4.7 Article

Agrobacterium sp. ZX09 β-Glucan Attenuates Enterotoxigenic Escherichia coli-Induced Disruption of Intestinal Epithelium in Weaned Pigs

Journal

Publisher

MDPI
DOI: 10.3390/ijms231810290

Keywords

beta-glucan; intestinal epithelium; enterotoxigenic Escherichia coli; weaned pigs

Funding

  1. Key Research and Development Program of Sichuan Province [2020YFN0147]
  2. National Natural Science Foundation of China [31972599]

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The study found that dietary beta-glucan (BGL) supplementation has a protective effect on intestinal epithelium exposed to enterotoxigenic Escherichia coli (ETEC). BGL supplementation improves intestinal absorption, reduces inflammation, enhances intestinal immunity and antioxidant capacity, and improves intestinal microbiota.
To explore the protective effect of dietary beta-glucan (BGL) supplementation on intestinal epithelium exposure to enterotoxigenic Escherichia coli (ETEC), thirty-two weaned pigs were assigned to four groups. Pigs were fed with a basal diet or basal diet containing 500 mg/kg BGL, and were orally infused with ETEC or culture medium. Results showed BGL supplementation had no influence on growth performance in weaned pigs. However, BGL supplementation increased the absorption of D-xylose, and significantly decreased the serum concentrations of D-lactate and diamine oxidase (DAO) in the ETEC-challenged pigs (p < 0.05). Interestingly, BGL significantly increased the abundance of the zonula occludens-1-(ZO-1) in the jejunal epithelium upon ETEC challenge (p < 0.05). BGL supplementation also increased the number of S-phase cells and the number of sIgA-positive cells, but significantly decreased the number of total apoptotic cells in the jejunal epithelium upon ETEC challenge (p < 0.05). Moreover, BGL significantly increased the duodenal catalase (CAT) activity and the ileal total superoxide dismutase (T-SOD) activity in the ETEC-challenged pigs (p < 0.05). Importantly, BGL significantly decreased the expression levels of critical inflammation related proteins such as the tumor necrosis factor-alpha (TNF-alpha), interlukin-6 (IL-6), myeloid differentiation factor 88 (MyD88), and nuclear factor-kappa B (NF-kappa B) in the jejunal and ileal mucosa upon ETEC challenge (p < 0.05). BGL also elevated the propanoic acid content and the abundance of Lactobacillus and Bacillus in the colon upon ETEC challenge (p < 0.05). These results suggested BGL could alleviate the ETEC-induced intestinal epithelium injury, which may be associated with suppressed inflammation and improved intestinal immunity and antioxidant capacity, as well as the improved intestinal macrobiotic.

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