Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
J Clin Microbiol. 2024 Mar 13;62(3):e0166923. doi: 10.1128/jcm.01669-23. Epub 2024 Feb 21.
Interlaboratory agreement of viral load assays depends on the accuracy and uniformity of quantitative calibrators. Previous work demonstrated poor agreement of secondary cytomegalovirus (CMV) standards with nominal values. This study re-evaluated this issue among commercially produced secondary standards for both BK virus (BKV) and CMV, using digital polymerase chain reaction (dPCR) to compare the materials from three different manufacturers. Overall, standards showed an improved agreement compared to prior work, against nominal values in both log copies/mL and log international unit (IU)/mL, with bias from manufacturer-assigned nominal values of 0.0-0.9 log units (either copies or IU)/mL. Standards normalized to IU and those values assigned by dPCR rather than by real-time PCR (qPCR) showed better agreement with nominal values. The latter reinforces prior conclusions regarding the utility of using such methods for quantitative value assignment in reference materials. Quantitative standards have improved over the last several years, and the remaining bias from nominal values might be further reduced by universal implementation of dPCR methods for value assignment, normalized to IU.
Interlaboratory agreement of viral load assays depends on accuracy and uniformity of quantitative calibrators. Previous work, published in JCM several years ago, demonstrated poor agreement of secondary cytomegalovirus (CMV) standards with nominal values. This study re-evaluated this issue among commercially produced secondary standards for both BK virus (BKV) and CMV, using digital polymerase chain reaction (dPCR) to compare the materials from three different manufacturers. Overall, standards showed an improved agreement compared to prior work, against nominal values, indicating a substantial improvement in the production of accurate secondary viral standards, while supporting the need for further work in this area and for the broad adaption of international unit (IU) as a reporting standard for quantitative viral load results.
病毒载量检测的实验室间一致性取决于定量校准品的准确性和均一性。先前的工作表明,次要巨细胞病毒 (CMV) 标准品与标称值的一致性较差。本研究使用数字聚合酶链反应 (dPCR) ,对来自三个不同制造商的材料进行比较,重新评估了商用生产的 BK 病毒 (BKV) 和 CMV 次要标准品在这方面的问题。总体而言,与之前的工作相比,这些标准品与标称值在对数拷贝/ml 和对数国际单位 (IU)/ml 方面的一致性有所提高,与制造商分配的标称值的偏差在 0.0-0.9 个对数单位(无论是拷贝还是 IU)/ml。与 IU 标准化的标准品以及由 dPCR 而不是实时 PCR (qPCR) 分配的值显示出与标称值更好的一致性。后者强化了之前关于在参考物质中使用此类方法进行定量赋值的结论。定量标准品在过去几年中得到了改进,通过普遍采用 dPCR 方法对 IU 进行标准化赋值,可以进一步降低与标称值的剩余偏差。
病毒载量检测的实验室间一致性取决于定量校准品的准确性和均一性。几年前发表在《临床微生物学杂志》(JCM)上的先前工作表明,次要巨细胞病毒 (CMV) 标准品与标称值的一致性较差。本研究使用数字聚合酶链反应 (dPCR) ,对来自三个不同制造商的材料进行比较,重新评估了商用生产的 BK 病毒 (BKV) 和 CMV 次要标准品在这方面的问题。与之前的工作相比,总体而言,标准品与标称值的一致性有所提高,这表明在生产准确的次要病毒标准品方面取得了重大进展,同时支持在该领域进一步开展工作,并广泛采用 IU 作为定量病毒载量结果的报告标准。