Standardized One-Step Real-Time Reverse Transcription-PCR Assay for Universal Detection and Quantification of Hepatitis Delta Virus from Clinical Samples in the Presence of a Heterologous Internal-Control RNA
Author(s) -
Caroline Scholtès,
Vinca Icard,
Majid Amiri,
Philippe Chevallier-Queyron,
MaryAnne Trabaud,
Christophe Ramière,
Fabien Zoulim,
Patrice André,
Paul Dény
Publication year - 2012
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.06829-11
Subject(s) - virology , heterologous , biology , reverse transcriptase , real time polymerase chain reaction , reverse transcription polymerase chain reaction , hepatitis delta , rna , hepatitis c virus , virus , hepatitis b virus , microbiology and biotechnology , messenger rna , gene , genetics
As for other chronic viral diseases, quantification of hepatitis delta virus (HDV) loads may be useful for patient management. We describe a one-step quantitative reverse transcription-PCR assay that is reliable and automatable and meets the regulatory authorities' standards for accurate quantification of the major HDV genotypes. It includes an internal control and uses in vitro-transcribed RNAs as standards. Its linearity range is 500 to 1.7 × 10(11) copies/ml, its sensitivity is around 150 copies/ml, its repeatability is around 15%, and its reproducibility is below 0.25 log(10) copies/ml.
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