4.7 Article

Polysaccharides from soybean residue fermented by Neurospora crassa alleviate DSS-induced gut barrier damage and microbiota disturbance in mice

Journal

FOOD & FUNCTION
Volume 13, Issue 10, Pages 5739-5751

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2fo00137c

Keywords

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Funding

  1. National Natural Science Foundation of China [31960463]
  2. Natural Science Foundation of Jiangxi Province [20212BAB206090]

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Soluble polysaccharides (FSRP) derived from Neurospora crassa-fermented soybean residue can alleviate colitis in mice by reducing inflammation, enhancing gut barrier function, and modulating gut microbiota homeostasis.
Soluble polysaccharides derived from microbial fermentation of agricultural by-products were considered as potential functional ingredients, primarily having probiotic properties. Herein, soluble polysaccharides (FSRP) were isolated from soybean residue fermented by Neurospora crassa, and FSRP mainly contained rhamnose, arabinose, fucose, mannose, glucose, and galactose, according to GC-MS analysis. To further investigate the protective effect of FSRP against colitis, dextran sulfate sodium induction (DSS)-treated mice were orally gavaged with FSRP (200 mg kg(-1) d(-1)) or inulin (400 mg kg(-1) d(-1), a positive control) for 7 d. The results showed that DSS-treated mice displayed symptoms of body weight loss, atrophy, and histopathological changes of colon, as well as gut barrier damage, which were recovered after FSRP supplementation (similar to inulin). Furthermore, the beneficial effects of FSRP were linked to a decreased inflammatory response and increased protein expression of E-cadherin, claudin-1 and ZO-1. Illumina-MiSeq sequencing analysis revealed that FSRP increased microbial diversity and altered community structure. Specifically, FSRP could modulate the abundance of inflammation-related bacteria (such as Tenericutes, Clostridia, and Bacilli) to ameliorate colitis symptoms. Therefore, FSRP can relieve DSS-induced colitis, which is closely associated with reduced levels of inflammatory factors, improved gut barrier function and gut microbiota homeostasis.

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