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Patients with familial adenomatous polyposis harbor colonic biofilms containing tumorigenic bacteria
Author(s) -
Christine M. Dejea,
Payam Fathi,
John M. Craig,
Annemarie Boleij,
Rahwa Taddese,
Abby L. Geis,
Xinqun Wu,
Christina E. DeStefano Shields,
Elizabeth M. Hechenbleikner,
David L. Huso,
Robert A. Anders,
Francis M. Giardiello,
Elizabeth C. Wick,
Hao Wang,
Shaoguang Wu,
Drew M. Pardoll,
Franck Housseau,
Cynthia L. Sears
Publication year - 2018
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aah3648
Subject(s) - familial adenomatous polyposis , colorectal cancer , microbiome , adenomatous polyposis coli , adenomatous polyps , medicine , bacteria , biofilm , gastroenterology , biology , cancer , pathology , genetics , colonoscopy
Individuals with sporadic colorectal cancer (CRC) frequently harbor abnormalities in the composition of the gut microbiome; however, the microbiota associated with precancerous lesions in hereditary CRC remains largely unknown. We studied colonic mucosa of patients with familial adenomatous polyposis (FAP), who develop benign precursor lesions (polyps) early in life. We identified patchy bacterial biofilms composed predominately of Escherichia coli and Bacteroides fragilis Genes for colibactin ( clbB ) and Bacteroides fragilis toxin ( bft ), encoding secreted oncotoxins, were highly enriched in FAP patients' colonic mucosa compared to healthy individuals. Tumor-prone mice cocolonized with E. coli (expressing colibactin), and enterotoxigenic B. fragilis showed increased interleukin-17 in the colon and DNA damage in colonic epithelium with faster tumor onset and greater mortality, compared to mice with either bacterial strain alone. These data suggest an unexpected link between early neoplasia of the colon and tumorigenic bacteria.

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