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

被引:25
作者
Song, Jae-Hoon [1 ,2 ]
Ko, Kwan Soo [2 ,3 ]
Suh, Ji Yoeun
Oh, Won Sup [1 ]
Kang, Cheol-In [1 ]
Chung, Doo Ryeon [1 ]
Peck, Kyong Ran [1 ]
Lee, Nam Yong [1 ]
Lee, Wee Gyo [4 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Infect Dis,Lab Med, Seoul, South Korea
[2] Asian Pacific Res Fdn Infect Dis ARFID, Seoul, South Korea
[3] Sungkyunkwan Univ, Sch Med, Dept Mol Cell Biol, Suwon, South Korea
[4] Ajou Univ, Sch Med, Dept Lab Med, Suwon, South Korea
关键词
vancomycin-resistant enterococci; teicoplanin; VanD-vanA;
D O I
10.1093/jac/dkn025
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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.
引用
收藏
页码:838 / 844
页数:7
相关论文
共 25 条
[1]   Mutations leading to increased levels of resistance to glycopeptide antibiotics in VanB-type enterococci [J].
Baptista, M ;
Depardieu, F ;
Reynolds, P ;
Courvalin, P ;
Arthur, M .
MOLECULAR MICROBIOLOGY, 1997, 25 (01) :93-105
[2]   Emergence of vancomycin-resistant enterococci in Australia: Phenotypic and genotypic characteristics of isolates [J].
Bell, JM ;
Paton, JC ;
Turnidge, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (08) :2187-2190
[3]  
Bonten M J, 2001, Lancet Infect Dis, V1, P314, DOI 10.1016/S1473-3099(01)00145-1
[4]   Vancomycin-resistant enterococci [J].
Cetinkaya, Y ;
Falk, P ;
Mayhall, CG .
CLINICAL MICROBIOLOGY REVIEWS, 2000, 13 (04) :686-+
[5]  
*CLIN LAB STAND I, 2006, M100S16 CLSI
[6]   Emergence of vanA genotype vancomycin-resistant enterococci with low or moderate levels of teicoplanin resistance in Korea [J].
Eom, JS ;
Hwang, IS ;
Hwang, BY ;
Lee, JG ;
Lee, YJ ;
Cheong, HJ ;
Park, YH ;
Park, SC ;
Kim, WJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (04) :1785-1786
[7]  
*EUCAST, 2004, EUR ANT MIC BREAKP T
[8]   Effects of antibiotics on nosocomial epidemiology of vancomycin-resistant enterococci [J].
Harbarth, S ;
Cosgrove, S ;
Carme, Y .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (06) :1619-1628
[9]   Amino acid substitutions in the VanS sensor of the VanA-type vancomycin-resistant enterococcus strains result in high-level vancomycin resistance and low-level teicoplanin resistance [J].
Hashimoto, Y ;
Tanimoto, K ;
Ozawa, Y ;
Murata, T ;
Ike, Y .
FEMS MICROBIOLOGY LETTERS, 2000, 185 (02) :247-254
[10]   Multilocus sequence typing scheme for Enterococcus faecium [J].
Homan, WL ;
Tribe, D ;
Poznanski, S ;
Li, M ;
Hogg, G ;
Spalburg, E ;
van Embden, JDA ;
Willems, RJL .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :1963-1971