Abstract |
Dietary glutamine (Gln) or arginine (Arg) supplementation is beneficial for intestinal health; however, whether Gln or Arg may confer protection against Enterotoxigenic Escherichia coli (ETEC) infection is not known. To address this, we used an ETEC-infected murine model to investigate the protective effects of Gln and Arg. Experimentally, we pre-treated mice with designed diet of Gln or Arg supplementation prior to the oral ETEC infection and then assessed mouse mortality and intestinal bacterial burden. We also determined the markers of intestinal innate immunity in treated mice, including secretory IgA response ( SIgA), mucins from goblet cells, as well as antimicrobial peptides from Paneth cells. ETEC colonized in mouse small intestine, including duodenum, jejunum, and ileum, and inhibited the mRNA expression of intestinal immune factors, such as polymeric immunoglobulin receptor (pIgR), cryptdin-related sequence 1C (CRS1C), and Reg3γ. We found that dietary Gln or Arg supplementation decreased bacterial colonization and promoted the activation of innate immunity (e.g., the mRNA expression of pIgR, CRS1C, and Reg3γ) in the intestine of ETEC-infected mice. Our results suggest that dietary arginine or glutamine supplementation may inhibit intestinal ETEC infection through intestinal innate immunity.
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Authors | Gang Liu, Wenkai Ren, Jun Fang, Chien-An Andy Hu, Guiping Guan, Naif Abdullah Al-Dhabi, Jie Yin, Veeramuthu Duraipandiyan, Shuai Chen, Yuanyi Peng, Yulong Yin |
Journal | Amino acids
(Amino Acids)
Vol. 49
Issue 12
Pg. 1945-1954
(Dec 2017)
ISSN: 1438-2199 [Electronic] Austria |
PMID | 28299479
(Publication Type: Journal Article)
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Chemical References |
- Anti-Infective Agents
- Protective Agents
- Glutamine
- Arginine
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Topics |
- Animals
- Anti-Infective Agents
(metabolism)
- Arginine
(pharmacology)
- Bacterial Load
(drug effects)
- Dietary Supplements
- Enterotoxigenic Escherichia coli
(drug effects)
- Escherichia coli Infections
(drug therapy, immunology)
- Female
- Gene Expression Regulation
(drug effects)
- Glutamine
(pharmacology)
- Ileum
(drug effects, immunology)
- Immunity, Innate
(drug effects)
- Intestinal Mucosa
(drug effects, immunology, physiopathology)
- Jejunum
(drug effects, immunology)
- Mice
- Protective Agents
(pharmacology)
- Signal Transduction
(drug effects)
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