Abstract
As the richest component in human milk oligosaccharides (HMOs), 2’-fucosyllactose (2’-FL) can reduce the colonization of harmful microbiota in vivo, thus lowering the risk of infection; however, the mechanism for this is still unclear. In this study, a model of Escherichia coli O157 infection in healthy adult mice was established to explore the effect of 2’-FL intervention on E. coli O157 colonization and its protective effects on mice. The results showed that 2’-FL intake reduced E. coli O157 colonization in mice intestine by more than 90% (p < 0.001), and it also reduced intestinal inflammation, increased the content of fecal short-chain fatty acids, and enhanced intestinal barrier function. These beneficial effects were attributed to the increased expression of mucins such as MUC2 (increased by more than 20%, p < 0.001), and inhibition of E. coli O157 cell adhesion (about 30% reduction, p < 0.001), and were associated with the modulation of gut microbiota composition. 2’-FL significantly increased the abundance of Akkermansia, a potential probiotic, which may represent the fundamental means by which 2’-FL enhances the expression of mucin and reduces the colonization of harmful bacteria. The current study may support the use of 2’-FL in the prevention of foodborne pathogen infections in human.
Highlights
Can reduce the colonization of harmful microbiota in vivo, lowering the risk of infection; the mechanism for this is still unclear
The present study aims to investigate the protective effect of 2’-FL against E. coli O157:H7 infection in mice model
To research the correlation between gut microbiota and other sample indicators, we introduced an environment factors analysis and built a correspondence analysis (CCA) model for microbiota samples and five main factors, including colon infection rates, overall amount of short-chain fatty acids (SCFAs), MUC2 expression and IL-6 and tumor necrosis factor-α (TNF-α) expression in the colon
Summary
Can reduce the colonization of harmful microbiota in vivo, lowering the risk of infection; the mechanism for this is still unclear. The results showed that 2’-FL intake reduced E. coli O157 colonization in mice intestine by more than 90% (p < 0.001), and it reduced intestinal inflammation, increased the content of fecal short-chain fatty acids, and enhanced intestinal barrier function. These beneficial effects were attributed to the increased expression of mucins such as MUC2 (increased by more than 20%, p < 0.001), and inhibition of E. coli O157 cell adhesion (about 30% reduction, p < 0.001), and were associated with the modulation of gut microbiota composition. Many companies have added 2’-FL to infant formula in an attempt to close the gap between formula
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