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Clinical implications of vancomycin-resistant Enterococcus faecium (VRE) with VanD phenotype and vanA genotype.
DC Field | Value | Language |
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dc.contributor.author | Song, JH | - |
dc.contributor.author | Ko, KS | - |
dc.contributor.author | Suh, JY | - |
dc.contributor.author | Oh, WS | - |
dc.contributor.author | Kang, CI | - |
dc.contributor.author | Chung, DR | - |
dc.contributor.author | Peck, KR | - |
dc.contributor.author | Lee, NY | - |
dc.contributor.author | Lee, WG | - |
dc.date.accessioned | 2011-01-11T02:38:43Z | - |
dc.date.available | 2011-01-11T02:38:43Z | - |
dc.date.issued | 2008 | - |
dc.identifier.issn | 0305-7453 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/1078 | - |
dc.description.abstract | OBJECTIVES: To investigate the clinical implications of vancomycin-resistant Enterococcus faecium (VRE) with VanD phenotype and vanA genotype (VanD-vanA VRE). METHODS: We tested in vitro and in vivo efficacies of teicoplanin against VanD-vanA VRE strains. Change in teicoplanin MICs was monitored during incubation with teicoplanin. In vitro and in vivo time-kill assay and survival analysis using a mouse peritonitis model were performed. RESULTS: Teicoplanin MICs of VanD-vanA VRE strains increased to 128 mg/L within 48 h when they were cultured with 120 mg/L teicoplanin. In vitro and in vivo time-kill assay showed that VanD-vanA VRE strains were not eliminated by 120 mg/L teicoplanin in contrast to vancomycin-susceptible E. faecium and VanD-vanB strains. The survival rate of mice infected with VanD-vanA VRE strains treated with teicoplanin was comparable with that of untreated mice. CONCLUSION: Data suggest that teicoplanin would fail in the treatment of VanD type VRE infections if the strains contained the vanA gene, which cannot be detected in the clinical microbiology laboratory. | - |
dc.language.iso | en | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Anti-Bacterial Agents | - |
dc.subject.MESH | Bacterial Proteins | - |
dc.subject.MESH | Blood | - |
dc.subject.MESH | Carbon-Oxygen Ligases | - |
dc.subject.MESH | Colony Count, Microbial | - |
dc.subject.MESH | Enterococcus faecium | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Gram-Positive Bacterial Infections | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Mice, Inbred ICR | - |
dc.subject.MESH | Microbial Sensitivity Tests | - |
dc.subject.MESH | Microbial Viability | - |
dc.subject.MESH | Peritonitis | - |
dc.subject.MESH | Survival Analysis | - |
dc.subject.MESH | Teicoplanin | - |
dc.subject.MESH | Vancomycin Resistance | - |
dc.title | Clinical implications of vancomycin-resistant Enterococcus faecium (VRE) with VanD phenotype and vanA genotype. | - |
dc.type | Article | - |
dc.identifier.pmid | 18230690 | - |
dc.identifier.url | http://jac.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=18230690 | - |
dc.contributor.affiliatedAuthor | 이, 위교 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1093/jac/dkn025 | - |
dc.citation.title | The Journal of antimicrobial chemotherapy | - |
dc.citation.volume | 61 | - |
dc.citation.number | 4 | - |
dc.citation.date | 2008 | - |
dc.citation.startPage | 838 | - |
dc.citation.endPage | 844 | - |
dc.identifier.bibliographicCitation | The Journal of antimicrobial chemotherapy, 61(4). : 838-844, 2008 | - |
dc.identifier.eissn | 1460-2091 | - |
dc.relation.journalid | J003057453 | - |
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