Ribonuclease-resistant RNA controls (armored RNA) for reverse transcription-PCR, branched DNA, and genotyping assays for hepatitis C virus

Background: Comparison and evaluation of molecular diagnostic assays for th e detection and quantification of hepatitis C virus (HCV) RNA have been lim ited by the lack of RNA controls and calibrators. Armored RNA(R) technology is a means for producing RNA that is completely protected from plasma ribo nucleases. This method produces recombinant pseudoviral particles that are noninfectious and contain predefined RNA sequences, Methods: A consensus 412-base sequence from the 5'NCR/Core region of HCV su btype 2b was derived from 34 individually sequenced HCV genotype 2b variant s. A DNA fragment encoding the consensus HCV-2b sequence was synthesized de novo, cloned, and expressed as an Armored RNA control. The resulting HCV-2 b Armored RNA (AR-HCV-2b) contained the complete HCV-2b consensus RNA seque nce encapsidated within a protective protein coat. Results: AR-HCV-2b was fully recoverable from human plasma incubated at 4 d egrees C for >300 days. The particles were tested in three clinical assay f ormats: Amplicor(TM) HCV Monitor 1.0, Quantiplex(TM) HCV RNA 2.0, and INNO- LiPA(TM) HCV II. When added into seronegative, nonviremic plasma, AR-HCV-2b showed reproducible signals and linear dilutions in both the Amplicor and Quantiplex assays. AR-HCV-2b was correctly identified as subtype 2b in the INNO-LiPA line probe assay. Conclusion: The HCV-2b Armored RNA control is a versatile, durable, ribonuc lease-resistant viral RNA control that is compatible in three different cli nical assay formats. (C) 1999 American Association for Clinical Chemistry.