Abstract
A 2 h single-tube, reverse-transcription(RT)-PCR/hybridization assay using the TaqMan format for rapid diagnostic screening of enterovirus (EV) infections was optimized for the real-time LightCycler (LC) technology. For low EV load clinical samples an additional 30 min reamplification step using a novel primer-mix/probe design resulted in a 100% concordance with AMPLICOR EV PCR Test and in-house RT-PCR. Combined with maximum specificity, the sensitivity of LC-PCR was 10- to 100-fold higher compared to AMPLICOR EV Test.
Publication types
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Comparative Study
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Evaluation Study
MeSH terms
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Enterovirus / genetics
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Enterovirus / isolation & purification*
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Enterovirus Infections / diagnosis*
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Enterovirus Infections / virology
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Feces / virology
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Fluorescent Dyes*
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Humans
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Pharynx / virology
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Polymerase Chain Reaction / methods*
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RNA, Viral / analysis
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RNA, Viral / blood
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RNA, Viral / cerebrospinal fluid
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Reverse Transcriptase Polymerase Chain Reaction
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Sensitivity and Specificity
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Taq Polymerase / metabolism*
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Time Factors
Substances
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Fluorescent Dyes
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RNA, Viral
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Taq Polymerase