多重聚合酶链反应
多路复用
微阵列
分子诊断学
生物
放大器
聚合酶链反应
分子生物学
分子信标
计算生物学
数字聚合酶链反应
微生物学
DNA
多重位移放大
实时聚合酶链反应
寡核苷酸
基因
生物信息学
遗传学
基因表达
作者
Hongna Liu,Kathryn Heflin,Jing Han,Matt S. Conover,Leslie Wagner,Jacques-Charles Bertrand,Phillip Ewing,Stanley Lu,Scott Clemmons,John Watts,Song Li
标识
DOI:10.1166/jbn.2019.2783
摘要
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™, 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 × 10 5 –1.7 × 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.
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