4.6 Article

Immunomodulation of Antimicrobial Peptides Expression in the Gastrointestinal Tract by Probiotics in Response to Stimulation by Salmonella minnesota Lipopolysaccharides

期刊

PROBIOTICS AND ANTIMICROBIAL PROTEINS
卷 13, 期 4, 页码 1157-1172

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SPRINGER
DOI: 10.1007/s12602-021-09746-y

关键词

Probiotics; Innate immunity; Antimicrobial peptides; Avian beta defensins; Cytokines; Salmonella minnesota

资金

  1. South Valley University, Qena, Egypt
  2. Egyptian Ministry of Higher Education and Scientific Research, Mission Sector, Cairo, Egypt

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The study aimed to investigate the effects of probiotics-feeding on the expression and localization of avian beta defensins and proinflammatory cytokines in the gastrointestinal tract. The results suggest that probiotics-feeding may enhance the immune defense system mediated by AvBDs against infection by Gram-negative bacteria.
The aim was to determine whether probiotics-feeding can affect the expression and localization of avian beta defensins (AvBDs) and proinflammatory cytokines in response to Salmonella minnesota lipopolysaccharide (LPS) in the gastrointestinal tract. One-day-old male Chunky broiler chicks were fed with or without 0.4% probiotics for 7 days (P-group and non-P-group, respectively). Then, they were orally challenged with no LPS (0-LPS), 1 mu g LPS (1-LPS), or 100 mu g LPS (100-LPS) (n = 5, each), in experiment 1, and with no LPS and 1 mu g LPS (n = 6, each) in experiment 2. Five hours after LPS challenge, the proventriculi and ceca were collected. A total of seven and eight AvBDs were identified in proventriculus and cecum, respectively. The density of ir-AvBD12 in the surface epithelium of proventriculus increased in the P-group in response to 1-LPS and 100-LPS stimulation. In experiment 1, the expression of two AvBDs in the proventriculus and six AvBDs in the cecum of 1-LPS chicks was higher in P-group than in the non-P-group. Results of experiment 2 showed similar tendency to experiment 1. These results suggest that probiotics-feeding may enhance the immunodefense system mediated by AvBDs but not by cytokine, against infection by Gram-negative bacteria.

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