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

被引:9
作者
Ji, Tuo [1 ,2 ,3 ]
Zhang, Junlong [1 ,2 ,3 ]
Gao, Yuzhi [1 ,2 ,3 ]
Zhao, Cheng [1 ,2 ,3 ,4 ]
Gao, Xuzhu [1 ,2 ,3 ,4 ]
机构
[1] Jiangsu Univ, Dept Cent Lab, Lianyungang Hosp, Lianyungang, Peoples R China
[2] Canc Hosp Lianyungang, Peoples Hosp Lianyungang City 2, Dept Cent Lab, Lianyungang, Peoples R China
[3] Xuzhou Med Univ, Dept Cent Lab, Lianyungang Hosp, Lianyungang, Peoples R China
[4] 161 Xingfu Rd, Lianyungang, Peoples R China
关键词
Staphylococcus haemolyticus; Recombinase polymerase amplification; Lateral flow strips; Point-of-care rapid testing; PCR; ASSAY;
D O I
10.1016/j.aca.2023.341534
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
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 degrees 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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页数:9
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