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dc.contributor.authorMatsumura, Yasufumien
dc.contributor.authorYamamoto, Masakien
dc.contributor.authorHiguchi, Takeshien
dc.contributor.authorKomori, Toshiakien
dc.contributor.authorTsuboi, Fusayukien
dc.contributor.authorHayashi, Akihikoen
dc.contributor.authorSugimoto, Yoshihisaen
dc.contributor.authorHotta, Gouen
dc.contributor.authorMatsushima, Akien
dc.contributor.authorNagao, Mikien
dc.contributor.authorTakakura, Shunjien
dc.contributor.authorIchiyama, Satoshien
dc.contributor.alternative松村, 康史ja
dc.date.accessioned2013-08-19T07:16:27Z-
dc.date.available2013-08-19T07:16:27Z-
dc.date.issued2012-08-
dc.identifier.issn0924-8579-
dc.identifier.urihttp://hdl.handle.net/2433/178036-
dc.description.abstractIn 2010, a total of 1327 clinical Escherichia coli isolates from five hospitals in the Kyoto and Shiga regions of Japan were analysed by PCR. The prevalences of plasmid-mediated AmpC β-lactamase (pAmpC)-producers, extended-spectrum β-lactamase (ESBL)-producers and co-producers of pAmpC and ESBL were 1.7%, 9.7% and 0.3%, respectively. Less than one-half of the pAmpC-producers were reported to be resistant to third-generation cephalosporins, cephamycins and β-lactam/β-lactam inhibitors using the old 2009 Clinical and Laboratory Standards Institute (CLSI) breakpoints. CMY-2 was the most prevalent pAmpC type (95%), and CTX-M-14 (38%), CTX-M-15 (26%) and CTX-M-27 (19%) were the most prevalent ESBL types. The worldwide O25b-ST131-B2 clone accounted for 11% of pAmpC-producers and 41% of ESBL-producers. The O25b-ST131-B2 clone was characterised by a CTX-M-27- or CTX-M-15-type ESBL and ciprofloxacin-non-susceptibility with quadruple mutations in the quinolone resistance-determining regions (S83L and D87N in GyrA and S80I and E84V in ParC). A significant proportion of pAmpC-producers and the O25b-ST131-B2 clone were found in Japan by a recent regional surveillance programme.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier B.V.en
dc.rights© 2012 Elsevier B.V.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.rightsThis is not the published version. Please cite only the published version.en
dc.subjectESBLen
dc.subjectAmpCen
dc.subjectST131en
dc.subjectCTX-M-27en
dc.subjectPrevalenceen
dc.subject.meshAnti-Bacterial Agents/pharmacologyen
dc.subject.meshBacterial Proteins/biosynthesisen
dc.subject.meshBacterial Proteins/geneticsen
dc.subject.meshCeftazidime/pharmacologyen
dc.subject.meshCiprofloxacin/pharmacologyen
dc.subject.meshDNA Gyrase/biosynthesisen
dc.subject.meshDNA Gyrase/geneticsen
dc.subject.meshDrug Resistance, Bacterialen
dc.subject.meshEscherichia coli/classificationen
dc.subject.meshEscherichia coli/drug effectsen
dc.subject.meshEscherichia coli/enzymologyen
dc.subject.meshEscherichia coli/isolation & purificationen
dc.subject.meshEscherichia coli Infections/epidemiologyen
dc.subject.meshEscherichia coli Infections/microbiologyen
dc.subject.meshEscherichia coli Proteins/biosynthesisen
dc.subject.meshEscherichia coli Proteins/geneticsen
dc.subject.meshGenes, Bacterialen
dc.subject.meshHospitalsen
dc.subject.meshHumansen
dc.subject.meshJapan/epidemiologyen
dc.subject.meshMicrobial Sensitivity Testsen
dc.subject.meshPhylogenyen
dc.subject.meshPlasmids/geneticsen
dc.subject.meshPlasmids/metabolismen
dc.subject.meshPrevalenceen
dc.subject.meshbeta-Lactamases/biosynthesisen
dc.subject.meshbeta-Lactamases/geneticsen
dc.titlePrevalence of plasmid-mediated AmpC β-lactamase-producing Escherichia coli and spread of the ST131 clone among extended-spectrum β-lactamase-producing E. coli in Japan.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleInternational journal of antimicrobial agentsen
dc.identifier.volume40-
dc.identifier.issue2-
dc.identifier.spage158-
dc.identifier.epage162-
dc.relation.doi10.1016/j.ijantimicag.2012.04.013-
dc.textversionauthor-
dc.identifier.pmid22743014-
dcterms.accessRightsopen access-
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