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Fusobacteriumnucleatum Adheres to Clostridioides difficile via the RadD Adhesin to Enhance Biofilm Formation in Intestinal Mucus.
Engevik, Melinda A; Danhof, Heather A; Auchtung, Jennifer; Endres, Bradley T; Ruan, Wenly; Bassères, Eugénie; Engevik, Amy C; Wu, Qinglong; Nicholson, Maribeth; Luna, Ruth Ann; Garey, Kevin W; Crawford, Sue E; Estes, Mary K; Lux, Renate; Yacyshyn, Mary Beth; Yacyshyn, Bruce; Savidge, Tor; Britton, Robert A; Versalovic, James.
Affiliation
  • Engevik MA; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas; Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, Texas. Electronic address: melinda.engevik@bcm.edu.
  • Danhof HA; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas.
  • Auchtung J; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas; Department of Food Science and Technology, University of Nebraska-Lincoln, Lincoln, Nebraska.
  • Endres BT; Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, Texas.
  • Ruan W; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas; Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, Texas.
  • Bassères E; Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, Texas.
  • Engevik AC; Department of Surgical Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Wu Q; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas; Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, Texas.
  • Nicholson M; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Luna RA; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas; Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, Texas.
  • Garey KW; Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, Texas.
  • Crawford SE; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas.
  • Estes MK; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas; Department of Surgical Sciences, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Lux R; Department of Periodontics, University of California Los Angeles School of Dentistry, Los Angeles, California.
  • Yacyshyn MB; Department of Medicine Division of Digestive Diseases University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Yacyshyn B; Department of Medicine Division of Digestive Diseases University of Cincinnati College of Medicine, Cincinnati, Ohio.
  • Savidge T; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas; Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, Texas.
  • Britton RA; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas.
  • Versalovic J; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas; Texas Children's Microbiome Center, Department of Pathology, Texas Children's Hospital, Houston, Texas.
Gastroenterology ; 160(4): 1301-1314.e8, 2021 03.
Article in En | MEDLINE | ID: mdl-33227279
ABSTRACT
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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Clostridioides difficile / Fusobacterium nucleatum / Clostridium Infections / Adhesins, Bacterial / Gastrointestinal Microbiome Limits: Humans Language: En Journal: Gastroenterology Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Clostridioides difficile / Fusobacterium nucleatum / Clostridium Infections / Adhesins, Bacterial / Gastrointestinal Microbiome Limits: Humans Language: En Journal: Gastroenterology Year: 2021 Document type: Article
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