4.8 Article

Fusobacterium nucleatum Adheres to Clostridioides difficile via the RadD Adhesin to Enhance Biofilm Formation in Intestinal Mucus

期刊

GASTROENTEROLOGY
卷 160, 期 4, 页码 1301-+

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2020.11.034

关键词

Clostridioides difficile; MUC2; Mucus; Biofilm

资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases [P30-DK-56338]
  2. National Institutes of Health [K01DK123195-01, KO1DK12186901, T32DK07644, F32AI136404, R01AI123278, U01AI124290]
  3. BioGaia AB (Stockholm, Sweden)

向作者/读者索取更多资源

The study revealed that certain mucus-associated bacteria can promote colonization and biofilm formation of C difficile, with some patients infected with C difficile harboring high levels of Fusobacterium species. The interaction between pathogenic C difficile and F nucleatum in the intestinal mucus layer is shown to be unique.
BACKGROUND & AIMS: 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. METHODS: 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. RESULTS: 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. Consistent with our bioreactor data, publicly available data sets and patient stool samples showed that a subset of patients with C difficile infection harbored high levels of Fusobacterium species. We observed colocalization of C difficile and F nucleatum in an aggregation assay using adult patients and stool of pediatric patients with inflammatory bowel disease and in tissue sections of patients with CDI. C difficile strains were found to coaggregate with F nucleatum subspecies in vitro; an effect that was inhibited by blocking or mutating the adhesin RadD on Fusobacterium and removal of flagella on C difficile. Aggregation was shown to be unique between F nucleatum and C difficile, because other gut commensals did not aggregate with C difficile. Addition of F nucleatum also enhanced C difficile biofilm formation and extracellular polysaccharide production. CONCLUSIONS: Collectively, these data show a unique interaction of between pathogenic C difficile and F nucleatum in the intestinal mucus layer.

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