Relationship between Vancomycin MIC and Virulence Gene Expression in Clonal Complexes of Methicillin-Susceptible Staphylococcus aureus Strains Isolated from Left-sided Endocarditis

dc.contributor.authorPericàs, Juan M.
dc.contributor.authorCervera, Carlos
dc.contributor.authorGarcía de la Mària, Cristina
dc.contributor.authorSharma-Kuinkel, Batu K.
dc.contributor.authorGonzales, Rachelle
dc.contributor.authorMoreno Camacho, Ma. Asunción
dc.contributor.authorAlmela, M. (Manel)
dc.contributor.authorFalces Salvador, Carles
dc.contributor.authorQuintana, Eduard
dc.contributor.authorFuster Pelfort, David
dc.contributor.authorMarco Reverté, Francesc
dc.contributor.authorBayer, Arnold S.
dc.contributor.authorFowler, Vance G.
dc.contributor.authorMiró Meda, José M. (José María), 1956-
dc.contributor.authorHospital Clinic Endocarditis Study Group
dc.date.accessioned2020-05-27T17:49:47Z
dc.date.available2021-07-01T05:10:19Z
dc.date.issued2020-02-21
dc.date.updated2020-05-27T17:49:48Z
dc.description.abstractHigher vancomycin MICs have been associated with more complicated courses and higher mortality rates in patients with Staphylococcus aureus bacteremia and infective endocarditis (IE). The aim of this study was to investigate whether the strains belonging to the cohort of 93 patients from a previously published study in which patients with strains with vancomycin MICs of ≥1.5 μg/ml presented higher mortality rates and systemic emboli than patients with strains with vancomycin MICs of <1.5 μg/ml had specific patterns of virulence factors, clonal complex (CC) types, or the ability to form biofilms. Vancomycin MICs were determined by Etest, and the isolates underwent spa typing to infer the CC, biofilm studies, a thrombin-induced platelet microbicidal assay, and multiplex PCR for the presence of virulence genes. We found no differences in genes encoding adhesins, toxins, or other putative virulence genes according to the vancomycin MIC group. CC30, CC34, and CC45 represented nearly half of the isolates, and there was no association with the vancomycin MIC. agr subgroups I and III predominated, with no association with the vancomycin MIC. Isolates with higher vancomycin MICs exhibited a poorer ability to form biofilms with and without the presence of vancomycin (2.03 versus 2.48 [P < 0.001], respectively, for isolates with higher vancomycin MICs and 2.60 versus 2.87 [P = 0.022], respectively, for isolates with lower vancomycin MICs). In the multivariable analysis, efb and V8 were risk factors for major emboli (adjusted odds ratio [aOR] = 7.5 and 95% confidence interval [CI] = 1.2 to 46.6 for efb, and aOR = 3.9 and 95% CI = 1.1 to 14.1 for V8), whereas no genotypic predictors of in-hospital mortality were found. No clear associations between genes encoding virulence factors, agr type, clonal complexes, mortality, and major embolic events according to vancomycin MIC group were found.
dc.format.extent14 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec695888
dc.identifier.issn0066-4804
dc.identifier.pmid31907181
dc.identifier.urihttps://hdl.handle.net/2445/162700
dc.language.isoeng
dc.publisherAmerican Society for Microbiology
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1128/AAC.01579-19
dc.relation.ispartofAntimicrobial Agents and Chemotherapy, 2020, vol. 64, num. 3, p. e01579-19
dc.relation.urihttps://doi.org/10.1128/AAC.01579-19
dc.rights(c) American Society for Microbiology, 2020
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationEndocarditis
dc.subject.classificationInfeccions per estafilococs
dc.subject.classificationAntibiòtics
dc.subject.otherEndocarditis
dc.subject.otherStaphylococcal infections
dc.subject.otherAntibiotics
dc.titleRelationship between Vancomycin MIC and Virulence Gene Expression in Clonal Complexes of Methicillin-Susceptible Staphylococcus aureus Strains Isolated from Left-sided Endocarditis
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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