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首页> 外文期刊>Journal of Clinical Microbiology >Revised approach for identification and detection of ampicillin and vancomycin resistance in Enterococcus species by using MicroScan panels.
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Revised approach for identification and detection of ampicillin and vancomycin resistance in Enterococcus species by using MicroScan panels.

机译:使用MicroScan面板鉴定和检测肠球菌中氨苄青霉素和万古霉素耐药性的修订方法。

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The frequency of antimicrobial agent-resistant enterococci is increasing, making accurate identification and screening for susceptibility essential. We evaluated the ability of MicroScan Positive Breakpoint Combo Type 6 panels (Dade MicroScan Inc., West Sacramento, Calif.) to identify Enterococcus species and to detect ampicillin and vancomycin resistance. A total of 398 well-characterized Enterococcus isolates from two institutions were inoculated into MicroScan panels, into conventional biochemical assays, and into ampicillin and vancomycin agar dilution media. Resistance was verified by the broth macrodilution method. MicroScan panels accurately detected resistance to ampicillin in 132 of 132 enterococcal isolates, while three isolates for which the MICs were < 16 micrograms/ml were classified incorrectly by MicroScan panels as resistant. No beta-lactamase-producing enterococci were detected. All 64 isolates showing resistance to vancomycin (MICs > or = 32 micrograms/ml) were correctly classified by MicroScan panels. Seven isolates for which the vancomycin MICs were 8 and 16 micrograms/ml were incorrectly classified as susceptible by MicroScan panels, while eight isolates for which the MICs were 4 micrograms/ml were incorrectly labeled as intermediate. Fourteen of these 15 isolates were subsequently identified as motile enterococci. Overall, there were three major errors in susceptibility testing for ampicillin and 15 minor errors for vancomycin. Conventional testing confirmed the identity of 181 Enterococcus faecalis isolates, 157 E. faecium isolates, and 60 isolates of other species; however, 56 of these 60 isolates were misidentified by the MicroScan panels. After recognition of this problem, a revised approach which included tests for pigment, motility, and sucrose fermentation was devised. In combination with these additional assays, the conventional MicroScan panels accurately identified the 56 originally misidentified isolates. In summary, the ability of MicroScan panels to detect vancomycin and ampicillin resistance in enterococci was confirmed. Our study found that the inability of MicroScan panels to identify enterococci other than E. faecalis and E. faecium can be compensated for by the addition of standard assays.
机译:耐药菌耐药肠球菌的频率在增加,因此准确鉴定和筛查药敏性至关重要。我们评估了MicroScan 6型阳性断点组合板(加利福尼亚州西萨克拉曼多的Dade MicroScan Inc.)鉴定肠球菌种类并检测氨苄青霉素和万古霉素耐药性的能力。将来自两个机构的总共398个特征明确的肠球菌菌株接种到MicroScan面板,常规生化分析以及氨苄青霉素和万古霉素琼脂稀释培养基中。抗性通过肉汤大稀释法验证。 MicroScan小组在132个肠球菌分离株中的132个中准确检测了对氨苄西林的抗性,而MicroScan小组将MIC≤16微克/ ml的三个分离株错误地归类为抗性。未检测到产生β-内酰胺酶的肠球菌。所有显示出对万古霉素耐药性的分离株(MICs≥32微克/ ml)均由MicroScan面板正确分类。 MicroScan板将万古霉素MIC分别为8和16微克/毫升的7个分离物错误地分类为易感,而MIC为4微克/毫升的8个分离物被错误地标记为中间体。随后将这15株分离物中的14株鉴定为运动性肠球菌。总体而言,氨苄西林药敏试验存在三个主要错误,万古霉素存在15个次要错误。常规测试确认了181株粪肠球菌,157株粪肠球菌和60株其他物种的菌群。但是,这60个分离株中有56个被MicroScan小组误认了。在认识到这个问题之后,设计了一种修正的方法,其中包括色素,活力和蔗糖发酵的测试。结合这些附加的检测方法,常规的MicroScan面板可以准确地识别出56个最初被错误识别的分离株。总之,证实了MicroScan面板检测肠球菌中万古霉素和氨苄青霉素抗性的能力。我们的研究发现,通过添加标准检测方法可以弥补MicroScan面板无法识别粪肠球菌和粪肠球菌以外的肠球菌的问题。

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