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Clinical implications of vancomycin-resistant Enterococcus faecium (VRE) with VanD phenotype and vanA genotype

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 durin...

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Published in:Journal of antimicrobial chemotherapy 2008-04, Vol.61 (4), p.838-844
Main Authors: Song, Jae-Hoon, Ko, Kwan Soo, Suh, Ji Yoeun, Oh, Won Sup, Kang, Cheol-In, Chung, Doo Ryeon, Peck, Kyong Ran, Lee, Nam Yong, Lee, Wee Gyo
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container_end_page 844
container_issue 4
container_start_page 838
container_title Journal of antimicrobial chemotherapy
container_volume 61
creator Song, Jae-Hoon
Ko, Kwan Soo
Suh, Ji Yoeun
Oh, Won Sup
Kang, Cheol-In
Chung, Doo Ryeon
Peck, Kyong Ran
Lee, Nam Yong
Lee, Wee Gyo
description 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.
doi_str_mv 10.1093/jac/dkn025
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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.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkn025</identifier><identifier>PMID: 18230690</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Animals ; Anti-Bacterial Agents - pharmacology ; Anti-Bacterial Agents - therapeutic use ; Antibiotics ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Bacteria ; Bacterial Proteins - genetics ; Biological and medical sciences ; Blood - microbiology ; Carbon-Oxygen Ligases - genetics ; Chemotherapy ; Colony Count, Microbial ; Drug resistance ; Enterococcus faecium ; Enterococcus faecium - drug effects ; Enterococcus faecium - genetics ; Enterococcus faecium - isolation &amp; purification ; Female ; Genotype &amp; phenotype ; Gram-Positive Bacterial Infections - drug therapy ; Gram-Positive Bacterial Infections - microbiology ; Medical sciences ; Mice ; Mice, Inbred ICR ; Microbial Sensitivity Tests ; Microbial Viability ; Peritonitis - drug therapy ; Peritonitis - microbiology ; Pharmacology. Drug treatments ; Survival Analysis ; teicoplanin ; Teicoplanin - pharmacology ; Teicoplanin - therapeutic use ; Vancomycin Resistance - genetics ; vancomycin-resistant enterococci ; VanD-vanA</subject><ispartof>Journal of antimicrobial chemotherapy, 2008-04, Vol.61 (4), p.838-844</ispartof><rights>The Author 2008. 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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. 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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.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>18230690</pmid><doi>10.1093/jac/dkn025</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Anti-Bacterial Agents - pharmacology
Anti-Bacterial Agents - therapeutic use
Antibiotics
Antibiotics. Antiinfectious agents. Antiparasitic agents
Bacteria
Bacterial Proteins - genetics
Biological and medical sciences
Blood - microbiology
Carbon-Oxygen Ligases - genetics
Chemotherapy
Colony Count, Microbial
Drug resistance
Enterococcus faecium
Enterococcus faecium - drug effects
Enterococcus faecium - genetics
Enterococcus faecium - isolation & purification
Female
Genotype & phenotype
Gram-Positive Bacterial Infections - drug therapy
Gram-Positive Bacterial Infections - microbiology
Medical sciences
Mice
Mice, Inbred ICR
Microbial Sensitivity Tests
Microbial Viability
Peritonitis - drug therapy
Peritonitis - microbiology
Pharmacology. Drug treatments
Survival Analysis
teicoplanin
Teicoplanin - pharmacology
Teicoplanin - therapeutic use
Vancomycin Resistance - genetics
vancomycin-resistant enterococci
VanD-vanA
title Clinical implications of vancomycin-resistant Enterococcus faecium (VRE) with VanD phenotype and vanA genotype
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