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Microbial genomic analysis reveals the essential role of inflammation in bacteria-induced colorectal cancer.

Nature communications | 2014

Enterobacteria, especially Escherichia coli, are abundant in patients with inflammatory bowel disease or colorectal cancer (CRC). However, it is unclear whether cancer is promoted by inflammation-induced expansion of E. coli and/or changes in expression of specific microbial genes. Here we use longitudinal (2, 12 and 20 weeks) 16S rRNA sequencing of luminal microbiota from ex-germ-free mice to show that inflamed Il10(-/-) mice maintain a higher abundance of Enterobacteriaceae than healthy wild-type mice. Experiments with mono-colonized Il10(-/-) mice reveal that host inflammation is necessary for E. coli cancer-promoting activity. RNA-sequence analysis indicates significant changes in E. coli gene catalogue in Il10(-/-) mice, with changes mostly driven by adaptation to the intestinal environment. Expression of specific genes present in the tumour-promoting E. coli pks island are modulated by inflammation/CRC development. Thus, progression of inflammation in Il10(-/-) mice supports Enterobacteriaceae and alters a small subset of microbial genes important for tumour development.

Pubmed ID: 25182170 RIS Download

Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK073338
  • Agency: NIH HHS, United States
    Id: P40 OD010995
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK047700
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK034987
  • Agency: NCI NIH HHS, United States
    Id: P30 CA016086
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK053347
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK47700
  • Agency: NIDDK NIH HHS, United States
    Id: R01DK053347
  • Agency: NIH HHS, United States
    Id: 5P40OD010995
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK73338

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