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dc.contributor.authorGhotaslou, R
dc.contributor.authorSefidan, FY
dc.contributor.authorAkhi, MT
dc.contributor.authorAsgharzadeh, M
dc.contributor.authorAsl, YM
dc.date.accessioned2018-08-26T07:15:04Z
dc.date.available2018-08-26T07:15:04Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/45257
dc.description.abstractIntroduction: Enzymatic inactivation is one of the most important mechanisms of resistance to aminoglycosides. The aim of this study was to investigate the prevalence of armA and diversity of the genes encoding aminoglycoside-modifying enzymes (AMEs) and their associations with resistance phenotypes in Enterobacteriaceae isolates. Methods: Three hundred and seven Enterobacteriaceae isolates were collected from five hospitals in northwest Iran. The disk diffusion method for amikacin, gentamicin, tobramycin, kanamycin, and streptomycin, as well as the minimum inhibitory concentration for amikacin, gentamicin, tobramycin, and kanamycin were done for susceptibility testing. Thirteen AME genes and armA methylase were screened using the PCR and sequencing assays. Results: Two hundred and twenty (71.7%) of isolates were resistant to aminoglycosides and 155 (70.5%) of them were positive for aminoglycoside resistance genes. The most prevalent AME genes were ant(3 '')-Ia and aph(3 '')-Ib with the frequency 35.9% and 30.5%, respectively. Also, 21 (9.5%) of resistant isolates were positive for armA methylase gene. Conclusions: The prevalence of resistance to aminoglycoside is high and AME genes frequently are disseminated in Enterobacteriaceae isolates. There is an association between phenotypic resistance and the presence of some aminoglycoside genes.
dc.language.isoEnglish
dc.relation.ispartofMICROBIAL DRUG RESISTANCE
dc.subjectaminoglycoside-modifying enzymes
dc.subjectarmA
dc.subjectEnterobacteriaceae
dc.titleDissemination of Genes Encoding Aminoglycoside-Modifying Enzymes and armA Among Enterobacteriaceae Isolates in Northwest Iran
dc.typeArticle
dc.citation.volume23
dc.citation.issue7
dc.citation.spage826
dc.citation.epage832
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1089/mdr.2016.0224


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