Bundeswehr Institute of Microbiology (IMB), Munich, Germany.
Quality Control for Molecular Diagnostics (QCMD), Unit 5, Technology Terrace, Todd Campus, West of Scotland Science Park, Glasgow G20 0XA, United Kingdom.
J Clin Virol. 2024 Dec;175:105741. doi: 10.1016/j.jcv.2024.105741. Epub 2024 Oct 21.
Diagnostic capabilities and correspondent External Quality Assessments (EQA) are key for outbreak preparedness. To support diagnostic facilities with a quality assessment of newly established monkeypox virus (MPXV) molecular diagnostic workflows, Quality Control for Molecular Diagnostics (QCMD) and the Bundeswehr Institute of Microbiology (IMB) piloted an international EQA study conducting four challenges from autumn 2022 to summer 2023 during the global mpox outbreak.
To assess the performance (sensitivity/specificity) of molecular assays used by diagnostic laboratories.
Inactivated EQA panels were prepared and distributed containing seven samples of clade Ia and clade IIb MPXV strains at different viral concentrations, two specificity controls with other zoonotic orthopoxviruses (vaccinia and cowpox virus) and a negative control. Assessment was based on reported qualitative testing results.
In this outbreak-related EQA study, a total of 192 laboratories from 37 countries reported 346 qualitative datasets. Overall, core samples were correctly detected by approximately 92 % of participants in all four challenges. While sensitivity performance was acceptable in at least 90 % of datasets correctly reported even for educational MPXV-positive samples with low viral concentration [10 genome equivalents (GE)/mL], several laboratories reported the educational specificity controls as false positives or were unable to differentiate MPXV from related orthopoxviruses.
Mpox is now a globally occurring infection with a demand for quality-assured diagnostic capabilities. The newly established EQA scheme presented here, offers a multi-purpose panel for orthopoxviruses with a focus on MPXV which will continue to ensure diagnostic quality in clinical settings with up-to-date sample panels.
诊断能力和相应的外部质量评估(EQA)是暴发准备的关键。为了支持诊断机构对新建立的猴痘病毒(MPXV)分子诊断工作流程进行质量评估,分子诊断质量控制(QCMD)和联邦国防军微生物研究所(IMB)在全球猴痘暴发期间,于 2022 年秋季至 2023 年夏季,试点了一项国际 EQA 研究,开展了四项挑战。
评估诊断实验室使用的分子检测方法的性能(灵敏度/特异性)。
制备并分发了灭活的 EQA 面板,其中包含七种不同病毒浓度的 Ia 分支和 IIb 分支 MPXV 菌株样本、两种具有其他人畜共患正痘病毒(牛痘和牛痘病毒)特异性的对照样本和一个阴性对照。评估基于报告的定性检测结果。
在这项与暴发相关的 EQA 研究中,来自 37 个国家的 192 个实验室报告了 346 个定性数据集。总体而言,在所有四项挑战中,大约 92%的参与者正确检测到核心样本。虽然对于低病毒浓度(10 个基因组当量(GE)/mL)的教育性 MPXV 阳性样本,灵敏度性能在至少 90%的正确报告数据集中可接受,但一些实验室报告说教育性特异性对照是假阳性,或无法区分 MPXV 与相关正痘病毒。
猴痘现在是一种在全球范围内发生的感染,需要有质量保证的诊断能力。这里提出的新 EQA 方案提供了一个多用途的正痘病毒检测面板,重点是 MPXV,该方案将继续确保临床环境中诊断质量,采用最新的样本面板。