Center for Advanced Measurement Science, National Institute of Metrology, Beijing, 100029, China.
College of Food Sciences & Technology, Shanghai Ocean University, Shanghai, 201306, China.
Anal Bioanal Chem. 2023 Mar;415(7):1333-1337. doi: 10.1007/s00216-023-04518-9. Epub 2023 Jan 21.
Human monkeypox has attracted attention recently. Monkeypox virus (MPXV) keeps evolving as it spreading around the world rapidly, which may threaten the health of more and more people. Here, we have developed a high order reference method based on digital PCR (dPCR) for MPXV detection, of which the limits of quantification (LoQ) and detection (LoD) are 38 and 6 copies/reaction, respectively. Pseudovirus reference materials (RM) containing the conserved F3L gene has been developed, and the homogeneity assessment showed that the RM was homogeneous. The reference value with its expanded uncertainty determined by the established dPCR is (2.74 ± 0.46) × 10 copies/μL. Six different MPXV test kits were accessed by the RM. Four out of six test kits cannot reach their claimed LoDs. The poor analytical sensitivity might cause false-negative results, which lead to incorrect diagnosis and treatment. The establishment of a high order reference method of dPCR and pseudovirus RM is very useful for improving the accuracy and reliability of MPXV detection.
近期,人类猴痘病毒引起了广泛关注。随着猴痘病毒在全球范围内迅速传播,该病毒不断进化,可能会威胁到越来越多人的健康。在这里,我们开发了一种基于数字 PCR(dPCR)的高等级参考方法,用于检测猴痘病毒,其定量下限(LoQ)和检测下限(LoD)分别为 38 和 6 拷贝/反应。我们已经开发了含有保守 F3L 基因的假病毒参考材料(RM),均匀性评估表明 RM 是均匀的。通过建立的 dPCR 确定的参考值及其扩展不确定度为(2.74±0.46)×10 拷贝/μL。使用 RM 评估了六种不同的猴痘病毒检测试剂盒,其中四种试剂盒无法达到其声称的 LoD。较差的分析灵敏度可能导致假阴性结果,从而导致错误的诊断和治疗。建立 dPCR 和假病毒 RM 的高等级参考方法对于提高猴痘病毒检测的准确性和可靠性非常有用。