Escherichia coliClbS is a colibactin resistance protein

被引:50
作者
Bossuet-Greif, Nadege [1 ,2 ,3 ,4 ]
Dubois, Damien [1 ,2 ,3 ,4 ,5 ]
Petit, Claude [1 ,2 ,3 ,4 ,6 ]
Tronnet, Sophie [1 ,2 ,3 ,4 ]
Martin, Patricia [1 ,2 ,3 ,4 ,5 ]
Bonnet, Richard [7 ]
Oswald, Eric [1 ,2 ,3 ,4 ,5 ]
Nougayrede, Jean-Philippe [1 ,2 ,3 ,4 ]
机构
[1] INRA, USC 1360, Toulouse, France
[2] INSERM, UMR 1043, Toulouse, France
[3] CNRS, UMR 5282, Toulouse, France
[4] Univ Toulouse, UPS, Toulouse, France
[5] CHU Toulouse, Serv Bacteriol Hyg, Toulouse, France
[6] INP ENVT ESC, Toulouse, France
[7] Univ Auvergne, INSERM UMR 1071, INRA USC 2018, Clermont Ferrand, France
关键词
COLON-TUMOR GROWTH; GENOTOXIN COLIBACTIN; CROSS-LINKS; BIOSYNTHESIS; MECHANISM; ANTIBIOTICS; PERSISTENCE; POLYKETIDE; BACTERIA; BREAKS;
D O I
10.1111/mmi.13272
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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 clbSuvrB double mutant inactivated for DNA repair by nucleotide excision but was suppressed in a clbSclbA 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.
引用
收藏
页码:897 / 908
页数:12
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