| Literature DB >> 26560421 |
Nadège Bossuet-Greif1,2,3,4, Damien Dubois1,2,3,4,5, Claude Petit1,2,3,4,6, Sophie Tronnet1,2,3,4, Patricia Martin1,2,3,4,5, Richard Bonnet7, Eric Oswald1,2,3,4,5, Jean-Philippe Nougayrède1,2,3,4.
Abstract
The genomic pks island codes for the biosynthetic machinery that produces colibactin, a peptide-polyketide metabolite. Colibactin is a genotoxin that contributes to the virulence of extra-intestinal pathogenic Escherichia coli and promotes colorectal cancer. In this work, we examined whether the pks-encoded clbS gene of unknown function could participate in the self-protection of E. coli-producing colibactin. A clbS mutant was not impaired in the ability to inflict DNA damage in HeLa cells, but the bacteria activated the SOS response and ceased to replicate. This autotoxicity phenotype was markedly enhanced in a clbS uvrB double mutant inactivated for DNA repair by nucleotide excision but was suppressed in a clbS clbA double mutant unable to produce colibactin. In addition, ectopic expression of clbS protected infected HeLa cells from colibactin. Thus, ClbS is a resistance protein blocking the genotoxicity of colibactin both in the procaryotic and the eucaryotic cells.Entities:
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Year: 2015 PMID: 26560421 DOI: 10.1111/mmi.13272
Source DB: PubMed Journal: Mol Microbiol ISSN: 0950-382X Impact factor: 3.501