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Evaluation of the Xpert vanA/vanB Assay Using Enriched Inoculated Broths for Direct Detection of vanB Vancomycin-Resistant Enterococci

机译:使用丰富的接种肉汤直接检测vanB抗万古霉素肠球菌的Xpert vanA / vanB分析方法的评估

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摘要

Rapid and accurate detection of VRE (vancomycin-resistant enterococci) is required for adequate antimicrobial treatment and infection prevention measures. Previous studies using PCR for the detection of VRE, including Cepheid's Xpert vanA/vanB assay, reported accurate detection of vanA VRE; however, many false-positive results were found for vanB VRE. This is mainly due to nonenterococcal vanB genes, which can be found in the gut flora. Our goal was to optimize the rapid and accurate detection of vanB VRE and to improve the positive predictive value (PPV) by limiting false-positive results. We evaluated the use of the Xpert vanA/vanB assay on rectal swabs and on enriched inoculated broths for the detection of vanB VRE. By adjusting the cycle threshold (C-T) cutoff value to 30 appeared to be true negative. In conclusion, this study shows that the Cepheid's Xpert vanA/vanB assay performed on enriched inoculated broths with an adjusted cutoff C-T value is a useful and rapid tool for the detection of vanB VRE.
机译:需要快速,准确地检测VRE(耐万古霉素的肠球菌),以进行充分的抗菌治疗和预防感染的措施。先前使用PCR检测VRE的研究(包括造父变星的Xpert vanA / vanB分析)报告了对vanA VRE的准确检测。但是,发现vanB VRE有许多假阳性结果。这主要是由于在肠菌群中发现了非肠球菌的vanB基因。我们的目标是优化vanB VRE的快速准确检测,并通过限制假阳性结果来提高阳性预测值(PPV)。我们评估了Xpert vanA / vanB测定法在直肠拭子和富集接种肉汤上的使用,以检测vanB VRE。通过将循环阈值(C-T)调整为30,截止值为真负值。总而言之,这项研究表明,造父变星的Xpert vanA / vanB测定法是在富集的接种肉汤中以截止C-T值进行调整的,它是检测vanB VRE的有用且快速的工具。

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