an initial BW of 6.49 ± 0.02 kg were randomly assigned to 3 dietary treatments with 8 replicate pens, each of per treatment and 6 pigs. Pigs were fed a basal diet ( <b>CON</b>, controls), the basal diet supplemented with 100 mg/kg olaquindox and 75 mg/kg aureomycin ( <b>OA</b>) or the basal diet supplemented with 5 × 10 <sup>10</sup> cfu/kg <i>L. reuteri</i> LR1 for a 14-d period. At the end of study, the ADG, ADFI, and G:F were calculated, and 1 randomly selected pig from each pen was euthanized for sample collection. The LR1 increased ADG (22.73%, <i>P</i> &lt; 0.05) compared with CON. The villus height of the ileum was increased ( <i>P</i> &lt; 0.05) and crypt depth in duodenum was reduced ( <i>P</i> &lt; 0.05), along with increased ( <i>P</i> &lt; 0.05) villus height to crypt depth ratio of the jejunum and ileum by LR1 compared with CON and OA. LR1 increased ( <i>P</i> &lt; 0.05) ileal mucosal content of IL-22 and transforming growth factor-β compared with OA. Compared with CON, LR1 increased ( <i>P</i> &lt; 0.05) and OA decreased ( <i>P</i> &lt; 0.05) the ileal content of secretory immunoglobulin A ( <b>sIgA</b>), and the abundance of transcripts of porcine β-defensin 2 and protegrin 1-5. Compared with CON, LR1 increased ( <i>P</i> &lt; 0.05) tight junction protein zonula occludens-1 and occludin transcripts in the mucosa of the jejunum and ileum, and those of mucin-2 in ileal mucosa. The relative expression of toll-like receptor 2 ( <b>TLR2</b>) and TLR4 were increased ( <i>P</i> &lt; 0.05) in ileal mucosa in pigs fed LR1 compared with CON. In conclusion, these data indicated that dietary LR1 supplementation at 5 × 10 <sup>10</sup> cfu/kg improved growth performance, intestinal morphology, and intestinal barrier function in weaned pigs. </p>

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          Most cited references34

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          Toll-like receptors and their crosstalk with other innate receptors in infection and immunity.

          Toll-like receptors (TLRs) are germline-encoded pattern recognition receptors (PRRs) that play a central role in host cell recognition and responses to microbial pathogens. TLR-mediated recognition of components derived from a wide range of pathogens and their role in the subsequent initiation of innate immune responses is widely accepted; however, the recent discovery of non-TLR PRRs, such as C-type lectin receptors, NOD-like receptors, and RIG-I-like receptors, suggests that many aspects of innate immunity are more sophisticated and complex. In this review, we will focus on the role played by TLRs in mounting protective immune responses against infection and their crosstalk with other PRRs with respect to pathogen recognition. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Lactobacillus reuteri induces gut intraepithelial CD4 + CD8αα + T cells

            The small intestine contains CD4+CD8αα+ double-positive intraepithelial T lymphocytes (DP IELs), which originate from intestinal CD4+ T cells through downregulation of the transcription factor ThPOK and have regulatory functions. DP IELs are absent in germ-free mice, suggesting that their differentiation depends on microbial factors. We found that DP IEL numbers in mice varied in different vivaria, correlating with the presence of Lactobacillus reuteri. This species induced DP IELs in germ-free mice and conventionally raised mice lacking these cells. L. reuteri did not shape DP–IEL–TCR repertoire, but generated indole derivatives of tryptophan that activated the aryl-hydrocarbon receptor in CD4+ T cells, allowing ThPOK downregulation and differentiation into DP IELs. Thus, L. reuteri together with a tryptophan-rich diet can reprogram intraepithelial CD4+ T cells into immunoregulatory T cells.
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              Gut Microbiota Dysbiosis in Postweaning Piglets: Understanding the Keys to Health.

              Weaning is a critical event in the pig's life cycle, frequently associated with severe enteric infections and overuse of antibiotics; this raises serious economic and public health concerns. In this review, we explain why gut microbiota dysbiosis, induced by abrupt changes in the diet and environment of piglets, emerges as a leading cause of post-weaning diarrhea, even if the exact underlying mechanisms remain unclear. Then, we focus on nonantimicrobial alternatives, such as zinc oxide, essential oils, and prebiotics or probiotics, which are currently evaluated to restore intestinal balance and allow a better management of the crucial weaning transition. Finally, we discuss how in vitro models of the piglet gut could be advantageously used as a complement to ex vivo and in vivo studies for the development and testing of new feed additives.
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                Author and article information

                Journal
                Journal of Animal Science
                Oxford University Press (OUP)
                0021-8812
                1525-3163
                June 2018
                June 04 2018
                April 12 2018
                June 2018
                June 04 2018
                April 12 2018
                : 96
                : 6
                : 2342-2351
                Affiliations
                [1 ]State Key Laboratory of Livestock and Poultry Breeding, Ministry of Agriculture Key Laboratory of Animal Nutrition and Feed Science in South China, Guangdong Public Laboratory of Animal Breeding and Nutrition, Guangdong Key Laboratory of Animal Breeding and Nutrition, Institute of Animal Science, Guangdong Academy of Agricultural Sciences, Guangzhou, China
                Article
                10.1093/jas/sky129
                6095392
                29659876
                8f16c1b4-7d0d-4014-be93-f5f6d4adcd23
                © 2018

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