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利用数字 PCR 开发人鼻病毒 RNA 参考物质。

Development of Human Rhinovirus RNA Reference Material Using Digital PCR.

机构信息

Biometrology Group, Korea Research Institute of Standards and Science (KRISS), Daejeon 34113, Republic of Korea.

School of Biomedical Engineering, Korea University, Seoul 02841, Republic of Korea.

出版信息

Genes (Basel). 2023 Dec 14;14(12):2210. doi: 10.3390/genes14122210.

Abstract

The human rhinovirus (RV) is a positive-stranded RNA virus that causes respiratory tract diseases affecting both the upper and lower halves of the respiratory system. RV enhances its replication by concentrating RNA synthesis within a modified host membrane in an intracellular compartment. RV infections often occur alongside infections caused by other respiratory viruses, and the RV virus may remain asymptomatic for extended periods. Alongside qualitative detection, it is essential to accurately quantify RV RNA from clinical samples to explore the relationships between RV viral load, infections caused by the virus, and the resulting symptoms observed in patients. A reference material (RM) is required for quality evaluation, the performance evaluation of molecular diagnostic products, and evaluation of antiviral agents in the laboratory. The preparation process for the RM involves creating an RV RNA mixture by combining RV viral RNA with RNA storage solution and matrix. The resulting RV RNA mixture is scaled up to a volume of 25 mL, then dispensed at 100 µL per vial and stored at -80 °C. The process of measuring the stability and homogeneity of RV RMs was conducted by employing reverse transcription droplet digital polymerase chain reaction (RT-ddPCR). Digital PCR is useful for the analysis of standards and can help to improve measurement compatibility: it represents the equivalence of a series of outcomes for reference materials and samples being analyzed when a few measurement procedures are employed, enabling objective comparisons between quantitative findings obtained through various experiments. The number of copies value represents a measured result of approximately 1.6 × 10 copies/μL. The RM has about an 11% bottle-to-bottle homogeneity and shows stable results for 1 week at temperatures of 4 °C and -20 °C and for 12 months at a temperature of -80 °C. The developed RM can enhance the dependability of RV molecular tests by providing a precise reference value for the absolute copy number of a viral target gene. Additionally, it can serve as a reference for diverse studies.

摘要

人鼻病毒(RV)是一种正链 RNA 病毒,可引起影响呼吸道上下两部分的呼吸道疾病。RV 通过在细胞内隔室内的改良宿主膜内集中 RNA 合成来增强其复制。RV 感染通常与其他呼吸道病毒感染同时发生,RV 病毒可能在很长一段时间内无症状。除了定性检测外,从临床样本中准确量化 RV RNA 以探索 RV 病毒载量、病毒感染以及患者观察到的相关症状之间的关系至关重要。参考物质(RM)是质量评估、分子诊断产品性能评估以及实验室抗病毒药物评估所必需的。RM 的制备过程包括通过将 RV 病毒 RNA 与 RNA 储存溶液和基质混合来制备 RV RNA 混合物。将得到的 RV RNA 混合物放大至 25 mL 体积,然后以 100 µL/管分装并储存在-80°C。通过采用反转录液滴数字聚合酶链反应(RT-ddPCR)来测量 RV RM 的稳定性和均一性。数字 PCR 可用于标准分析,有助于提高测量的兼容性:当采用少数测量程序时,它代表了一系列参考材料和被分析样品的结果等同性,从而实现了通过各种实验获得的定量结果之间的客观比较。拷贝数值代表大约 1.6×10 拷贝/μL 的测量结果。RM 具有约 11%的瓶间均一性,在 4°C 和-20°C 下可稳定保存 1 周,在-80°C 下可稳定保存 12 个月。开发的 RM 可以通过为病毒靶基因的绝对拷贝数提供精确的参考值来增强 RV 分子检测的可靠性。此外,它可以作为各种研究的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0cc0/10742479/7376ec4a4f84/genes-14-02210-g001.jpg

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