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首页> 外文期刊>Journal of biomedical nanotechnology >Development of the iCubate Molecular Diagnostic Platform Utilizing Amplicon Rescue Multiplex Polymerase Chain Reaction
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Development of the iCubate Molecular Diagnostic Platform Utilizing Amplicon Rescue Multiplex Polymerase Chain Reaction

机译:利用扩增子救援多重聚合酶链反应的近辅助分子诊断平台的发展

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We utilized Amplicon-Rescue Multiplex PCR (ARM-PCR) and microarray hybridization to develop and validate the iC-GPC Assay, a multiplexed, in vitro diagnostic test that identifies five of the most common gram positive bacteria and three clinically relevant resistance markers associated with bloodstream infections (BSI). The iC-GPC Assay is designed for use with the iC-System (TM), which automates sample preparation, ARM-PCR, and microarray detection within a closed cassette. Herein, we determined the limit of detection for each of the iC-GPC Assay targets to be between 3.0 x 10(5)-1.7 x 10(7) CFU/mL, well below clinically relevant bacterial levels for positive blood cultures. Additionally, we tested 106 strains for assay inclusivity and observed a target performance of 99.4%. 95 of 96 non-target organisms tested negative for cross-reactivity, thereby assuring a high level of assay specificity. Overall performance above 99% was observed for iC-GPC Assay reproducibility studies across multiple sites, operators and cassette lots. In conclusion, the iC-GPC Assay is capable of accurately and rapidly identifying bacterial species and resistance determinants present in blood cultures containing gram positive bacteria. Utilizing molecular diagnostics like the iC-GPC Assay will decrease time to treatment, healthcare costs, and BSI-related mortality.
机译:我们利用扩增子 - 抢救多重PCR(ARM-PCR)和微阵列杂交,以开发和验证IC-GPC测定,多路复用的体外诊断试验,其鉴定五种最常见的革兰氏阳性细菌和三种临床相关的阻力标记血流感染(BSI)。 IC-GPC测定设计用于IC-System(TM),其在封闭的盒内自动制备样品制备,ARM-PCR和微阵列检测。在此,我们确定每种IC-GPC测定靶标的检测极限在3.0×10(5)-1.7×10(7)CFU / mL之间,远低于临床相关的血液培养物的细菌水平。此外,我们测试了106个菌株以进行测定包容性,并观察到99.4%的目标性能。 96个非靶生物的95个对交叉反应性的阴性测试,从而确保了高水平的测定特异性。对于多个地点,操作员和盒式批量的IC-GPC测定可重复性研究,观察到99%以上的总体性能。总之,IC-GPC测定能够准确且快速地识别含有革兰氏阳性细菌的血液培养物中存在的细菌种类和抗性决定簇。利用IC-GPC测定等分子诊断将减少治疗,医疗费用和BSI相关死亡率的时间。

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