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用于严重急性呼吸综合征冠状病毒 2 检测的分子信标分析方法的建立。

Molecular Beacon Assay Development for Severe Acute Respiratory Syndrome Coronavirus 2 Detection.

机构信息

CICS-UBI-Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Av. Infante D. Henrique, 6200-506 Covilhã, Portugal.

C4-Cloud Computing Competence Centre, UBIMedical, Universidade da Beira Interior, Estrada Municipal 506, 6200-284 Covilhã, Portugal.

出版信息

Sensors (Basel). 2021 Oct 22;21(21):7015. doi: 10.3390/s21217015.

Abstract

The fast spread of SARS-CoV-2 has led to a global pandemic, calling for fast and accurate assays to allow infection diagnosis and prevention of transmission. We aimed to develop a molecular beacon (MB)-based detection assay for SARS-CoV-2, designed to detect the ORF1ab and S genes, proposing a two-stage COVID-19 testing strategy. The novelty of this work lies in the design and optimization of two MBs for detection of SARS-CoV-2, namely, concentration, fluorescence plateaus of hybridization, reaction temperature and real-time results. We also identify putative G-quadruplex (G4) regions in the genome of SARS-CoV-2. A total of 458 nasopharyngeal and throat swab samples (426 positive and 32 negative) were tested with the MB assay and the fluorescence levels compared with the cycle threshold (Ct) values obtained from a commercial RT-PCR test in terms of test duration, sensitivity, and specificity. Our results show that the samples with higher fluorescence levels correspond to those with low Ct values, suggesting a correlation between viral load and increased MB fluorescence. The proposed assay represents a fast (total duration of 2 h 20 min including amplification and fluorescence reading stages) and simple way of detecting SARS-CoV-2 in clinical samples from the upper respiratory tract.

摘要

SARS-CoV-2 的快速传播导致了全球大流行,因此需要快速、准确的检测方法来进行感染诊断和传播预防。我们旨在开发一种基于分子信标的(MB)SARS-CoV-2 检测方法,用于检测 ORF1ab 和 S 基因,提出了一种两阶段的 COVID-19 检测策略。这项工作的新颖之处在于设计和优化了用于检测 SARS-CoV-2 的两个 MB,即浓度、杂交的荧光平台、反应温度和实时结果。我们还鉴定了 SARS-CoV-2 基因组中的假定 G-四联体(G4)区域。使用 MB 检测法对总共 458 份鼻咽和咽喉拭子样本(426 份阳性和 32 份阴性)进行了检测,并根据检测持续时间、灵敏度和特异性,将荧光水平与商业 RT-PCR 检测获得的循环阈值(Ct)值进行了比较。我们的结果表明,荧光水平较高的样本对应于 Ct 值较低的样本,表明病毒载量与 MB 荧光增加之间存在相关性。该检测方法代表了一种快速(包括扩增和荧光读取阶段在内,总时长为 2 小时 20 分钟)、简便的方法,可用于检测上呼吸道临床样本中的 SARS-CoV-2。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e2c/8587319/b9f490b512db/sensors-21-07015-g001.jpg

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