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AIEC colonization and pathogenicity: influence of previous antibiotic treatment and preexisting inflammation
Maryline Drouet1, Cécile Vignal, Elisabeth Singer
1University Lille Nord de France, Lille, France.
Background:
Inflammatory bowel diseases (IBD) patients are abnormally colonized by adherent-invasive Escherichia coli (AIEC). NOD2 gene mutations impair intracellular bacterial clearance. We evaluated the impact of antibiotic treatment on AIEC colonization in wildtype (WT) and NOD2 knockout mice (NOD2KO) and the consequences on intestinal inflammation.
Methods:
After 3 days of antibiotic treatment, mice were infected for 2 days with 10⁹ CFU AIEC and sacrificed 1, 5, and 60 days later. In parallel, mice were challenged with AIEC subsequent to a dextran sodium sulfate (DSS) treatment and sacrificed 9 days later. Ileum, colon, and mesenteric tissues were sampled for AIEC quantification and evaluation of inflammation.
Results:
Without antibiotic treatment, AIEC was not able to colonize WT and NOD2KO mice. Compared with nontreated animals, antibiotic treatment led to a significant increase in ileal and colonic colonization of AIEC in WT and/or NOD2KO mice. Persistent AIEC colonization was observed until day 5 only in NOD2KO mice, disappearing at day 60. Mesenteric translocation of AIEC was observed only in NOD2KO mice. No inflammation was observed in WT and NOD2KO mice treated with antibiotics and infected with AIEC. During DSS-induced colitis, colonization and persistence of AIEC was observed in the colon. Moreover, a dramatic increase in clinical, histological, and molecular parameters of colitis was observed in mice infected with AIEC but not with a commensal E. coli strain.
Conclusions:
Antibiotic treatment was necessary for AIEC colonization of the gut and mesenteric tissues and persistence of AIEC was dependent on NOD2. AIEC exacerbated a preexisting DSS-induced colitis in WT mice.
Insights
Antibiotic treatment enables adherent-invasive Escherichia coli (AIEC) gut colonization. NOD2 gene function influences AIEC persistence and exacerbation of inflammatory bowel disease (IBD) models.
Area of Science:
- Microbiology
- Immunology
- Gastroenterology
Background:
- Inflammatory bowel diseases (IBD) are linked to abnormal gut colonization by adherent-invasive Escherichia coli (AIEC).
- Mutations in the NOD2 gene impair the host's ability to clear intracellular bacteria, potentially affecting AIEC interactions.
- Understanding the interplay between antibiotic use, AIEC, and host genetics is crucial for IBD management.
Purpose of the Study:
- To investigate the impact of antibiotic treatment on AIEC colonization in wildtype (WT) and NOD2 knockout (NOD2KO) mice.
- To assess the consequences of AIEC colonization on intestinal inflammation in these models.
- To determine the role of NOD2 in AIEC persistence and translocation.
Main Methods:
- Mice (WT and NOD2KO) received antibiotic treatment followed by AIEC infection, with sampling at various time points.
- A separate cohort underwent dextran sodium sulfate (DSS) treatment followed by AIEC challenge to model colitis.
- AIEC colonization, mesenteric translocation, and inflammatory markers were quantified in ileum, colon, and mesenteric tissues.
Main Results:
- Antibiotic treatment was essential for AIEC colonization in both WT and NOD2KO mice.
- AIEC persisted longer in the ileum and colon of NOD2KO mice compared to WT mice.
- AIEC exacerbated DSS-induced colitis in WT mice, increasing clinical and histological inflammation.
- Mesenteric translocation of AIEC was observed exclusively in NOD2KO mice.
Conclusions:
- Antibiotic administration is a prerequisite for AIEC gut and mesenteric colonization.
- NOD2 plays a critical role in controlling AIEC persistence and preventing mesenteric translocation.
- AIEC can worsen pre-existing colitis, highlighting its pathogenic potential in IBD contexts.
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