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Updated: Dec 13, 2025

An In Vitro Batch-culture Model to Estimate the Effects of Interventional Regimens on Human Fecal Microbiota
Published on: July 31, 2019
Dynamics of Structural and Functional Changes in Gut Microbiota during Treatment with a Microalgal β-Glucan,
Harrison B Taylor1, Radhika Gudi1, Robert Brown1
1Department of Microbiology and Immunology, College of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Abstract:
Previously, we have shown that oral administration of yeast derived β-1,3/1,6-d-glucan enhances immune regulation and alters the composition of the gut microbiota. However, it is not known if other structurally distinct β-glucans have similar properties. Here, using C57BL/6 mice, we show the potential of a microalgae derived β-1,3-d-glucan, paramylon (PM), in shaping the gut microbiota and modulating the susceptibility to colitis. The community structure within the gut microbiota showed progressive changes including selective enrichment of specific communities and lowered community richness and diversity during prolonged oral treatment with PM. Compared to control mice, the gut microbiota of PM-treated mice had significantly higher abundance of Verrucomicrobia and lower abundance of Firmicutes. Specific taxa that were significantly more abundant in PM-treated mice include Akkermansia muciniphila and several Bacteroides members. Predictive functional analysis revealed overrepresentation of carbohydrate metabolism function in the fecal microbiota of PM recipients compared to controls, and this function was linked to Bacteroides spp. Prolonged pretreatment with PM not only diminished susceptibility to dextran sulfate sodium induced colitis severity, but also caused enhanced immune regulation. Overall, this study demonstrates the prebiotic properties of PM and the potential benefits of its prolonged oral consumption to gut health.
Insights
Paramylon, a microalgae-derived beta-glucan, reshapes gut microbiota, increasing beneficial bacteria like Akkermansia muciniphila. This prebiotic effect enhances immune regulation and reduces colitis severity in mice.
Area of Science:
- Microbiology
- Immunology
- Nutrition Science
Background:
- Oral administration of yeast-derived beta-1,3/1,6-d-glucan influences immune regulation and gut microbiota.
- The effects of other structurally distinct beta-glucans on the gut microbiota and immune system are less understood.
Purpose of the Study:
- To investigate the impact of microalgae-derived beta-1,3-d-glucan, paramylon (PM), on gut microbiota composition and its modulation of colitis susceptibility.
- To assess the potential prebiotic properties and immune-regulatory effects of paramylon.
Main Methods:
- Oral administration of paramylon to C57BL/6 mice over a prolonged period.
- Analysis of gut microbiota community structure using sequencing techniques.
- Assessment of susceptibility to dextran sulfate sodium (DSS)-induced colitis.
- Evaluation of immune regulation markers.
Main Results:
- Prolonged PM treatment altered gut microbiota structure, decreasing richness and diversity while enriching specific taxa like Verrucomicrobia (including Akkermansia muciniphila) and decreasing Firmicutes.
- Functional analysis indicated an enrichment of carbohydrate metabolism pathways, linked to Bacteroides species.
- PM pretreatment significantly reduced the severity of DSS-induced colitis.
- Enhanced immune regulation was observed in PM-treated mice.
Conclusions:
- Paramylon exhibits prebiotic properties, significantly altering gut microbiota composition and function.
- Prolonged oral consumption of PM demonstrates potential benefits for gut health by enhancing immune regulation and reducing colitis susceptibility.
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