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Insight into phylogenomic bias of blaVIM-2 or blaNDM-1 dissemination amongst carbapenem resistant Pseudomonas aeruginosa

dc.contributor.authorFortunato, Gianuario
dc.contributor.authorVaz-Moreira, Ivone
dc.contributor.authorGajic, Ina
dc.contributor.authorManaia, Célia M.
dc.date.accessioned2023-04-13T17:23:51Z
dc.date.available2023-04-13T17:23:51Z
dc.date.issued2023-05-01
dc.description.abstractObjectives: Pseudomonas aeruginosa (P. aeruginosa) are ubiquitous opportunistic pathogens that combine intrinsic and acquired multidrug resistance phenotypes. Due to different types of acquired genes, carbapenem resistance has been expanding in this species. This study hypothesised that the spread of carbapenem resistance among P. aeruginosa is influenced by phylogenomic features, being distinct for different genes. Methods: To test this hypothesis, the genomes of P. aeruginosa harbouring bla VIM-2 or bla NDM-1 genes were compared. The bla VIM-2 gene was selected because, although frequent, it is almost restricted to this species and bla NDM-1 gene due to its wide interspecies distribution. A group of genomes harbouring the genes bla VIM-2 (n = 116) or bla NDM-1 (n = 27), available in GenBank, was characterised based on core phylogenomic analysis, functional categories in the accessory genome and mobile genetic elements flanking the selected genes. Results: Most bla VIM-2 gene hosts belonged to multilocus sequence types (ST) ST111 (n = 32 of 116) and ST233 (n = 27 of 116) and were reported in Europe (n = 75 of 116). The bla NDM-1 gene hosts were distributed by different STs (ST38, ST773, ST235, ST357 and ST654), frequently from Asia (n = 11 of 27). Significant differences in the prevalence of functional protein/enzyme annotations per number of accessory genomes were observed between bla VIM-2+ and bla NDM-1+. The bla VIM-2 gene was frequently inserted in the Tn402-like and Tn21 transposons family and rarely in IS6100, while bla NDM-1 gene was preferentially flanked by ISAba125 and ble MBL genes or associated with IS91 insertion sequence. Conclusion: The hypothesis that carbapenem resistance gene acquisition is not random among phylogenomic lineages was confirmed, suggesting the importance of phylogeny in the dissemination of antibiotic resistance genes.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.ijantimicag.2023.106788pt_PT
dc.identifier.eid85152530843
dc.identifier.issn0924-8579
dc.identifier.pmid36924802
dc.identifier.urihttp://hdl.handle.net/10400.14/40819
dc.identifier.wos000984352600001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectBeta-lactamasespt_PT
dc.subjectMobile genetic elementspt_PT
dc.subjectPhylogenetic diversitypt_PT
dc.subjectAntibiotic resistancept_PT
dc.titleInsight into phylogenomic bias of blaVIM-2 or blaNDM-1 dissemination amongst carbapenem resistant Pseudomonas aeruginosapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue5
oaire.citation.titleInternational Journal of Antimicrobial Agentspt_PT
oaire.citation.volume61
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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