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dc.contributor.authorSánchez Urtaza, Sandra
dc.contributor.authorOcampo Sosa, Alain
dc.contributor.authorRodríguez Grande, Jorge
dc.contributor.authorEl-Kholy, Mohammed A.
dc.contributor.authorShawky, Sherine M.
dc.contributor.authorAlcorta Calvo, Miren Itziar
dc.contributor.authorGallego Andrés, Lucía
dc.date.accessioned2024-04-19T15:29:22Z
dc.date.available2024-04-19T15:29:22Z
dc.date.issued2023
dc.identifier.citationFrontiers in Cellular and Infection Microbiology 13 : (2023) // Article ID 1332736es_ES
dc.identifier.issn2235-2988
dc.identifier.urihttp://hdl.handle.net/10810/66813
dc.description.abstractMultidrug resistant Acinetobacter baumannii is one of the most important nosocomial pathogens worldwide. During the last decades it has become a major threat for healthcare settings due to the high antibiotic resistance rates among these isolates. Many resistance determinants are coded by conjugative or mobilizable plasmids, facilitating their dissemination. The majority of plasmids harbored by Acinetobacter species are less than 20 Kb, however, high molecular weight elements are the most clinically relevant since they usually contain antibiotic resistance genes. The aim of this work was to describe, classify and determine the genetic content of plasmids harbored by carbapem resistant A. baumannii isolates belonging to predominant clonal lineages circulating in hospitals from Alexandria, Egypt. The isolates were subjected to S1-Pulsed Field Gel Electrophoresis experiments to identify high molecular weight plasmids. To further analyze the plasmid content and the genetic localization of the antibiotic resistance genes, isolates were sequenced by Illumina Miseq and MinION Mk1C and a hybrid assembly was performed using Unicycler v0.5.0. Plasmids were detected with MOBsuite 3.0.3 and Copla.py v.1.0 and mapped using the online software Proksee.ca. Replicase genes were further analyzed through a BLAST against the Acinetobacter Plasmid Typing database. Eleven plasmids ranging in size from 4.9 to 205.6 Kb were characterized and mapped. All isolates contained plasmids, and, in many cases, more than two elements were identified. Antimicrobial resistance genes such as blaOXA-23, blaGES-like, aph(3’)-VI and qacEΔ1 were found in likely conjugative large plasmids; while virulence determinants such as septicolysin or TonB-dependent receptors were identified in plasmids of small size. Some of these resistance determinants were, in turn, located within transposons and class 1 integrons. Among the identified plasmids, the majority encoded proteins belonging to the Rep_3 family, but replicases of the RepPriCT_1 (Aci6) family were also identified. Plasmids are of high interest as antibiotic resistance control tools, since they may be used as genetic markers for antibiotic resistance and virulence, and also as targets for the development of compounds that can inhibit transfer processes.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectAcinetobacter baumanniies_ES
dc.subjectplasmidses_ES
dc.subjectreplicon typinges_ES
dc.subjectantibiotic resistance geneses_ES
dc.subjectwhole genome sequencinges_ES
dc.titlePlasmid content of carbapenem resistant Acinetobacter baumannii isolates belonging to five International Clones collected from hospitals of Alexandria, Egyptes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2024 Sánchez-Urtaza, Ocampo-Sosa, Rodríguez-Grande, El-Kholy, Shawky, Alkorta and Gallego. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fcimb.2023.1332736/fulles_ES
dc.identifier.doi10.3389/fcimb.2023.1332736
dc.departamentoesBioquímica y biología moleculares_ES
dc.departamentoesInmunología, microbiología y parasitologíaes_ES
dc.departamentoeuBiokimika eta biologia molekularraes_ES
dc.departamentoeuImmunologia, mikrobiologia eta parasitologiaes_ES


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© 2024 Sánchez-Urtaza, Ocampo-Sosa, Rodríguez-Grande, El-Kholy, Shawky, Alkorta and Gallego. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Except where otherwise noted, this item's license is described as © 2024 Sánchez-Urtaza, Ocampo-Sosa, Rodríguez-Grande, El-Kholy, Shawky, Alkorta and Gallego. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.