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Article: Influence of the microenvironment on modulation of the host response by typhoid toxin

TitleInfluence of the microenvironment on modulation of the host response by typhoid toxin
Authors
KeywordsAtaxia-telangiectasia mutated (ATM)
bacterial genotoxins
colitis
immune response
immunomodulation
microenviroment
senescence
typhoid toxin
Issue Date6-Apr-2021
PublisherCell Press
Citation
Cell Reports, 2021, v. 35, n. 1 How to Cite?
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.


Persistent Identifierhttp://hdl.handle.net/10722/347819
ISSN

 

DC FieldValueLanguage
dc.contributor.authorMartin, Océane CB-
dc.contributor.authorBergonzini, Anna-
dc.contributor.authorLopez Chiloeches, Maria-
dc.contributor.authorPaparouna, Eleni-
dc.contributor.authorButter, Deborah-
dc.contributor.authorTheodorou, Sofia DP-
dc.contributor.authorHaykal, Maria M-
dc.contributor.authorBoutet-Robinet, Elisa-
dc.contributor.authorTebaldi, Toma-
dc.contributor.authorWakeham, Andrew-
dc.contributor.authorRhen, Mikael-
dc.contributor.authorGorgoulis, Vassilis G-
dc.contributor.authorMak, Tak-
dc.contributor.authorPateras, Ioannis S-
dc.contributor.authorFrisan, Teresa-
dc.date.accessioned2024-10-01T00:30:30Z-
dc.date.available2024-10-01T00:30:30Z-
dc.date.issued2021-04-06-
dc.identifier.citationCell Reports, 2021, v. 35, n. 1-
dc.identifier.issn2639-1856-
dc.identifier.urihttp://hdl.handle.net/10722/347819-
dc.description.abstract<p>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.</p>-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofCell Reports-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAtaxia-telangiectasia mutated (ATM)-
dc.subjectbacterial genotoxins-
dc.subjectcolitis-
dc.subjectimmune response-
dc.subjectimmunomodulation-
dc.subjectmicroenviroment-
dc.subjectsenescence-
dc.subjecttyphoid toxin-
dc.titleInfluence of the microenvironment on modulation of the host response by typhoid toxin-
dc.typeArticle-
dc.identifier.doi10.1016/j.celrep.2021.108931-
dc.identifier.pmid33826883-
dc.identifier.scopuseid_2-s2.0-85103781998-
dc.identifier.volume35-
dc.identifier.issue1-
dc.identifier.eissn2211-1247-
dc.identifier.issnl2211-1247-

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