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Activity of Ceftazidime-Avibactam against Clinical and Isogenic Laboratory Pseudomonas aeruginosa Isolates Expressing Combinations of Most Relevant β-Lactam Resistance Mechanisms.

dc.contributor.authorTorrens, Gabriel
dc.contributor.authorCabot, Gabriel
dc.contributor.authorOcampo-Sosa, Alain A
dc.contributor.authorConejo, M Carmen
dc.contributor.authorZamorano, Laura
dc.contributor.authorNavarro, Ferran
dc.contributor.authorPascual, Alvaro
dc.contributor.authorMartinez-Martinez, Luis
dc.contributor.authorOliver, Antonio
dc.contributor.funderAstraZeneca Pharmaceutical Spain
dc.contributor.funderMinisterio de Ciencia e Innovación of Spain
dc.contributor.funderInstituto de Salud Carlos III
dc.date.accessioned2023-01-25T08:35:00Z
dc.date.available2023-01-25T08:35:00Z
dc.date.issued2016-09-23
dc.description.abstractThe activity of ceftazidime-avibactam was compared with that of ceftazidime alone and meropenem against a collection of 190 Pseudomonas aeruginosa clinical isolates recovered from a multicenter study of bloodstream infections. The addition of avibactam increased ceftazidime susceptibility in the complete collection of strains (64.7% to 91.1%) and particularly among subsets of isolates showing AmpC hyperproduction (10.9% to 76.1%) or multidrug resistance (MDR) profiles (27% to 77.8%). The MICs of ceftazidime-avibactam, in contrast with those of ceftazidime or meropenem, remained at ≤4 μg/ml for a panel of 16 P. aeruginosa PAO1 isogenic mutants expressing multiple combinations of the most relevant β-lactam resistance mechanisms.
dc.description.versionSi
dc.identifier.citationTorrens G, Cabot G, Ocampo-Sosa AA, Conejo MC, Zamorano L, Navarro F, et al. Activity of Ceftazidime-Avibactam against Clinical and Isogenic Laboratory Pseudomonas aeruginosa Isolates Expressing Combinations of Most Relevant β-Lactam Resistance Mechanisms. Antimicrob Agents Chemother. 2016 Sep 23;60(10):6407-10.
dc.identifier.doi10.1128/AAC.01282-16
dc.identifier.essn1098-6596
dc.identifier.pmcPMC5038310
dc.identifier.pmid27480848
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5038310/pdf
dc.identifier.unpaywallURLhttps://europepmc.org/articles/pmc5038310?pdf=render
dc.identifier.urihttp://hdl.handle.net/10668/10328
dc.issue.number10
dc.journal.titleAntimicrobial agents and chemotherapy
dc.journal.titleabbreviationAntimicrob Agents Chemother
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen Macarena
dc.page.number6407-6410
dc.provenanceRealizada la curación de contenido 10/03/2025
dc.publisherAmerican Society for Microbiology
dc.pubmedtypeJournal Article
dc.relation.projectIDREIPI RD12/0015
dc.relation.projectIDRD16/00016
dc.relation.publisherversionhttps://journals.asm.org/doi/10.1128/AAC.01282-16?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed
dc.rights.accessRightsRestricted Access
dc.subjectAzabicyclo Compounds
dc.subjectDrug Combinations
dc.subjectMeropenem
dc.subjectPseudomonas aeruginosa
dc.subjectbeta-Lactam Resistance
dc.subject.decsCeftazidima
dc.subject.decsMeropenem
dc.subject.decsEsguinces y distensiones
dc.subject.decsPseudomonas aeruginosa
dc.subject.decsLactamas
dc.subject.decsResistencia a múltiples medicamentos
dc.subject.decsEstudio multicéntrico
dc.subject.decsSepsis
dc.subject.meshCeftazidime
dc.subject.meshHumans
dc.subject.meshMicrobial Sensitivity Tests
dc.subject.meshThienamycins
dc.titleActivity of Ceftazidime-Avibactam against Clinical and Isogenic Laboratory Pseudomonas aeruginosa Isolates Expressing Combinations of Most Relevant β-Lactam Resistance Mechanisms.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number60
dspace.entity.typePublication

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