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dc.contributor.authorRobledo Garrido, Marta es_ES
dc.contributor.authorÁlvarez, Beatrizes_ES
dc.contributor.authorGonzález Gutiérrez, Sheilaes_ES
dc.contributor.authorRuano-Gallego, Davides_ES
dc.contributor.authorFernández, Luis Ángeles_ES
dc.contributor.authorCruz Calahorra, Fernando de la es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-02-24T15:17:14Z
dc.date.available2023-02-24T15:17:14Z
dc.date.issued2022-12es_ES
dc.identifier.issn0305-1048es_ES
dc.identifier.issn1362-4962es_ES
dc.identifier.otherBIO2017-89081-Res_ES
dc.identifier.otherPID2020-117923GB-I00es_ES
dc.identifier.urihttps://hdl.handle.net/10902/27894
dc.description.abstractGenetic interventions on microbiomes, for clinical or biotechnological purposes, remain challenging. Conjugation-based delivery of genetic cargo is still unspecific and limited by low conjugation rates. Here we report an approach to overcome these problems, based on a synthetic bacterial adhesion system. Mating assemblers consist on a synthetic adhesion formed by the expression on the surface of donor and target cells of specific nanobodies (Nb) and their cognate antigen (Ag). The Nb?Ag bridge increased 1?3 logs transfer of a variety of plasmids, especially in liquid media, confirming that cell-cell docking is a main determinant limiting mating efficiency. Synthetic cell-to-cell adhesion allows efficient conjugation to targeted recipients, enhancing delivery of desired genes to a predefined subset of prey species, or even specific pathogenic strains such as enterohemorrhagic Escherichia coli (EHEC), within a bacterial community. The synthetic conjugation enhancer presented here optimizes plasmid delivery by selecting the target hosts with high selectivity.es_ES
dc.description.sponsorshipFUNDING: Spanish Science and Innovation Ministry (MCIN) [PID2020-117923GB-I00 to F.d.l.C.]; MCIN/AEI and FEDER [BIO2017-89081-R]; MCIN/AEI and NextGeneration EU/PRTR [PLEC2021-007739 to L.A.F.]. Conflict of interest statement. None declared ACKNOWLEDGEMENTS: We thank R. Fernandez-López for providing us with the BWmKate2 strain and, along with M. P. Garcillan-Barcia, for helpful discussions. We also thank E. Zechner for providing the pAR106 plasmid, and I. Rosenshine for EHEC strains and V. Campa for technical assistance in setting up the microscopy assay.es_ES
dc.format.extent13 p.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rightsAttribution 4.0 International*
dc.rights© The Author(s) 2022es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceNucleic Acids Research, 2022, gkac1164es_ES
dc.titleTargeted bacterial conjugation mediated by synthetic cell-to-cell adhesionses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1093/nar/gkac1164es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International