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A rapid and visual detection of Staphylococcus haemolyticus in clinical specimens with RPA-LFS

底漆(化妆品) 重组酶聚合酶扩增 环介导等温扩增 化学 溶血葡萄球菌 琼脂糖凝胶电泳 琼脂糖 聚合酶链反应 分子生物学 纳米技术 色谱法 DNA 基因 葡萄球菌 生物 遗传学 材料科学 金黄色葡萄球菌 细菌 生物化学 有机化学
作者
Tuo Ji,Junlong Zhang,Yuzhi Gao,Cheng Zhao,Xuzhu Gao
出处
期刊:Analytica Chimica Acta [Elsevier BV]
卷期号:1273: 341534-341534 被引量:8
标识
DOI:10.1016/j.aca.2023.341534
摘要

Staphylococcus haemolyticus (S. haemolyticus), which is highly prevent in the hospital environment, is an etiological factor for nosocomial infections. Point-of-care rapid testing (POCT) of S. haemolyticus is not possible with the currently used detection methods. Recombinase polymerase amplification (RPA) is a novel isothermal amplification technology with high sensitivity and specificity. The combination of RPA and lateral flow strips (LFS) can achieve rapid pathogen detection, enabling POCT. This study developed an RPA-LFS methodology using a specific probe/primer pair to identify S. haemolyticus. A basic RPA reaction was performed to screen the specific primer from 6 primer pairs targeting mvaA gene. The optimal primer pair was selected based on agarose gel electrophoresis, and the probe was designed. To eliminate false-positive results caused by the byproducts, base mismatches were introduced in the primer/probe pair. The improved primer/probe pair could specifically identify the target sequence. To explore the optimal reaction conditions, the effects of reaction temperature and duration of the RPA-LFS method were systematically investigated. The improved system enabled optimal amplification at 37 °C for 8 min, and the results were visualized within 1 min. The S. haemolyticus detection sensitivity of the RPA-LFS method, whose performance was unaffected by contamination with other genomes, was 0.147 CFU/reaction. Furthermore, we analyzed 95 random clinical samples with RPA-LFS, quantitative polymerase chain reaction (qPCR), and traditional bacterial-culture assays and found that the RPA-LFS had 100% and 98.73% compliance rates with the qPCR and traditional culture method, respectively, which confirms its clinical applicability. In this study, we designed an improved RPA-LFS assay based on the specific probe/primer pair for the detection of S. haemolyticus via rapid POCT, free from the limitations of the precision instruments, helping to make diagnoses and treatment decisions as soon as possible.
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