Accuracy of quantitative viral secondary standards: a re-examination

• Published in: Journal of clinical microbiology 2024-03, Vol.62 (3), p.e0166923
• Main Authors: Hayden, R T, Su, Y, Tang, L, Zhu, H, Gu, Z, Glasgow, H L, Sam, S S, Caliendo, A M
• Format: Article
• Language: English
• Subjects: BK Virus - genetics; Cytomegalovirus - genetics; Cytomegalovirus Infections - diagnosis; DNA, Viral; Humans; Real-Time Polymerase Chain Reaction - methods; Viral Load - methods; Virology
• ISSN: 0095-1137; 1098-660X; 1098-660X
• DOI: 10.1128/jcm.01669-23

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.