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Effects of probe binding mutations in an assay designed to detect parvovirus B19: Implications for the quantitation of different virus genotypes
Quantitative real-time PCR is being widely used in the identification of plasma donations that contain high levels of parvovirus B19, to ensure their exclusion from start pools used in the manufacture of plasma derived medicinal products. In this study, the primers and probe of one such published as...
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Published in: | Journal of virological methods 2007, Vol.139 (1), p.97-99 |
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creator | Baylis, Sally A. Fryer, Jacqueline F. Grabarczyk, Piotr |
description | Quantitative real-time PCR is being widely used in the identification of plasma donations that contain high levels of parvovirus B19, to ensure their exclusion from start pools used in the manufacture of plasma derived medicinal products. In this study, the primers and probe of one such published assay, are examined for their ability to quantify different genotypes of parvovirus B19. Under standard assay conditions, there is a failure to detect and quantify one genotype 3 subtype. Alterations in assay conditions can restore quantitation of this subtype. |
doi_str_mv | 10.1016/j.jviromet.2006.09.002 |
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subjects | Biological and medical sciences Fundamental and applied biological sciences. Psychology Genotype Microbiology Mutation Parvovirus B19 Parvovirus B19, Human - classification Parvovirus B19, Human - genetics Parvovirus B19, Human - isolation & purification Plasma Polymerase Chain Reaction - methods Real-time PCR Techniques used in virology Variants Virology |
title | Effects of probe binding mutations in an assay designed to detect parvovirus B19: Implications for the quantitation of different virus genotypes |
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