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Effect of depolymerized sodium alginate on Salmonella Typhimurium infection in human enterocyte-like HT-29-Luc cells and BALB/c mice

•Alginate (HM-NA) is a highly viscous polysaccharide in brown algae.•Depolymerized alginate (LM-NA) is less viscous with low molecular weight (∼50kDa).•Both alginates inhibited S. Typhimurium adhesion and invasion in HT-29-Luc cells.•Both alginates (2%) in the diet suppressed S. Typhimurium infectio...

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Published in:Journal of functional foods 2017-01, Vol.28, p.122-126
Main Authors: Kuda, Takashi, Hirano, Shino, Yokota, Yasushi, Eda, Mika, Takahashi, Hajime, Kimura, Bon
Format: Article
Language:English
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Summary:•Alginate (HM-NA) is a highly viscous polysaccharide in brown algae.•Depolymerized alginate (LM-NA) is less viscous with low molecular weight (∼50kDa).•Both alginates inhibited S. Typhimurium adhesion and invasion in HT-29-Luc cells.•Both alginates (2%) in the diet suppressed S. Typhimurium infection in mouse liver.•LM-NA (2.5%) drinking water inhibited S. Typhimurium infection in liver and spleen. Depolymerized low-molecular-weight sodium alginate (LM-NA) has been developed as functional component for beverages. Solubility of LM-NA is far higher than that of general high-molecular-weight sodium alginate (HM-NA). To evaluate the effects of the alginates on infection of food related pathogens, the adhesion and invasion of Salmonella Typhimurium in human enterocyte-like HT-29-Luc cells and the infection in BALB/c mice were studied. Both the alginates (0.1% w/v) inhibited the adhesion and invasion in HT-29-Luc cells by 70–80%. Dietary intake of both alginates (2% w/v) reduced the infection in the liver of BALB/c mice from 5.0 to 4.4 log CFU/g tissue. Drinking water containing LM-NA (2.5% w/v) also reduced the infection in the liver from 5.5 to 4.6 log CFU/g tissue and in the spleen from 4.6 to 3.6 log CFU/g tissue. These results suggest that LM-NA can exert positive immunomodulatory effects and would be useful as a functional food material.
ISSN:1756-4646
2214-9414
DOI:10.1016/j.jff.2016.11.009