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A fibrolytic potential in the human ileum mucosal microbiota revealed by functional metagenomic
Author(s) -
Orlane Patrascu,
Fabienne Béguet-Crespel,
Ludovica Marinelli,
Emmanuelle Le Chatelier,
AnneLaure Abraham,
Marion Leclerc,
Christophe Klopp,
Nicolas Terrapon,
Bernard Henrissat,
Hervé M. Blottière,
Joël Doré,
Christel BéraMaillet
Publication year - 2017
Publication title -
scientific reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.24
H-Index - 213
ISSN - 2045-2322
DOI - 10.1038/srep40248
Subject(s) - metagenomics , ileum , bacteroides , biology , glycoside hydrolase , microbiome , polysaccharide , microbiology and biotechnology , human gastrointestinal tract , clostridia , glycan , clostridiales , gut flora , human microbiome project , bifidobacterium , small intestine , digestion (alchemy) , gastrointestinal tract , gene , biochemistry , clostridiaceae , bacteria , genetics , lactobacillus , chemistry , glycoprotein , chromatography , toxin
The digestion of dietary fibers is a major function of the human intestinal microbiota. So far this function has been attributed to the microorganisms inhabiting the colon, and many studies have focused on this distal part of the gastrointestinal tract using easily accessible fecal material. However, microbial fermentations, supported by the presence of short-chain fatty acids, are suspected to occur in the upper small intestine, particularly in the ileum. Using a fosmid library from the human ileal mucosa, we screened 20,000 clones for their activities against carboxymethylcellulose and xylans chosen as models of the major plant cell wall (PCW) polysaccharides from dietary fibres. Eleven positive clones revealed a broad range of CAZyme encoding genes from Bacteroides and Clostridiales species, as well as Polysaccharide Utilization Loci (PULs). The functional glycoside hydrolase genes were identified, and oligosaccharide break-down products examined from different polysaccharides including mixed-linkage β-glucans. CAZymes and PULs were also examined for their prevalence in human gut microbiome. Several clusters of genes of low prevalence in fecal microbiome suggested they belong to unidentified strains rather specifically established upstream the colon, in the ileum. Thus, the ileal mucosa-associated microbiota encompasses the enzymatic potential for PCW polysaccharide degradation in the small intestine.

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