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Outbreak of Vancomycin-Susceptible Enterococcus faecium Containing the Wild-Type vanA Gene

机译:含有野生型vanA基因的万古霉素易感肠球菌的暴发

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摘要

Accurate detection of vancomycin-resistant enterococci (VRE) is essential in preventing transmission in health care settings. Chromogenic media are widely used for screening VRE because of fast turnaround times (TAT) and high sensitivity. We report an outbreak of Enterococcus faecium bearing vanA yet susceptible to vancomycin (vancomycin-variable Enterococcus [VVE]). Between October 2009 to March 2011, clinical and screening specimens (n = 14,747) were screened for VRE using VRE-selective medium and/or PCR. VVE isolates were genotyped to determine relatedness. Plasmids from these isolates were characterized by sequencing. Overall, 52 VVE isolates were identified, comprising 15% of all VRE isolates identified. Isolates demonstrated growth on Brilliance VRE agar (Oxoid) at 24 h of incubation but did not grow on brain heart infusion agar with 6 μg/ml vancomycin (Oxoid) or bile esculin azide agar with 6 μg/ml vancomycin (Oxoid) and were susceptible to vancomycin. Genotyping of 20 randomly selected VVE isolates revealed that 15/20 were identical, while 5 were highly related. PCR of the VVE transposon confirmed the presence of vanHAXY gene cluster; however, vanS (sensor) and vanR (regulator) genes were absent. The outbreak was controlled through routine infection control measures. We report an emergence of a fit strain of E. faecium containing vanA yet susceptible to vancomycin. Whether this new strain represents VRE has yet to be determined; however, unique testing procedures are required for reliable identification of VVE.
机译:准确检测耐万古霉素的肠球菌(VRE)对于防止在医疗机构中传播至关重要。由于快速周转时间(TAT)和高灵敏度,生色介质被广泛用于筛选VRE。我们报告了暴发性肠球菌vanA感染但对万古霉素(万古霉素可变肠球菌[VVE])敏感。在2009年10月至2011年3月之间,使用VRE选择性培养基和/或PCR对临床和筛查样本(n = 14,747)进行了VRE筛查。对VVE分离株进行基因分型以确定相关性。通过测序来表征来自这些分离物的质粒。总体上,鉴定出52种VVE分离株,占鉴定出的所有VRE分离株的15%。分离物在培养24小时后显示在Brilliance VRE琼脂(类毒素)上生长,但在含有6μg/ ml万古霉素(Oxoid)的脑心浸液琼脂或含6μg/ ml万古霉素(Oxoid)的胆汁叠氮化琼脂中未生长。万古霉素。对20个随机选择的VVE分离株进行基因分型,发现15/20是相同的,而5个是高度相关的。 VVE转座子的PCR证实了vanHAXY基因簇的存在。然而,缺少vanS(传感器)和vanR(调节子)基因。通过常规感染控制措施控制了暴发。我们报告出现了含有vanA但对万古霉素敏感的粪肠球菌的合适菌株。该新菌株是否代表VRE尚待确定;但是,要可靠地识别VVE,需要独特的测试程序。

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