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dc.contributor.authorGianecini, Ricardo Aes
dc.contributor.authorRomero, María Mercedeses
dc.contributor.authorOviedo, Claudiaes
dc.contributor.authorVacchino, Martines
dc.contributor.authorGalarza, Patricia G.es
dc.date.accessioned2020-12-04T09:07:16Z-
dc.date.available2020-12-04T09:07:16Z-
dc.date.issued2017-06-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/1813-
dc.descriptionFil: Gianecini, Ricardo. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas; Argentina.es
dc.descriptionFil: Romero, Maria de Las Mercedes. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas; Argentina.es
dc.descriptionFil: Oviedo, Claudia. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas; Argentina.es
dc.descriptionFil: Vacchino, Martin. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas; Argentina.es
dc.descriptionFil: Galarza, Patricia. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas; Argentina.es
dc.description.abstractBackground: The emergence of Neisseria gonorrhoeae strains with decreased susceptibility to cephalosporins represents a major concern globally. The aim of this study was to examine the phenotypic and molecular characteristics of N. gonorrhoeae isolates with decreased susceptibility to ceftriaxone and cefixime in Argentina. Methods: A total of 1987 isolates were collected during 2009 and 2013. The susceptibility to penicillin G, tetracycline, ciprofloxacin, cefixime, ceftriaxone, and azithromycin was determined using the agar dilution method. The major extended-spectrum cephalosporin resistance determinants (penA, mtrR, and porB1b) were sequenced in 42 N. gonorrhoeae isolates that showed decreased susceptibility to ceftriaxone (minimum inhibitory concentration [MIC], 0.06-0.125 mg/L) and cefixime (MIC, 0.125-0.25 mg/L). Genotyping by N. gonorrhoeae multiantigen sequence typing (NG-MAST) was performed. Results: Between 2009 and 2013, there was a shift in the modal MICs for ceftriaxone. Among the 42 isolates exhibiting decreased susceptibility to ceftriaxone and cefixime, 95.2% were resistant to penicillin G, 95.2% to tetracycline, 97.6% to ciprofloxacin, and 33.3% to azithromycin. Thirty-five (83.3%) of the 42 isolates had a mosaic penA allele XXXIV, which has been previously associated with resistance to ceftriaxone and cefixime as well as treatment failures. The isolates that contained the mosaic penicillin-binding protein 2 (PBP2) XXXIV were associated with NG-MAST ST1407 or closely related genotypes. Conclusions: In Argentina, N. gonorrhoeae isolates with decreased susceptibility to cefixime and ceftriaxone have now emerged, mostly due to the introduction of the internationally spread multidrug-resistant NG-MAST ST1407.es
dc.formatpdf -
dc.language.isoenes
dc.publisherLippincott, Williams & Wilkinses
dc.relationdatasets-
dc.relation.ispartofSexually transmitted diseaseses
dc.rightsOpen Access-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.sourceSexually Transmitted Diseases 2017; 44(6):351-355-
dc.subjectAntibacterianoses
dc.subjectArgentinaes
dc.subjectCefiximaes
dc.subjectCeftriaxonaes
dc.subjectResistencia a las Cefalosporinases
dc.subjectGonorreaes
dc.subjectHumanoses
dc.subjectPruebas de Sensibilidad Microbianaes
dc.subjectTipificación Moleculares
dc.subjectNeisseria gonorrhoeaees
dc.subjectFilogeniaes
dc.subjectVigilancia de Guardiaes
dc.subjectAnálisis de Secuencia de ADNes
dc.titleEmergence and spread of Neisseria gonorrhoeae isolates with decreased susceptibility to extended-spectrum Cephalosporins in Argentina, 2009 to 2013es
dc.typeArtículoes
dc.rights.licenseCreative Commons Attribution 4.0 International License-
dc.identifier.doi10.1097/OLQ.0000000000000603-
anlis.essnrd1-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.openairetypeArtículo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.deptInstituto Nacional de Enfermedades Infecciosas (INEI)-
crisitem.author.deptDepartamento de Bacteriología-
crisitem.author.deptServicio de Enfermedades de Transmisión Sexual-
crisitem.author.deptAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.deptInstituto Nacional de Enfermedades Infecciosas (INEI)-
crisitem.author.deptDepartamento de Bacteriología-
crisitem.author.deptServicio de Enfermedades de Transmisión Sexual-
crisitem.author.deptAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.deptInstituto Nacional de Enfermedades Infecciosas (INEI)-
crisitem.author.deptDepartamento de Bacteriología-
crisitem.author.deptServicio de Enfermedades de Transmisión Sexual-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Enfermedades Infecciosas (INEI)-
crisitem.author.parentorgDepartamento de Bacteriología-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Enfermedades Infecciosas (INEI)-
crisitem.author.parentorgDepartamento de Bacteriología-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Enfermedades Infecciosas (INEI)-
crisitem.author.parentorgDepartamento de Bacteriología-
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