Cited 76 times in
Characterization of IncF plasmids carrying the blaCTX-M-14 gene in clinical isolates of Escherichia coli from Korea.
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김주원 | - |
dc.contributor.author | 배일권 | - |
dc.contributor.author | 이경원 | - |
dc.contributor.author | 정석훈 | - |
dc.date.accessioned | 2014-12-20T16:36:09Z | - |
dc.date.available | 2014-12-20T16:36:09Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 0305-7453 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/93026 | - |
dc.description.abstract | OBJECTIVES: The purpose of this study was to investigate the molecular epidemiology of CTX-M-14-producing Escherichia coli clinical isolates from Korea. METHODS: A total of 138 non-duplicate E. coli clinical isolates showing reduced susceptibility or resistance to ceftazidime and/or cefotaxime were included in the study. Resistance genes, genetic environment, R plasmid size and replicon type, sequence type (ST) and XbaI-macrorestriction patterns were determined. RESULTS: Among 138 isolates, 35 were found to carry the bla(CTX-M-14) gene. The ISEcp1 element was identified in the upstream region of the bla(CTX-M-14) gene in 32 isolates. The bla(CTX-M-14) gene was located on an IncF plasmid in 21 isolates, on an IncA/C plasmid in 1 isolate, on the chromosome in 8 isolates and on both the chromosome and an IncF plasmid in 5 isolates. The most prevalent ST was ST405 (n = 8), followed by ST354 (n = 4), ST38 (n = 3), ST69 (n = 3) and the intercontinental ST, ST131 (n = 3). PFGE and multilocus sequence typing experiments demonstrated no major clonal relationship among the CTX-M-14-producing isolates. CONCLUSIONS: The bla(CTX-M-14) gene was probably mobilized by IncF plasmids, which can readily spread in E. coli, causing horizontal dissemination of the resistance gene in Korea. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 1263~1268 | - |
dc.relation.isPartOf | JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY | - |
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 | Bacterial Typing Techniques | - |
dc.subject.MESH | Cefotaxime/pharmacology | - |
dc.subject.MESH | Ceftazidime/pharmacology | - |
dc.subject.MESH | DNA, Bacterial/chemistry | - |
dc.subject.MESH | DNA, Bacterial/genetics | - |
dc.subject.MESH | DNA, Bacterial/metabolism | - |
dc.subject.MESH | Deoxyribonucleases, Type II Site-Specific/metabolism | - |
dc.subject.MESH | Escherichia coli/classification | - |
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/epidemiology* | - |
dc.subject.MESH | Escherichia coli Infections/microbiology* | - |
dc.subject.MESH | Gene Transfer, Horizontal | - |
dc.subject.MESH | Korea/epidemiology | - |
dc.subject.MESH | Molecular Epidemiology | - |
dc.subject.MESH | Molecular Sequence Data | - |
dc.subject.MESH | Molecular Typing | - |
dc.subject.MESH | Plasmids* | - |
dc.subject.MESH | Polymorphism, Restriction Fragment Length | - |
dc.subject.MESH | Sequence Analysis, DNA | - |
dc.subject.MESH | beta-Lactam Resistance | - |
dc.subject.MESH | beta-Lactamases/genetics* | - |
dc.title | Characterization of IncF plasmids carrying the blaCTX-M-14 gene 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 | Juwon Kim | - |
dc.contributor.googleauthor | Il Kwon Bae | - |
dc.contributor.googleauthor | Seok Hoon Jeong | - |
dc.contributor.googleauthor | Chulhun L. Chang | - |
dc.contributor.googleauthor | Chae Hoon Lee | - |
dc.contributor.googleauthor | Kyungwon Lee | - |
dc.identifier.doi | 10.1093/jac/dkr106 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A00943 | - |
dc.contributor.localId | A01802 | - |
dc.contributor.localId | A02649 | - |
dc.contributor.localId | A03619 | - |
dc.relation.journalcode | J01237 | - |
dc.identifier.eissn | 1460-2091 | - |
dc.identifier.pmid | 21415040 | - |
dc.subject.keyword | replicon sequence typing | - |
dc.subject.keyword | IncA/C plasmid | - |
dc.subject.keyword | sequence type 131 | - |
dc.contributor.alternativeName | Kim, Ju Won | - |
dc.contributor.alternativeName | Bae, Il Kwon | - |
dc.contributor.alternativeName | Lee, Kyung Won | - |
dc.contributor.alternativeName | Jeong, Seok Hoon | - |
dc.contributor.affiliatedAuthor | Kim, Ju Won | - |
dc.contributor.affiliatedAuthor | Bae, Il Kwon | - |
dc.contributor.affiliatedAuthor | Lee, Kyung Won | - |
dc.contributor.affiliatedAuthor | Jeong, Seok Hoon | - |
dc.rights.accessRights | free | - |
dc.citation.volume | 66 | - |
dc.citation.number | 6 | - |
dc.citation.startPage | 1263 | - |
dc.citation.endPage | 1268 | - |
dc.identifier.bibliographicCitation | JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, Vol.66(6) : 1263-1268, 2011 | - |
dc.identifier.rimsid | 27979 | - |
dc.type.rims | ART | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.