Cited 63 times in
CTX-M-14 and CTX-M-15 enzymes are the dominant type of extended-spectrum beta-lactamase in clinical isolates of Escherichia coli from Korea
DC Field | Value | Language |
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dc.contributor.author | 배일권 | - |
dc.contributor.author | 이경원 | - |
dc.contributor.author | 정석훈 | - |
dc.date.accessioned | 2015-04-24T17:45:54Z | - |
dc.date.available | 2015-04-24T17:45:54Z | - |
dc.date.issued | 2009 | - |
dc.identifier.issn | 0022-2615 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/106025 | - |
dc.description.abstract | This study was performed to assess the prevalence and genotypes of plasmid-borne extended-spectrum beta-lactamases (ESBLs) and AmpC beta-lactamases in Escherichia coli in Korea. A total of 576 isolates of E. coli was collected from 12 Korean hospitals during May and July 2007. A phenotypic confirmatory test detected ESBLs in 82 (14.2 %) of the 576 E. coli isolates. The most common types of ESBLs identified were CTX-M-14 (n=32) and CTX-M-15 (n=27). The prevalence and diversity of the CTX-M mutants, including CTX-M-15, CTX-M-27 and CTX-M-57, with significant hydrolytic activity against ceftazidime were increased. PCR experiments detected genes encoding plasmid-borne AmpC beta-lactamases in 15/56 cefoxitin-intermediate or cefoxitin-resistant isolates, and the most common type of AmpC beta-lactamase identified was DHA-1 (n=10). These data suggest that the incidence of ESBLs in E. coli has increased as a result of the dissemination of CTX-M enzymes in Korea. In addition, CTX-M-22, CTX-M-27 and CTX-M-57 have appeared in Korea. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 261~266 | - |
dc.relation.isPartOf | JOURNAL OF MEDICAL MICROBIOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Anti-Bacterial Agents/pharmacology | - |
dc.subject.MESH | DNA, Bacterial/genetics | - |
dc.subject.MESH | Escherichia coli/enzymology* | - |
dc.subject.MESH | Escherichia coli/genetics | - |
dc.subject.MESH | Escherichia coli/isolation & purification | - |
dc.subject.MESH | Escherichia coli Infections/microbiology* | - |
dc.subject.MESH | Escherichia coli Proteins/biosynthesis* | - |
dc.subject.MESH | Escherichia coli Proteins/genetics | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Korea | - |
dc.subject.MESH | Microbial Sensitivity Tests/methods | - |
dc.subject.MESH | Polymerase Chain Reaction/methods | - |
dc.subject.MESH | beta-Lactamases/biosynthesis* | - |
dc.subject.MESH | beta-Lactamases/classification | - |
dc.subject.MESH | beta-Lactamases/genetics* | - |
dc.subject.MESH | beta-Lactams/pharmacology | - |
dc.title | CTX-M-14 and CTX-M-15 enzymes are the dominant type of extended-spectrum beta-lactamase in clinical isolates of Escherichia coli from Korea | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Laboratory Medicine (진단검사의학) | - |
dc.contributor.googleauthor | Wonkeun Song | - |
dc.contributor.googleauthor | Hyukmin Lee | - |
dc.contributor.googleauthor | Kyungwon Lee | - |
dc.contributor.googleauthor | Seok Hoon Jeong | - |
dc.contributor.googleauthor | Il Kwon Bae | - |
dc.contributor.googleauthor | Jae-Seok Kim | - |
dc.contributor.googleauthor | Hyo-Sun Kwak | - |
dc.identifier.doi | 10.1099/jmm.0.004507-0 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A01802 | - |
dc.contributor.localId | A02649 | - |
dc.contributor.localId | A03619 | - |
dc.relation.journalcode | J01583 | - |
dc.identifier.eissn | 1473-5644 | - |
dc.identifier.pmid | 19141747 | - |
dc.contributor.alternativeName | Bae, Il Kwon | - |
dc.contributor.alternativeName | Lee, Kyung Won | - |
dc.contributor.alternativeName | Jeong, Seok Hoon | - |
dc.contributor.affiliatedAuthor | Bae, Il Kwon | - |
dc.contributor.affiliatedAuthor | Lee, Kyung Won | - |
dc.contributor.affiliatedAuthor | Jeong, Seok Hoon | - |
dc.citation.volume | 58 | - |
dc.citation.number | pt2 | - |
dc.citation.startPage | 261 | - |
dc.citation.endPage | 266 | - |
dc.identifier.bibliographicCitation | JOURNAL OF MEDICAL MICROBIOLOGY, Vol.58(pt2) : 261-266, 2009 | - |
dc.identifier.rimsid | 56981 | - |
dc.type.rims | ART | - |
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