Center for Advanced Measurement of Science, National Institute of Metrology, Beijing, 100029, China.
Kunming National High-level Biosafety Research Center for Non-Human Primates, Center for Biosafety Mega-Science, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, 650107, China.
Talanta. 2023 Jun 1;258:124462. doi: 10.1016/j.talanta.2023.124462. Epub 2023 Mar 21.
More than forty antigen testing kits have been approved to response the prevalence of SARS-CoV-2 and its variant strains. However, the approved antigen testing kits are not capable of quantitative detection. Here, we successfully developed a lateral flow immunoassay based on colloidal gold nanoparticles (CGNP-based LFIA) for nucleocapsid (N) protein of SARS-CoV-2 quantitative detection. Delta strain (NMDC60042793) of SARS-CoV-2 have been cultured and analyzed by our developed digital PCR and LFIA methods to explore the relationship between N protein amount and N gene level. It indicated that the linear relationship (y = 47 ×) between N protein molecule number and N gene copy number exhibited very well (R = 0.995), the virus titers and N protein amount can be roughly estimated according to nucleic acid testing. Additionally, detection limits (LODs) of nine approved antigen testing kits also have been evaluated according to the Guidelines for the registration review of 2019-nCoV antigen testing reagents. Only three antigen testing kits had LODs as stated in the instructions, the LODs of Kits have been converted into the N gene and N protein levels, according to the established relationships among virus titer vers. N gene and antigen. Results demonstrated that the sensitivity of nucleic acid testing is at least 1835 times higher than that of antigen testing. We expect that the relationship investigation and testing kits evaluation have the important directive significance to precise epidemic prevention.
已经有四十多种抗原检测试剂盒获批用于应对 SARS-CoV-2 及其变异株的流行。然而,获批的抗原检测试剂盒不具备定量检测能力。在这里,我们成功开发了一种基于胶体金纳米颗粒(CGNP 基 LFIA)的侧向流动免疫分析(LFIA)方法,用于定量检测 SARS-CoV-2 的核衣壳(N)蛋白。我们开发的数字 PCR 和 LFIA 方法对 SARS-CoV-2 的 Delta 株(NMDC60042793)进行了培养和分析,以探讨 N 蛋白量与 N 基因水平之间的关系。结果表明,N 蛋白分子数与 N 基因拷贝数之间的线性关系(y = 47 ×)表现得非常好(R = 0.995),根据核酸检测可以大致估计病毒滴度和 N 蛋白量。此外,还根据 2019-nCoV 抗原检测试剂注册审查指南评估了九种已批准的抗原检测试剂盒的检测限(LOD)。只有三种抗原检测试剂盒的 LOD 符合说明书中的规定,根据病毒滴度与 N 基因和抗原之间的关系,将试剂盒的 LOD 转换为 N 基因和 N 蛋白水平。结果表明,核酸检测的灵敏度至少比抗原检测高 1835 倍。我们期望这项关系研究和检测试剂盒评估对精准防控具有重要的指导意义。