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Comparative Performance of Reagents and Platforms for Quantitation of Cytomegalovirus DNA by Digital PCR
Author(s) -
Randall T. Hayden,
Z. Gu,
Soya S. Sam,
Yilun Sun,
Li Tang,
Stanley Pounds,
Angela M. Caliendo
Publication year - 2016
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.01474-16
Subject(s) - digital polymerase chain reaction , viral load , reagent , cytomegalovirus , biology , quantitative analysis (chemistry) , correlation , pairwise comparison , real time polymerase chain reaction , virology , chromatography , polymerase chain reaction , chemistry , mathematics , statistics , virus , herpesviridae , viral disease , genetics , geometry , gene
A potential benefit of digital PCR is a reduction in result variability across assays and platforms. Three sets of PCR reagents were tested on two digital PCR systems (Bio-Rad and RainDance), using three different sets of PCR reagents for quantitation of cytomegalovirus (CMV). Both commercial quantitative viral standards and 16 patient samples (n = 16) were tested. Quantitative accuracy (compared to nominal values) and variability were determined based on viral standard testing results. Quantitative correlation and variability were assessed with pairwise comparisons across all reagent-platform combinations for clinical plasma sample results. The three reagent sets, when used to assay quantitative standards on the Bio-Rad system, all showed a high degree of accuracy, low variability, and close agreement with one another. When used on the RainDance system, one of the three reagent sets appeared to have a much better correlation to nominal values than did the other two. Quantitative results for patient samples showed good correlation in most pairwise comparisons, with some showing poorer correlations when testing samples with low viral loads. Digital PCR is a robust method for measuring CMV viral load. Some degree of result variation may be seen, depending on platform and reagents used; this variation appears to be greater in samples with low viral load values.

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