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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
善始善终完成签到 ,获得积分10
1秒前
落寞的土豆完成签到 ,获得积分10
2秒前
1touzansi完成签到 ,获得积分10
3秒前
清脆如娆完成签到 ,获得积分0
5秒前
里清水完成签到 ,获得积分10
5秒前
欧斌完成签到,获得积分10
6秒前
山复尔尔完成签到 ,获得积分10
6秒前
自觉的宇完成签到 ,获得积分10
6秒前
麦当劳没有Creazy4完成签到,获得积分20
10秒前
fishswim1完成签到,获得积分10
11秒前
lin完成签到,获得积分10
11秒前
Twelve完成签到,获得积分10
12秒前
科研顺利完成签到,获得积分10
13秒前
13秒前
木鱼完成签到,获得积分10
14秒前
14秒前
yhyhyhyh完成签到,获得积分10
14秒前
kkkkkk的应助被科研通管家采纳,获得30
14秒前
桐桐的应助被科研通管家采纳,获得10
14秒前
15秒前
李爱国的应助被科研通管家采纳,获得10
15秒前
klicking完成签到,获得积分10
15秒前
zhaosiqi完成签到,获得积分10
18秒前
19秒前
好困发布了新的文献求助10
19秒前
木鱼发布了新的文献求助10
20秒前
Rxtdj完成签到 ,获得积分10
20秒前
顺心的一德完成签到,获得积分10
20秒前
拓跋幻枫完成签到,获得积分10
22秒前
赵浩宇完成签到 ,获得积分10
22秒前
爱学数学的数学小白完成签到,获得积分10
25秒前
孙士淼完成签到 ,获得积分10
25秒前
含蓄凡白完成签到 ,获得积分10
26秒前
包容的忆灵完成签到 ,获得积分10
28秒前
28秒前
matafeiyan完成签到,获得积分10
28秒前
可带玉米完成签到,获得积分10
29秒前
Joy完成签到,获得积分10
30秒前
maple完成签到 ,获得积分10
31秒前
史克珍香完成签到 ,获得积分10
32秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
Deformation and Fracture of the Lumbar Vertebral End Plate 500
CLSI C56QG Examples of Hemolyzed, Icteric, and Lipemic/Turbid Samples Quick Guide 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7802584
求助须知:如何正确求助?哪些是违规求助? 9336575
关于积分的说明 20480466
捐赠科研通 7394103
什么是DOI,文献DOI怎么找? 3326910
关于科研通互助平台的介绍 2473975
邀请新用户注册赠送积分活动 2344920