School of Life Sciences and Biopharmaceutics, GuangDong Pharmaceutical University, Guangzhou, China.
Department of Pediatrics, Affiliated Shenzhen Maternity & Child Healthcare Hospital, Southern Medical University, Shenzhen, China.
J Med Virol. 2022 Sep;94(9):4502-4507. doi: 10.1002/jmv.27886. Epub 2022 Jun 10.
The outbreak of COVID-19 epidemic has enabled the establishment and application of various rapid detection methods. It is particularly important to establish a fast and accurate detection method for enterovirus, which will be beneficial for clinical diagnosis, epidemic prevention and control, and timely traceability. Through establishing an ultra-fast reverse transcription-polymerase chain reaction (RT-PCR) equipment, this study aimed to evaluate the sensitivity and specificity of the testing method of enterovirus nucleic acids based on ultra-fast real-time fluorescence RT-PCR technology. A total of 61 cases were sampled, which were then transported and preserved. After the nucleic acid extraction, the nucleic acids of the same sample were tested with the enterovirus nucleic acid detection kit produced by Guangzhou Da An Gene Company and the ultra-fast RT-PCR equipment system established in this study. ABI7500Fast and Ahram biosystems S1 fast equipment were used for amplification detection. If the sample had an S-shaped amplification curve in the FAM channel and the Ct value ≤40.00, the result was positive. The sensitivity, precision, and accuracy of the detection method were then verified. This study established a novel testing method to achieve enterovirus nucleic acid detection within 24 min. The sensitivity detection limit of the method was 1.0 × 10 copies/ml. The coefficients of variation for repeated detection of the high, medium, and low concentration samples were 2.644%, 1.674%, and 4.281%, respectively, with good detection repeatability. In addition, a total of 29 cases were positive by the ultra-fast RT-PCR detection method in 61 suspected samples, which was consistent with the conventional fluorescent RT-PCR method. The established rapid detection method can greatly shorten the time for providing a detection report, which may greatly improve the efficiency of diagnosis and treatment.
新型冠状病毒肺炎疫情的爆发,促使各种快速检测方法得以建立和应用。建立一种快速、准确的肠道病毒检测方法尤为重要,这将有利于临床诊断、疫情防控和及时溯源。本研究通过建立超快速逆转录-聚合酶链反应(RT-PCR)设备,旨在评估基于超快速实时荧光 RT-PCR 技术的肠道病毒核酸检测方法的灵敏度和特异性。共采集 61 例样本,进行运输和保存。提取核酸后,采用广州达安基因股份有限公司生产的肠道病毒核酸检测试剂盒和本研究建立的超快速 RT-PCR 设备系统对同一批样本的核酸进行检测。ABI7500Fast 和 Ahram biosystems S1 fast 设备用于扩增检测。如果样本在 FAM 通道中出现 S 型扩增曲线,且 Ct 值≤40.00,则结果为阳性。然后验证检测方法的灵敏度、精密度和准确性。本研究建立了一种新型检测方法,可在 24 分钟内实现肠道病毒核酸检测。该方法的灵敏度检测限为 1.0×10 拷贝/ml。对高、中、低浓度样本进行重复检测的变异系数分别为 2.644%、1.674%和 4.281%,具有良好的检测重复性。此外,在 61 例疑似样本中,超快速 RT-PCR 检测方法共检出 29 例阳性,与常规荧光 RT-PCR 方法一致。建立的快速检测方法可大大缩短提供检测报告的时间,从而可能极大地提高诊断和治疗的效率。