Authors: Mary A. Williamson Mt(ascp) Phd,L. Michael Snyder Md
Samples with low viral load may be untypable. Sequencing methods are less effective than hybridization methods in genotyping samples with mixed genotypes.
HEPATITIS C VIRUS (HCV) RNA, QUANTITATIVE VIRAL LOAD: MOLECULAR ASSAY
Definition
The HCV viral load assay quantifies HCV RNA in the plasma of HCV-infected individuals. The HCV test is standardized against the first WHO International Standard for HCV RNA for nucleic acid amplification technology assays (NIBSC code 96/790).
Normal range:
Not detected when the result is below the level of detection of the assay.
Use
Methods
Branched DNA assay (bDNA; Siemens): A signal amplification technology that detects the presence of specific nucleic acids by measuring the signal generated by branched, labeled DNA probes; a reliable method that provides consistent results in the higher range of the assay.
Real-time PCR: Reverse transcription followed by amplification and quantification of the targeted DNA molecule; generally offers both a wider range of quantification and a lower limit of detection than the bDNA method.
Used in the management of HCV-infected individuals undergoing antiviral therapy.
Limitations
PCR inhibitors in the specimen may lead to underestimation of viral quantitation or false-negative results in rare cases. However, current technologies include internal controls which if not amplified during the PCR, will not give a result rather than a false-negative result.
HEPATITIS D VIRUS (HDV; DELTA HEPATITIS) ANTIBODY
Definition
HDV is a subviral agent that is dependent on the HBV virus for its life cycle; therefore, HDV infection cannot occur in the absence of HBV infection.