Publication:
Pangenome of Acinetobacter baumannii uncovers two groups of genomes, one of them with genes involved in CRISPR/Cas defence systems associated with the absence of plasmids and exclusive genes for biofilm formation.

dc.contributor.authorMangas, Eugenio L
dc.contributor.authorRubio, Alejandro
dc.contributor.authorÁlvarez-Marín, Rocío
dc.contributor.authorLabrador-Herrera, Gema
dc.contributor.authorPachón, Jerónimo
dc.contributor.authorPachón-Ibáñez, María Eugenia
dc.contributor.authorDivina, Federico
dc.contributor.authorPérez-Pulido, Antonio J
dc.date.accessioned2023-02-08T14:39:29Z
dc.date.available2023-02-08T14:39:29Z
dc.date.issued2019
dc.description.abstractAcinetobacter baumannii is an opportunistic bacterium that causes hospital-acquired infections with a high mortality and morbidity, since there are strains resistant to virtually any kind of antibiotic. The chase to find novel strategies to fight against this microbe can be favoured by knowledge of the complete catalogue of genes of the species, and their relationship with the specific characteristics of different isolates. In this work, we performed a genomics analysis of almost 2500 strains. Two different groups of genomes were found based on the number of shared genes. One of these groups rarely has plasmids, and bears clustered regularly interspaced short palindromic repeat (CRISPR) sequences, in addition to CRISPR-associated genes (cas genes) or restriction-modification system genes. This fact strongly supports the lack of plasmids. Furthermore, the scarce plasmids in this group also bear CRISPR sequences, and specifically contain genes involved in prokaryotic toxin-antitoxin systems that could either act as the still little known CRISPR type IV system or be the precursors of other novel CRISPR/Cas systems. In addition, a limited set of strains present a new cas9-like gene, which may complement the other cas genes in inhibiting the entrance of new plasmids into the bacteria. Finally, this group has exclusive genes involved in biofilm formation, which would connect CRISPR systems to the biogenesis of these bacterial resistance structures.
dc.identifier.doi10.1099/mgen.0.000309
dc.identifier.essn2057-5858
dc.identifier.pmcPMC6927304
dc.identifier.pmid31626589
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927304/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1099/mgen.0.000309
dc.identifier.urihttp://hdl.handle.net/10668/14956
dc.issue.number11
dc.journal.titleMicrobial genomics
dc.journal.titleabbreviationMicrob Genom
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAcinetobacter baumannii
dc.subjectCRISPR
dc.subjectbacterial genomics
dc.subjectbiofilm
dc.subjectplasmids
dc.subjecttoxin–antitoxin
dc.subject.meshAcinetobacter baumannii
dc.subject.meshBacteria
dc.subject.meshBacterial Proteins
dc.subject.meshBiofilms
dc.subject.meshCRISPR-Cas Systems
dc.subject.meshClustered Regularly Interspaced Short Palindromic Repeats
dc.subject.meshGenome, Bacterial
dc.subject.meshGenomics
dc.subject.meshPhylogeny
dc.subject.meshPlasmids
dc.titlePangenome of Acinetobacter baumannii uncovers two groups of genomes, one of them with genes involved in CRISPR/Cas defence systems associated with the absence of plasmids and exclusive genes for biofilm formation.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number5
dspace.entity.typePublication

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