Emergency Medicine, College of Medicine, Korea University Guro Hospital, Seoul, Republic of Korea.
Departments of Laboratory Medicine, College of Medicine, Korea University Guro Hospital, Seoul, Republic of Korea.
PLoS One. 2021 Mar 3;16(3):e0248042. doi: 10.1371/journal.pone.0248042. eCollection 2021.
A newly identified coronavirus, designated as severe acute respiratory syndrome coronavirus 2 (SARS CoV-2), has spread rapidly from its epicenter in China to more than 150 countries across six continents. In this study, we have designed three reverse-transcription loop-mediated isothermal amplification (RT-LAMP) primer sets to detect the RNA-dependent RNA polymerase (RdRP), Envelope (E) and Nucleocapsid protein (N) genes of SARS CoV-2. For one tube reaction, the detection limits for five combination SARS CoV-2 LAMP primer sets (RdRP/E, RdRP/N, E/N, RdRP/E/N and RdRP/N/Internal control (actin beta)) were evaluated with a clinical nasopharyngeal swab sample. Among the five combination, the RdRP/E and RdRP/N/IC multiplex LAMP assays showed low detection limits. The sensitivity and specificity of the RT-LAMP assay were evaluated and compared to that of the widely used Allplex™ 2019-nCoV Assay (Seegene, Inc., Seoul, South Korea) and PowerChek™ 2019-nCoV Real-time PCR kit (Kogenebiotech, Seoul, South Korea) for 130 clinical samples from 91 SARS CoV-2 patients and 162 NP specimens from individuals with (72) and without (90) viral respiratory infections. The multiplex RdRP (FAM)/N (CY5)/IC (Hex) RT-LAMP assay showed comparable sensitivities (RdRP: 93.85%, N: 94.62% and RdRP/N: 96.92%) to that of the Allplex™ 2019-nCoV Assay (100%) and superior to those of PowerChek™ 2019-nCoV Real-time PCR kit (RdRP: 92.31%, E: 93.85% and RdRP/E: 95.38%).
一种新鉴定的冠状病毒,被指定为严重急性呼吸综合征冠状病毒 2(SARS-CoV-2),已迅速从其在中国的发源地传播到六大洲的 150 多个国家。在这项研究中,我们设计了三个逆转录环介导等温扩增(RT-LAMP)引物组,用于检测 SARS-CoV-2 的 RNA 依赖性 RNA 聚合酶(RdRP)、包膜(E)和核衣壳蛋白(N)基因。对于一个管反应,用临床鼻咽拭子样本评估了五个组合 SARS-CoV-2 LAMP 引物组(RdRP/E、RdRP/N、E/N、RdRP/E/N 和 RdRP/N/内部对照(肌动蛋白β)的检测限。在这五个组合中,RdRP/E 和 RdRP/N/IC 多重 LAMP 检测显示出较低的检测限。评估了 RT-LAMP 检测的灵敏度和特异性,并与广泛使用的 Allplex™2019-nCoV 检测试剂盒(Seegene,Inc.,韩国首尔)和 PowerChek™2019-nCoV 实时 PCR 试剂盒(Kogenebiotech,韩国首尔)进行了比较,共检测了 91 例 SARS-CoV-2 患者的 130 份临床样本和 72 例病毒性呼吸道感染患者和 90 例无病毒呼吸道感染患者的 162 份 NP 标本。多重 RdRP(FAM)/N(CY5)/IC(Hex)RT-LAMP 检测与 Allplex™2019-nCoV 检测试剂盒(100%)具有相当的灵敏度(RdRP:93.85%,N:94.62%和 RdRP/N:96.92%),优于 PowerChek™2019-nCoV 实时 PCR 试剂盒(RdRP:92.31%,E:93.85%和 RdRP/E:95.38%)。