Publication:
Genomic Background and Phylogeny of cfiA-Positive Bacteroides fragilis Strains Resistant to Meropenem-EDTA.

dc.contributor.authorValdezate, Sylvia
dc.contributor.authorCobo, Fernando
dc.contributor.authorMonzón, Sara
dc.contributor.authorMedina-Pascual, María J
dc.contributor.authorZaballos, Ángel
dc.contributor.authorCuesta, Isabel
dc.contributor.authorPino-Rosa, Silvia
dc.contributor.authorVillalón, Pilar
dc.date.accessioned2023-02-09T10:50:01Z
dc.date.available2023-02-09T10:50:01Z
dc.date.issued2021-03-16
dc.description.abstractBacteroides fragilis shows high antimicrobial resistance (AMR) rates and possesses numerous AMR mechanisms. Its carbapenem-resistant strains (metallo-β-lactamase cfiA-positive) appear as an emergent, evolving clade. This work examines the genomes, taxonomy, and phylogenetic relationships with respect to other B. fragilis genomes of two B. fragilis strains (CNM20180471 and CNM20200206) resistant to meropenem+EDTA and other antimicrobial agents. Both strains possessed cfiA genes (cfiA14b and the new cfiA28), along with other AMR mechanisms. The presence of other efflux-pump genes, mexAB/mexJK/mexXY-oprM, acrEF/mdtEF-tolC, and especially cusR, which reduces the entry of carbapenem via the repression of porin OprD, may be related to meropenem-EDTA resistance. None of the detected insertion sequences were located upstream of cfiA. The genomes of these and other B. fragilis strains that clustered together in phylogenetic analyses did not meet the condition of >95% average nucleotide/amino acid identity, or >70% in silico genome-to-genome hybridization similarity, to be deemed members of the same species, although 95% average nucleotide/amino acid identity, or >70% in silico genome-to-genome hybridization similarity, to be deemed members of the same species, although 70% in silico genome-to-genome hybridization similarity, to be deemed members of the same species, although Carbapenem-resistant strains may be considered a distinct clonal entity, and their surveillance is recommended given the ease with which they appear to acquire AMR.
dc.identifier.doi10.3390/antibiotics10030304
dc.identifier.issn2079-6382
dc.identifier.pmcPMC8001070
dc.identifier.pmid33809460
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001070/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2079-6382/10/3/304/pdf?version=1615885956
dc.identifier.urihttp://hdl.handle.net/10668/17512
dc.issue.number3
dc.journal.titleAntibiotics (Basel, Switzerland)
dc.journal.titleabbreviationAntibiotics (Basel)
dc.language.isoen
dc.organizationHospital Universitario Virgen de las Nieves
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBacteroides fragilis
dc.subjectcarbapenems
dc.subjectcfiA14
dc.subjectcfiA28
dc.subjectdivision II
dc.subjectmultidrug resistance
dc.subjectporin inactivation
dc.subjectsusceptibility
dc.titleGenomic Background and Phylogeny of cfiA-Positive Bacteroides fragilis Strains Resistant to Meropenem-EDTA.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number10
dspace.entity.typePublication

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