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dc.contributor.author이미애*
dc.date.accessioned2018-05-30T08:14:02Z-
dc.date.available2018-05-30T08:14:02Z-
dc.date.issued2006*
dc.identifier.issn1076-6294*
dc.identifier.otherOAK-3272*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/243486-
dc.description.abstractCefoxitin-resistant Escherichia coli and Klebsiella pneumoniae are relatively prevalent in Korea, suggesting dissemination of plasmid-mediated AmpC β-lactamases. In this study, 238 isolates of cefositin-resistant E. coli and K, pneumoniae (not including subspecies ozaenae and rhinoscleromatis) were collected in 2003 from 16 Korean hospitals. The prevalence of plasmid-mediated AmpC β-lactamases was determined by PCR. The AmpC gene alleles detected in E. coli and K. pneumoniae were blaDHA-1, 10 (8.6%) and 93 (76.2%); blaCMY-1-like, 14 (12.1%) and 2 (1.6%); and blaCMY-2-like, 38 (32.7%) and 1 (0.8%) isolates, respectively. The genes identified were blaDHA-1, blaCMY10-like, and blaCMY-2-like, and a new variant, blaCMY-18. Plasmid-mediated AmpC gene allele-positive isolates were present both in large city and in small province hospitals, as well as in isolates from outpatients. The proportions of plasmid-mediated AmpC gene-positive isolates were similar in both expanded spectrum β-lactamase (ESBL)-producing and -nonproducing isolates. In conclusion, DHA-1, CMY-2-like, and CMY-10-like plasmid-mediated AmpC β-lactamase-producing K. pneumoniae and E. coli isolates are widely disseminated in both large city and small province hospitals. Absence of blaCMY-1 and detection of a novel variant of blaCMY-2, blaCMY-18, indicate continued evolution of the prototype genes. Similar proportions of plasmid-mediated AmpC gene-positive isolates in both ESBL-producing and -nonproducing isolates suggest unhindered future spread of these resistances. © Mary Ann Liebert, Inc.*
dc.languageEnglish*
dc.titlePrevalence of plasmid-mediated AmpC β-lactamases in Escherichia coli and Klebsiella pneumoniae in Korea*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume12*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage44*
dc.relation.lastpage49*
dc.relation.journaltitleMicrobial Drug Resistance*
dc.identifier.doi10.1089/mdr.2006.12.44*
dc.identifier.wosidWOS:000236686300009*
dc.identifier.scopusid2-s2.0-33646075082*
dc.author.googleLee K.*
dc.author.googleLee M.*
dc.author.googleShin J.H.*
dc.author.googleLee M.H.*
dc.author.googleKang S.H.*
dc.author.googlePark A.J.*
dc.author.googleYong D.*
dc.author.googleChong Y.*
dc.contributor.scopusid이미애(7409114044)*
dc.date.modifydate20240118124940*
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의과대학 > 의학과 > Journal papers
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