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Biology subjects

Henrick, B.

Publications and source records attributed to Henrick, B..

2 recordsLinked to original sources

Novel plant-derived bioactive compounds shape the human gut microbiome in vitro

Mounting evidence supports the potential of dietary bioactive compounds to reduce chronic disease risk. Recently, the biological activity of N-trans-caffeoyltyramine (NCT) and N-trans-feruloyltyramine (NFT) has been hypothesized to drive regulation of gut permeability,but the impact of these components on the human gut microbiome composition has not been studied. The aim of this work is to determine whether purified NCT and NFT, or a hemp hull product containing NCT and NFT (Brightseed(R) Bio Gut Fiber), can impact the gut microbiome using an in vitro fermentation assay. To address this question, we treated three fecal inocula, representative of the human gut microbiome, with Bio Gut Fiber and NCT/NFT and evaluated their respective impact against starch and methylcellulose as controls. We found strong changes exerted by Bio Gut Fiber and NCT/NFT on the gut microbiome relative to starch and methylcellulose, with distinct responses across all microbial communities. Among communities treated with Bio Gut Fiber, we saw increased community productivity and increased community diversity. Further, to determine whether changes found in gut microbiome profiles were dose-dependent, we tested different concentrations of NCT/NFT and found a dose-dependent impact on the resulting microbial compositions. Through this work, we provide novel insight into the potential of bioactive components to shape the gut microbiome, highlighting the potential for plant-derived bioactives to improve the human gut microbiome and host health.

microbiology↗

Bifidobacteria-mediated immune system imprinting early in life

Immune-microbe interactions early in life influence an individuals risk of developing allergies, asthma and some autoimmune disorders. Breastfeeding helps guide the development of healthy immune-microbe relationships, in part by providing nutrients to specialized microbes that in turn benefit the host and its developing immune system. Such bacteria having co-evolved with humans are associated with reduced risks of immune mediated diseases but are increasingly rare in modern societies. Here we map an immunological sequence of events, triggered by microbial colonization that distinguish children with different gut bacterial composition. Lack of bifidobacterial species is associated with elevated markers of intestinal inflammation and immune dysregulation and in a randomized trial of breastfed infants, the infant-adapted Bifidobacterium infantis EVC001 silenced intestinal Th2 and Th17 immune responses, while inducing IFN{beta}, and its metabolites skew T-cell polarization in vitro, from Th2 towards Th1, suggesting a healthier immune imprinting during the first critical months of life. HIGHLIGHTSAn ordered sequence of immune changes after birth, driven by microbial interactions Low gut Bifidobacterium abundance is associated with markers of intestinal inflammation Feeding B. infantis EVC001 silenced intestinal Th2 and Th17 but upregulates IFN{beta} B. infantis EVC001 metabolites and/or enteric cytokines skew naive T-cell polarization towards Th1 and away from Th2

immunology↗