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dc.contributor.authorÇiçek, Ayşegül Çopur
dc.contributor.authorSaral, Ayşegül
dc.contributor.authorIraz, Meryem
dc.contributor.authorCeylan, Ayşenur
dc.contributor.authorDüzgün, Azer Özad
dc.contributor.authorPeleg, Anton Y.
dc.contributor.authorSandallı, Cemal
dc.date.accessioned2020-12-19T20:03:13Z
dc.date.available2020-12-19T20:03:13Z
dc.date.issued2014
dc.identifier.citationCicek, A.C., Saral, A:, Iraz, M., Ceylan, A., Duzgun, A.O., Peleg, A.Y., Sandalli, C., (2014).OXA- and GES-type beta-lactamases predominate in extensively drug-resistant Acinetobacter baumannii isolates from a Turkish University Hospital.Clinical Microbiology and Infection, 20(5), 410-415.https://doi.org/10.1111/1469-0691.12338
dc.identifier.issn1198-743X
dc.identifier.issn1469-0691
dc.identifier.urihttps://doi.org/10.1111/1469-0691.12338
dc.identifier.urihttps://hdl.handle.net/11436/3124
dc.descriptionDUZGUN, AZER OZAD/0000-0002-6301-611X; DUZGUN, AZER OZAD/0000-0002-6301-611X; SARAL, AYSEGUL/0000-0002-7757-6812; Peleg, Anton/0000-0002-2296-2126; SANDALLI, Cemal/0000-0002-1298-3687en_US
dc.descriptionWOS: 000337674400019en_US
dc.descriptionPubMed: 23957892en_US
dc.description.abstractWe determined the antibiotic susceptibility and genetic mechanisms of resistance in clinical strains of Acinetobacter baumannii from Istanbul, Turkey. A total of 101 clinical strains were collected between November 2011 and July 2012. Antimicrobial susceptibility was performed using the Vitek 2 Compact system and E-test. Multiplex PCR was used for detecting bla(OXA-51-like), bla(OXA-23-like), bla(OXA-40-like) and bla(OXA-58-like) genes. ISAba1, bla(IMP-like), bla(VIM-like), bla(GES), bla(VEB), bla(PER-2), aac-3-Ia and aac-6'-Ib and NDM-1 genes were detected by PCR and sequencing. By multiplex PCR, all strains were positive for bla(OXA-51), 79 strains carried bla(OXA-23) and one strain carried bla(OXA-40). bla(OXA-51) and bla(OXA-23) were found together in 79 strains. ISAba1 element was detected in 81 strains, and in all cases it was found upstream of bla(OXA-51). GES-type carbapenemases were found in 24 strains (GES-11 in 16 strains and GES-22 in 8 strains) while bla(PER-2), bla(VEB-1), bla(NDM-1), bla(IMP)- and bla(VIM)-type carbapenemases were not observed. Aminoglycoside modifying enzyme (aac-3-Ia and aac-6'Ib) genes were detected in 13 and 15 strains, respectively. Ninety-seven (96%) A. baumannii strains were defined as MDR and of these, 98% were extensively drug resistant (sensitive only to colistin). Colistin remains the only active compound against all clinical strains. As seen in other regions, OXA-type carbapenemases, with or without an upstream ISAba1, predominate but GES-type carbapenemases also appear to have a significant presence. REP-PCR analysis was performed for molecular typing and all strains were collected into 12 different groups. To our knowledge, this is the first report of GES-11 and OXA-40 in A. baumannii from Turkey.en_US
dc.description.sponsorshipRecep Tayyip Erdogan UniversityRecep Tayyip Erdogan University [BAP-2012.106.01.11, BAP-2011.102.03.3]; Australian National Health and Medical Research CouncilNational Health and Medical Research Council of Australia [APP1047916, APP1010114]en_US
dc.description.sponsorshipThis study was supported by grants from Recep Tayyip Erdogan University (BAP-2012.106.01.11 and BAP-2011.102.03.3). AYP was supported by the Australian National Health and Medical Research Council (APP1047916 and APP1010114).en_US
dc.language.isoengen_US
dc.publisherElsevier Sci Ltden_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcinetobacter baumanniien_US
dc.subjectAntimicrobial agentsen_US
dc.subjectGES-11en_US
dc.subjectGES-22en_US
dc.subjectOXA-40en_US
dc.titleOXA- and GES-type beta-lactamases predominate in extensively drug-resistant Acinetobacter baumannii isolates from a Turkish University Hospitalen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Temel Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorÇiçek, Ayşegül Çopur
dc.contributor.institutionauthorSandallı, Cemal
dc.identifier.doi10.1111/1469-0691.12338
dc.identifier.volume20en_US
dc.identifier.issue5en_US
dc.identifier.startpage410en_US
dc.identifier.endpage415en_US
dc.ri.editoaen_US
dc.relation.journalClinical Microbiology and Infectionen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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