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dc.rights.licenseopenen_US
dc.contributor.authorLOOT, Céline
dc.contributor.authorMILLOT, Gael
dc.contributor.authorRICHARD, Egill
dc.contributor.authorVIT, Claire
dc.contributor.authorDARRACQ, Baptiste
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPARISSI, Vincent
hal.structure.identifierHub Bioinformatique et Biostatistique - Bioinformatics and Biostatistics HUB
dc.contributor.authorLEMOINE, Frédéric
dc.contributor.authorNIAULT, Théophile
dc.contributor.authorCURY, Jean
dc.contributor.authorROCHA, Eduardo
dc.contributor.authorMAZEL, Didier
dc.date.accessioned2023-05-17T08:24:12Z
dc.date.available2023-05-17T08:24:12Z
dc.date.created2022-09-13
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/182187
dc.description.abstractEnIntegrons are genetic elements found exclusively in bacteria. They are well known for their role in disseminating antibiotic resistance genes among pathogens and more generally for enabling bacteria to rapidly adapt to changing environmental conditions. Integrons constitute a natural system to capture, stockpile, shuffle, express and disseminate genes embedded in cassettes. All these events are governed by the integron integrase through site-specific recombination between integron att sites (attC and attI sites). Here, we demonstrate that integron integrase can efficiently catalyze the insertion of cassettes in bacterial genomes, outside the att sites carried by the integron system. Surprisingly, analysis of more than 5 × 10 to the power of 5 independent clones revealed that the genome recombination sites differ greatly, in terms of sequence and structure, from both classical attC and attI recombination sites. We named theses new sites attG. Notably, among these a few are driving integration at very high rates. We also showed that, once inserted in genomes, cassettes can be expressed if located near a bacterial promoter. Moreover, even if occurring at low frequency, genome inserted cassettes can be excised precisely or imprecisely, inducing in this latter case, chromosomal modifications. These results unveil a new route for antibiotic resistance dissemination and expand the role of integrons in bacterial genome evolution.
dc.description.sponsorshipEtude de l'impact des intégrons chromosiques sur l'évolution des bactéries - ANR-21-CE12-0002en_US
dc.description.sponsorshipIntegrative Biology of Emerging Infectious Diseasesen_US
dc.language.isoENen_US
dc.rights.urihttp://hal.archives-ouvertes.fr/licences/copyright/
dc.subject.enBacterial evolution
dc.subject.enantibiotic resistance
dc.subject.ensite-specific recombination
dc.subject.enIntegron
dc.subject.encassette dynamics
dc.subject.enattC sites
dc.subject.engenome-wide mapping
dc.title.enA new route for integron cassette dissemination among bacterial genomes
dc.typeDocument de travail - Pré-publicationen_US
dc.identifier.doi10.1101/2022.09.11.507474en_US
dc.subject.halSciences du Vivant [q-bio]/Biochimie, Biologie Moléculaire/Biologie moléculaireen_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.institutionCNRSen_US
bordeaux.import.sourcehal
hal.identifierpasteur-03826688
hal.version1
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.au=LOOT,%20C%C3%A9line&MILLOT,%20Gael&RICHARD,%20Egill&VIT,%20Claire&DARRACQ,%20Baptiste&rft.genre=preprint


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