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Searching for links between environmental and clinical mecA+ Staphylococcus aureus: a comparative genomics study

dc.contributor.authorRocha, Jaqueline
dc.contributor.authorSilva, Vanessa
dc.contributor.authorPoeta, Patrícia
dc.contributor.authorBotelho, João
dc.contributor.authorManaia, Célia M.
dc.date.accessioned2023-07-20T14:12:34Z
dc.date.available2023-07-20T14:12:34Z
dc.date.issued2023-10-15
dc.description.abstractStaphylococcus aureus integrate the list of highly virulent and antibiotic resistant pathogens, mainly due to the mecA gene, associated with methicillin resistance. Given the ubiquity of this species, the aim of this study was to investigate whether closely related mecA+ S. aureus found in the environment can be also thrive as clinical isolates and if the respective accessory genome may suggest bacterial adaptation. The genomes of environmental (water, animal facilities, food products, n = 111) isolates were compared with closely related genomes of clinical origin (human patients, n = 103). These genomes, available in the public database NCBI, were analysed for phylogeny, accessory genome, and presence of selected clinically relevant genes (n = 104). The genomes of environmental isolates belonged to 18 multi-locus sequence types (MLSTs), 11 of which also included clinical genomes, a result confirmed based on core-genome analysis. Genes significantly (p ≤ 0.05) more frequent among environmental genomes were related with resistance to β-lactams (blaI, blaPCI), aminoglycosides (ant(6)-Ia), macrolides (mph(C), erm(B)), enterotoxins (seg, sei, sem, sen, seo, seu) and serine protease functions (splB), among others. Genes significantly more frequent among clinical genomes were associated with resistance to macrolides (erm(C)), phenicols (fexA), fosfomycin (murA), the leucocidin virulence gene (lukS-PV), and serine protease functions (splA, splE). It is suggested that mecA+ S. aureus can be exchanged between clinical and environmental settings, with accessory traits (particularly antibiotic resistance, virulence and stress response) possibly being associated with the habitat. The interplay between phylogeny and accessory genome is an interesting contribution to better understanding the ecology and evolution of mecA+ S. aureus.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.scitotenv.2023.165078pt_PT
dc.identifier.eid85163486022
dc.identifier.issn0048-9697
dc.identifier.pmid37356759
dc.identifier.urihttp://hdl.handle.net/10400.14/41814
dc.identifier.wos001029934200001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.uricreativecommons.org/licenses/by-nc/2.0/pt_PT
dc.subjectAnimalspt_PT
dc.subjectComparative genomicspt_PT
dc.subjectFoodpt_PT
dc.subjectHumanspt_PT
dc.subjectmecA Staphylococcus aureuspt_PT
dc.subjectWaterpt_PT
dc.titleSearching for links between environmental and clinical mecA+ Staphylococcus aureus: a comparative genomics studypt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleScience of the Total Environmentpt_PT
oaire.citation.volume895pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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