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

J Clin Microbiol. 2012 Jun;50(6):2126-8. doi: 10.1128/JCM.06829-11. Epub 2012 Mar 14.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Hepatitis D / virology*
  • Hepatitis Delta Virus / isolation & purification*
  • Humans
  • Real-Time Polymerase Chain Reaction / methods*
  • Real-Time Polymerase Chain Reaction / standards*
  • Reference Standards
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Viral Load / methods*