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dc.contributor.authorMengeloglu, F.Z.
dc.contributor.authorÇopur Çiçek, A.
dc.contributor.authorKoçoğlu, E.
dc.contributor.authorSandalli, C.
dc.contributor.authorBudak, E.E.
dc.contributor.authorÖzgümüş, O.B.
dc.date.accessioned2020-12-19T20:05:54Z
dc.date.available2020-12-19T20:05:54Z
dc.date.issued2014
dc.identifier.issn0374-9096
dc.identifier.urihttps://hdl.handle.net/11436/3501
dc.descriptionPubMed: 24506715en_US
dc.description.abstractThe dissemination of antibiotic resistance genes between bacteria leads to serious problems in the treatment of infectious diseases. It has been shown that resistance genes can also be carried by the integrons. There are limited studies regarding the carriage of class 1 and 2 integrons in Adnetobacter baumannii and Pseudomonas aeruginosa clinical strains in Turkey. The aims of this study were to investigate the carriage rates of class 1 and class 2 integrans in A.baumannii and P.aeruginosa strains isolated from clinical samples in Abant Izzet Baysal University Hospital, and to characterize the antibiotic resistance gene cassettes in these integrans by sequence analyses. A total of 137 strains (77 Abaumannii and 60 P.aeruginosa) isolated from various clinical specimens (56% were sputum, 19% wound, 11 % urine, 11 % blood, 3% catheter), between March 2010-December 2012, were included in the study. The identification and antibiotic susceptibility tests of the isolates were performed by Vitek 2 Compact (bioMérieux, France) and BD Phoenix 100 (Becton Dickinson, USA) systems. The presence of intégrons were screened by PCR method using specific primer pairs targeting class 1 (intll) and 2 (intl2) integrase regions. All the samples that revealed integran amplification were subjected to DNA sequence analysis, both in the forms of cloned products and PCR amplicons. In the study, the highest susceptibility rates were found against colistin 96% and tigecycline 78% in A.baumannii, and against piperacillin/tazobactam 97% and piperacillin 93% in P.aeruginosa isolates. The highest resistance rate was determined for piperacillin/tazobactam 95% in A.baumannii strains. The presence of intll gene was detected in 33% (26/77) of A.baumannii and 10% (6/60) of P.aeruginosa isolates. When variable regions in intl1 positive strains were amplified by PCR, eight (8/77, 10%) A.baumannii and three (3/60, 5%) P.aeruginosa strains were found to harbor antibiotic resistance gene cassettes. Intl2 gene was not detected in any of the isolates. Resistance to piperacillin/tazobactam, ceftazidime, cefepime, ceftriaxone and ampicillin/sulbactam was detected as the common resistance pattern in all integron-positive A.baumannii strains, whereas resistance to ceftazidime, gentamicin and ciprofloxacin was the common pattern in all integron-positive P.aeruginosa strains. DNA sequence analysis of variable regions of integrons indicated that two separate gene cassette arrays (aacCl-aadA1 and aac(3)-1) were carried by A.baumannii strains, and two types of gene cassette arrays (bla QXA-30-aadA1 and bla0XA-11- cmlA7) were carried by P.aeruginosa strains. To our best knowledge, this is the first report of the gene sequence of blaQXA-11-cmlA7 defined in an integron gene cassette of P.aeruginosa.en_US
dc.language.isoturen_US
dc.publisher0-Belirleneceken_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAdnetobacter baumanniien_US
dc.subjectGene casetteen_US
dc.subjectIntegronen_US
dc.subjectPseudomonas aeruginosaen_US
dc.titleCarriage of class 1 and 2 integrons in acinetobacter baumannii and Pseudomonas aeruginosa isolated from clinical specimens and a novel gene cassette array: BlaOXA-11-cmlA7 [Klinik Örneklerden izole Edilen Acinetobacter baumannii ve Pseudomonas aeruginosa Suşlarinin Sinif 1 ve 2 integran Taşiyiciligi ve Yeni Bir Gen Kaseti Birlikteliği: Bla0XA-11-cmlA7]en_US
dc.title.alternativeKlinik Örneklerden izole Edilen Acinetobacter baumannii ve Pseudomonas aeruginosa Suşlarinin Sinif 1 ve 2 integran Taşiyiciligi ve Yeni Bir Gen Kaseti Birlikteliği: Bla0XA-11-cmlA7en_US
dc.typearticleen_US
dc.contributor.departmentRTEÜen_US
dc.identifier.volume48en_US
dc.identifier.issue1en_US
dc.identifier.startpage48en_US
dc.identifier.endpage58en_US
dc.relation.journalMikrobiyoloji Bultenien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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