重组酶聚合酶扩增
化学
多路复用
重组酶
多重位移放大
逆转录酶
多重聚合酶链反应
聚合酶链反应
逆转录聚合酶链式反应
实时聚合酶链反应
聚合酶
生物传感器
分子生物学
病毒学
DNA
基因
遗传学
生物化学
生物
基因表达
DNA提取
重组
作者
Yating Song,Bach Ma,Jia Li,Jiangbing Shuai,Mingzhou Zhang
出处
期刊:Talanta
[Elsevier]
日期:2024-08-01
卷期号:: 126775-126775
标识
DOI:10.1016/j.talanta.2024.126775
摘要
Bovine viral diarrhea virus (BVDV), bovine epidemic fever virus (BEFV), and bovine respiratory syncytial virus (BRSV) cause respiratory symptoms in cattle. The absence of rapid, precise, and easily accessible diagnostic methods poses difficulties for herders and veterinary epidemiologists during outbreaks of major infectious animal diseases. Considering the mixed infection of viruses, a multiple-detection method, reverse transcription recombinase polymerase amplification (mRT-RPA) combined with a lateral flow biosensor (LFB), was established to simultaneously detect the three pathogens. This technique is based on the specific binding of three differently labeled RT-RPA products (DNA sequences) to antibodies on the three test lines of the LFB, achieving multiplex detection through the presence or absence of coloration on the LFB test lines. The fluorescence values of the LFB test lines are recorded by a test strip reader. The mRT-RPA-LFB assay completes detection at a constant temperature of 41 °C within 33 min. The limits of detection (LODs) for BVDV, BEFV and BRSV were 2.62 × 10
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