Comparative Performance of Reagents and Platforms for Quantitation of Cytomegalovirus DNA by Digital PCR

被引:25
作者
Hayden, R. T. [1 ]
Gu, Z. [1 ]
Sam, S. S. [3 ]
Sun, Y. [2 ]
Tang, L. [2 ]
Pounds, S. [2 ]
Caliendo, A. M. [4 ]
机构
[1] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN USA
[3] Miriam Hosp, Providence, RI 02906 USA
[4] Brown Univ, Dept Med, Alpert Med Sch, Providence, RI 02912 USA
关键词
REAL-TIME PCR; VIRAL LOAD; VARIABILITY; STANDARDS;
D O I
10.1128/JCM.01474-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:2602 / 2608
页数:7
相关论文
共 21 条
[1]   ROBUST TESTS FOR EQUALITY OF VARIANCES [J].
BROWN, MB ;
FORSYTHE, AB .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1974, 69 (346) :364-367
[2]   Tolerance of Droplet-Digital PCR vs Real-Time Quantitative PCR to Inhibitory Substances [J].
Dingle, Tanis C. ;
Sedlak, Ruth Hall ;
Cook, Linda ;
Jerome, Keith R. .
CLINICAL CHEMISTRY, 2013, 59 (11) :1670-1672
[3]   EBV viral load detection in clinical virology [J].
Gaertner, Barbara ;
Preiksaitis, Jutta K. .
JOURNAL OF CLINICAL VIROLOGY, 2010, 48 (02) :82-90
[4]  
Hayden RT, 2008, J CLIN MICROBIOL, V46, P157, DOI 10.1128/JCM.01252-07
[5]   Comparison of Droplet Digital PCR to Real-Time PCR for Quantitative Detection of Cytomegalovirus [J].
Hayden, R. T. ;
Gu, Z. ;
Ingersoll, J. ;
Abdul-Ali, D. ;
Shi, L. ;
Pounds, S. ;
Caliendo, A. M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (02) :540-546
[6]   Factors Contributing to Variability of Quantitative Viral PCR Results in Proficiency Testing Samples: a Multivariate Analysis [J].
Hayden, R. T. ;
Yan, X. ;
Wick, M. T. ;
Rodriguez, A. B. ;
Xiong, X. ;
Ginocchio, C. C. ;
Mitchell, M. J. ;
Caliendo, A. M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (02) :337-345
[7]   High-Throughput Droplet Digital PCR System for Absolute Quantitation of DNA Copy Number [J].
Hindson, Benjamin J. ;
Ness, Kevin D. ;
Masquelier, Donald A. ;
Belgrader, Phillip ;
Heredia, Nicholas J. ;
Makarewicz, Anthony J. ;
Bright, Isaac J. ;
Lucero, Michael Y. ;
Hiddessen, Amy L. ;
Legler, Tina C. ;
Kitano, Tyler K. ;
Hodel, Michael R. ;
Petersen, Jonathan F. ;
Wyatt, Paul W. ;
Steenblock, Erin R. ;
Shah, Pallavi H. ;
Bousse, Luc J. ;
Troup, Camille B. ;
Mellen, Jeffrey C. ;
Wittmann, Dean K. ;
Erndt, Nicholas G. ;
Cauley, Thomas H. ;
Koehler, Ryan T. ;
So, Austin P. ;
Dube, Simant ;
Rose, Klint A. ;
Montesclaros, Luz ;
Wang, Shenglong ;
Stumbo, David P. ;
Hodges, Shawn P. ;
Romine, Steven ;
Milanovich, Fred P. ;
White, Helen E. ;
Regan, John F. ;
Karlin-Neumann, George A. ;
Hindson, Christopher M. ;
Saxonov, Serge ;
Colston, Bill W. .
ANALYTICAL CHEMISTRY, 2011, 83 (22) :8604-8610
[8]   Marked variability of BK virus load measurement using quantitative real-time PCR among commonly used assays [J].
Hoffman, Noah G. ;
Cook, Linda ;
Atienza, Ederlyn E. ;
Limaye, Ajit P. ;
Jerome, Keith R. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2008, 46 (08) :2671-2680
[9]  
Holden MJ, 2011, EXPERT REV MOL DIAGN, V11, P741, DOI [10.1586/erm.11.50, 10.1586/ERM.11.50]
[10]   Considerations for Digital PCR as an Accurate Molecular Diagnostic Tool [J].
Huggett, Jim F. ;
Cowen, Simon ;
Foy, Carole A. .
CLINICAL CHEMISTRY, 2015, 61 (01) :79-88