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Hybrid metagenome assemblies link carbohydrate structure with function in the human gut microbiome. | LitMetric

AI Article Synopsis

  • - Complex carbohydrates that can't be digested in the small intestine are broken down by gut microbes in the large intestine, creating beneficial metabolic products that can impact host health and affect other microbes.
  • - The study investigates how different carbohydrate structures influence the composition of gut microbiota and the succession of microbes that digest these carbohydrates, yet this relationship remains partially understood.
  • - Researchers identified 509 high-quality genomes associated with various bacteria, discovering that certain species with starch-binding genes became more abundant when exposed to starch, highlighting the potential of uncultured microbes for starch degradation in future research.

Article Abstract

Complex carbohydrates that escape small intestinal digestion, are broken down in the large intestine by enzymes encoded by the gut microbiome. This is a symbiotic relationship between microbes and host, resulting in metabolic products that influence host health and are exploited by other microbes. However, the role of carbohydrate structure in directing microbiota community composition and the succession of carbohydrate-degrading microbes, is not fully understood. In this study we evaluate species-level compositional variation within a single microbiome in response to six structurally distinct carbohydrates in a controlled model gut using hybrid metagenome assemblies. We identified 509 high-quality metagenome-assembled genomes (MAGs) belonging to ten bacterial classes and 28 bacterial families. Bacterial species identified as carrying genes encoding starch binding modules increased in abundance in response to starches. The use of hybrid metagenomics has allowed identification of several uncultured species with the functional potential to degrade starch substrates for future study.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458734PMC
http://dx.doi.org/10.1038/s42003-022-03865-0DOI Listing

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