Development of a rapid, internally controlled, two target, real-time RT-PCR for detection of rubella virus.

Helene Schulz, Mackenzie Neale, Vanessa Zubach, Alberto Severini, Joanne Hiebert

Journal of virological methods 2022 May

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Rubella surveillance in elimination setting relies on rapid molecular detection of the virus. In this study a multiplex real-time RT-PCR assay for the detection of rubella virus was validated. The assay includes three independent probes with unique reporter dyes for the simultaneous detection of the rubella viral coding regions for envelope glycoprotein E1 and non-structural p150 protein, and an endogenous control (human RNaseP). Using dilution series of synthetic RNAs, the limits of detection were determined to be at least 50 copies of rubella RNA. The assay is reproducible with low intra-assay and inter-assay coefficients of variation for both the E1 and the p150 targets. After testing 62 confirmed rubella positive and 165 rubella negative archival clinical samples, the sensitivity and specificity of the multiplex assay were 98.4 and 100 %, respectively. No cross reactivity was identified with clinical specimens positive for eleven other viruses. This multiplex assay successfully detected nine viral genotypes including the predominant genotypes 1E, 1G, 1J, and 2B as well as the 1a vaccine genotype. Crown Copyright © 2022. Published by Elsevier B.V. All rights reserved.

Citation

Helene Schulz, Mackenzie Neale, Vanessa Zubach, Alberto Severini, Joanne Hiebert. Development of a rapid, internally controlled, two target, real-time RT-PCR for detection of rubella virus. Journal of virological methods. 2022 May;303:114500