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利用基于微阵列的核酸检测法直接鉴定血培养中的革兰氏阳性菌和耐药决定因子:对微阵列检测结果不确定的深入分析。

Direct identification of Gram-positive bacteria and resistance determinants from blood cultures using a microarray-based nucleic acid assay: in-depth analysis of microarray data for undetermined results.

出版信息

Clin Chem Lab Med. 2015 Jun;53(7):1013-24. doi: 10.1515/cclm-2014-0669.

DOI:10.1515/cclm-2014-0669
PMID:25536666
Abstract

BACKGROUND

The Verigene Gram-Positive Blood Culture (BC-GP) nucleic acid assay (Nanosphere, Inc., Northbrook, IL, USA) is a newly developed microarray-based test with which 12 Gram-positive bacterial genes and three resistance determinants can be detected using blood culture broths. We evaluated the performance of this assay and investigated the signal characteristics of the microarray images.

METHODS

At the evaluation stage, we tested 80 blood cultures that were positive for various bacteria (68 bacteria covered and 12 not covered by the BC-GP panel) collected from the blood of 36 patients and 44 spiked samples. In instances where the automated system failed and errors were called, we manually inspected microarray images, measured the signal intensities of target spots, and reclassified the results.

RESULTS

With the manual analysis of the microarray images of 14 samples for which error calls were reported, we could obtain correct identification results for 12 samples without the need for retesting, because strong signals in the target spots were clearly discriminable from background noise. With our interpretation strategy, we could obtain 97.1% sensitivity and 100% specificity for bacterial identification by using the BC-GP assay. The two unidentified bacteria were viridans group streptococci, which produced weaker target signals. During the application stage, among 25 consecutive samples positive for Gram-positive bacteria, we identified two specimens with error calls as Streptococcus spp. by using manual analysis.

CONCLUSIONS

With help of the manual review of the microarray images, the BC-GP assay could successfully identify species and resistance markers for many clinically important Gram-positive bacteria.

摘要

背景

Verigene 革兰氏阳性菌血培养(BC-GP)核酸检测(Nanosphere,Inc.,美国伊利诺伊州诺斯布鲁克)是一种新开发的微阵列检测方法,可使用血培养肉汤检测 12 种革兰氏阳性细菌基因和 3 种耐药决定因素。我们评估了该检测方法的性能,并研究了微阵列图像的信号特征。

方法

在评估阶段,我们测试了 80 份来自 36 名患者和 44 份添加样本的血液中阳性的各种细菌(68 种细菌涵盖,12 种不涵盖 BC-GP 面板)的血培养物。在自动系统出现故障并发出错误警报的情况下,我们手动检查微阵列图像,测量目标点的信号强度,并重新分类结果。

结果

通过对 14 份报告错误警报的样本的微阵列图像进行手动分析,我们可以获得 12 份样本的正确鉴定结果,而无需重新测试,因为目标点的强信号明显可与背景噪声区分开来。通过我们的解释策略,我们可以通过 BC-GP 检测获得 97.1%的细菌鉴定敏感性和 100%的特异性。两种未识别的细菌是草绿色链球菌,其产生的目标信号较弱。在应用阶段,在 25 份连续阳性的革兰氏阳性菌样本中,我们通过手动分析鉴定出两份标本为链球菌属。

结论

通过微阵列图像的手动审查,BC-GP 检测可以成功鉴定许多临床重要的革兰氏阳性菌的种和耐药标记。

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