| Literature DB >> 33826883 |
Océane C B Martin1, Anna Bergonzini2, Maria Lopez Chiloeches2, Eleni Paparouna3, Deborah Butter1, Sofia D P Theodorou3, Maria M Haykal4, Elisa Boutet-Robinet5, Toma Tebaldi6, Andrew Wakeham7, Mikael Rhen8, Vassilis G Gorgoulis9, Tak Mak7, Ioannis S Pateras3, Teresa Frisan10.
Abstract
Bacterial genotoxins cause DNA damage in eukaryotic cells, resulting in activation of the DNA damage response (DDR) in vitro. These toxins are produced by Gram-negative bacteria, enriched in the microbiota of inflammatory bowel disease (IBD) and colorectal cancer (CRC) patients. However, their role in infection remains poorly characterized. We address the role of typhoid toxin in modulation of the host-microbial interaction in health and disease. Infection with a genotoxigenic Salmonella protects mice from intestinal inflammation. We show that the presence of an active genotoxin promotes DNA fragmentation and senescence in vivo, which is uncoupled from an inflammatory response and unexpectedly associated with induction of an anti-inflammatory environment. The anti-inflammatory response is lost when infection occurs in mice with acute colitis. These data highlight a complex context-dependent crosstalk between bacterial-genotoxin-induced DDR and the host immune response, underlining an unexpected role for bacterial genotoxins.Entities:
Keywords: Ataxia-telangiectasia mutated (ATM); bacterial genotoxins; colitis; immune response; immunomodulation; microenviroment; senescence; typhoid toxin
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Year: 2021 PMID: 33826883 DOI: 10.1016/j.celrep.2021.108931
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423