<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Engevik MA</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIAID NIH HHS</funding><pagination>1301-1314.e8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7956072</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>160(4)</volume><pubmed_abstract>&lt;h4>Background &amp; aims&lt;/h4>Although Clostridioides difficile infection (CDI) is known to involve the disruption of the gut microbiota, little is understood regarding how mucus-associated microbes interact with C difficile. We hypothesized that select mucus-associated bacteria would promote C difficile colonization and biofilm formation.&lt;h4>Methods&lt;/h4>To create a model of the human intestinal mucus layer and gut microbiota, we used bioreactors inoculated with healthy human feces, treated with clindamycin and infected with C difficile with the addition of human MUC2-coated coverslips.&lt;h4>Results&lt;/h4>C difficile was found to colonize and form biofilms on MUC2-coated coverslips, and 16S rRNA sequencing showed a unique biofilm profile with substantial cocolonization with Fusobacterium species. </pubmed_abstract><journal>Gastroenterology</journal><pubmed_title>Fusobacteriumnucleatum Adheres to Clostridioides difficile via the RadD Adhesin to Enhance Biofilm Formation in Intestinal Mucus.</pubmed_title><pmcid>PMC7956072</pmcid><funding_grant_id>K01 DK123195</funding_grant_id><funding_grant_id>F32 AI136404</funding_grant_id><funding_grant_id>P30 DK056338</funding_grant_id><funding_grant_id>R01 AI123278</funding_grant_id><funding_grant_id>U01 AI124290</funding_grant_id><funding_grant_id>P30 DK123704</funding_grant_id><pubmed_authors>Britton RA</pubmed_authors><pubmed_authors>Versalovic J</pubmed_authors><pubmed_authors>Auchtung J</pubmed_authors><pubmed_authors>Endres BT</pubmed_authors><pubmed_authors>Nicholson M</pubmed_authors><pubmed_authors>Lux R</pubmed_authors><pubmed_authors>Wu Q</pubmed_authors><pubmed_authors>Yacyshyn B</pubmed_authors><pubmed_authors>Engevik AC</pubmed_authors><pubmed_authors>Luna RA</pubmed_authors><pubmed_authors>Savidge T</pubmed_authors><pubmed_authors>Ruan W</pubmed_authors><pubmed_authors>Crawford SE</pubmed_authors><pubmed_authors>Engevik MA</pubmed_authors><pubmed_authors>Yacyshyn MB</pubmed_authors><pubmed_authors>Estes MK</pubmed_authors><pubmed_authors>Danhof HA</pubmed_authors><pubmed_authors>Basseres E</pubmed_authors><pubmed_authors>Garey KW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fusobacteriumnucleatum Adheres to Clostridioides difficile via the RadD Adhesin to Enhance Biofilm Formation in Intestinal Mucus.</name><description>&lt;h4>Background &amp; aims&lt;/h4>Although Clostridioides difficile infection (CDI) is known to involve the disruption of the gut microbiota, little is understood regarding how mucus-associated microbes interact with C difficile. We hypothesized that select mucus-associated bacteria would promote C difficile colonization and biofilm formation.&lt;h4>Methods&lt;/h4>To create a model of the human intestinal mucus layer and gut microbiota, we used bioreactors inoculated with healthy human feces, treated with clindamycin and infected with C difficile with the addition of human MUC2-coated coverslips.&lt;h4>Results&lt;/h4>C difficile was found to colonize and form biofilms on MUC2-coated coverslips, and 16S rRNA sequencing showed a unique biofilm profile with substantial cocolonization with Fusobacterium species. </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-22T01:46:18.849Z</modification><creation>2025-04-05T20:06:02.646Z</creation></dates><accession>S-EPMC7956072</accession><cross_references><pubmed>33227279</pubmed><doi>10.1053/j.gastro.2020.11.034</doi></cross_references></HashMap>