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dc.contributor.authorKayacan, Cigdem Bal
dc.contributor.authorAktas, Zerrin
dc.date.accessioned2021-03-04T13:27:26Z
dc.date.available2021-03-04T13:27:26Z
dc.date.issued2008
dc.identifier.citationAktas Z., Kayacan C. B. , "Investigation of metallo-beta-lactamase producing strains of Pseudomonas aeruginosa and Acinetobacter baumannii by E-test, disk synergy and PCR", SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, cilt.40, sa.4, ss.320-325, 2008
dc.identifier.issn0036-5548
dc.identifier.otherav_7c856ac0-f227-4654-997b-a0b8edd75270
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/85154
dc.identifier.urihttps://doi.org/10.1080/00365540701704698
dc.description.abstractCarbapenem non-susceptible Pseudomonas aeruginosa and Acinetobacter baumannii strains were tested for the presence of metallo-beta-lactamases (MBLs) by EDTA-synergy screening. Imipenem hydrolysis was investigated by a bioassay and IMP-/VIM-encoding genes by PCR. No blaIMP/VIM related genes or imipenemase activity were detected although E-test found all strains as MBL-positive. Disk synergy tests with 0.5M EDTA determined 63.6-100%, while those with 0.1M EDTA detected 0-7.7% of isolates as MBL producers. Most strains were susceptible to EDTA. In conclusion, for MBL-screening purposes, EDTA-synergy results change with molarity of EDTA, but even if some false positives are encountered, 0.1M EDTA seems to be acceptable.
dc.language.isoeng
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectBULAŞICI HASTALIKLAR
dc.subjectİmmünoloji
dc.titleInvestigation of metallo-beta-lactamase producing strains of Pseudomonas aeruginosa and Acinetobacter baumannii by E-test, disk synergy and PCR
dc.typeMakale
dc.relation.journalSCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume40
dc.identifier.issue4
dc.identifier.startpage320
dc.identifier.endpage325
dc.contributor.firstauthorID185669


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