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Hepatitis C virus subtyping in Uttarakhand, India: a comparative study.


ABSTRACT: The objective of this study was to compare Reverse Hybridisation Assay with conventional sequencing for determination of Hepatitis C Virus Genotype and Subtypes. Anti-HCV antibody was determined followed by HCV RNA extraction which was used for (1) viral load determination (2) qualitative real-time PCR RHA for genotyping and (3) conventional sequencing. Compared to conventional sequencing, accuracy of RHA results was 96.55% for determination of genotype (κ = 0.93) and 89.66% for subtype (κ = 0.85). Sensitivity, specificity, negative predictive value (NPV) and positive predictive value (PPV) of the qualitative PCR were 82.29%, 100%, 44.44% and 100% respectively with an accuracy of 86.84%. RHA is a less time consuming and cheaper method for determination of HCV genotype and subtype yet results must be interpreted with caution and quality control monitoring should be strictly followed to ensure validity.

Supplementary information

The online version contains supplementary material available at 10.1007/s13337-021-00729-9.

SUBMITTER: Chatterjee K 

PROVIDER: S-EPMC8473521 | biostudies-literature | 2021 Sep

REPOSITORIES: biostudies-literature

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Hepatitis C virus subtyping in Uttarakhand, India: a comparative study.

Chatterjee Kuhu K   Kalita Deepjyoti D   Omar Balram Ji BJ   Gupta Rohit R   Jha Mithilesh Kumar MK   Gupta Pratima P  

Virusdisease 20210817 3


The objective of this study was to compare Reverse Hybridisation Assay with conventional sequencing for determination of Hepatitis C Virus Genotype and Subtypes. Anti-HCV antibody was determined followed by HCV RNA extraction which was used for (1) viral load determination (2) qualitative real-time PCR RHA for genotyping and (3) conventional sequencing. Compared to conventional sequencing, accuracy of RHA results was 96.55% for determination of genotype (κ = 0.93) and 89.66% for subtype (κ = 0.8  ...[more]

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