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dc.contributor.authorAghazadeh, M
dc.contributor.authorHojabri, Z
dc.contributor.authorMahdian, R
dc.contributor.authorNahaei, MR
dc.contributor.authorRahmati, M
dc.contributor.authorHojabri, T
dc.contributor.authorPirzadeh, T
dc.contributor.authorPajand, O
dc.date.accessioned2018-08-26T06:05:24Z
dc.date.available2018-08-26T06:05:24Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41754
dc.description.abstractIn order to gain a better understanding of the role of several mechanisms in antibiotic resistance in Pseudomonas aeruginosa clinical isolates obtained from CF and burn patients, we evaluated gene expression of efflux pumps MexAB-OprM and MexXY(-OprA), the natural ?-lactamase AmpC and outer membrane porin protein OprD. Also, the presence of genes encoding Ambler classes A, B ?-lactamases and aminoglycoside modifying enzymes (AMEs) was examined.Piperacillin-tazobactam and amikacin retained the highest in vitro activities among 21 CF and 27 burn P. aeruginosa isolates. Based on Enterobacterial Repetitive Intergenic Consensus (ERIC) PCR, 15 distinct patterns were detected. There were 5 CF and 6 burn isolates harbored PER-1 and VEB-1, respectively. Among AMEs, involved in resistance of anti-Pseudomonas aminoglycosides, aac(6')-Ib was the most prevalent gene. Among CF isolates, mexA overexpression was the most prevalent mechanism (47.6%) followed by mexX (42.8%), ampC (9.5%) and oprD downregulation (4.7%). Among burn isolates, the prevalence of mexX, mexA, and ampC overexpression was 62.9%, 74%, and 11.1%, respectively. Downregulation of oprD was observed in 14.8% of burn isolates.Among CF isolates, mexX and mexA overexpression were the major contributing factors to aminoglycoside (gentamicin) and carbapenem (meropenem) resistance, respectively while among burn isolates, AMEs in conjunction with mexX hyperexpression were identified to be responsible for aminoglycoside resistance. Also mexA overexpression was partially associated with carbapenem resistance. Moreover, cephalosporin resistance was linked to overexpression of mexA and/or mexX. The impact of interplay between different resistance mechanisms on resistant phenotypes was more complicated among burn than CF isolates.
dc.language.isoEnglish
dc.relation.ispartofInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
dc.subjectAmikacin
dc.subjectAnti-Bacterial Agents
dc.subjectBacterial Outer Membrane Proteins
dc.subjectBacterial Proteins
dc.subjectBurns
dc.subjectCephalosporinase
dc.subjectCystic Fibrosis
dc.subjectDrug Resistance, Multiple, Bacterial
dc.subjectEscherichia coli Proteins
dc.subjectGene Expression Regulation, Bacterial
dc.subjectHumans
dc.subjectMembrane Transport Proteins
dc.subjectMicrobial Sensitivity Tests
dc.subjectPenicillanic Acid
dc.subjectPiperacillin
dc.subjectPorins
dc.subjectPseudomonas Infections
dc.subjectPseudomonas aeruginosa
dc.subjectbeta-Lactamases
dc.titleRole of efflux pumps: MexAB-OprM and MexXY(-OprA), AmpC cephalosporinase and OprD porin in non-metallo-?-lactamase producing Pseudomonas aeruginosa isolated from cystic fibrosis and burn patients.
dc.typearticle
dc.citation.volume24
dc.citation.spage187
dc.citation.epage92
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1016/j.meegid.2014.03.018


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